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Bristol-Myers Squibb is a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases.
One shared journey is moving us forward at Bristol-Myers Squibb. Around the world, we are passionate about making an impact on the lives of patients with serious disease. Empowered to apply our individual talents and ideas so that we can learn and grow together. Driven to make a difference, from innovative research to hands-on community support. Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives.
The position is in a dynamic, professional lab responsible for both aseptic and non–sterile manufacturing support of small molecules and biologics, and provides exciting opportunities to contribute to the development of drugs at the forefront of the industry. Among the responsibilities for the successful candidates. Responsible for the day to day operation of a GMP microbiology laboratory that supports sterile and non-sterile manufacture of clinical supplies.
An international pharmaceutical company is seeking a pharmaceutical microbiologist for an exciting position in a laboratory, supporting early and late phase clinical manufacturing. The position is in a dynamic, professional lab responsible for both aseptic and non–sterile manufacturing support of small molecules and biologics, and provides exciting opportunities to contribute to the development of drugs at the forefront of the industry.
Among the responsibilities for the successful candidates:
• Responsible for the day to day operation of a high sample load GMP pharmaceutical microbiology laboratory
• Management of a staff of 8 bacteriologists to support clinical manufacturing of parenteral and oral solid dose products
• Oversee training of the staff
• Responsible for assuring timely revision of SOP’s, and other procedural documents.
• Responsible for quality event investigations as they relate to laboratory operations as well as implementation of appropriate CAPA’s.
• Provides guidance and feedback to drug development teams and regulatory functions in responding to health authorities worldwide
• Interacts with IT groups to assure that electronic notebooks are functioning properly and to introduce new methods into the electronic notebook environment.
• Acquires, reviews and/or approves in GMP compliant manner, data related to methods development and testing of GMP and development materials.
• Supervision and training of junior personnel.
• Maintains data in electronic notebooks.
• Prepares reports for methods, validation, and technology transfer.
• Sustains up to date knowledge on applicable department and site standard practices related to GMP’s.
• Assists in purchase and implementation of new technology.
• Serves as a member of interdisciplinary departmental teams, providing scientific and operational input to development plans.
• Drafts responses and corrective actions to internal compliance questions related to their work.
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