Biotech Science Jobs

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Electrical Engineer - Life Science & Biotech Industries Position Summary: The successful Electrical Engineering candidate will develop and execute project tasks and deliverables, be a collaborative team player, and have a strong drive to deliver quality project designs to customers. This person will develop and implement the electrical and special systems concepts and design, coordinating with i...

Senior Project Manager – Life Science & Biotech Industries Job Qualifications: Bachelor of Science, Engineering discipline 10+ years PM experience PE registration preferred PMP Certification preferred LEED Accreditation preferred FDA regulated manufacturing experience required cGMP compliance/verification Job Description: Qualified candidates will offer 7+ years of project management exp...

Smaller, well established international sponsor with a stateside site in NJ has an immediate need for a perm Southeast based Medical Science Liaison. Excellent pay, bonus, and benefits available. No relo assistance available as this is a home based opportunity when incumbent is traveling. Territory: Florida, Georgia, South Carolina, and North Carolina). The Medical Science Liaison will function a...

Smaller, well established international sponsor with a stateside site in NJ has an immediate need for a perm Southeast based Medical Science Liaison. Excellent pay, bonus, and benefits available. No relo assistance available as this is a home based opportunity when incumbent is traveling. Territory: Florida, Georgia, South Carolina, and North Carolina). The Medical Science Liaison will function a...

Alpha Executive Search Partners specializes in recruiting appropriate candidates for a full range of positions within their select book of Life Science Clients located across the United States. Types of candidates we are looking to identify: · Pharmaceutical · Biotechnology · Medical Device · Research and Development · Chemistry (Inorganic, Organic, Analytical) · Laboratory · Food Science ...

CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Director of Quality Control Sunnyvale, CA Unspecified Apply Apply Director of Quality Control Sunnyvale, CA Unspecified Apply Job Details If you are a Director of Quality Control with experience, please read on! Located in Sunnyvale CA, we are a industry leading, biotechnology research company....

Director of Formulations and CMC: Boston-area pharmaceutical company is seeking a technically strong leader to join their formulation/CMC group as a Director. You must live and work in the Boston area, have expertise with injectable formulations and have strong understanding of CMC aspects. You must also have prior experience working with CROs/CMOs for selection and managing them. BS, MS, or Ph....

Responsibilities - Provides guidance and direction to procedure authors (SMEs) to ensure the procedure development process, content and format comply with RA and Corporate requirements - Liaise with Drug Safety department to ensure the Pharmacovigilance System Master File (PSMF) is updated following related changes in RA SOPs and WPs. . The project management support involves the building and m...

Contract Clinical SAS programmer Responsibilities: • Participate in the programming, testing and documentation of study data sets and tables, listings & figures (TLFs) in accordance with standards and validation procedures. • Apply standard tools developed for the study or project. Participate in development of new standards and tools. • Follow all company SOP and guidelines in the creat...

Work with Head, Central Clinical Trial Operations to: Responsible for the operational strategy of assigned clinical trials, including operational planning and execution according to study objectives and adequate preparation and training of teams supporting the study. Leads the cross-functional Clinical Trial Team functions contributing to the relevant clinical trial(s) and relevant vendors to en...

We are looking for a Sr. SAS Programmer with a minimum of 7 years of SAS Programming experience in Pharmaceutical, Biotechnology, or CRO environment. Must be very proficient in CDISC (SDTM and ADaM) and have experience working with Efficacy ADaM domains. Long term contract, no specific end date. Description: - Generates and validated analysis datasets, tables, listings, and figures - Writes SAS...

Our client, an exciting and growing medical device/diagnostics sponsor company located in the Southern CA area is looking for a Director of their Medical Affairs division. The Director of Medical Affairs will lead the post-market scientific and technical activities for the company's biomarker tests, starting with the FDA-cleared tests already on the market. Key areas of focus include medical educ...

If you have a strong work ethic and enjoy a fast-paced environment, we would like to invite you to apply. This company has very high growth potential and you will be getting in early to accelerate your career into the fast growth phase. Description of Duties: - Design high quality, reliable medical products such as single-use devices or disposables. - Engineering leadership of all phases of des...

Mid-Size Contract Research Organization (CRO) with a global reach is currently seeking Senior Clinical Project Managers for the Research Triangle Park, NC and Houston, TX. Responsibilities: • Sponsor liaison ensuring high sponsor satisfaction • Project assessment and initiation • Resource planning and procurement • Project implementation • Ensure effective communication channels exist and ar...

My client company, a biopharmaceutical company specializing in nucleic acid delivery is seeking a formulation scientist to join their pharmaceutical development team. You must have experience mentoring and advising junior scientist, you must have project management skills, and you must have a strong scientific background with formulations of nucleic acids. This is an exciting opportunity for Bosto...

Job Description POSITION SUMMARY The Director, Strategic Business Development will shape and drive adoption of Healthagen's analytical services for a specific client base within the healthcare industry: pharmaceutical manufacturers, biotechnology companies, and medical device firms. The Director will lead client account management for the Healthagen Outcomes business unit, with responsibility fo...

TalentMine is actively seeking contract SAS Programmers for one of our Pharmaceutical clients in New Jersey. This opportunity offers an excellent potential for growth and development. We are looking for a Sr. SAS Programmer with a minimum of 6 years of SAS Programming experience in Pharmaceutical, Biotechnology, or CRO environment. Essential Responsibilities: - Perform statistical programming ac...

Purpose: To deliver an industry superior sponsor-experience and project performance (time, quality/level of service and cost of awarded projects) that exceed the clients' expectations and specifications. To oversee and coordinate all internal and external activities to ensure the smooth, timely and accurate flow of information required to meet the purpose of the role. To strengthen the client ...

Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include sit...

Work with Head, Central Clinical Trial Operations to: Responsible for the operational strategy of assigned clinical trials, including operational planning and execution according to study objectives and adequate preparation and training of teams supporting the study. Leads the cross-functional Clinical Trial Team functions contributing to the relevant clinical trial(s) and relevant vendors to en...