
Senior Validation Specialist
1 week ago
Ensure quality oversight for validation, qualification, and equipment replacement projects within manufacturing environments. Review and approve acceptance test protocols and reports in line with applicable procedures and standards. Collaborate with cross-functional teams to organize, plan, and ensure efficient execution of qualification activities.
">About You
Candidates should have experience with process validation methodologies (IQ, OQ, PQ), New Product Introduction (NPI) and technology transfers across manufacturing sites, and knowledge of cGMP, GAMP, and relevant regulatory requirements.
Strong analytical skills are required, along with an understanding of quality risk management principles and validation lifecycle.
A Bachelor's degree in Pharmaceutical Engineering, Life Sciences, or a related field is necessary.
Gaining experience with CIP/SIP, Autoclave, and buffer preparation processes will be advantageous.
This role involves leading and managing the product transfer process for new product introductions (NPI) and site-to-site technology transfers. It also requires continuous improvement of validation practices and documentation.
About UsWe are committed to providing a comprehensive benefits package that supports the well-being and development of our employees.
The successful candidate will receive training and development opportunities to enhance their skills and knowledge.
Our company is dedicated to fostering a culture of innovation, collaboration, and excellence.
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