About the Company
Lonza is a global partner to the pharmaceutical, biotech and nutrition industries. We help our customers to enable new medicines and deliver advanced products to patients and consumers. Our products and services range from active pharmaceutical ingredients to cell & gene therapies, to nutrition ingredients and much more. We are committed to using science and technology to improve lives and contribute to a healthier world.
Job Description
We are seeking a highly motivated and detail-oriented Finished Products Chemist to join our Quality Control team in Gaithersburg, MD. In this high-demand role, you will be instrumental in ensuring the quality and integrity of our biopharmaceutical finished products. The successful candidate will perform a variety of analytical tests, interpret data, troubleshoot issues, and contribute to continuous improvement initiatives within our state-of-the-art laboratory. This position offers weekly pay and the opportunity to work in a dynamic, fast-paced environment at the forefront of pharmaceutical innovation.
Key Responsibilities
- Perform routine and non-routine analytical testing on finished biopharmaceutical products using techniques such as HPLC, GC, UV/Vis spectroscopy, Karl Fischer, and dissolution.
- Accurately record, analyze, and interpret experimental data, ensuring compliance with cGMP, ICH guidelines, and company SOPs.
- Troubleshoot analytical instrumentation and methods, escalating complex issues to senior chemists or supervisors.
- Prepare and review technical documents, including method validation protocols, reports, and standard operating procedures.
- Participate in out-of-specification (OOS) and out-of-trend (OOT) investigations, identifying root causes and implementing corrective actions.
- Maintain laboratory equipment, ensuring proper calibration, maintenance, and cleanliness.
- Contribute to continuous improvement projects aimed at enhancing laboratory efficiency, data integrity, and analytical capabilities.
- Adhere to all safety regulations and maintain a safe working environment.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, or a related scientific field.
- Minimum of 3 years of experience in a GMP/GLP analytical laboratory, preferably within the pharmaceutical or biopharmaceutical industry.
- Proficiency with various analytical techniques, including HPLC, GC, UV/Vis, and Karl Fischer titration.
- Strong understanding of cGMP, ICH guidelines, and regulatory requirements.
- Excellent problem-solving skills and attention to detail.
- Ability to work independently and collaboratively in a team environment.
- Strong written and verbal communication skills.
Preferred Qualifications
- Master's degree in Chemistry or a related field.
- Experience with LIMS (Laboratory Information Management System).
- Knowledge of statistical analysis software for data interpretation.
- Prior experience with method development or validation.
Perks & Benefits
- Competitive weekly pay structure.
- Comprehensive health, dental, and vision insurance.
- 401(k) retirement plan with company match.
- Paid time off and holidays.
- Professional development and training opportunities.
- Tuition reimbursement program.
- Life and disability insurance.
- On-site fitness center (at select locations).
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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