Laboratory Equipment Validation Specialist
3 weken geleden
About the Opportunity
The Quality Analytical Laboratory at Teva Pharmaceuticals is responsible for analytical testing, including APIs, excipients, packaging materials, and drug products, to ensure quality and consistency in production. To expand this responsibility, we are looking for an Equipment Qualification Engineer to join our team.
Key Responsibilities
- Assess, qualify, and implement high-end laboratory equipment, such as GC, UPLC/HPLC, FT-IR, and UV-VIS, ensuring compliance with regulatory requirements.
- Determine priorities and manage project execution across multiple departments.
- Oversee the timely completion of validation documentation, including contractor activities.
- Present project status to stakeholders and senior management.
- Develop training instructions, calibration procedures, operational manuals, equipment specifications, and reports.
Requirements
- Minimum HBO in chemistry or related field.
- Organizational capabilities and experience with scientific analytical approaches.
- Good knowledge of laboratory equipment and experience in calibration, qualification, and validation.
- 4-5 years of experience in the Pharmaceutical industry or equivalent GMP environment, with at least 1 year of experience in laboratory equipment validation.
- Team player with sound communication skills and proactive approach.
- Excellent English writing skills.
Pre-Employment Screening
Teva Pharmaceuticals will conduct pre-employment screening and verification prior to the confirmation of any offer of employment.
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