Senior Technician Analytical QC

dsm-firmenich•Exton, PA

1d•$50,000 - $70,000•Onsite

About The Position

The Senior Technician Analytical QC supports the accurate and timely testing and inspection of current products 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.

Requirements

Associates 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)
Must have excellent writing, editing and proofing skills
Proficient using MS Word, Excel and Outlook

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 9001and/or 13485 standards.
Performs OOS investigations with oversite from the Supervisor.

Benefits

A competitive compensation package, with comprehensive health and welfare benefits
A place to grow and develop.
A company that is purpose-led and performance-driven in a corporate culture that values people and planet.
The opportunity to work on growing brands and build on a strong foundation.
The chance to make improvements and make an impact on the business.
annual incentive pay
a retirement savings plan
health care coverage
paid time off
recognition programs