Technical Supervisor PC
On-siteMiami, Florida, United States
Job Summary
Direct manufacturing methods, processes, and operations for new or existing products while ensuring effective use of material, equipment, and personnel. Align staffing requirements with production schedules and adjust work plans to meet efficiency targets. Participate in troubleshooting to maintain quality, yields, and cycle times, and conduct investigations of non-conforming events using data and problem-solving skills. Interpret policies to enforce safety and compliance with environmental regulations, and audit areas for cGMP adherence. Train and certify employees on regulatory requirements, revise documentation as needed, and coordinate equipment repairs to minimize downtime. Motivate teams to achieve goals and represent the department in new product development efforts.
Required Qualifications
- Bachelor degree
- Minimum two (2) years of related work experience or training, within the pharmaceutical industry
- Equivalent work-related experience of (6) years
- Experience reading and interpreting production schedules
- Experience reading and interpreting SOPs
- Experience reading and interpreting cGMPs
- Experience reading and interpreting FDA guidelines
- Technical knowledge of the manufacturing environment
- Specific knowledge related to assigned department
- Basic understanding of engineering/scientific fundamentals that are applicable to area under supervision
- Flexibility to work different shifts/schedules
- Computer literacy with the ability to use various computer and related software programs to perform duties
- Ability to facilitate teams of exempt/non-exempt employees to audit work areas
- Ability to identify non-compliance of requirements
- Ability to develop/oversee action plans for corrective action
- Ability to lift and/or move at least 50 pounds
Desired Qualifications
- Experience within the pharmaceutical industry
- Knowledge with the various aspects of the Transdermal manufacturing
- Six-Sigma Green belt certification
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