Analytical Chemist (cGMP) — Method Dev & Validation

PMRS; Horsham (PA); On-site; USD 65,000 - 90,000; Full time

Job summary

PMRS is seeking skilled laboratory professionals to support analytical testing in a cGMP environment. You will work with HPLC/UHPLC, conduct method development and validation, and ensure compliance with USP, ICH, and CFR guidelines.

Collaboration with cross-functional teams is essential for meeting client and regulatory deadlines. The role involves maintaining instruments, preparing regulatory documentation, and contributing to continuous improvement in a fast-paced lab setting.

Qualifications

• Bachelor's Degree in chemistry from an accredited US college or university.
• Experience in a lab is preferred but not required.
• Background and Credit Check required as part of the hiring process.

Responsibilities

• Perform analytical tests on raw materials, in-process materials, stability, and finished products.
• Schedule and calibrate equipment; maintain lab instruments and inventory.
• Develop and validate analytical methods; adhere to SOPs in a cGMP environment.
• Prepare documentation for product license applications/regulatory filings.
• Collaborate with cross-functional teams and communicate progress to meet deadlines.
• Train employees in lab techniques and cGMP procedures.

Skills

Analytical instrumentation

HPLC/UHPLC

Method development/validation

cGMP compliance

Liaising with customers/suppliers

Regulatory knowledge (USP/ICH/CFR)

Laboratory maintenance

Prioritization & time management

Education

Bachelor's Degree in chemistry

Tools

LIMS

TrackWise

OpenLAB

Excel

Word

Job description

PMRS is seeking skilled laboratory professionals to support analytical testing in a cGMP environment. You will work with HPLC/UHPLC, conduct method development and validation, and ensure compliance with USP, ICH, and CFR guidelines.

Collaboration with cross-functional teams is essential for meeting client and regulatory deadlines. The role involves maintaining instruments, preparing regulatory documentation, and contributing to continuous improvement in a fast-paced lab setting.