QC Analytical Chemist: GMP, Method Transfer & Validation

Jubilant Pharma, LLC; Pennsylvania; On-site; USD 75,000 - 110,000; Full time

Job summary

Jubilant Radiopharma is seeking an experienced Analytical Chemist for a 12-month temporary role in our Quality Control laboratory. The role focuses on analytical method transfer, qualification, validation, and continuous improvement to meet GMP and regulatory standards.

The ideal candidate holds a Chemistry/Biochemistry degree, 7+ years in pharma analytics, and hands-on experience with HPLC, GC, LCMS, and related instrumentation, along with strong technical writing and data governance skills.

Qualifications

• Bachelor’s degree in Chemistry or Biochemistry is required.
• GMP, pharmacopoeias (USP, Ph. Eur., BP) knowledge is essential.
• Experience in analytical method qualification (transfer, verification, validation) is required.

Responsibilities

• Execute analytical method transfers in the QC lab.
• Qualify compendial methods, processes, and equipment.
• Analyze samples from validations, batches, and transfers.
• Review and optimize analytical methods and SOPs.
• Develop and maintain laboratory procedures and instructions.
• Train team members on new methods, equipment, and software.
• Prepare analytical validation protocols and reports.
• Ensure calibration and qualification documentation integrity.

Skills

Regulatory compliance

Data integrity & governance

Technical writing

Cross-functional collaboration

Education

Bachelor’s degree in Chemistry or Biochemistry

Member of Ordre des chimistes du Québec

Tools

HPLC

GC

LCMS

Spectrophotometry

Infrared spectroscopy

Titration

Wet chemistry

AAS

TrackWise

SAP

Job description

Jubilant Radiopharma is seeking an experienced Analytical Chemist for a 12-month temporary role in our Quality Control laboratory. The role focuses on analytical method transfer, qualification, validation, and continuous improvement to meet GMP and regulatory standards.

The ideal candidate holds a Chemistry/Biochemistry degree, 7+ years in pharma analytics, and hands-on experience with HPLC, GC, LCMS, and related instrumentation, along with strong technical writing and data governance skills.