Packaging Supervisor
Title: Packaging Supervisor
Location: Tampa, FL
Industry: Pharmaceutical
Hours: 2nd shift, Monday-Friday, 3pm-11:30pm with possible weekends
Salary: Competitive industry compensation package and benefits (401k, health, vision/dental, eligibility for annual performance bonus)
Employment Type: Direct hire
Environment
This client is one of the world s leading suppliers to the pharmaceutical, biotech, and specialty ingredients markets. We create products that support a healthier lifestyle and enhance one s quality of life.
Summary
Supervises and directs all work activities in the packaging department, including production schedule, material exchange, personnel and processes. Work closely with other functions to ensure compliance with good manufacturing practices at all times.
Key Accountabilities- Provides work direction and leadership to ensure teams members are in compliance with processes, procedures and instructions for all activities on the shop floor.
- Manage the day-today operations and maintenance of all process and upkeep of the packaging facility.
- Review production schedule and provide inputs to Master Scheduler, batch records and quality events.
- Responsible for quality event investigations and documentation issues are resolved in a timely fashion.
- Responsible for hiring, coaching and performance management of employees.
- Provides on-the-floor training to support technical and cGMP training in addition to other related training.
- Responsible for purchases of indirect materials and overtime in support of the packaging department need.
- Communicate with key stakeholders such as Project Managers, QA, and other related functions.
- Adhere to all defined Safety and Sustainability requirements and expectations and seek clarification whenever Safety and Sustainability requirements and expectations are either unknown or unclear
- Promptly report identified Safety and Sustainability issues, problems, deficiencies, errors, incidents, and/or opportunities to management and correct where possible
- Stop work where deemed necessary to maintain safety
Qualifications:- Minimum high school diploma or GED, AS/AA or BS degree is preferred
- Minimum of 6 years' experience in a cGMP pharmaceutical setting, preferably with oral solid dosage.
- CMO (contract manufacturing organization) experience is highly preferred.
- Proven ability to lead and manage a team effectively in a manufacturing environment.
- Strong knowledge of good manufacturing practices and regulatory requirements.
- Outstanding communication and problem-solving skills to identify and address operational needs.
- Ability to work overtime and be hands-on as needed.
ADA/EOE
IND123
SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model partnering closely with clients to understand not only the role, but the company s culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.
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The Staffing Resource Group, Inc