Laboratory Technician

Position: Quality Control Analyst

Work Location: Netherlands (Must be ready to Commute or Relocate to Bilthovan, Netherlands)

Note: Freshers can apply from a chemistry background...

Responsibilities:

Analytical Testing:

• Perform routine and non-routine analysis of raw materials, intermediates, and finished products using analytical techniques.
• Conduct assays, HPLC, GC, and other tests according to established protocols and procedures.

Documentation and Reporting:

• Maintain accurate and detailed records of all testing activities.
• Prepare and review documentation, including test procedures, protocols, and analytical reports.

Instrumentation:

• Operate and maintain analytical instruments, including but not limited to HPLC, GC, and dissolution apparatus.
• Troubleshoot and calibrate instruments as needed.

Quality Compliance:

• Ensure compliance with cGMP regulations and Company Pharma's quality standards.
• Participate in internal and external audits as required.

Method Validation:

• Assist in method development, validation, and transfer activities.
• Collaborate with the R&D and QA teams to implement new testing methods.

Requirements:

Education:

• Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.

Experience:

• 0- 3 years of experience in a pharmaceutical QC laboratory setting.

Analytical Skills:

• Proficient in various analytical techniques, including HPLC, GC, and wet chemistry methods.

Documentation Skills:

• Strong documentation and record-keeping skills.

Regulatory Knowledge:

• Familiarity with cGMP regulations and quality standards.

Communication:

• Effective communication skills and the ability to work in a collaborative team environment.

Benefits:

1. Competitive salary based on experience.
2. Comprehensive health and wellness benefits.
3. Opportunities for professional development and training.
4. Positive and inclusive work culture.