Specialist, Quality Control

Job Description

Our Quality Assurance group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements.  Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.

Specialist, Technician Biologist | Quality Control with In Vivo Release Testing (IRT) in our Manufacturing Division, Quality Laboratory Operations Team.

Position Responsibilities:

• This role will perform testing in support of releasing vaccines to market. 
• Work is on site, task-oriented, of moderate complexity, and is assigned, monitored, and directed by area management or designee. 
• Support IRT activities with the execution of general operational tasks, which may be associated with facilities, scheduling, assembly, coordination, delivery, and maintenance of study or program-related information. 
• Conduct laboratory procedures in compliance with established testing methods/protocols/sops. 
• Document study data in technical notebooks or approved electronic files.
• Review and entry of data in validated systems.
• Support during audits and inspections.
• Rotating holidays and weekend Saturday, Sunday work.

Education Minimum Requirement

• Bachelor degree in biological sciences or a related field.

Required Experience and Skills 

• Rodent handling and dosing techniques.
• Rodent observations of physical signs, differentiating and understanding normal rodent demeanor and appearance.
• Rodent gross examinations and necropsy.

Preferred Experience and Skills

• Intraperitoneal (IP) and intracranial (IC) routes intramuscular (IM), intravenous (IV), and subcutaneous (SQ) routes of administration.
• Familiarity working with and/or around BSL2 materials.
• Working in an GMP and/or GLP setting.
• Effective computer, scientific, organizational, and documentation skills.
• Excellent interpersonal and communication (verbal and written) skills and attention to detail.
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.

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We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues t