Specialist Clinical Supplies Quality Assurance
We are seeking a skilled professional to fill the role of Specialist Clinical Supplies Quality Assurance. This position is critical in maintaining the global clinical supply chain via disposition activities for sourced drug product.
This position reports to the Associate Director Clinical Supplies Quality (Disposition Lead) and is key to ensuring the integrity of our products. The Specialist Clinical Supplies Quality Assurance will be responsible for evaluating and disposing of clinical supply materials, ensuring they meet all applicable policies and procedures of our organization and comply with governing regulations.
* Evaluate and dispose of clinical supply materials to ensure conformance to company policies and compliance with regulatory requirements.
* Serve as the point of contact for Sourced Drug Product releases and Shelf-Life Extensions, both ongoing projects and new initiatives.
* Provide support and coordination for quality control laboratory activities related to Sourced Drug Product testing.
This role requires a strong understanding of current Good Manufacturing Practices (cGMPs) and regulatory requirements as they apply to the pharmaceutical field or a related area. The successful candidate will have experience in batch disposition, reviewing and approving investigations, deviation management support, and Corrective/Preventative Actions (CAPAs).
Requirements:
* Bachelor's degree with a technical emphasis in an appropriate scientific or engineering or other closely related field required.
* Minimum of 3 years' experience in the pharmaceutical or equivalent industry Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations.
* Familiarity with batch disposition (release) activities is a strongly preferred skill necessary for success in this position; prior batch disposition experience is a plus.
About Us:
We are a research-driven biopharmaceutical company dedicated to delivering innovative health solutions and advancing the prevention and treatment of diseases that threaten people and animals around the world.
Our Commitment:
We are committed to fostering an inclusive and diverse workplace where employees can grow and develop their careers. We believe that diverse ideas come together in an inclusive environment to drive breakthrough innovation.
Contact Information:
Please submit your application through our website.
* Job Title: Specialist Clinical Supplies Quality Assurance
* Salary: Competitive
* Employment Type: Full-Time
* Location: Switzerland
* Language: English
* Education: Bachelor's degree with a technical emphasis in an appropriate scientific or engineering or other closely related field
* Experience: Minimum of 3 years' experience in the pharmaceutical or equivalent industry Good Manufacturing Practice (GMP) related field including Technical, Engineering, Quality or Operations
We offer a comprehensive benefits package, including medical, dental, and vision insurance, a 401(k) plan, paid time off, and more.
About Our Company:
We are a leader in the pharmaceutical industry, with a presence in Switzerland since 1963. Our company has a regional office and manufacturing/packaging facility in Lucerne, with approximately 1,000 employees working collaboratively across four locations.
Why Work Here:
At our company, you'll have the opportunity to work with a talented team of professionals who share a passion for making a difference in people's lives. We offer a dynamic and inclusive work environment that fosters growth, development, and innovation.
Equal Opportunity Employer:
We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace where employees can grow and develop their careers.