QA Lead, Quality Systems - Cell Therapy (GMP)

Cellipont

Research Forest (TX)

On-site

USD 90,000 - 115,000

Full time

14 days+
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Benefits offered by this job

401K strong employer match
Tuition Reimbursement
Flexible work schedules
Employee Referral Bonuses

Job summary

Cellipont in Research Forest is seeking a QA Lead for Quality Systems to ensure compliance with Good Manufacturing Practices (GMP). This role includes supervising the Quality Management System and leading cross-functional teams.

The ideal candidate will have a BS in Life Sciences, at least 8 years of experience in the biopharmaceutical industry, and a strong background in quality assurance. The position offers a competitive benefits package and opportunities for growth.

Qualifications

  • Minimum 8 years of experience in a regulated pharmaceutical industry.
  • At least 6 years of experience in a Quality Assurance position with a focus on QMS.
  • Strong familiarity with GMP processes within the pharmaceutical industry.

Responsibilities

  • Key contact for QMS including Deviations, CAPAs, Effectiveness Checks, and Change Controls.
  • Generate monthly and annual compliance metrics for the site.
  • Perform internal audits of manufacturing and support areas.

Skills

Strong technical and quality background
Ability to apply scientific and regulatory principles
Excellent communication skills

Education

BS in a Life Sciences discipline

Job description

Cellipont in Research Forest is seeking a QA Lead for Quality Systems to ensure compliance with Good Manufacturing Practices (GMP). This role includes supervising the Quality Management System and leading cross-functional teams.

The ideal candidate will have a BS in Life Sciences, at least 8 years of experience in the biopharmaceutical industry, and a strong background in quality assurance. The position offers a competitive benefits package and opportunities for growth.

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