Quality Assurance Pharmaceutical Jobs in Burlington, MA

Randstad Life Sciences US - Burlington, MA, United States

and the prescribed requalification cadence. Education & Qualifications BS or MS degree, preferably in Sciences or Engineering 7-10 years of Quality Assurance experience in pharmaceutical industry OR BS degree with 2-5

from: linkedin.com - 14 days ago

Tandym Group - Bedford, MA, United States

Our client, a leader in the pharmaceutical industry, is seeking a QA Senior Associate to join their team. **This job is 5 days onsite in Bedford, MA** **W2 Only** As a Senior Specialist, Quality

from: linkedin.com - 9 days ago

Novo Nordisk - Lexington, MA

of experience. 5+ years of experience within GLP Quality Assurance. Demonstrates commitment and consistent achievement of goals through constructive collaboration with colleagues. Excels at navigating

from: Pharmadiversityjobboard.com - 10 days ago

Kelly Science, Engineering, Technology & Telecom - Westborough, MA, United States

that are designed to mitigate the risks identified through the Risk Management process. Qualifications: Bachelor’s degree 5 years Quality Assurance/Quality Engineering experience in the medical device

from: linkedin.com - 9 days ago

Kelly Science, Engineering, Technology & Telecom - Westborough, MA, United States

. Develops process improvement plans using a variety of Quality and Continuous Process Improvement tools. Qualifications: Bachelor s degree 2. 5 years Quality Assurance/Quality Engineering experience

from: linkedin.com - 9 days ago

Talnt - Boston, Massachusetts

. Qualifications: Bachelors degree or higher in a technical or scientific discipline. Minimum of 10 years' experience in a GMP-related field, with at least 7 years in quality assurance within the pharmaceutical

from: resume-library.com - 10 days ago

Natick, MA, United States

skills and qualities of a Quality Assurance Specialist: BS/MS Degree (preferred in a scientific discipline) 1-4 years of experience in a GMP pharmaceutical setting Broad understanding of cGMP, especially

from: linkedin.com - 15 days ago

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

Central Admixture Pharmacy Services, Inc. - Woburn , Massachusetts 01801 , United States

. Participates in cleanroom product introduction activities. Prepares records and monitors results for pharmaceutical quality assurance testing. Level II additionally may: Assist in training/mentoring of new IV

from: jobtarget.com (+1 source) - 14 days ago

EPM Scientific - Boston, MA, United States

degree (e.g., MS, PhD, JD) preferred. Minimum of 10 years of progressive leadership experience in regulatory affairs and quality assurance within the pharmaceutical or biotechnology industry, with a focus

from: linkedin.com - 12 days ago