Biotech Jobs in Lexington, North Carolina

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COMPANY OVERVIEW: Herbalife is a global nutrition company that has helped people pursue a healthy, active life since 1980. Our nutrition, weight-management and personal care products are available exclusively through dedicated independent Distributors in more than 80 countries. Our Mission is to change people’s lives by providing the best business opportunity in direct selling and the best nutrit...
Director, Quality (GMP), Emerging Pharma, RTP, NC Area Our client, an RTP-based pharmaceutical company in high growth mode, is actively recruiting for a very sharp and capable Quality Leader to drive all GMP Quality efforts. This is a building role. Seek exceedingly competent Quality Director with demonstrated ability to design, develop, implement and manage a top-notch Quality organization. Com...
Quality Assurance Director We are currently seeking a Quality Assurance Director to join our team in Raleigh, North Carolina. Job Description: The Quality Assurance Director is responsible for ensuring that all quality systems are cGMP compliant at sites used for the manufacture, packaging, and testing of active ingredients, excipients, labeling, packaging materials, drug products, and clinical...
The primary objective of this role is to provide support to Pharmaceutical manufacturing sites. This would include providing on-site support to US manufacturing sites at the time of regulatory inspections and major investigations. Drive changes to corporate procedures; execute training associated with these changes, and assistance with medical assessments, complaint investigations, and review of f...
We’re Grifols, an international plasma manufacturer headquartered in Barcelona, Spain. We serve healthcare professionals and patients in over 90 countries, have an unmatched record of product safety, and are the largest plasmapheresis company in the world. We offer full healthcare benefits, tuition reimbursement, and some of our Academy courses even count for college credit! If you enjoy providin...
Our client, a global leader in the pharmaceutical industry is seeking a Microbiologist I to join the Holly Springs, NC location. duties : Support organization and start-up of the QC Microbiology laboratory. Perform facility validation testing and routine EM and clean Utility testing. Responsible for sampling water, clean steam, environmental monitoring, compressed gases, media fill support, and...
Occupational Summary: Manage the development, coordination and implementation of clinical operations site management and clinical monitoring responsibilities for assigned projects with guidance, including trial-specific processes and systems, and daily supervision of the Clinical Operations team responsible for site management and clinical monitoring. Responsibilities: Provide leadership for th...
Senior Quality Assurance Specialist PharmaCore (www.pharmacore.com) is seeking a highly motivated, energetic, results-oriented individual to join our Quality Assurance team of dedicated professionals focused on customer service and quality. We are currently accepting resumes for the position of Senior Quality Assurance Specialist. The successful candidate will hold a BS/BA or MS degree in Chemis...
Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...
Must have: AS or BS (Biology or Chemistry) 1 year experience in QC Environmental Monitoring QC, QA, and/or GMP experience Ability to lift up to 40 pounds Responsibilities: Collection and testing of qualified Utility systems including Clean Steam, WFI and compressed gases. Execute environmental sampling of Classified Areas including active air sampling, surface sampling and non-viable air sa...
Senior Scientist (LC/MS/MS) Sciex API 3000/4000 Also seek Bionalytical Scientists and Project Manager / Principal Investigators in NC, NJ and Utah Scientist: Employee performs laboratory functions required for extraction and/or analysis of drugs from biological samples in support of pharmaceutical discovery, validation and sample analysis studies. Work is performed using bioanalytical division ...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Essential Job Duties: The duties and responsibilities of this position include; conducting market intelligence research, writing papers and reports, preparing presentations and developing course content. The researcher will also conduct detailed analysis of nonwoven products, markets and trends. Other Work/Responsibilities: Minimum Experience/Education: Ph.D. or equivalent doctorate (e.g., M.D...
Essential Job Duties: The employee will be responsible for developing mathematical models to understand the disease ecology of multi-pathogen systems under the supervision of Dr. Kevin Gross. Other Work/Responsibilities: The employee will disseminate the products of his or her research in a scholarly manner. These may include, but are not limited to, peer-reviewed publications and presentations...
I. Overview: The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. II. Department Summary: As a membe...
I. Overview: The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. II. Department Summary: As a membe...
I. Overview: The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. II. Department Summary: As a membe...
Essential Job Duties: The candidate selected for this position will report to the leader of the sweetpotato breeding and genetics program. He/she will lead and coordinate a project focused on the development of improved processing sweetpotatoes. We are seeking a highly motivated, organized and independent breeder who is a good communicator capable of coordinating a multidisciplinary project. The ...
This opportunity is with a top global company that seeks a Senior Statistical Programmer for their growing team! To summarise the role, it involves but it not limited to: Supporting/Leading studies and a small group of programmers Working vastly on Phase II - III ISS/ISE CDISC/SDTM ADaM Requirements for the position include: Minimum of Bachelors Degree in Computer Science, Mathematics, or r...
Our client, a growing RTP-based Contract Research Organization, is actively recruiting for 2 Senior/Lead CRAs to oversee and manage clinical trial sites and activities, acting as a Lead on select projects. We seek experienced Clinical Research Associates who enjoy leading, training and driving the process forward. These Senior CRAs will assure that the CRA function and sites are in compliance wit...

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