
Manager, Quality Operations (Onsite - Acton, MA)
Job Description
Job Summary
Reporting directly to the Senior Director of Quality Operations, the Quality Operations Manager provides oversight of a variety of analytical functions that occur in the QC department supporting validation, testing, and reporting of in-process, pre and post sterile release, and Environmental monitoring samples. This role also ensures activities occur in an efficient and cGMP compliant manner. The role will have formal people management responsibilities.Job Title: Quality Operations Manager
Department: Quality
FLSA Status: Exempt
Position Overview:
Reporting directly to the Senior Director of Quality Operations, the Quality Operations Manager provides oversight of a variety of analytical functions that occur in the QC department supporting validation, testing, and reporting of in-process, pre and post sterile release, and Environmental monitoring samples. This role also ensures activities occur in an efficient and cGMP compliant manner. The role will have formal people management responsibilities.
Responsibilities:
- Manages various QC/QA program(s)/processes within the department (training, sample management, data review and reporting) and serves as subject matter expert (SME).
- Coordinates and facilities QC/QA activities to meet commitments on-time
- Ensure QC/QA personnel have appropriate training and competency
- Leads planning, coordination and/or review of test method validations, test method transfers and/or equipment qualification/requalification, as required
- Assist in troubleshooting of test methods and/or equipment as required
- Authors, review, and/or approves data, SOPs, COAs, DHRs and other documents as needed
- Monitor, track publish and report QC/QA metrics (NCMR, CAPA, etc.) at the Operations meetings. As necessary analyze QC/QA metrics to identify trends and actions necessary to correct adverse trends
- Ensure all QC/QA records and DHR documentation adhere to cGMP/GDP expectations
- Leads compliance related teams working towards the goal of continuous improvement
- May be required to lead NCMR, OOT investigations/deviations and to identify corrective actions to prevent reoccurrence
- Integral part of Plant Leadership team and serves as QC/QA representative in cross-functional, cross-departmental working teams
- Participates in internal and external quality audits
- Manage Supervisors and Technicians to ensure
- Recruits, coaches, and develops organizational talent
- Perform other duties as assigned
Education and Experience:
Minimum Requirements:
- BS degree in scientific discipline; and/or equivalent combination of education and experience
- Minimum of 8 years’ experience of relevant experience in Quality Control / Quality Assurance
- Minimum 2 years’ managerial experience
- Minimum 2 years’ experience in Operations Quality Management
- Must possess strong leadership and analytical skills with team-focused attitude
- Experience leading or supporting FDA and ISO 13485 inspections preferred
- Ability to prioritize objectives from multiple projects, adhere to scheduled timelines while maintaining flexibility and attention to detail
Preferred Skills/Competencies:
- Excellent interpersonal, verbal, and written communication skills
- Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities
- Ability to communicate and work effectively at multiple levels within the organization
- Advanced PC skill, word processing, spreadsheet, and database
NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite
Additional Information:
Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $110,900.00 - $166,325.00 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: • Medical, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) • And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education.Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!
At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.