Quality Control Chemist - Pharmaceutical

Quality Control Chemist - Pharmaceutical

Position : 159572

Salary/Hourly Rate: $34/hr – $36/hr

Our client is a leading pharmaceutical contract development and manufacturing organization (CDMO), specializing in oral solid dosage and ingestible powder products. They partner with pharmaceutical companies to support drug development and manufacturing needs with a strong focus on quality, compliance, and innovation.

Responsibilities:

• Perform QC testing of raw materials and finished products—including tablets, capsules, and other dosage forms—using analytical techniques such as HPLC, UPLC, GC, UV‑Vis, FT‑IR, dissolution apparatus, and particle size analysis.
• Interpret and report analytical results while maintaining detailed and accurate laboratory records.
• Ensure compliance with regulatory standards, including FDA and EMA guidelines.
• Operate, calibrate, and maintain analytical instruments and laboratory equipment.
• Collaborate with cross‑functional teams, including R&D and production, to support product development and release.
• Provide technical support and training to junior staff as needed.

Required Experience &

Skills:

• 3–7 years of experience in a pharmaceutical analytical laboratory.
• Proficiency with HPLC/UPLC, GC, UV‑Vis, FT‑IR, and dissolution apparatus.
• Strong documentation skills aligned with cGMP guidelines.
• Ability to troubleshoot analytical techniques and instrumentation.
• Excellent attention to detail and strong problem‑solving capabilities.

Preferred Experience &

Skills:

• Experience working in a CDMO environment.
• Familiarity with ingestible powder and oral solid dosage product testing.
• Knowledge of international regulatory standards and quality systems.

Education Requirements:

• Bachelor’s degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related scientific field.

Benefits:

• Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).

Equal Opportunity

Employer:

As a woman‑owned firm, we value diversity. We are an equal opportunity and affirmative action employer and will consider all applications without regard to race, sex (including gender, pregnancy, sexual orientation and gender identity), age, color, religion or creed, national origin or ancestry, veteran status, disability (physical or mental), genetic information, citizenship or any other characteristic protected by law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

EOE/M/F/D/V/SO

• Seniority level:
  Mid‑Senior level
• Employment type:
  
  Full‑time
• Job function:
  Quality Assurance
• Industry: Staffing and Recruiting