Industry: Biopharmaceutical 

Duration: 12 months (possible extension)

We are seeking an QC Chemist to support pharmaceutical manufacturing and process development for solid oral dosage forms (tablets/capsules). In this role, you will:

• Support process development, optimization, validation (process, cleaning, packaging) from R&D through commercial launch.
• Troubleshoot and improve manufacturing processes, investigate issues, and implement CAPAs.
• Coordinate with cross-functional teams (R&D, Quality, Manufacturing, Planning) for new product introductions and site transfers.
• Analyze data using statistical tools (JMP, R, PowerBI, Python) to support decision-making and compliance.
• Prepare technical reports and support audits (FDA, MHRA, QA).

Qualifications:

• PhD in Chemistry or MS in Pharmaceutical Sciences with at least 1 year of experience in MS&T or formulation.
• Experience with solid oral dosage processes (granulation, compression, coating, encapsulation, packaging).
• Strong technical writing and documentation skills.
• Familiarity with cGMP, process validation, and digital tools (PowerBI, Python, JMP, R).

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)