Requisition ID 15337BR
Title Senior Manager, Quality Control
Job Category Management
Job Description Position Purpose:
Direct and coordinate the activities of Quality Control organizations to support the production of insulin products and devices through testing programs which meet or exceed business, regulatory, and customer requirements in accordance with the Novo Nordisk Way. Overall responsibility for Chemistry, Microbiology, Physical Testing and EM testing, equipment, personnel, facilities, and budget.
Education: Bachelor’s Degree in Chemistry, Microbiology or related field
Experience:
7-10+ years of laboratory experience in the pharmaceutical industry or related field
3+ years supervisory experience.
3 + years experience in Sterile Product Quality Assurance with a demonstrable knowledge base in Sterile Product cGMP’s and knowledge of Aseptic Production to include environmental monitoring
Experience training others to perform laboratory work
Experience with method validation and/or method transfer
Experience leading or managing projects
Technical/Process/Functional Knowledge:
Working knowledge of GMPs and compendial requirements (USP/EP/JP)
Demonstrated ability to write technical and scientific documents and reports
Demonstrated ability to present technical and scientific information to others
Ability to willingly work with customers in a cooperative manner.
Department Quality Control
Position Location US - Clayton, NC
City Clayton
State/Provinces US - NC
Degree Required Bachelor's Degree Required
Percent Travel 10 - 20%
Title Senior Manager, Quality Control
Job Category Management
Job Description Position Purpose:
Direct and coordinate the activities of Quality Control organizations to support the production of insulin products and devices through testing programs which meet or exceed business, regulatory, and customer requirements in accordance with the Novo Nordisk Way. Overall responsibility for Chemistry, Microbiology, Physical Testing and EM testing, equipment, personnel, facilities, and budget.
Education: Bachelor’s Degree in Chemistry, Microbiology or related field
Experience:
7-10+ years of laboratory experience in the pharmaceutical industry or related field
3+ years supervisory experience.
3 + years experience in Sterile Product Quality Assurance with a demonstrable knowledge base in Sterile Product cGMP’s and knowledge of Aseptic Production to include environmental monitoring
Experience training others to perform laboratory work
Experience with method validation and/or method transfer
Experience leading or managing projects
Technical/Process/Functional Knowledge:
Working knowledge of GMPs and compendial requirements (USP/EP/JP)
Demonstrated ability to write technical and scientific documents and reports
Demonstrated ability to present technical and scientific information to others
Ability to willingly work with customers in a cooperative manner.
Department Quality Control
Position Location US - Clayton, NC
City Clayton
State/Provinces US - NC
Degree Required Bachelor's Degree Required
Percent Travel 10 - 20%
