Production - COMPLIANCE SPECIALIST
Omni Inclusive
Compliance Specialist
Location: Devens, MA Local Candidates Only *There are 2 openings for this role*
Top Must Haves:
- 1-3 years of experience in investigations and a Bachelor's Degree
Major Duties and Responsibilities:
- Conducts and manages resolution of deviations, root cause investigations, impact assessments and CAPAs as a Lead Investigator
- Liaises with many different groups/organizations as a Lead Investigator
- Proactively identifies and facilitates resolution of obstacles to timely completion
- Proactively manages progression of investigation and CAPA to timely closure
- Leads and participates in cross-functional investigation teams
- Presents investigation findings to key stakeholders and site management
- Uses Quality Risk Management and Operational Excellence principles to facilitate risk-based decision-making, drive continuous improvement, and eliminate waste
Knowledge and Skill:
- Required BS in chemical/biochemical engineering, biological sciences, or a related discipline with 1-3 years relevant experience
- Prior experience in leading cGMP investigations utilizing formal Root Cause Analysis tools preferred
- Demonstrated basic project management skills(organization, collaboration, multi-tasking and communication), attention to detail, and the ability to perform well in a team-based environment are required
- Excellent verbal & written communications skills, including ability to present information clearly and concisely
- Excellent interpersonal and collaboration skills necessary to interface with and influence all levels of the organization
- Prior experience with SOPs, cGMPs and the know how to work within a regulatory environment
- Prior experience in/Knowledge of cell culture, recovery, and/or purification biopharmaceutical manufacturing
Vacancy posted more than 2 months ago
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