About the Company
Thermo Fisher Scientific is the world leader in serving science, with annual revenue exceeding $40 billion and over 100,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner, and safer. We provide innovative technologies, analytical instruments, lab equipment, reagents, consumables, and software to pharmaceutical and biotech companies, hospitals and clinical diagnostic labs, universities, research institutions, and government agencies. We are deeply committed to fostering a culture of inclusion, innovation, and continuous improvement, driving scientific breakthroughs that impact lives worldwide.
Job Description
We are seeking a highly motivated and detail-oriented Manufacturing Chemist specializing in Quality Control (QC) to join our dynamic team in Boston, MA. In this critical on-site role, you will be instrumental in ensuring the highest quality standards for our high-volume production of chemical reagents and products used in life science research and diagnostics. You will perform essential analytical testing, troubleshoot instrumentation, interpret complex data, and contribute to continuous improvement initiatives within our state-of-the-art manufacturing facility. This position offers a fantastic opportunity to contribute directly to the integrity of products that make a real difference in scientific discovery and healthcare innovation.
Key Responsibilities
- Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, Karl Fischer, titrations).
- Ensure all testing is conducted in strict compliance with cGMP, ISO, and company quality standards and procedures.
- Operate, maintain, troubleshoot, and calibrate laboratory equipment and instrumentation to ensure accurate and reliable results.
- Accurately record and document all test results, observations, and calculations in laboratory notebooks and LIMS (Laboratory Information Management System).
- Investigate out-of-specification (OOS) results, conduct thorough root cause analysis, and implement effective corrective and preventive actions (CAPA).
- Review and approve batch records and other critical manufacturing documentation.
- Participate in method development, validation, and transfer activities as needed to enhance laboratory capabilities.
- Provide expert technical support to manufacturing operations to efficiently resolve quality-related issues and ensure smooth production.
- Contribute to the continuous improvement of QC processes, procedures, and overall laboratory efficiency and compliance.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, or a closely related scientific field.
- 3+ years of progressive experience in a Quality Control or Analytical Chemistry role within a high-volume manufacturing environment (pharmaceutical, biotech, or chemical preferred).
- Proficiency with a range of analytical techniques including HPLC, GC, UV-Vis spectroscopy, and titrations.
- Strong foundational understanding of cGMP, GLP, and ISO quality systems.
- Excellent data analysis, troubleshooting, and problem-solving skills with a meticulous attention to detail.
- Ability to work effectively both independently and collaboratively in a fast-paced, high-volume production setting.
- Exceptional organizational skills, attention to detail, and ability to manage multiple priorities.
- Proficient in using laboratory information management systems (LIMS) and Microsoft Office Suite.
Preferred Qualifications
- Master's degree in Chemistry or a related scientific field.
- Experience with statistical process control (SPC) and lean manufacturing principles.
- Demonstrated knowledge of method validation and transfer protocols.
- Familiarity with regulatory submissions and participating in internal and external audits.
- Experience working with automated laboratory systems and robotics.
Perks & Benefits
- Competitive annual salary and performance-based bonuses.
- Comprehensive medical, dental, and vision insurance plans starting day one.
- 401(k) retirement plan with robust company matching contributions.
- Generous paid time off, including vacation, sick leave, and company holidays.
- Tuition reimbursement and extensive professional development opportunities.
- Employee assistance program for personal and professional support.
- On-site fitness center and comprehensive wellness programs.
- Life and disability insurance for peace of mind.
- Employee stock purchase plan with company contributions.
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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