QC Chemist

We are seeking a highly skilled QC Chemist to join our dynamic team. In this role, you will conduct comprehensive testing of raw materials and finished products using a range of advanced analytical techniques. You will ensure the highest quality standards and regulatory compliance in a fast-paced pharmaceutical environment.

• Conduct raw material and finished product testing using chromatography (HPLC, UPLC, GC), spectroscopy (UV-Vis, FT-IR), dissolution apparatus, and other analytical techniques.
• Independently process and report analytical results, ensuring clear documentation of findings.
• Maintain accurate laboratory records and follow methods, specifications, and protocols to ensure reproducibility and compliance with regulatory requirements.
• Identify and troubleshoot issues with analytical instruments and techniques.
• Ensure products meet regulatory standards, in-house, and regulatory quality specifications.
• Collaborate with the quality assurance team to ensure compliance with Good Manufacturing Practices (GMP) or other industry standards.
• Operate analytical instruments and equipment, ensuring they are calibrated and functioning properly.
• Perform routine maintenance, troubleshooting, and calibration of laboratory instruments.
• Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.
• Ensure all work is compliant with international regulations, such as FDA and EMA.
• Work with R&D and production teams to support product development, scale-up, and product release.
• Provide technical support and training to junior team members or other departments when necessary.

• Proven hands-on experience in a pharmaceutical analytical laboratory.
• 3-7 years of experience with analytical instruments (HPLC/UPLC, GC, Dissolution apparatus, UV-Vis spectrometer, FT-IR) is highly preferred.
• Current Good Manufacturing Practices (cGMP), FDA, and other regulatory requirements knowledge.
• Proficiency in dissolution, FT-IR, GC, UV-VIS, KF, TLC, and other analytical techniques.
• Basic computer knowledge including MS Word, Excel, and Outlook.

• Bachelor's degree (minimum) in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.
• Ability to document and record analytical experiments and results in detail as per cGMP guidelines.
• Excellent attention to detail and problem-solving skills.
• Ability to interpret and report complex data clearly.
• Knowledge of regulatory guidelines (e.g., GMP, GLP).

The role is based in a laboratory setting with exposure to chemicals, reagents, and specialized equipment. The team consists of approximately 10 people. This position may require standing for extended periods and the ability to lift moderate weights (about 25 lbs). Willingness to work overtime may be necessary depending on project deadlines. The workplace fosters growth with new leadership and offers a collaborative atmosphere.

This is a Contract to Hire position based out of East Windsor, NJ.

The pay range for this position is $35.00 - $35.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in East Windsor,NJ.

This position is anticipated to close on Jan 14, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $35