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Senior Quality Control Chemist

Kindeva Drug Delivery
Los Angeles, CA Full Time
POSTED ON 2/11/2025
AVAILABLE BEFORE 5/11/2025

19901 Nordhoff St, Northridge, CA 91324, USA Req #1656

06 February 2025

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

This is an exciting opportunity as a Senior Quality Control Chemist to work with a cross-functional team. This individual will perform complex and routine analytical processes for the testing of in-process, finished product, and stability pharmaceutical products.

Role Responsibilities :

  • Leading safety initiatives and training while driving completion of new product and continuous improvement projects.
  • Prepare sample solutions, standards, and reagents.
  • Perform wet chemical and instrumental analysis, including FTIR, HPLC, UV Spectrophotometer, Dissolution, Instron, Texture Analyzer, and Gas Chromatography.
  • Perform 1 : 1 and group training with peers and cross-functional teams as necessary. Mentor other analysts on best lab practices, techniques, and instrument troubleshooting.
  • Meet multiple testing cycle time requirements through scheduling, testing, and documentation review.
  • Author, review, and update lab documentation such as SOPs, worksheets, specifications, and methods to reflect current processes.
  • Author, execute, and support qualification, calibration, and maintenance of quality control laboratory equipment.
  • Lead resolution of non-conformances and investigations in the quality control laboratory.
  • Ensure timely completion of CAPA.
  • Lead part of the introduction of new analytical techniques and equipment to the quality control laboratory.
  • Ability to work flexible hours as needed to support production demands.
  • Support the lab as a Subject Matter Expert on test methods, equipment, and / or processes.
  • Work in a safe manner, take responsibility for personal safety and the safety of others. Participate in Pro-active Safety (OTSS, S&A) and raise documentation for safety incidents as required (NMs & MIs). Complete safety training 100% OTIF.

Basic Qualifications :

  • Bachelor’s degree or higher in a science discipline from an accredited university, Chemistry preferred.
  • Minimum 7 years analytical testing experience.
  • Firm understanding of GMP / GLP.
  • Proficient in technical lab investigations.
  • Demonstrated strong oral and written communication skills.
  • Experience with various lab instruments such as GC and HPLC.
  • Kindeva Drug Delivery is an Equal Opportunity / Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state, or local law.

    Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

    The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and / or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits).

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