Pharmaceutical Product Development Jobs in Woburn, MA

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Regulatory Project Manager (Part time)  

Tandym Group - Woburn, MA, United States

in a related field Working knowledge of global regulatory agency regulations, guidelines, and submissions and nonclinical, clinical, and CMC (bio)pharmaceutical drug / product development Direct hands

from: linkedin.com - 14 days ago

Scientist  

Tandym Group - Woburn, MA, United States

A leader in the pharmaceutical industry is seeking a Scientist to join their team. Reporting to the Associate Director of Analytical Development, the Scientist will be responsible for the development

from: linkedin.com - 23 days ago

Principle Device Quality Engineer, Combination Product Lead & Risk Management  

Biogen - Cambridge, Massachusetts

in the areas of development and commercialization of combination products.Thorough understanding of Design Controls and cGMP requirements compliant with ISO 13485 and the QSR (21 CFR Part 820) as per 21 CFR 820

from: snapjobsearch.com - 5 days ago

Director, CMC  

Zevra Therapeutics - Boston, MA, United States

, Pharmaceutical Science, Pharmaceutical or Chemical Engineering or related field. Masters or Doctorate degrees a plus. · Strong scientific knowledge and understanding of product development with relevance

from: linkedin.com - 6 days ago

Director, Regulatory Affairs Vaccines CMC  

Takeda - Boston, MA, United States

years Regulatory CMC experience combined with 5 years relevant vaccines or biologics experience (e.g. Pharmaceutical Development, Process Development, Analytical Development, Production, Quality Assurance

from: linkedin.com - 6 days ago

Quality Assurance Specialist I  

Cambridge Isotope Laboratories, Inc. - Tewksbury, Massachusetts

, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL

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from: resume-library.com - 3 days ago

Director Global Market Access  

Vertex Pharmaceuticals - Boston, MA, United States

, Countries, Marketing and Clinical Development counterparts to ensure value and access optimization Qualifications 8+ years of direct biotechnology / pharmaceutical industry experience and/or payer experience

from: linkedin.com - 11 days ago

Vice President Regulatory Affairs Quality Assurance  

EPM Scientific - Boston, MA, United States

on oncology products. Extensive knowledge of global regulatory requirements and guidelines governing the development and commercialization of oncology therapies. Proven track record of successfully leading

from: linkedin.com - 12 days ago

Senior Specialist, Clinical Supplies Project Manager  

Merck - Boston, MA

partner organizations such as Clinical Sciences and Study Management (CSSM), Regulatory, Chemistry, Manufacturing and Controls (CMC), Pharmaceutical Sciences, Formulation Development, and Global Development

from: Pharmadiversityjobboard.com - Yesterday

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Medical Device System Engineer  

ACL Digital - Cambridge, MA, United States

) • Relevant experience (pharmaceutical industry, combination products, medical devices, etc.) Nice to haves: Systems engineering background, lab experience. This position reports into the Systems Engineering

from: linkedin.com - 14 days ago


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