Sr. Manager, Quality Operations (Onsite)
About The Position
Join Insulet's growing team and lead critical Quality Control operations that help deliver innovative, life-changing medical devices to patients around the world. As a Senior Manager, Quality Control, you'll oversee laboratory testing, validation, lot release, compliance, and continuous improvement initiatives while leading and developing a high-performing team in a fast-paced, highly automated manufacturing environment. This is an exciting opportunity for an experienced quality leader to drive operational excellence, collaborate across global teams, support FDA and ISO compliance efforts, and make a meaningful impact as Insulet continues its rapid growth and expansion.
Requirements
- BS degree in scientific discipline; and/or equivalent combination of education and experience
- Minimum of 10+ years’ experience of relevant experience in Quality Control / Quality Assurance
- Minimum 2+ years’ managerial experience in a manufacturing environment
- Must possess strong leadership, analytical and communication skills with team-focused attitude
- Experience leading or supporting FDA and ISO 13485 inspections preferred
- Highly effective leadership skills.
- Excellent interpersonal, verbal and written communication skills
- Problem Solver
- 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 as well as across global sites.
- Advanced PC skills, word processing, spreadsheet, and database
- Highly proficient with industry standards sampling plans (ANSI z1.4 & z1.9)
- Ability to prioritize objectives from multiple projects, adhere to scheduled timelines while maintaining flexibility and attention to detail
- Experience working in a highly automated/high volume manufacturing environment
- Lead and support a multi-shift operation
- CAPA Management to drive improvement
- Strong workflow management experience.
Responsibilities
- Manages various processes within the department (shift schedules, workflow, training, sample management, data review and reporting) and serves as subject matter expert (SME).
- Coordinates and facilities QC activities to meet commitments on-time.
- Ensure QC personnel have appropriate training.
- Leads planning, coordination and/or review of test method validations, test method transfers and/or equipment qualification/requalification
- Assist in troubleshooting of test methods and/or equipment as required
- Responsibility as global lead for Lot testing/qualification activities.
- Collaborate with other department leaders as appropriate.
- Authors, review, and/or approves data, SOPs, COAs, and DHRs
- Monitor, track and publish department metrics.
- Ensure all QC records and DHR documentation adhere to cGMP/GDP expectations
- Responsible for final lot release
- 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
- Serves as QC representative in cross-functional, cross-departmental working teams and/or working with outside vendors to meet all QC needs
- Participates in internal and external quality audits
- Recruit, coach, and develop organizational talent
- Perform other duties as assigned
Benefits
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- And additional employee wellness programs
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Manager
