Validation Pharmaceutical Contract Jobs in Cambridge, MA

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Clinical Scientist III  

Randstad Life Sciences US - Cambridge, MA, United States

This position is anticipated to open within the next couple of months** We are seeking a PhD, PharmD, or MD Clinical Scientist for our Global Pharmaceutical Client in Cambridge, MA. Very attractive

from: linkedin.com - 12 days ago

Principal Commissioning/Validation Engineer III  

TalentBurst, an Inc 5000 company - Framingham, MA, United States

Industry: Biotechnology Position: Principal Commissioning/Validation Engineer III Location: Framingham, MA - 01701 Duration: 06 months contract (+Possibility of extension) Requirements : BSc/BEng

from: linkedin.com (+1 source) - 10 days ago

Regulatory Operations Associate  

Validation Associates LLC - Boston, MA, US

electronic document management systems; ? Familiarity with system validation practices; Contract: 6 month contract, strong possibility of extension or permanent. Preferred Experience: - B.S. w/ 1 + years

from: jobvertise.com - 14 days ago

Senior Commissioning Engineer  

TalentBurst, an Inc 5000 company - Framingham, MA, United States

Position: Principal Commissioning/Validation Engineer III , Req#: SNFIJP00008706 Location: Framingham, MA (100% onsite) Duration: 6 Months Contract Job Description: Education and Experience: BSc/BEng

from: linkedin.com - 10 days ago

Senior Network Engineer : Only w2 /No c2c  

Fortira Inc. - Groton, MA, United States

validation. Strong attention to safety a must. Experience in pharmaceutical manufacturing is a plus. Job Type: Contract

from: linkedin.com - 5 days ago

principal commissioning validation engineer  

Randstad - framingham, massachusetts

in the Framingham, NY area. This position involves writing and executing commissioning, qualification, and validation protocols for pharmaceutical facilities and equipment, resolving discrepancies, and ensuring $63.49 - $88.89 per hour

from: randstadusa.com - 9 days ago

Associate Director, GMP Quality Control  

Sumitovant Biopharma - Marlborough, MA, US

of method validation, transfer, and stability studies consistent with regulatory, quality, and pharmaceutical best practices (e.g., USP, ICH). Experience with managing external CMO and contract laboratory

from: jobvertise.com - 3 days ago


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