QC Chemist II

Job Description

Job Description

Job Title: Chemist II – Stability Testing (Quality Control)
Job Location: Fall River, MA (On-site)
Schedule: 8:00 AM – 5:00 PM (May vary based on business needs)
Classification: Full-Time, Exempt
Relocation Assistance: Up to $6,000 available
Work Authorization: US Citizen, Green Card, H1B Transfer, TN Visa, OPT-EAD

About the Role:

We are seeking a QC Chemist II – Stability Testing to join our Quality Control Department. The selected candidate will be responsible for performing and overseeing stability testing for pharmaceutical formulations under various environmental conditions, ensuring data integrity, and compliance with cGMP guidelines.

Key Responsibilities:

• Conduct routine and advanced stability testing in a laboratory setting.

• Operate and maintain instruments such as HPLC, GC, ICP, Karl Fischer, and Particle Size Analyzers.

• Perform raw material testing and release.

• Lead investigations into out-of-specification (OOS) or deviations and document findings.

• Ensure adherence to cGMP, Good Documentation Practices (GDP), and data integrity principles.

• Prepare and review documentation, including lab notebooks and reports.

• Participate in audits and ensure inspection readiness.

• Collaborate with cross-functional teams, including QA and manufacturing.

• Support training and mentoring of junior team members.

• Execute additional duties as assigned by departmental leadership.

Required Qualifications:

• Bachelor’s degree (BS/BA) in Chemistry or a related physical science.

• Minimum 3 years of experience in formulation stability testing in a pharmaceutical setting.

• Working knowledge of analytical instruments including HPLC, GC, ICP, Karl Fischer, and particle size analyzers.

• Familiarity with MDI (Metered Dose Inhaler) testing is a strong plus.

• Experience with various dosage forms (liquid, solid, tablets, capsules) is desirable.

• Strong command of English – spoken and written.

• Proficiency with Microsoft Office and scientific software.

• Excellent analytical, documentation, and communication skills.

• Must be authorized to work in the United States and be available to work on-site full-time.

Preferred Qualifications:

• Experience working with inhalation products (MDIs).

• Previous work in a fast-paced, regulated pharmaceutical QC lab environment.

• Experience leading or contributing to laboratory investigations.

Work Environment Physical Requirements:

• Work in a cGMP laboratory or manufacturing environment requiring the use of personal protective equipment (PPE).

• Regular exposure to solvents, powders, and chemical substances.

• Must be able to stand or walk for 75% or more of an 8-hour shift.

• Must be able to lift up to 10 kg unassisted.

• Must be able to sit and work at a computer for extended periods.

Compensation Benefits:

• Competitive salary based on experience ($75K–$105K)

• Bi-weekly pay

• Paid Time Off (PTO)

• Health Insurance (Medical, Dental, Vision) – starts on Day 1

• Disability Insurance

• Overtime and shift differential as applicable

• 401(k) with company match

• Career advancement opportunities and ongoing training

• Company-sponsored events

Important Notes:

• Candidates must have prior pharmaceutical (not biopharma) experience.

• Chemistry background is highly preferred.

• Candidates should clearly indicate experience with formulations including MDI, liquid, solid, tablets, and capsules in their resume.

• No Green Card sponsorship available; H1B transfers are acceptable.