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Title Location Compensation Date/Time
Microbiologist (2JY3) (near Brookside, DE) 2009-06-02 9:56AM
For over a decade, JOULÉ Scientific has been providing unparalleledstaffing services for temporary, contract and direct-hire professionalsto the Pharmaceutical, BioTechnological, Specialty Chemical, andClinical Research Organizations. Currently we have an opening fora Microbiologist to support a major Pharmaceutical Company.The position is located near Brookside, DE.Job Description:The Microbiologist will be working at our client site in the LaboratoryServices Department performing Raw Materials Microbiological Testing,In-Process Microbiological Testing, and Finished product MicrobiologicalTesting for clients in the Biopharmaceutical Industry.Job RequirementsThe Microbiologist for our client must have at least 5 Years of Experiencedoing Micro Testing in the Pharmaceutical or Biotechnological IndustryHe or she is required to have Experience in the following:- Bio Burden- Endotoxin Testing- Background in Good Manufacturing Practices (GMP)Contact Information:Name: Matthew PepePhone: 1-800-810-5587 x302E-Mail: mpepe@jouleinc.comRef IF: 1150-MP-2JY3 Location: near Brookside, DE Compensation: competitivePrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Chemist (Camden, DE) Camden, DE 2009-06-09 10:32AM
Recycling facility looking for an experienced Chemist to create a new product line from recycled plastic. Candidates must be hands-on and creative thinkers. This is a full-time position that is on going with other product line opportunities to create. Location: Camden, DEPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Greenhouse Technician Needed (Newark) Newark $10-14/hour 2009-05-26 2:32PM
Responsibilities: Assists with all aspects of greenhouse/growth chamber plant propagation, greenhouse maintenance, seed handling, plant tissue harvesting for various analyses, and laboratory assistant tasks. Specific tasks for this job function are listed below: Greenhouse Work / Seed Handling • Plant soybean seeds, stake & tie soybean plants, harvest soybean plants, throw out or bring in greenhouse plant pots into greenhouses/growth chambers • Thresh soybean plants, and organize seed packets • Apply insecticides, fertilizers, etc., to plants • Clean greenhouse/growth chamber floors and benches with disinfectant cleaners • No heavy lifting required• Leaf tissue collection off of soybean plants for various tests Laboratory Work • Assist with various laboratory protocols (entomological, herbicide, or fungal screening)Qualifications: Assists technical personnel in general laboratory operations, maintaining laboratory facilities and equipment in accordance with Laboratory standards in order to help ensure the validity and integrity of experimental results. -All positions are on an on-call basis; managers will call you in at least one to two days before start of shift; hours are 8-4:30-All employees must be able to work in a controlled greenhouse environment and wear safety gear including gloves and glasses.* Candidates cannot start an assignment without successful drug and background clearances.* Long term/on-going contract assignments in Newark, DE.*CANDIDATES WILL NOT BE CONSIDERED WITHOUT AN ATTACHED WORD RESUME! Location: Newark Compensation: $10-14/hour This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Laboratory Assistant (Greenhouse - Part-Time) (Newark, DE) Newark, DE $14/hr; Temp/Contract approx. 6-7 months; Part-time 2009-06-04 4:23PM
Remember when your career dreams were limitless?They can be again when you work with Yoh LABORATORY ASSISTANT - NEWARK, DE Weve been delivering the best talent to Americas leading companies for the past 7 decades - longer than any of our competitors. These customers count on our experience, time-honored processes, responsiveness and market intelligence to build their businesses. Most importantly, they look to Yoh to deliver talent with fresh ideas and empowered minds who want to fulfill their potential. People like you. Lifes short. Live your dream. Tell us where you want to work. What you want to do. And well help get you there. Yoh National Accounts has an opening for a Lab Assistant in Newark, DE for one of the worlds leading biotechnology companies. This is a temp/contract position of approximately 7-8 months.Responsibilities: -Assists with all aspects of greenhouse/growth chamber plant propagation, greenhouse maintenance, seed handling, plant tissue harvesting for various analyses, and laboratory assistant tasks.-Greenhouse Work / Seed Handling-Plant soybean seeds, stake & tie soybean plants, harvest soybean plants, throw out or bring in greenhouse plant pots into greenhouses/growth chambers -Thresh soybean plants, and organize seed packets-Apply insecticides, fertilizers, etc., to plants -Clean greenhouse/growth chamber floors and benches with disinfectant cleaners -Leaf tissue collection off of soybean plants for various tests -Assist with various laboratory protocols (entomological, herbicide, or fungal screening) Qualifications: -Degree or Relevant Experience-Must have experience in greenhouse environment-Ability to lift heavy loads (50 lb seed boxes)-Background check and drug screen required before startDiscover all that’s possible with Yoh. Apply now. Location: Newark, DE Compensation: $14/hr; Temp/Contract approx. 6-7 months; Part-time This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Lab Technician (Histology) (Newark, DE) Newark, DE $15-$17/hr 2009-06-29 4:25PM
Remember when your career dreams were limitless?They can be again when you work with Yoh LAB TECHNICIAN - NEWARK, DE Weve been delivering the best talent to Americas leading companies for the past 7 decades - longer than any of our competitors. These customers count on our experience, time-honored processes, responsiveness and market intelligence to build their businesses. Most importantly, they look to Yoh to deliver talent with fresh ideas and empowered minds who want to fulfill their potential. People like you. Lifes short. Live your dream. Tell us where you want to work. What you want to do. And well help get you there. Yoh National Accounts has an opening for a Lab Assistant in Newark, DE for one of the worlds leading biotechnology companies. This is a temp/contract position of approximately 1 year. Hours are Mon-Thurs, 7:30am-3:30pm.Responsibilities: -With guidance from supervision, primary responsibility is to assist technical personnel in general laboratory operations and routing laboratory or information handling tasks in support of scientific research.-Perform tasks according to accepted methods and training prescribed by the work group.-Perform procedures in histology to include loading tissue processors, embedding, cutting, staining, coverslipping tissue slides.Qualifications: - Histotechnology certification preferred (not required)- Must have previous experience- Background check and drug screen required before startDiscover all that’s possible with Yoh. Apply now. Location: Newark, DE Compensation: $15-$17/hr This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Lab Technician (Histology) (Newark, DE) Newark, DE $15-$17/hr; Temporary/Contract Assignment 2009-07-14 3:26PM
Remember when your career dreams were limitless?They can be again when you work with Yoh LAB TECHNICIAN - NEWARK, DE Weve been delivering the best talent to Americas leading companies for the past 7 decades - longer than any of our competitors. These customers count on our experience, time-honored processes, responsiveness and market intelligence to build their businesses. Most importantly, they look to Yoh to deliver talent with fresh ideas and empowered minds who want to fulfill their potential. People like you. Lifes short. Live your dream. Tell us where you want to work. What you want to do. And well help get you there. Yoh National Accounts has an opening for a Lab Assistant in Newark, DE for one of the worlds leading biotechnology companies. This is a temp/contract position of approximately 1 year. Hours are Mon-Thurs, 7:30am-3:30pm.Responsibilities: -With guidance from supervision, primary responsibility is to assist technical personnel in general laboratory operations, handling tasks in support of scientific research.-Perform tasks according to accepted methods and training prescribed by the work group.-Perform procedures in histology to include loading tissue processors, embedding, cutting, staining, coverslipping tissue slides.Qualifications: - Histotechnology certification preferred (not required)- Must have previous experience- Background check and drug screen required before startDiscover all that’s possible with Yoh. Apply now. Location: Newark, DE Compensation: $15-$17/hr; Temporary/Contract Assignment This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Histology-Laboratory Technician (Newark) Newark $15-17.50 per hour 2009-07-16 9:05AM
Exciting opportunity for a Histology Laboratory Technician with a world leader in the Sciences. **We offer paid holidays and vacation.**Primary responsiblities:*loading tissue processors*embedding*cutting*staining*coverslipping tissuePrevious experience required and Histo-technology certification is preferred but not required. Location: Newark Compensation: $15-17.50 per hour This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Greenhouse Assistant (Newark, DE) Newark, DE $15.00 to $15.25 per hour 2009-05-29 10:37AM
Qualifications: Assists technical personnel in general laboratory operations, maintaining laboratory facilities and equipment in accordance with Laboratory standards in order to help ensure the validity and integrity of experimental results. Responsibilities: Assists with all aspects of greenhouse/growth chamber plant propagation, greenhouse maintenance, seed handling, plant tissue harvesting for various analyses, and laboratory assistant tasks. Specific tasks for this job function are listed below: Greenhouse Work / Seed Handling • Plant soybean seeds, stake & tie soybean plants, harvest soybean plants, throw out or bring in greenhouse plant pots into greenhouses/growth chambers • Thresh soybean plants, and organize seed packets • Apply insecticides, fertilizers, etc., to plants • Clean greenhouse/growth chamber floors and benches with disinfectant cleaners • Ability to lift heavy loads (50 lb seed boxes) • Leaf tissue collection off of soybean plants for various tests Laboratory Work • Assist with various laboratory protocols (entomological, herbicide, or fungal screening) Applicants must have at least a high school diploma, valid drivers license, and successfully complete a pre-employment drug screen and background check. Resumes should be submitted as a Word attachment.All positions are on an on-call basis; managers will call you in at least one to two days before start of shift; hours are 8-4:30 Location: Newark, DE Compensation: $15.00 to $15.25 per hourPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Part Time Lab Tech Needed (Newark, DE) Newark, DE $15.00/hour 2009-06-29 4:18PM
With guidance from supervision, the candidates primary responsibility is to assist technical personnel in general laboratory operations and routine laboratory or information handling tasks in support of scientific research. Perform tasks according to accepted methods and training prescribed by the work group.Histology procedures to include but are not limited to:*Loading tissue processors*Embedding, cutting, staining, and coverslipping tissue slidesPrevious experience required and histo-technology certification is preferred.*Candidates cannot begin an assignment without successful drug & background clearances.*Part time contract assignment in Newark, DE.*CANDIDATES MUST ATTACH A WORD RESUME TO BE CONTACTED!!! Location: Newark, DE Compensation: $15.00/hour This is a part-time job. This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Biologist (Newark) Newark $18-$22 per hour 2009-06-23 9:03AM
Exciting long-term temporary opportunity for a Biologist in Newark.The position requires the development of fermentation processes for the production of bio-based materials. The person in this position will be responsible for cultivation of microorganisms in flasks and fermenters, fermenter set-up and operation, harvesting, and analysis of samples and results. This individual must carry out research independently, anticipate potential problems, and implement preventative measures. He/She will act as a resource to others and may serve as a lead on a project or shift. Must be proficient in fermentation and multiple computer applications to provide data reports and analysis. This position requires participation in a 3 shift/5 day operation in a semi-works environment. B.S. in biology, biotech or related field, or the equivalent work experience. Demonstrated skill with set-up and operation of fermentors and complex apparatus for batch and continuous studies from bench top to 10L scale. Experienced in aseptic techniques and in the cultivation of microorganisms in flasks or fermentors. Demonstrated ability to write, review and follow operating procedures and protocols. Demonstrated observational skills and ability to make decisions based on the research goals and what is being observed in the experiment. Demonstrated ability to use computers and using standard software such as MS office and equipment interfacing programs. Experience with common laboratory instruments, i.e., spectrophotometers, pH, YSI, etc. Able to work independently and efficiently with the willingness to collaborate and work as a team. Light-to-medium lifting, some climbing, bending, stooping, reaching and ability to wear a respirator. Location: Newark Compensation: $18-$22 per hourPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Microbiologist (Newark, DE) Newark, DE $20 - 30 hr 2009-06-01 4:59PM
We are seeking a Microbiologist with the following specifications...Requirements:Must possess a BS in Life Sciences, Biology, Bio-Technology, Chemistry, etc.Must show at least 5 years of hands-on experience working in a Bio Lab5 yrs experienceGMP backgroundBioburden experienceBasic endotoxin experienceSynerfac Overview:Synerfac has over 2 decades of specialized recruitment in the following industries: Pharmaceutical, Bio Technological, Specialty Chemical, Clinical Research, Engineering, IT, Finance & Accounting, and Adminstrative. We also conduct passive searches for Executive level positions for clients throughout the nation.**Please call Nolan Donofry at 302-324-9400 or 1-800-562-7040, if you are interested in the position or if you would like to discuss any other opportunities. Thank you!! **********************Alt Contact: ndonofry@synerfac.com Location: Newark, DE Compensation: $20 - 30 hrPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Analytical Lab Technician (Wilmington) Wilmington $20-$23 per hour 2009-05-26 2:39PM
Analytical Lab Tech needed for a temporary assignment in Wilmington, DE. The assignment is scheduled to last for approximately 3 months. Recent graduates with little industry experience will be considered.As a laboratory technician, you will be responsible for analyzing customer and R&D samples from water and paper industries using various instrumental and wet chemistry techniques. (pH, conductivity, titration, ICP, IC, CE, etc). Specific Duties and Responsibilities: Safety - Good track record of safety practices. Careful Worker - Team player, consistent, high quality results while highly productive. Strong Computer Skills - Data entry, manipulation and analysis. Must be proficient in Microsoft Excel, Word and PowerPoint. Proficient Writing Skills - Must be able to keep a clear, well-organized lab notebook and to write safety reviews. Quick Learner Required Skills: Two to five years of working experience in an analytical lab or a chemical process lab. Knowledge of wet chemistry techniques and some basic analytical instrumentation. Be able to learn analytical test methods quickly and keep good lab notebook records. Familiarity of working in a mid to high volume lab environment. Hands-on experience on Laboratory Information Management System (LIMS) is a plus. Good communication skills.Must be authorized to work in the United StatesEducational Requirements: AAS degree in Laboratory Technology is preferred. BS candidates will be considered with very little experience. Location: Wilmington Compensation: $20-$23 per hourPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Project Chemist and Engineer (Dover, NJ) Dover, NJ $35 to 60K annually 2009-05-19 2:29PM
Frontier Performance Polymers Corporation locates in Dover, New Jersey and is a multi-disciplined engineering company focusing on delivering advanced material and system solutions to diverse industrial lightweight applications. We are looking for outstanding engineers to join our fast growing organization. Please visit www.frontierpolymer.com to learn more. Description:We are seeking several junior Project Engineer candidates with BS degree in chemistry, chemical engineering, materials, physics, mechanical engineering and related fields Responsibilities (include, but not limited to): Conduct research and development project under supervising of research engineers. Ensure that projects are completed successfully and meet the project deadlines and milestones. Execute experiments and collect data, and record all the data and discoveries in the laboratory notebook. Ensure the operations and functions of the laboratory equipment. Analyze the experimental data and results to optimize the performance and cost goals. Analyze experimental results and communicate it through written reports and oral presentations. Provide weekly and monthly technical reports. Present project progresses to internal management in weekly/monthly briefing or update meetings. Requirements• Must have hand-on experiences in handling experiments or laboratory equipments. • Willing to work long hours to get the job done.• Must be capable of handling multiple projects/tasks at the same time, and must have hand-on experience and execute project independently without the need of supervision. • Experience with technical report writing. • Must be comfortable in a fast-paced environment with challenging deadlines, multiple projects and assignments. • Strong work ethic and team player and can handle pressure. • Excellent oral and written communication skills are necessary. • The candidates must have creative thinking, good analytical skills and can demonstrate having experiences to execute assignment independently. Frontier offers competitive salary and benefit package including vacation, medical/dental insurance, profit-sharing and retirement - 401(k). For immediate consideration, please specify desired salary range and attach your resume in either Word or PDF format to: jobs@frontierpolymer.com Location: Dover, NJ Compensation: $35 to 60K annuallyPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Lab Assistant $50,000 2009-07-14 12:11PM
Seeking a laboratory assistant to join a research lab. Previous lab experience not needed. Pay is based on lab experience. Main duties include cleaning lab equipment and setting up for experiments. Apply for position #98374583 at DNAlabservices.com Compensation: $50,000Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Tactical Marketing Manager - Biotech (Newark, DE) Newark, DE $65K and up, depending on experience 2009-06-19 3:57PM
My stable and growing client is looking for a talented Tactical Marketing Manager.Qualifications:1. Bio or life science 2. 3 years of experience in biotech industry 3. 2 years of marketing experience 4. Drove a campaign and was able to measure results MOST importantResponsibilities:„Ï Develop, execute and measure the results of aggressive promotional and communication marketing campaigns to exceed revenue and profitability goals for existing services and products. Provide leadership in print, eMarketing, trade shows and sponsorship activities. „Ï Develop strategies and marketing plans to support the launches of new services and products under the guidance of strategic product management to develop early adaptors and to train sales and distributors. „Ï Measure customer satisfaction as recommendations for potential process improvement projects or product life cycle management. „Ï Perform market competitive analysis, SWOT, cost-volume-profit, and pricing analysis under supervision of strategic product management „Ï Perform market research to identify changes in customer needs and market demand under guidance of strategic product management. „Ï Prepare product and service comparison, maintain product and service list, maintain price list, generate marketing literatures (press release, product flyers, application notes, technical bulletins, direct mail, web content and other online marketing literatures). Interested? Please contact Lewis Keel:Lewis Keel, SPHRSenior Business Development ManagerSix Sigma Yellow Belt Volt Workforce Solutions | One Sentry Parkway, Suite 6000A | Blue Bell, PA 19422lkeel@volt.com | tf: 800-523-6609 | t: 610-834-3930 | c: 215-439-8658Recognized by FORTUNE Magazine as One of America¡¦s Most Admired Companies Location: Newark, DE Compensation: $65K and up, depending on experiencePrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Product Manager - Bioscience (Newark, DE) Newark, DE $75K and up, depending on experience 2009-06-19 3:41PM
My stable and growing client is looking to add a Product Manager to their team.This individual will be responsible for maintaining acceptable profit margins and product line vitality for products within business line in accordance with guidelines set forth by senior management. - Provide technical support to customers, sales staff and customer service group including on-site visits.- Generate and maintain technical and marketing documentation such as price lists, user¡¦s guides, MSDS,¡¦ technical bulletins, etc. for products under their supervision - Maintain and administer the product training program for products under their supervision. - Support new product introductions by supporting R&D through the Design„Ï process, validation studies, beta site studies and staff/customer training. - Support the Sales & Operations Planning process by monitoring sales, forecasts, industry trends, inventory, backorder issues and competitive products Ability to effectively communicate with customers and Sales & Marketing staff regarding technical product and market issues. - Investigates and resolves CCR¡¦s, communicates results to Marketing, Sales, Production, Executives and customerQualification Include:1. Minimum of a Bachelors of Science (BS) in Biological/Chemical or engineering disciplines2. Minimum of 3 years experience with product lines or other product management. 3. Working knowledge of quality control and quality assurance programs.4. Excellent computer skills5. Excellent research skills6. Very good written and verbal communication skillsPlease respond to Lewis Keel, Contact Informatino Below:Lewis Keel, SPHRSenior Business Development ManagerSix Sigma Yellow Belt Volt Workforce Solutions | One Sentry Parkway, Suite 6000A | Blue Bell, PA 19422lkeel@volt.com | tf: 800-523-6609 | t: 610-834-3930 | c: 215-439-8658Recognized by FORTUNE Magazine as One of America¡¦s Most Admired Companies Location: Newark, DE Compensation: $75K and up, depending on experiencePrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
QUALITY ASSURANCE ENGINEER (BIOMATERIALS) (WESTCHESTER, PA) WESTCHESTER, PA (In Job Posting) 2009-06-09 9:47PM
This is a leading company in the orthopedic trauma market. They develop, manufacture and market the AO ASIF system of internal fixation instruments and implants used by surgeons to repair difficult bone fractures. This concept was developed in Switzerland by Professors Maurice Müller, Martin Allgöwer, Robert Schneider and Hans Willenegger, who realized that conventional methods of fracture treatment (plaster casts) often led to poor results and partial disability. These surgeons, along with a group of metallurgists and scientists, formed the Swiss group known as the AO (Arbeitsgemeinschaft fur Osteosynthesefragen) ASIF (Association for the Study of Internal Fixation). The resulting system of carefully conceived stainless steel and titanium implants to hold fracture ends in precise alignment while healing takes place has revolutionized orthopaedic surgery and saved countless patients from varying degrees of disability.The AO products were originally produced and distributed by Mathys Medical and Straumann (later Stratec Holdings). This USA company was formed in 1974 and began marketing the AO ASIF system in North America in 1975. Early in 1999, said company and another company together agreed to merge into one company serving the orthopedic, spinal, maxillofacial and veterinary surgical specialties in North and South America and Europe. In 2004, this company continued its globalization with acquisition of Mathys Medical AG, to become the sole producer of AO ASIF instruments and implants, with the opportunity to serve surgeons in every corner of the world.Being a global leader in the orthopaedic trauma market and has expanded from its roots in orthopaedic trauma to include maxillofacial and spine surgery. The Maxillofacial division designs and markets products for use in mandible, orthognathic and cranial surgery, providing treatments for trauma applications and reconstructive surgery. They have developed surgical techniques and instrument and implant systems to treat deformity and degenerative disorders of the spine, as well as spinal trauma. Fantastic company with a great chance to move up. Great benefits tooJob Title: Quality Assurance Engineer - BioMaterials Job Requirements: This is one perm position located at the Development Center. The salary could be anywhere from $55 to $80K plus a bonus potential up to $7,750. Relocation is available for the right candidate. Candidates must have Biomaterials experience. Will be working with a five person QA team in Biomaterials.OVERALL RESPONSIBILITIES:Develop, implement and maintain Quality System requirements on assigned areas of Manufacturing, Supplier management, Process Validation and New Products Introduction. Areas of responsibility may include: Non-conforming product, CAPA, Calibration Systems, Supplier Auditing, Sterility, Measuring techniques, Design of tools and gages, Training, Statistical Support, Quality Planning, Experimental Protocols, Facilitation of Root Cause analysis, Risk Assessment and Complaint Investigation.POSITION DUTIES & RESPONSIBILITIES:General• Know and follow all laws and policies that apply to one’s job and maintain the highest levels of professionalism, ethics and compliance at all times.• Diligently participate in our compliance program- related activities as denoted by your supervisor or our Chief Compliance Officer.• Perform other related duties as required.The Quality Engineer assignments can be isolated but not limited to the following tasks:Manufacturing Support• Member of the Material Review Board (MRB). Communicate and resolve quality issues and apply root cause analysis to drive corrective and preventive actions.• Work on continuous improvement activities. These may include participating in, and/or leading Quality Improvement Teams.• Provide quality reports and review trending on assigned areas of responsibility.• Conduct failure investigations and problem analysis regarding customer complaints, stock evaluations, supplier quality issues, calibration out of tolerance conditions, and CAPA’s (internal or audit CAPA’s ).• Review and approve documents and drawings for manufacturing and product development (DCO’s, MC’s).• Support to Engineering, Manufacturing, Materials, Inspection, Distribution and/or Product Development Groups in order to assure quality and compliance of new and existing products.• Develop training course materials and conduct training for approved documentation and practices.New Products• Participate on cross- functional project teams.• Design gauging and develop tools and techniques to measure pertinent product parameters to assure product complies with engineering drawings.• Recommend, acquire and validate the necessary tools, equipment and technologies to support inspection and testing activities.• Develop and document Quality Plans to support new products.• Facilitate creation of PFMEA.• Ensure compliance issues are addressed for new products activities.• Participate on design reviews and risk analysis for new products. Validation• Provide process validation program oversight to ensure adequacy of validation activities and documentation in terms of regulatory compliance and technical/statistical soundness.• Review, assess and evaluate validation protocols (IQ, OQ, PQ) for compliance to procedures and regulations, statistical validity and approval.• Provide guidance to others for the generation of clear, concise and defendable protocols and reports.• Assist in determination of the need for validation.• Generate and/or maintain internal validation master plans as required. • Manage process monitoring activities including tracking, data collection and analysis, corrective action, and reporting. • Manage supplier validation activities including supplier assessment, protocol development, and generation of supplier validation master plan(s).• Lead continuous improvement activities for the validation program to ensure efficiency, effectiveness and compliance.Supplier Management• Coordinate and participate on supplier audits and technical assessments.• Assist purchasing with identification and qualification of suppliers and alternate manufacturing locations.• Administrate Supplier Management Program and measures effectiveness.• Manage Supplier CAPA activities including root cause analysis, definition of corrective actions and verification of actions. • Coordinate Quality Plans and inspection/test methods between suppliers.• Visit suppliers for the purpose of quality issues investigation and capability analysis.• Assist purchasing in resolution of supplier complaints. PROFESSIONAL EXPERIENCE & EDUCATIONAL REQUIREMENTS:BS degree in Sciences, Business, Engineering or related technical field.Experience in the medical and/or pharmaceutical field. Two (2) years QE experience preferred.Knowledge of FDA’s QSR and ISO regulations preferred.Working knowledge of Geometric Dimensioning and Tolerancing, Blueprint Reading, Basic Metrology, Gage design, Design/Process FMEA and Quality Plan Development.Strong Statistical ability and experience including Gage Repeatability and Reproducibility, Statistical Process Control, Process Capability and Design of Experiments. ASQ Certified Quality Engineer, Lean Manufacturing and/or Six Sigma certification preferred.Demonstrated excellent interpersonal and communication skills.Working knowledge of Word Processing and Spreadsheet software required (MS Word and Excel knowledge desired).Knowledge of Manufacturing materials and processes preferred (machining, sheet metal, electropolishing, passivation, hard coating, anodizaton, etc.)Attention to detail and ability to meet deadlines. Ability to manage multiple projects/requirements in a fast-paced environment.Ability to work independently with minimum supervision for application of QE principles and Techniques.Ability to work effectively in a team environment.DEVELOPMENT CENTER ONLY REQUIREMENTS: Knowledge of Manufacturing Clean Rooms, ISO Class 7 and ISO Class 8 (Class 100,000 and 10,000).Strong environmental monitoring knowledge for Clean rooms.Experience with Biomaterial, Ceramic and Polymer medical devices is a plus.Strong Pharma/Medical Device Manufacturing and R&D experience.Knowledge of sterile packaging and sterilization validations. Location: WESTCHESTER, PA Compensation: (In Job Posting)Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
PLM/CAx Systems Analyst (West Chester, PA) West Chester, PA (In the Posting) 2009-06-09 10:03PM
This Ideal candidate should have a background in Drafting or Design. A Mechanical Engineer background is a plus. Candidates must have discrete manufacturing experience, does not have to be medical device. Candidates do not need to be IT guru\"s, they just need to have an understanding of IT. Ideal candidate comes from a Product Development Engineering or Manufacturing Engineering. Must be able to support and house information for organization, must have experience with Finite Analysis, must be able to help engineers diagnose problems with manufacturing. Candidates must have CAD, PRO/E Wildfire, Windchill experience. Must have configuration, implementation and trouble shooting experience. A degree is ideal but not a must for a great candidate. This individual will be the go to guy for the Product Development group. Must be able to hit the ground running and handle large scale projects. The company just implemented Windchill.Will entertain H1B or OPT candidates. Pay is between $80k and 100k depending on experience and education. Great benefits and wonderful oppty to move up in the company eventually.Relocation assistance is available for this position.• Support of North American PLM/CAx System users. • Provide troubleshooting and software problem resolution to issues related to the use of all PLM/CAx applications particularly Pro/E Wildfire 3 and Windchill 9. • Provide user mentoring & support for applying specific standards to business processes executed by use of PLM/CAx System applications. • Route issues to IT Help Desk as appropriate. • Track and report all trouble reports and support calls • Deploy corporate standard PLM/CAx client Application configuration settings. • Coordinate corporate PLM/CAx System software rollouts. • Know and follow all laws and policies that apply to ones job, and maintain the highest levels of professionalism, ethics and compliance at all times. • Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer. • Other duties as assigned. Location: West Chester, PA Compensation: (In the Posting)Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Sr. Regulatory Affairs Dir/Oncology/Biologics (Northern NJ) Northern NJ 200K + Plus LTI 140 + 20% Bonus Relo Assistance 2009-06-19 7:24AM
Senior Director, Regulatory Affairs Oncology- Strong Biologics (Northern N.J.)Senior Director, Regulatory Affairs Oncology This has been upgraded to a Senior Director that must have significant Biologics and BLA background My name is Volora Howell, I am a sr. recruiter for Pharma Search, my client is based in Northern NJ is seeking an experience Senior RA Director with Oncology Drug experience with a heavy BLA /Biologics background. Relo assistance is provided Up to 200K base LTI 140K 20% bonus Department Name : Regulatory Affairs Location/Territory Name : Northern , NJ Job Description : The incumbent is responsible for but not limited to the following: Develop and guide the regulatory strategy ! for the approval of assigned Oncology products. Aid and supervise the preparation of regulatory submissions in the US, Canada, and Latin America. Serve as the Regulatory International Product Team (IPT) member for Oncology and provide regulatory leadership. Monitor Oncology programs so they comply with the required Health Authority Regulations and Laws. Interact with Health Authorities to address regulatory issues and to maintain the product development plan on schedule. Coordinate regulatory project activities with global counterparts. Job Qualifications : BS degree required in associated functional discipline (Life Sciences, Chemistry, Toxicology, Pharmacology, Pharmacy or Nursing). PhD, PharmD, or comparable degree in the life sciences highly desired. Sr. RA Director: Minimum 10-12 years of regulatory experience plus 2-3 years of additional related experience (i.e., clinical development, medical writing, medical affair! s). Must have experience in interacting with the appropriate regulatory bodies and in Oncology Drug Development. Must possess in-depth knowledge of appropriate Code of Federal Regulations, Regulatory Guidance Documents and ICH Regulations. Experience with electronic submissions highly desirable and having completed filings (i.e., NDA’s, BLA’s, IND’s) to health authorities. History of working in complex team environments with numerous/diverse stakeholders. ------------------------------------- Location: Northern NJ Compensation: 200K + Plus LTI 140 + 20% Bonus Relo AssistancePrincipals only. Recruiters, please dont contact this job poster.Phone calls about this job are ok.Please do not contact job poster about other services, products or commercial interests.
Experienced Analytical/Bio-Chemist Needed (New Castle County, DE) New Castle County, DE Commensurate with experience 2009-06-05 11:24AM
Our client, located in New Castle County, DE, is currently seeking an Experienced Analytical/Bio-Chemist to join their team!This is a contract to hire position.Requirements:Must possess a Bachelors Degree in Life Sciences: Biology, Bio-Technology, Chemistry, etc.Must have at least 5 years of hands-on expereince working in a laboratory environment.GMP backgroundELISAProtein AnalysisChemical AnalysisHPLCGLInterested candidates should forward their resumes to Mary Holmes at mholmes@penntechnical.com or for more information, feel free to give me a call at my office at (800) 230-8852, anytime between 8am and 5:30pm Monday-Thursday and until 5pm Friday. Also, please be sure to check out our website at www.penntechnical.com for free access to our easy to search database of 200+ open positions. Location: New Castle County, DE Compensation: Commensurate with experiencePrincipals only. Recruiters, please dont contact this job poster.Phone calls about this job are ok.Please do not contact job poster about other services, products or commercial interests.
Experienced Microbiologist Needed (New Castle County, DE) New Castle County, DE Commensurate with experience 2009-06-05 10:55AM
Our client, located in the New Castle County, DE, is currently seeking an Experienced Microbiologist to join their team!This is a contract to hire position.Candidates must have at least 5 years hands-on experience in a laboratory setting.GMP backgroundBioburden experience and basic endotoxin experienceInterested candidates should forward their resumes to Mary Holmes at mholmes@penntechnical.com or for more information, feel free to give me a call at my office at (800) 230-8852, anytime between 8am and 5:30pm Monday-Thursday and until 5pm Friday. Also, please be sure to check out our website at www.penntechnical.com for free access to our easy to search database of 200+ open positions. Location: New Castle County, DE Compensation: Commensurate with experiencePrincipals only. Recruiters, please dont contact this job poster.Phone calls about this job are ok.Please do not contact job poster about other services, products or commercial interests.
Complaint Specialist (West Chester, PA) West Chester, PA Commensurate with Experience 2009-06-23 8:39AM
This is a 3 month contract with the possibility of turning into a direct position with our client. Overview:Complaint Handling Unit (CHU) member responsible for supporting Post Market Regulatory Affairs activities associated with complaint handling and MDR submissions. Additionally these activities may include Non-Conformance Investigations, Field Actions, Documentation Management and Metrics. The Complaint Specialist will be responsible for the oversight and direct support of technical evaluations and investigational tasks required for complaint processing/closure. The Complaint Specialist will communicate with Quality Engineers, Manufacturing, Product Development and other functional experts as needed to ensure clear understanding/investigation of applicable issues.Specific Responsibilities:Direct interface with in-house and field staff employees, surgeons and hospital personnel when taking complaint/adverse event information. Need to ask questions to ensure understanding of the event. Data entry of complaint/AE information into company database.Perform reviews of complaint investigations. Be proactive. Ask questions when assessing completed investigations for level of completeness. Be able to discuss and understand the investigation findings. Facilitate applicable documentation corrections as necessary to support compliance, using “good documentation practices”. Prior to closure, perform an analytical review of the complaint file. Prepare a complaint file summary addressing the alleged product complaint.Responsible for processing and closing complaints in a timely manner.Act as a CHU liaison with other departments for Post Market RA activities.Review trend data with Product Development and Manufacturing on a routine basis to ensure complaint trends are investigated and reported to management. Responsible for the maintenance of individual and departmental metrics, as applicable. Prepare, organize and summarize routine weekly, monthly, and quarterly reports for department management use.Ability to function as an “Expert User” of department database(s).Monitor department databases for continuous improvement opportunities. Maintain current knowledge of the FDA regulations (frequent reading of the trade press/emails, FDA news bulletins, attending job-related webinars, or outside courses when appropriate); consider innovative solutions to meet changing regulatory compliance goals.Provide support to internal and external customers regarding complaints or other post market activities as needed. Provide assistance to bring resolution to complex cross functional issues.Requirements:BS Degree, engineering or science degree highly preferred. RAC or ASQ certifications a plus.Strict attention to detail.Must be able to work in an open office environment.Must be able to work independently and prioritize with little supervision. Strong written and oral communication and interpersonal (listening) skills.Must have ability to lead efforts aimed at the identification of problematic situations, the reporting of issues, and the development of resolutions and decision making.Minimum 3 years experience in a regulated industry (medical device or pharmaceutical). Post market regulatory, quality or compliance areas preferred. Familiarity with basic quality tools and techniques.Analytical and Critical thinking skills are essential.Excellent organizational and time management skills.Proficient with complaint handling software, ERP systems, and Microsoft Windows applications. Ability to read and understand a Risk Analysis Report.Qualifications should be submitted to:Mike Coultermcoulter@arstaf.com Location: West Chester, PA Compensation: Commensurate with Experience This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Research Assistant in Biotech Company Competitive compensation, benefits and 401K matching plan offered 2009-06-11 10:41PM
POSITION Research Assistant (ELC0010)LOCATIONNewark, DelawareJOB DESCRIPTIONElcriton Inc. is looking for a research assistant that can perform daily tasks in standard molecular biology and microbiology techniques. Specific tasks would include polymerase chain reaction (PCR) amplification of DNA, recombinant DNA manipulation (e.g. constructing gene expression plasmids), cloning recombinant DNA into Escherichia coli, solid and liquid E. coli cell culture and analytical assays (HPLC, GC, optical density measurements, etc.). Good candidates must have experience with most if not all these techniques and most importantly impeccable aseptic-culture technique. Candidates will also perform regular laboratory maintenance and management duties. REQUIREMENTSExperience in molecular biology, microbiological and aseptic technique are a must. This position requires a high level of recombinant DNA manipulation knowledge, and preferably laboratory experience in applying such knowledge to E. coli. Additionally, ideal candidates will have considerable knowledge of microbial physiology with an emphasis on anaerobic metabolism. Candidates must have or show significant promise to acquire laboratory management skills, and should be experienced in keeping superb documentation of experiments. A master’s degree in biology, bioengineering, chemical engineering, microbiology or a related field as well as laboratory experience is required. Candidates with a Bachelor’s degree and three or more years experience in related research/work will be considered. Candidates must have strong laboratory skills and will spend upwards of 80% of their time in the lab. They must also be able to work under the direction of a PhD level scientist, but eventually assume responsibility for some of their own experiments and projects. Excellent written and verbal communication skills in English are essential.Elcriton, Inc. is a high-tech, bioengineering start-up company that is looking for motivated and innovative personnel to contribute to our company goals. We offer a competitive compensation and benefits package, in addition to 401(k)/profit sharing matching plans.Elcriton, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex or national origin.HOW TO APPLYIn order to apply, please email Bryan Tracy at b_tracy3@yahoo.com. In the subject line, please reference the specific solicitation as “ELC0010 – research assistant,” and include a cover-letter and resume (with at least 3 references from the past 4 years) as attachments to the email. Compensation: Competitive compensation, benefits and 401K matching plan offeredPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Scientific transcriptionist/editor (Anywhere) Anywhere fees negotiable 2009-05-29 5:35AM
I am a trained scientific transcriptionist and can edit scientific papers/manuscripts. I have experieince in publishing as well. I take transcription through various media. If you need experienced help, I can help you. Can provide a local, -Wilmington, - scientific reference. I can handle most any need. Location: Anywhere Compensation: fees negotiable Telecommuting is ok.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Chemistry student negotiable 2009-01-15 10:12PM
Chemistry student with expertise in organic and computational chemistry wanted for project Compensation: negotiable Telecommuting is ok. OK to highlight this job opening for persons with disabilitiesPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.PostingID: 994679949
LIMS Installer/Administrator (Exton, PA) Exton, PA open 2009-07-14 11:03AM
LIMS Systems AdministratorJob Summary This position is responsible for installing, configuring, and maintaining a laboratory information management system (LIMS) in a GMP facility, as well as integrating LIMS with other systems. The LIMS Systems Administrator will also be the primary administrator within the quality management system and be required to configure, maintain and upgrade this system. The position will also perform end-user training and support functions for related administered systems. Will establish and document standards and procedures related to GxP systems. Essential Functions LIMS systems installation, administration, and systems integrationQuality management system administration (Trackwise)Develop Standard Operating Procedures for use in GxP FacilityProvide Levels 1, 2 and 3 help desk supportand end-user trainingOther duties as assignedScope Measures:Makes recommendations on IT related budget items and assists in the writing of policies and procedures that affect the organization. Will work closely with the business users of the systems being administered to ensure the business goals are being met.Knowledge/Skills/Abilities Required:BS/BA in MIS, CIS or related field or equivalent experience required5-7 years of IT experience with at least 3 years in a GxP environment requiredLIMS administration experience requiredStrong knowledge of cGMP/ICH/FDA regulations with 21 CFR Part 11 and GAMP knowledge a plusExperience with change control and software validation preferredMicrosoft Active Directory experience a plusSQL DBA experience is a plusCisco experience is a plusMust be able to lift up to 50lbsMust be available to work after hours and weekends when necessary. Must be available for after-hours supportPlease refer to job code 4331-JM when responding to this ad. Location: Exton, PA Compensation: open OK to highlight this job opening for persons with disabilitiesPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Sr. Clinical QA/Auditor Specialist (Exton, PA) Exton, PA Open 2009-07-14 11:03AM
Sr. Clinical QA/Auditor SpecialistIn this position the incumbent shall independently conduct a series of detailed GCP audits of Phase I – III domestic and international clinical research trials and/or GCP-related systems and processes to assure compliance with all applicable government regulations, federal guidelines, company standard operating procedures, and industry standards. Audits will be performed on external investigator sites, vendors/CROs, trial master files (TMFs), data/CRFs, study reports, and GCP-related systems/processes for clinical trials.Essential Functions Plans, schedules, and conducts QA audits to assure adherence to company Standard Operating Procedures, and any applicable regulatory requirements. Audits clinical investigator, trial master files, system/process, document and vendor audits/assessments. Reviews audit responses for acceptability; elevates issues that are above incumbents abilities or that cannot be resolved. Recommends corrective action to compliance issues and/or observations as needed to insure corrective action is implemented. Monitors clinical operations corrective action process to insure corrective actions are being appliedWorks with supervisor to develop and maintain standard operating procedures. Provides support to management during regulatory sponsor monitor inspections, as needed. Other projects and responsibilities may be added at the companys discretion.Job requirements and qualifications:BA/BS degree in biological sciences, nursing or related discipline, or equivalent experience requiredStrong knowledge of government regulations, guidelines and standards for investigation of new pharmaceutical products is requiredExperience in QA audits of Clinical InvestigatorsExperience in QA audits of Clinical documents associated with clinical trialsExperience in system/process auditsExperience in development of SOPsWorking knowledge and understanding of drug development and global clinical regulatory environmentAbility to manage multiple projectsEffective organizational skillsEffective team player and detail orientedStrong attention to detail, good organizational skills, ability to work independentlySolid oral and written communication skills with ability to communicate effectively and professionally with medical personnelKnowledge Requirements:Knowledge of the code of federal regulations, European Directives, ICH/GCP practices and clinical auditing processes experience. Experience: A minimum of 3-5 years working experience as a clinical quality assurance auditor. Travel is required, 25-35%, physical requirements, on-call schedules, and etc.Please refer to job code 4330-JM when responding to this ad. Location: Exton, PA Compensation: Open OK to highlight this job opening for persons with disabilitiesPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Biotechnology Applications Mgr (Wash DC) Wash DC to $120K 2009-05-18 10:20PM
Position MUST HAVEs :Graduate degree preferred in Biological, Medical, or Computer Sciences 5- 10 years management of scientific applications for software developmentUnderstanding & experience in Computational Biology, Bioinformatics, & Biostatistics Understanding of setting software requirements and development of prototypesUnderstanding & experience in predictive modelsOverview:Excellent organizational skills, and experience managing science/computer related programs, with the knowledge of government systems and an understanding of specialized software Responsibilities:Ability to simultaneously coordinate tasks for multiple proposals. Project timelines for projects Track milestonesExcellent organizational skills and detail oriented. Ability to create budget projections based on historical data and budget record keeping. Excellent interpersonal skills Understanding of the following:Bioinformatics Computational Biology Biomedical Statistical modeling Biomedical modeling algorithms Predictive models or algorithms Creating a software prototype You will perform the following tasks: Coordinate various aspects of the Applications programs Tracking and providing assistance with proposals Assisting with scientific posters and presentations Ensuring all program tasks are completed in a timely manner Education Level – Minimum of a Bachelors degree. Experience level - Minimum of 7 years managing a program Company:Large Consulting Company-Federal Government is the primary client REPLY: knowltongroup@yahoo.com Location: Wash DC Compensation: to $120KPrincipals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Analytical Laboratory Technician (Newark ) Newark up to $23.00 per hour 2009-06-29 12:36PM
Exciting temporary opportunity for an Analytical Laboratory Technician in Newark, DE. This position is customer service oriented that provides the opportunity to interact with a wide variety of customers in a dynamic environment. This position reports to the Fermentation Technology Leader and provies analytical support to the research facility on a weekly basis and consultation with customers on an as needed basis. Job responsiblilties include and are not limited to: analyzing samples generated in the fermentation facility using standard analytical equipment such as HPLC, GC, bio-analyzer, colorimetric assays, spectrophotometers, and robotic liquid handling systems. Successful candidate is responsible for analyzing, organizing, archiving, and communicating to customers in a timely fashion.Must have BS or MS in analytical chemistry or biochemistry with more than 1-2 years working experience. Working knowledge of biological systems is a plus, but not required. Demonstrated ability to manipulate large amounts of data using spreadsheets. There are paid holidays and vacation associated with this temporary assignment and medical and dental benefits are available.To apply, please email your resume as a Word document.All candidates are required to pass a pre-employment drug screen, background and respirator clearance prior to starting an assignment. Location: Newark Compensation: up to $23.00 per hour This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.
Fermentation Research Technician (Newark, DE) Newark, DE up to $23/hr 2009-06-26 8:32AM
Position Description:The position, located at the Fermentation Research Facility, requires the development of fermentation processes for the production of bio-based materials. The person in this position will be responsible for cultivation of microorganisms in flasks and fermenters, fermenter set-up and operation, harvesting, and analysis of samples and results. This individual must carry out research independently, anticipate potential problems, and implement preventative measures. He/She will act as a resource to others and may serve as a lead on a project or shift. Must be proficient in fermentation and multiple computer applications to provide data reports and analysis. This position requires participation in a 3 shift/5 day operation in a semi-works environment.Skills/Experience:• B.S. in biology, biotechnology or related field, or the equivalent work experience preferred. (Biology/Microbiology/Biotechnology/Fermentation)• Demonstrated skill with set-up and operation of fermenters and complex apparatus for batch and continuous studies from bench top to 10-liter scale.• Experienced in aseptic techniques and in the cultivation of microorganisms in flasks or fermentors• Key resource to other laboratory associates in area of microbial fermentation operation• Demonstrated ability to write, review and follow operating procedures and protocols• Strong mechanical and troubleshooting skills • Demonstrated observational skills and ability to make decisions based on the research goals and what is being observed in the experiment• Demonstrated ability to use computers and execute tasks using standard software such as MS Word, Excel, and equipment interfacing programs• Experience with common laboratory instruments, i.e., spectrophotometers, pH, YSI, etc.• Ability to work independently and efficiently• Demonstrated willingness to collaborate and work as a team; effective interpersonal and communication skills• Strong track record of delivering quality research results• Good record keeping and organization abilities• Demonstrated ability to analyze data and to communicate scientific observations concisely and accurately• Light-to-medium lifting, some climbing, bending, stooping, reaching and ability to wear a respirator*Candidates cannot start an assignment without successful drug and background clearances.*Six month assignments in Newark, DE. Location: Newark, DE Compensation: up to $23/hr This is a contract job.Principals only. Recruiters, please dont contact this job poster.Please, no phone calls about this job!Please do not contact job poster about other services, products or commercial interests.