Artech Information System LLC Verified 9d ago
Lead Quality Investigator
Andover, MA, United States On-site
Salary not listedPaySalary not listed
TypeContract
Work settingOn-site
Verified listing
JobFig found this opening at its original source and checks that it remains available.
About the role
The Andover Site Operations Management group is looking for an individual to fill a Lead Investigator position within the Andover Site Investigations group. The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture.
What you'll bring
- A BS or MS
- A minimum qualifications to BS + 4-6 yrs experience or MS + 2-4 yrs experience in a pharmaceutical and/or biological manufacturing operation with a strong technical background in a cGMP and Quality environment is required.
- The incumbent must be a collaborative team player with strong coordination, facilitation and writing skills
- The Andover Site Operations Management group is looking for an individual to fill a Lead Investigator position within the Andover Site Investigations group.
- The Andover Site Investigation group is responsible for overseeing investigations for all GMP manufacturing suites in Andover, including both mammalian and bacterial based processes in support of commercial and clinical Drug Substance manufacture.
- This position will report to the Manager of Investigations within the Site Operations Management Function.
- Prior experience with investigations including conducting and writing investigations and in use of continuous improve methodology preferred.
- preferably in a scientific or engineering discipline preferable.