Sr. Supervisor, Production Operations
Kindeva Drug Delivery · St. Louis County, MO · Yesterday
On-siteManagementFull-time
About the role
Lead People. Deliver Excellence. Improve Lives.
Responsibilities
- Directly supervise production personnel and lead operators.
- Manage staffing, scheduling, attendance, vacations, and overtime.
- Interview, hire, onboard, train, coach, and develop employees.
- Conduct performance evaluations and administer corrective action when appropriate.
- Ensure employees maintain required qualifications and training.
- Lead daily communication meetings while promoting accountability, safety, quality, and continuous improvement.
- Support employee relations and labor relations activities, including union environments when applicable.
- Lead daily manufacturing operations and ensure production schedule attainment.
- Ensure compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), safety requirements, and regulatory expectations.
- Review production documentation and investigate deviations and quality events.
- Cookordinate activities with Quality, Engineering, Maintenance, Planning, and Supply Chain.
- Drive continuous improvement initiatives and operational excellence programs.
- Support audits of aseptic processes and supporting areas for accuracy.
- Perform other duties as assigned.
Qualifications
- Associate degree in a scientific, technical, manufacturing, business, engineering, or related field and a minimum of five (5) years of supervisory experience in a manufacturing environment; OR a minimum of twelve (12) years of supervisory experience in pharmaceutical operations in lieu of a degree.
- Effective written and verbal communication skills.
- Proficiency with Microsoft Office applications, Kronos, and Veeva.
- Demonstrated reading comprehension and writing proficiency with the ability to communicate effectively within a diverse workforce.
- Self-starter and team player with strong interpersonal and coaching skills.
- Proven record of problem-solving, decision-making, and application of process improvement tools.
- Regular onsite attendance is required.
- Able to simultaneously manage multiple priorities across multiple functions.
- Able to work effectively under strict production, quality, time, and performance deadlines.
- Able to work beyond normal business hours, including weekends and holidays, as business needs require.
Preferred Qualifications
- Pharmaceutical manufacturing experience.
- Experience working in regulated manufacturing environments.
- Union leadership experience.
Physical Requirements
- Ability to stand upright for several consecutive hours absent of any medical restrictions that would prevent completion of required duties.
- Ability to occasionally bend, stoop, squat, carry, and lift up to 50 pounds.
- Ability to stand for extended periods and frequently walk between production areas while supervising operations.
- Specific vision abilities include close vision, color vision, and the ability to adjust and focus.
- Ability to work near moving machinery, in varying temperature environments, and while wearing required personal protective equipment (PPE) in designated manufacturing areas.