- Aequor (West Greenwich, RI)
- …ability to work nights long-term is critical to ensure continuity in this role. QA Senior Associate will be responsible for Quality On the Floor in support of ... would be nice to have. ONSITE 100% - PQA Sr . Associate (Nights)- No remote work 12-hour...Qualities of your ideal candidate? Has worked in similar drug manufacturing organization, within Quality or MFG… more
- Aequor (West Greenwich, RI)
- …of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time ... completed Preferred Qualifications: Bachelor's Degree & 4 year of Quality/ Manufacturing experience cGMP Experience Excellent written and verbal communication skills… more
- ThermoFisher Scientific (Plainville, MA)
- …facility houses automated isolator filling technology along with sophisticated drug substance manufacturing . **Location:** Plainville, MA (5 Commerce ... Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail… more
- Actalent (West Greenwich, RI)
- …ability to work nights long-term is critical to ensure continuity in this role. QA Senior Associate will be responsible for Quality On the Floor in support of ... would be nice to have. ONSITE 100 - PQA Sr . Associate Nights- 12-hour night shifts 7:00...of your ideal candidate? - Has worked in similar drug manufacturing organization within Quality or MFG… more
- US Tech Solutions (West Greenwich, RI)
- …of Manufacturing activities. This position requires working directly with Manufacturing staff during bulk drug substance operations to facilitate real-time ... are completed **Preferred Qualifications:** + Bachelor's degree and 2 years of Quality/ Manufacturing work experience + Experience working in a cGMP environment +… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- ** Associate Director, Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... product at CDMOs + Design and lead method validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and… more
