GLP QC Analyst: Lab Compliance & Stability

Cipla Holding B.V.; Bilthoven; On-site; EUR 38,000 - 54,000; Full time

Job summary

Cipla Holding B.V. in the Netherlands seeks a Quality Control Analyst to execute routine QC operations and stability studies, ensuring compliance with GLP guidelines and regulatory requirements.

Responsibilities include maintaining lab areas, reviewing intimation and specifications, calibrating instruments, using valid reagents and glassware, and documenting results in the data sheets as per procedures.

Qualifications

• Experience with GLP and QC testing per pharmaceutical standards.
• Maintaining laboratory areas and following safety precautions.
• Ability to analyze finished product and review documents.
• Knowledge of instrument calibration and use of reagents and glassware.
• Follow specifications and documentation practices per cGLP.

Responsibilities

• Ensure compliance with cGLP per QC procedures.
• Maintain laboratory work areas.
• Follow safety precautions in the lab.
• Analyze finished product.
• Review intimation documents for details and match with sample specs.
• Read relevant specifications and organize work to meet testing timelines.
• Be aware of potential issues affecting accuracy and take corrective actions.
• Ensure instruments/equipment meet performance specs and are calibrated.
• Use valid reagents and clean glassware for analysis.
• Follow instructions for preparation of solutions and testing per spec.
• Record data accurately and ensure proper data entry and validation.

Skills

Quality control

GLP compliance

Laboratory safety

Education

M. Sc, B. Pharm, M. Pharm

Tools

HPLC

Job description

Cipla Holding B.V. in the Netherlands seeks a Quality Control Analyst to execute routine QC operations and stability studies, ensuring compliance with GLP guidelines and regulatory requirements.

Responsibilities include maintaining lab areas, reviewing intimation and specifications, calibrating instruments, using valid reagents and glassware, and documenting results in the data sheets as per procedures.