The Company
One of the global leaders in generics and biopharmaceuticals, improving the lives of millions worldwide. They provide a full spectrum of products, from generic medicines, pharmaceutical raw materials & over-the-counter medicines. With a portfolio of more than 3,500 medicines, they can produce approximately 120 billion tablets & capsules per year.
 
Job Description
The Quality Analytical Laboratory is responsible for all analytical testing to support the production of Cytotoxic and Inhalation drug products. The laboratory executes a wide variety of analytical test packages to test APIs, excipients, packaging materials and drug products for release and stability purposes. The department is also responsible for transfer, validation and verification of analytical methods for testing of new drug products.

Responsibilities
• Assessing, qualification (incl. validation) and implementation of sophisticated high-end (computerized) Laboratory equipment.
• Determine priorities within own project, while keeping track of project execution across multiple departments.
• Oversees the timely completion of all validation documentation, including coordination of contractor activities.
• Present project status to stakeholders and (senior) management.
• Write training instructions, calibration, maintenance , operational procedures, equipment specification files and reports.
 
Requirements
• A minimum of HBO in chemistry or related field.
• Organizational capabilities is part of your nature.
• Experience with scientific analytical approaches.
• Good knowledge of laboratory equipment with experience in calibration, qualification and validation.
• Experience in the Pharmaceutical industry or an equivalent GMP environment for 4-5 years with at least 1 year experience on validation of laboratory equipment, commissioning and de-commissioning.
• Team player with sound communication skills and pro-active approach.
• Experience with writing required documents in English.
 
Other information
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