Senior Quality Control Analyst – 3rd Shift - Piedmont, South Carolina United States - 36968



JOB DESCRIPTION

Job #: 36968
Title: Senior Quality Control Analyst – 3rd Shift
Job Location: Piedmont, South Carolina - United States
Employment Type:
Salary: contact recruiter for details
Employer Will Recruit From: Regional
Relocation Paid?: NO

WHY IS THIS A GREAT OPPORTUNITY?


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JOB DESCRIPTION

Senior Quality Control Analyst – 3rd Shift

SUMMARY:

Expand your professional portfolio as a Quality Control Analyst with our client in Piedmont, SC. As the Quality Control Analyst, you will be responsible for daily laboratory testing of raw materials, in process and finished products. You will also provide support for environmental testing, validation, stability and other various laboratory and production testing. This is a direct-hire opportunity.

REWARDS:

  • Competitive pay
  • Health benefits
  • Direct-hire opportunity

REQUIREMENTS:

  • B.S. in Chemistry or related scientific field 4+ years related experience or M.S. in Chemistry or related scientific field 2+ years related experience (preferred)
  • Must be able to work 3rd shift
  • Experience working in an ISO or FDA regulated environment preferred
  • Familiarity with Empower
  • Excellent communication skills, including the ability to speak clearly, listen and gain clarification, respond well to questions, and write clearly and informatively
  • Ability to deal with problems involving several concrete variables in standardized situations

RESPONSIBILITIES:

  • Perform chemical testing using analytical instrumentation including HPLC, GC, FTIR, UV-VIS, etc.
  • Assist in sampling of raw materials upon receipt, when needed
    • Aid in maintaining quick turnaround time of raw material release
  • Familiar with Quality GMP documentation (hard copy and electronic) of testing results and assurance of laboratory data integrity
  • Maintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs
  • Experience with USP interpretation and testing
  • Support QC audit readiness with understanding of FDA and ISO regulations and requirements
  • Support on-time performance in the QC lab against the Production and laboratory schedules
  • Assist with maintenance and troubleshooting of QC lab equipment to minimize downtime
  • Assist with OOS investigations
  • Employ sound and compliant laboratory techniques and logic per industry standards (e.g., FDA, USP/NF, ISO, ANSI) and internal and customer requirements
  • Troubleshoot laboratory instrumentation and administer simple repairs as needed
  • Review batch records to ensure they are compliant with SOPs, WIs, and cGMPs
  • Perform all other duties as assigned or needed

QUALIFICATIONS

REQUIREMENTS:

  • B.S. in Chemistry or related scientific field 4+ years related experience or M.S. in Chemistry or related scientific field 2+ years related experience (preferred)
  • Must be able to work 3rd shift
  • Experience working in an ISO or FDA regulated environment preferred
  • Familiarity with Empower
  • Excellent communication skills, including the ability to speak clearly, listen and gain clarification, respond well to questions, and write clearly and informatively
  • Ability to deal with problems involving several concrete variables in standardized situations

Education:
University - Bachelor's Degree/3-4 Year Degree

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