QC Analytical Chemist- Torrance, California

Prime Matter Labs • Torrance, CA

60d • $32 - $35

About The Position

QC Analytical Chemist- Torrance, California Rate: $32.00 to $35.00 Analyzes Raw Materials, In-Process Samples and Finished Goods Includes the following: Other duties may be assigned. Analyzes compounds to determine chemical and physical properties. Complete routine review of QC test data and related documents for in-process samples, finished goods and stability samples. Monitor and trend QC data results Follows established procedures and documents all findings and results timely, concisely, clearly and accurately. Prepares standards and specifications for processes, facilities, products, and tests. Measures products for compliance to standards and specifications and reports same. Provide updates/escalations at daily and weekly site-specific and cross-site meetings. Experience with method development/qualification, tech transfer, QC testing, and laboratory deviations/investigations Experience with analytical testing methods (organoleptic, viscosity, pH, moisture, specific gravity, titration assays, FTIR) in cosmetic and OTC manufacturing environment to support QC testing, data reviews, & COA generation to support testing and release. Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211). Knowledge of regulatory requirements for data integrity and practices. Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits Assessment of GMP systems currently in place to ensure compliance. Proficiency in MS Word, Excel, Power Point and other applications Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment Works with development of formulas, processes, and methods for solution of technical problems. Provides input to the development of procedures. Strives toward continuous self-improvement in personal productivity. Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities A minimum of 3 years' experience and BS or BA. What we're offering: ●Competitive compensation package. ●Health, dental, and vision benefits. ●401K program. ●The spirit of a startup with the security of an established, profitable industry leader. ●The opportunity to make waves in a $250B industry. At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer.

Requirements

• Experience with method development/qualification, tech transfer, QC testing, and laboratory deviations/investigations
• Experience with analytical testing methods (organoleptic, viscosity, pH, moisture, specific gravity, titration assays, FTIR) in cosmetic and OTC manufacturing environment to support QC testing, data reviews, & COA generation to support testing and release.
• Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211). Knowledge of regulatory requirements for data integrity and practices.
• Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits
• Proficiency in MS Word, Excel, Power Point and other applications
• Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
• Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities
• A minimum of 3 years' experience and BS or BA.

Nice To Haves

• Demonstrated leadership and management skills, including establishing direction and goals, and building good work ethics for the team
• Supervising/managing experience.
• Experience with microbiological testing methods.

Responsibilities

• Analyzes compounds to determine chemical and physical properties.
• Complete routine review of QC test data and related documents for in-process samples, finished goods and stability samples.
• Monitor and trend QC data results
• Follows established procedures and documents all findings and results timely, concisely, clearly and accurately.
• Prepares standards and specifications for processes, facilities, products, and tests.
• Measures products for compliance to standards and specifications and reports same.
• Provide updates/escalations at daily and weekly site-specific and cross-site meetings.
• Assessment of GMP systems currently in place to ensure compliance.
• Works with development of formulas, processes, and methods for solution of technical problems.
• Provides input to the development of procedures.
• Strives toward continuous self-improvement in personal productivity.

Benefits

• Competitive compensation package.
• Health, dental, and vision benefits.
• 401K program.
• The spirit of a startup with the security of an established, profitable industry leader.
• The opportunity to make waves in a $250B industry.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Chemical Manufacturing
• Number of Employees: 101-250 employees