Quality Control Analytical Chemist I
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Job Location:
Torrance, CA - USA
Monthly Salary:
$ 26 - 29
Posted on:
15 hours ago
Vacancies:
1 Vacancy
Job Summary
QC Analytical Chemist I - Torrance California
Rate: $26.00 to $29.00
Analyzes raw material compounds bulk and finished goods 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.
Follows established procedures and documents all findings and results timely concisely clearly and accurately.
Prepares standards and specifications for processes facilities products and tests.
Provide updates/escalations at daily and weekly site-specific and cross-site meetings.
Aids in root cause analyses and corrective/preventive action (CAPA) initiatives related to quality issues including product Out-of-Specifications deviations and consumer complaints.
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.
Collaborate with cross-functional teams to support continuous improvement initiatives.
Assists in the development review writing and implementation of SOPs for quality functions to ensure compliance with all regulatory and GMP 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.
Assessment of GMP systems currently in place to ensure compliance and provides solutions to improve quality systems.
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.
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
May aid in monitoring and trending raw material in-process finished goods and stability data results
Preferred:
Demonstrated self-management skills including establishing direction and goals and building good work ethics for the team
Experience with microbiological testing methods.
Qualifications:
Minimum 3 years of experiencein a QC Laboratory or regulated manufacturing environmentpreferred(cosmetics or OTC drugs a plus).
Bachelors degree in a scientific or technical field (e.g. Chemistry Biology Pharmaceutical Sciences).
Working knowledge and understanding of GMP FDA regulations and quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211).
Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits
Strong attention to detail and organizational skills.
Effective written and verbal communication skills.
Proficiency in Microsoft Office and familiarity with electronic quality systems is a plus.
Maintains an exemplary attendance and punctuality performance record.
Adheres to all Prime Personnel Policies as established by the company.
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.
Rate: $26.00 to $29.00
Analyzes raw material compounds bulk and finished goods 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.
Follows established procedures and documents all findings and results timely concisely clearly and accurately.
Prepares standards and specifications for processes facilities products and tests.
Provide updates/escalations at daily and weekly site-specific and cross-site meetings.
Aids in root cause analyses and corrective/preventive action (CAPA) initiatives related to quality issues including product Out-of-Specifications deviations and consumer complaints.
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.
Collaborate with cross-functional teams to support continuous improvement initiatives.
Assists in the development review writing and implementation of SOPs for quality functions to ensure compliance with all regulatory and GMP 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.
Assessment of GMP systems currently in place to ensure compliance and provides solutions to improve quality systems.
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.
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
May aid in monitoring and trending raw material in-process finished goods and stability data results
Preferred:
Demonstrated self-management skills including establishing direction and goals and building good work ethics for the team
Experience with microbiological testing methods.
Qualifications:
Minimum 3 years of experiencein a QC Laboratory or regulated manufacturing environmentpreferred(cosmetics or OTC drugs a plus).
Bachelors degree in a scientific or technical field (e.g. Chemistry Biology Pharmaceutical Sciences).
Working knowledge and understanding of GMP FDA regulations and quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211).
Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits
Strong attention to detail and organizational skills.
Effective written and verbal communication skills.
Proficiency in Microsoft Office and familiarity with electronic quality systems is a plus.
Maintains an exemplary attendance and punctuality performance record.
Adheres to all Prime Personnel Policies as established by the company.
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.
Required Experience:
Manager
About Company
Prime Matter Labs offers tailored product development and production, adapting and innovating along with your business.
