Date Posted: 03/13/2026
Hiring Organization: Rose International
Position Number: 498343
Industry: Pharmaceutical/Healthcare
Job Title: Production Supervisor
Job Location: Menlo Park, CA, USA, 94025
Work Model: Onsite
Shift: 2nd Shift from 2:00 PM to 10:30 PM
Employment Type: Temporary
FT/PT: Full-Time
Estimated Duration (In months): 5
Min Hourly Rate($): 30.00
Max Hourly Rate($): 32.00
Must Have Skills/Attributes: Management, Manufacturing, Production Support
Experience Desired: Proven track record of supervising engineers/technicians and leading quality system projects (5+ yrs)
Required Minimum Education: Bachelor’s Degree
**C2C is not available**
Job Description
Required Education:
- Bachelor's Degree Required (Engineering, Life Sciences, or related field preferred)
Requirements:
- Minimum 5 years of quality experience in a regulated manufacturing environment
- Demonstrated initiative, problem-solving, and critical-thinking skills
- Demonstrated competency with financial systems and fiscal controls
- Strong technical knowledge of quality concepts, practices, and procedures
- Ability to work on complex problems involving multiple competing factors
- Experience with FDA, BSI, and EEO regulatory compliance
- Experience managing multiple concurrent projects
Overview: Abbott Laboratories is seeking a Production Supervisor (Lead Supervisor) to support Quality Systems within the Structural Heart business unit at the Menlo Park, CA facility. This role involves supervising engineers and technicians, leading medium-to-complex quality projects, ensuring regulatory compliance, and driving continuous improvement across quality systems and tools.
Responsibilities:
- Independently, or as a project team lead, identify, plan, and conduct medium-sized assigned projects with conventional and custom risk-managed execution plans
- Assist in developing direct reports through training, progressively challenging assignments, and formal performance reviews
- Lead complex technical projects with multiple inter-coordinating elements, applying new methods and considering system-wide impact
- Lead and/or participate in cross-functional teams to support organizational goals
- Complete documentation promptly and in accordance with business standards
- Serve as Subject Matter Expert (SME) or Independent Technical Expert (ITE); may interface with external firms or agencies
- Implement and maintain the effectiveness of the Quality System (FDA, BSI, EEO compliance)
- Monitor daily work operations and provide direction and guidance to exempt and non-exempt staff
- Interact regularly with internal and external customers; respond to requests and explain procedures
- Contribute to the development of operational policies and procedures
- Identify, develop, and implement processes to improve department performance
- Ensure sustaining support of the Quality System and regulatory compliance - **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
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I believe the best thing that Rose HR has going for it is the incredible responsiveness. Everyone is very quick to reply to any concerns, and contacts the contracted employees very quickly and efficiently.
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My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.
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I have been very pleased with my experience with Rose International. Everyone that I encountered was very helpful and courteous.
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