Job Description
Job DescriptionJob Title: Quality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to join our team. The ideal candidate will conduct quality control testing of raw materials and finished products using various analytical techniques. This role requires a strong understanding of chromatography, spectroscopy, and other analytical methods to ensure regulatory compliance and product quality.
Responsibilities
- Conduct quality control testing on raw materials and finished products using analytical techniques such as HPLC, UPLC, GC, UV-Vis, FT-IR, and dissolution apparatus.
- Interpret and report analytical results, maintaining accurate laboratory records, and ensuring compliance with regulatory requirements.
- Collaborate with the quality assurance team to ensure products meet in-house and regulatory quality specifications.
- Operate, maintain, and calibrate analytical instruments, ensuring they are functioning properly.
- Adhere to health and safety guidelines, ensuring a safe working environment in the laboratory.
- Ensure compliance with international regulations such as FDA and EMA.
- Work collaboratively with R&D and production teams to support product development and release.
- Provide technical support and training to junior team members or other departments.
Essential Skills
- 3-7 years of routine testing experience using HPLC and dissolution techniques.
- Proficiency in working with solid oral dosage forms, raw materials, and finished products.
- Experience with analytical instruments such as GC, FTIR, KF, and UV-VIS.
- Strong understanding of Pharma GMP practices.
- Competence in laboratory applications including wet chemistry, titration, and chromatography.
- Basic computer skills in MS Word, Excel, and Outlook.
Additional Skills & Qualifications
- Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, Biology, or a related field.
- Proven hands-on experience in a pharmaceutical analytical laboratory.
- Ability to document and record analytical experiments and results as per cGMP guidelines.
- Strong problem-solving skills and attention to detail.
- Knowledge of regulatory guidelines such as GMP and GLP.
Work Environment
The role is based in a laboratory setting, involving exposure to chemicals, reagents, and specialized equipment. The position may require standing for extended periods and the ability to lift moderate weight, approximately 25 pounds. A team of 10 professionals works collaboratively in this environment. Overtime may be required to meet project deadlines.
Job Type & Location
This is a Contract to Hire position based out of East Windsor, NJ.
Pay and Benefits
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)
Workplace Type
This is a fully onsite position in East Windsor,NJ.
Application Deadline
This position is anticipated to close on Jan 19, 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.