Senior QC Chemist – cGMP/GLP Pharma Testing

ACTalent; Boca Raton (FL); On-site; USD 56,000 - 76,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

HSA available

Job summary

Actalent is seeking a Quality Control Chemist to support analytical testing, method validation, and regulatory compliance in a pharmaceutical manufacturing setting. The role ensures the quality and release of raw materials, in-process materials, packaging components, and finished products in a cGMP environment.

The ideal candidate has a bachelor’s degree in a related science and 5+ years of QC experience, with hands-on use of GC, FTIR, TOC, UV-Vis, and related instruments, and experience with

Qualifications

• Minimum 5 years of quality control experience in pharmaceutical manufacturing.
• Bachelor’s degree in Chemistry, Pharmaceutical Sciences, Microbiology, or related field.
• Hands-on experience with GC, FTIR, TOC, UV-Vis and other analytical instruments.

Responsibilities

• Perform analytical testing of raw materials, in-process samples, finished products, and materials.
• Develop and maintain specifications, test methods, SOPs, and documentation.
• Conduct method validations, transfers, and suitability studies.
• Investigate OOS/OOT, deviations, CAPAs, change controls, and quality risk assessments.
• Review data and approve Certificates of Analysis (COAs).
• Manage qualification, calibration, maintenance, and documentation of lab equipment.
• Support audits and maintain inspection readiness.
• Ensure data integrity, GMP/GLP compliance.

Skills

QC in pharma

Analytical testing

Regulatory compliance

Technical writing

Education

Bachelor's degree in Chemistry or related field

Tools

GC

FTIR

TOC

UV-Vis

LIMS

Job description

Actalent is seeking a Quality Control Chemist to support analytical testing, method validation, and regulatory compliance in a pharmaceutical manufacturing setting. The role ensures the quality and release of raw materials, in-process materials, packaging components, and finished products in a cGMP environment.

The ideal candidate has a bachelor’s degree in a related science and 5+ years of QC experience, with hands-on use of GC, FTIR, TOC, UV-Vis, and related instruments, and experience with