Sr. Specialist, QC Compliance

26 Mar 2024

Vacancy expired!

Minimum 5-8+ years of QC and/or QA experience in a pharmaceutical cGMP setting.B.S. degree in relevant scientific discipline.Excellent technical writing skills and experience authoring deviations, investigations, and procedures in a cGMP setting.Knowledge of relevant and current FDA, EU, ICH guidelines and regulations.Excellent ability to communicate in a scientifically sound and understandable manner.Demonstrated ability to prioritise, manage and complete multiple projects and tasks in a fast-paced environment effectively and independently.Ability to collaborate effectively in a dynamic, cross-functional matrix environment.Ability to navigate through ambiguity and rapid growth and adapt to change.Here’s What You’ll Bring to the Table (Preferred Qualifications)MS in a relevant scientific discipline with 2-5+ years QC and/or QA experience in a pharmaceutical cGMP setting.Previous experience in a laboratory compliance function within QC or QA.

  • ID: #49554868
  • State: Massachusetts Norwood 02062 Norwood USA
  • City: Norwood
  • Salary: Depends on Experience
  • Job type: Permanent
  • Showed: 2023-03-26
  • Deadline: 2023-05-13
  • Category: Science/biotech