About the Company
Catalent is a global leader in providing advanced delivery technologies and development solutions for drugs, biologics, and consumer health products. With over 90 years of experience, we are dedicated to helping our partners bring more treatments to more patients faster, reliably, and safely. We foster a collaborative and innovative environment where every team member contributes to life-changing outcomes.
Job Description
We are seeking a highly motivated and detail-oriented QC Chemist to join our dynamic Quality Control team in Memphis, TN. This is an immediate opening for an individual who is passionate about ensuring the quality and safety of pharmaceutical products. The successful candidate will perform a variety of chemical and physical tests on raw materials, in-process samples, and finished products according to established procedures, supporting the release of critical medicines to patients. You will work in a fast-paced cGMP environment, utilizing advanced analytical instrumentation and contributing directly to our mission of delivering superior health outcomes.
Key Responsibilities
- Perform routine and non-routine analytical testing on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, Karl Fischer, and dissolution.
- Accurately record, analyze, and interpret experimental data, maintaining thorough documentation in laboratory notebooks and LIMS.
- Calibrate and maintain laboratory equipment, ensuring proper functionality and compliance with quality standards.
- Troubleshoot analytical instrumentation and methods under supervision.
- Adhere strictly to cGMP, GLP, and company SOPs to ensure data integrity and product quality.
- Participate in OOS (Out-of-Specification) investigations and laboratory investigations as required.
- Prepare reagents, standards, and samples according to written procedures.
- Contribute to the continuous improvement of laboratory operations and safety practices.
- Review and approve peer data and documentation for accuracy and completeness.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
- Minimum of 2 years of experience in a pharmaceutical or related regulated industry (cGMP/GLP environment).
- Proficiency in analytical techniques including HPLC, GC, UV-Vis, and Karl Fischer.
- Strong understanding of cGMP principles and data integrity requirements.
- Excellent attention to detail and ability to follow complex procedures precisely.
- Solid problem-solving skills and ability to troubleshoot analytical issues.
- Effective written and verbal communication skills.
Preferred Qualifications
- Master's degree in Chemistry or a related field.
- Experience with Empower 3 or other LIMS/CDS systems.
- Familiarity with compendial testing (USP, EP, JP).
- Experience in method validation or transfer activities.
Perks & Benefits
- Comprehensive health, dental, and vision insurance plans.
- 401(k) with company match.
- Paid time off and company holidays.
- Opportunities for professional development and career advancement.
- Tuition reimbursement program.
- On-site fitness center or wellness programs.
- Employee assistance program (EAP).
- Life and disability insurance.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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