Quality Associate

Primary Talent Partners
Cleveland, MS Full Time | Contractor
POSTED ON 6/2/2023 CLOSED ON 1/9/2024

What are the responsibilities and job description for the Quality Associate position at Primary Talent Partners?

Primary Talent Partners has a 6-month contract opportunity for a Quality Associate with a multinational pharmaceutical and biotechnology company located in Cleveland, MS.

Job Description:

Responsible for providing Quality support to Quality Operations Management. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and quality practices.

Essential Duties and Responsibilities:

· Perform in-depth internal assessments and evaluations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude.

· Assessments and information gathering may be through in-depth employee interviews, flow charting and other informational gathering techniques.

· Determine the logic, adequacy and effectiveness of processes, systems and related requirements.

· Develop plans to correct identified risks including areas of non-conformance, inform management and implement approved corrective action plans.

· Write, review, analyze and revise written Standard Operating Procedures (SOPs) and submit procedural changes as needed to meet Corporate, Divisional, Plant, Regulatory Requirements, etc.

· Support external assessments or audits.

#PTPStandard

Qualifications:

· To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

· Strong interpersonal skills and great attention to detail are necessary.

· Must be a strong team player with good problem solving, and good verbal and written communication skills.

· Must have the ability to manage people, encourage teamwork and drive decisions.

· Must be able to handle multiple projects concurrently, have computer experience and have knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices as appropriate.

Education and/or Experience:

Associate degree in business/scientific discipline and one to three years of relevant experience

Job Types: Full-time, Contract

Pay: $25.00 per hour

Schedule:

  • 8 hour shift
  • Monday to Friday

Work setting:

  • In-person

Education:

  • Associate (Required)

Experience:

  • quality assesments: 1 year (Preferred)
  • Good Manufacturing Practices: 1 year (Preferred)
  • pharmaceutical/biotech industry: 1 year (Preferred)

Work Location: In person

Salary : $25

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