Quality Control Analytical Chemist I

**QC Analytical Chemist I - Torrance, California

Rate: $26\.00 to $29\.00**

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Analyzes raw material compounds, bulk and finished goods to determine chemical and physical properties.

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Complete routine review of QC test data and related documents for in-process samples, finished goods and stability samples.

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Follows established procedures and documents all findings and results timely, concisely, clearly and accurately.

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Prepares standards and specifications for processes, facilities, products, and tests.

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Provide updates/escalations at daily and weekly site-specific and cross-site meetings.

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Aids in root cause analyses and corrective/preventive action (CAPA) initiatives related to quality issues, including product Out-of-Specifications, deviations and consumer complaints.

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Aids in improvements of the stability program, including initiating stability protocols, stability inventory schedules, stability pulls, ensuring timely testing of products, compiling stability reports, and trending data across the shelf-life of OTC products.

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Collaborate with cross-functional teams to support continuous improvement initiatives.

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Assists in the development, review, writing, and implementation of SOP's for quality functions to ensure compliance with all regulatory and GMP requirements.

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Experience with method development/qualification, tech transfer, QC testing, and laboratory deviations/investigations

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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.

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Assessment of GMP systems currently in place to ensure compliance and provides solutions to improve quality systems.

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Proficiency in MS Word, Excel, Power Point and other applications

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Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment

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Works with development of formulas, processes, and methods for solution of technical problems.

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Strives toward continuous self-improvement in personal productivity.

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Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities

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May aid in monitoring and trending raw material, in-process, finished goods and stability data results

Preferred:

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Demonstrated self-management skills, including establishing direction and goals, and building good work ethics for the team

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Experience with microbiological testing methods.

Qualifications:

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Minimum 3 years of experience in a QC Laboratory or regulated manufacturing environment preferred (cosmetics or OTC drugs a plus).

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Bachelor’s degree in a scientific or technical field (e.g., Chemistry, Biology, Pharmaceutical Sciences).

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Working knowledge and understanding of GMP, FDA regulations and quality systems, and regulatory requirements (21 CRF Part 11/ 210/ 211).

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Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits

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Strong attention to detail and organizational skills.

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Effective written and verbal communication skills.

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Proficiency in Microsoft Office and familiarity with electronic quality systems is a plus.

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Maintains an exemplary attendance and punctuality performance record.

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Adheres to all Prime Personnel Policies as established by the company

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What we are 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.