GMP Analytical Chemist | HPLC Methods & Lab Ops (Irvine)

Actalent

Irvine (CA)

On-site

USD 71,000 - 83,000

Full time

10 days ago
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Benefits offered by this job

Dental and vision coverage
Sign-on bonus
PTO & holidays

Job summary

Actalent, based in Irvine, CA, seeks an Analytical Chemist to perform analytical testing in a GMP-regulated lab, contribute to method development/validation, and collaborate across Quality and Manufacturing to support product development and commercial activities.

The role emphasizes data integrity, accurate reporting, and maintaining compliant records with attention to detail in a fast-paced environment.

Qualifications

  • Bachelor's degree in Chemistry or related field.
  • 2–5+ years of analytical chemistry experience in GMP-regulated labs.
  • Hands-on experience operating HPLC systems.
  • Experience with analytical method validation or transfer.
  • Pharmaceutical industry experience in product development or manufacturing.
  • Strong knowledge of GMP documentation, data integrity, and record-keeping.
  • Ability to interpret analytical data and communicate results in reports.
  • Attention to detail and commitment to quality and compliance.

Responsibilities

  • Perform analytical testing using HPLC in a GMP environment.
  • Execute method validation, transfer, and troubleshooting activities.
  • Analyze and interpret laboratory data with accuracy and integrity.
  • Author and review analytical documents and reports.
  • Collaborate with Quality, Manufacturing, and cross-functional teams.
  • Maintain compliant laboratory records and adhere to GMP practices.
  • Support continuous improvement of methods and workflows.

Skills

HPLC operation
Analytical testing
Data analysis
GMP compliance
Cross-functional collaboration
Technical writing
Attention to detail

Education

Bachelor's degree in Chemistry

Job description

Actalent, based in Irvine, CA, seeks an Analytical Chemist to perform analytical testing in a GMP-regulated lab, contribute to method development/validation, and collaborate across Quality and Manufacturing to support product development and commercial activities.

The role emphasizes data integrity, accurate reporting, and maintaining compliant records with attention to detail in a fast-paced environment.

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