Pharmaceutical Product Development Jobs in Andover, MA

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Senior Scientist (Downstream)  

Insight Global - Andover, MA, United States

pharmaceutical client based out of Andover, MA. This MSAT downstream purification team supports downstream development purification and optimization, mRNA drug substance process activities, and providing support

from: linkedin.com - 16 days ago

Quality Control Analyst I / Wet Chemistry  

Cambridge Isotope Laboratories, Inc. - Andover, Massachusetts

pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years

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from: resume-library.com (+1 source) - 2 days ago

Quality Control Laboratory Support Technician  

Cambridge Isotope Laboratories, Inc. - Andover, Massachusetts

that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Laboratory Support

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from: resume-library.com (+1 source) - 2 days ago

ISO Quality Specialist  

Cambridge Isotope Laboratories, Inc. - Andover, MA

development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The ISO Quality Specialist will be responsible for development

from: workable.com - More than 30 days ago

Group Leader, Research Products  

Cambridge Isotope Laboratories, Inc. - Andover, Massachusetts

that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Group Leader, RP is responsible

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from: resume-library.com - 15 days ago

Group Leader, Research Products  

Cambridge Isotope Laboratories, Inc. - Andover, MA

that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Group Leader, RP is responsible

from: workable.com - More than 30 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. ยท Strong scientific knowledge and understanding of product development with relevance

from: linkedin.com - 7 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 - 7 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 - 4 days ago

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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 - 15 days ago


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