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Quality Specialist
- Permanent
- Senior/Director & VP, Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP)
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Quality Specialist with a pharmaceutical company located in Boston, MA.
Job Responsibilities:
- Review executed API, drug product and packaging batch records
- Review deviations/investigations related to API and drug product manufacturing as well as packaging
- Assist with disposition of products in multiple phases of development, including commercial
- Review change control documentation
- Assist with managing corporate partnerships (tracking and managing deliverables)
Skills and Requirements:
- Ability to effectively prioritize and manage multiple projects and tasks
- Experience with small molecule and solid oral dosage forms required
- B.S. degree in life sciences, chemistry or equivalent and 5+ years GMP quality experience in a virtual Pharmaceutical/Biotech setting
If you are having difficulty in applying or if you have any questions, please contact Bri Copeland at 267-297-3280.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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