Production - Manufacturing Supervisor - Inspection & Packaging

DUTIES & RESPONSIBILITIES Responsible for coordinating the Parenteral Inspection and Packaging operation efficiencies, labor utilization and expenses in the shift assuring compliance with applicable policies, regulations, and procedures. The incumbent must comply with Corporate and HR Policies and; FDA, GMP, Environmental Health and Safety goals program, objective and regulations and; with current Good Manufacturing Practices required by the job function.

1. Coordinates daily Parenteral Lyophilization manufacturing activities and resources allocation including manufacturing areas sanitization (controlled and non-controlled areas), components preparation and lyophilization activities.
2. Provides continuity to the operations as required.
3. Verifies all the manufacturing documentation and ensure it is completed and in compliance.
4. Provides coaching and feedback to employees which includes employee disciplinary investigations and execution of disciplinary actions when necessary as per Company Policies.
5. Facilitates the coordination of any manufacturing related activities with support areas (eg. Maintenance, QA/QC, TS, SC, etc.) to ensure flawless execution on processes, equipment evaluations, product transfer and other activities.
6. Assists the Associate Director and the support groups to solve any production technical problem (eg. Process / equipment troubleshooting, QE’s, CAPA’s, yield, cycle time, quality and productivity).
7. Performs administrative functions such as personnel performance appraisals and development action plans, vacation schedules and approval, attendance (Kronos) administration for payroll processing, personnel leave of absences administration, budget activities and projections etc.
8. lops and revise manufacturing schedule to assure that the manufacturing activities are executed according with the production plans.
9. Provides alternatives and recommendations to improve and maximize processes and equipments.
10. Drives the decision making process balancing risks and benefits.
11. Promotes and model the BMS Core Behaviors, facilitating teamwork, providing coaching and feedback etc.
12. Supports all site Initiatives and any other assignments based on business needs.

MINIMUM REQUIREMENTS • BS Degree in Science and/or Engineering • Three (3) years supervisory experience in the Pharmaceutical Industry • Proven experience in aseptic areas maintenance (sanitization) is a must • Ability to interpret and analyze statistical data. • Knowledge in CGMP’s, OSHA, EPA and other regulatory standards • Knowledge of computers applications (Microsoft Word, Excel, Power Point) • Strong Supervisory skills • Excellent interpersonal skills and team work oriented • Excellent communications skills in Spanish /English • Capability to engage people

Weil Group is proud to be an Equal Employment Opportunity Employer.