Job Role: QC Chemist IIIndustry: Pharmaceuticals / Biotechnology / Clinical ResearchLocation: Fall River, MA, USAJob Type: Full-time, On-siteKey Responsibilities
- Execute analytical method validation, verification, and transfer
- Residue analysis as part of cleaning validation
- Routine and advanced testing of raw materials and finished products
- Operation of lab instruments (e.g., Karl Fisher, HPLC, GC, Particle Size, ICP)
- Lead and participate in investigations and deviation analysis
- Ensure compliance with cGMP, SOPs, lab safety, and data integrity
- Prepare reports and documentation aligned with Good Documentation Practices (GDP)
Required Qualifications
- Bachelor’s degree in Chemistry or related physical sciences
- experience in the pharmaceutical industry
- Proficient in English (reading, writing, speaking)
- Must be legally authorized to work in the US (US Citizen / Green Card / H1B Transfer / OPT-EAD / TN Visa)
Technical Skills Required
- Familiar with pharmaceutical dosage forms:
- Metered Dose Inhalers (MDIs) (preferred)
- Liquids, solids, tablets, capsules (acceptable)
- Experience with:
- GMP & SOPs
- Lab Safety & USP Standards
- Instruments: HPLC, GC, ICP, Karl Fisher, Particle Size Analyzer
Nice-to-Haves
- Experience in inhalation products (MDI)
- Experience across various dosage forms (liquid, solid, tablets, capsules)
- Strong analytical thinking and documentation skills
Work Environment & Conditions
- cGMP-compliant laboratory
- PPE required
- Involves standing/walking >75% of the shift
- May require lifting up to 10 kg
- Regular weekday hours (8:30 AM – 5:00 PM), with some weekends possible
Job Types: Full-time, ContractPay: $65,000.00 - $90,000.00 per yearBenefits:
- Flexible schedule
- Relocation assistance
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Work Location: In person