Senior Technician Analytical QC
About the role
The Senior Technician Analytical QC supports the accurate and timely testing and inspection of current product lines in their area of responsibility following customer requirements and/or established procedures. The Senior Technician Analytical QC works with all areas of Operations and R&D to ensure that dsm-firmenich products are of consistent and high quality by conducting standard and nonroutine laboratory tests, performing product inspections, and organizing data in a manner compliant with cGMPs.
At dsm-firmenich, we don’t just meet expectations – we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions – every single day. Whether it’s fragrance that helps you focus, alternative meat that’s better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you’re making a difference, we’ll make sure you’re growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They’re essential to our future. Because real progress only happens when we go beyond, together.
Responsibilities
- Conduct laboratory tests and inspections on raw materials, in-process, and finished products.
- Analyze and maintain all test data according to cGMPs.
- Conduct thorough batch record reviews as part of material approval process.
- Initiate NCRs as needed and execute the final disposition, including MRB transactions.
- Organize laboratory supplies and documentation.
- Authorized to release and transfer in-process and finished material in ERP system for sale, distribution, or further use.
- Perform routine equipment maintenance and calibration on equipment.
- Conduct routine environmental monitoring on controlled areas and water systems.
- Offer suggestions on improvement of methods and implement through change control process.
- Perform non-routine tests involved with method development/improvement, process optimization studies, and validation and qualification projects.
- Assist the Biomaterials Manufacturing and R&D teams as needed.
- Adhere to Biomedical Quality System procedures regarding ISO 9001 and/or 13485 standards.
- Performs OOS investigations with oversight from the Supervisor.
Requirements
- Associate’s degree in the biological or chemical sciences required; B.Sc. degree preferred.
- Minimum 5‑7 years experience with an associate’s degree; minimum 4 years with B.Sc. degree; minimum 1‑3 years with M.Sc. degree.
- Demonstrated progressive inspection and testing responsibilities in a laboratory setting.
- Experience working in QC laboratories and manufacturing clean rooms.
- Inspection and testing experience within a GMP or ISO 9001 and ISO 13485 environment.
- Knowledge of commonly used concepts, practices, and procedures within a QC environment.
- Basic knowledge & understanding of sampling techniques (ANSI/ASQC Z1.4‑2003).
Skills
- Excellent writing, editing and proofing skills.
- Proficient using MS Word, Excel and Outlook.
Benefits
- Competitive compensation package.
- Comprehensive health and welfare benefits.
- Opportunity to grow and develop.
- Purpose‑led, performance‑driven corporate culture that values people and planet.
- Chance to work on growing brands and build on a strong foundation.
- Opportunity to make improvements and make an impact on the business.
- Annual incentive pay.
- Retirement savings plan.
- Health care coverage.
- Paid time off.
- Recognition programs.
- Broad range of other benefits.
Pay
Salary: $50,000.00 - $70,000.00.