Jobs · Management · Missouri

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.

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