Jenny Osberg
Quality Leader M&A | Quality Systems | Ops Integration
- Role
- Sr Quality Manager, Acquisition Integration at Boston Scientific
- Location
- Minneapolis, MN, US
- LinkedIn followers
- 500 followers
About Jenny Osberg
As a transformational leader, Jenny connects each team member with a shared vision for the organization. Creating opportunities for learning and promoting growth within the organization, she encourages and challenges others to grow to their full potential.Mrs. Osberg is experienced with managing cross-functional relationships and building high performing teams. She is a results-oriented professional, highly collaborative and believes in strong partnerships. She values Lean Quality Engineering and Manufacturing along with Six Sigma Capabilities. She has experience with developing strategic marketing initiatives, new product introductions, quality operations, validation of utilities, facilities, and process equipment for pharmaceutical, biological, and medical device manufacturers. Her experience includes the creation and maturation of Quality Management Systems to meet requirements including 21 CFR 820 and ISO 13485. She has extensive knowledge in regulatory standards, risk management, process validation, cGMPs, global compliance and has lead efforts of compiling and assessing data for process optimization. Jenny also has experience in managing new facility cleanroom qualification as well as product and asset acquisition transfers.Jenny holds a B.S. in Chemical Engineering and also a Masters of Business Administration. She has experience in business development, marketing, management, product development, scale-up and commercialization, operations engineering, and project management.
Experience
Sr Quality Manager, Acquisition Integration
Nov 2021 — Present · Minneapolis, MN, US
Education
University of Oklahoma
Bachelor of Science, Chemical Engineering
University of St. Thomas
Master of Business Administration (M.B.A.), Business
Skills
- Product Transfer
- Supplier Quality
- Iso 14971
- Cqe
- Validation
- Process Validation
- Corrective and Preventive Action (Capa)
- 21 Cfr Part 11
- 21 Cfr
- Design Control
- Gamp
- Quality Auditing
- Spc
- Cleaning Validation
- Computer System Validation
- Fmea
- Change Control
- Minitab
- Dmaic
- New Product Qualification
- Quality System
- V&V
- Fda
- Quality Control
- Gmp
- U.s. Food and Drug Administration (Fda)
- Design of Experiments
- Medical Devices
- Capa
- Iso 13485
- Root Cause Analysis
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