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Simtra BioPharma Solutions

Sterile injectable drug manufacturing

Manufacturing Supervisor - Weekend PM

Machine & Process OperationConfirmed live in the last 24 hours
Full-timeBloomington, IN, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or GED is required.
  • At least two years of manufacturing or operations support experience is required.
  • At least one year of leadership experience is required.
  • Computer proficiency in Microsoft Word, Excel, and Outlook, and the ability to use enterprise software such as Microsoft Dynamics, Veeva, Power BI, or TrackWise.
  • Ability to stand or sit for extended periods.
  • Ability to lift up to 50 pounds.
  • Ability to push or pull heavy wheeled objects, such as tanks, carts, and pallet jacks.
  • Ability to perform overhead work, such as sanitizing walls and ceilings.
  • Physical coordination and flexibility to gown for clean room environments.
  • Ability to use applicable personal protective equipment, including safety shoes or toe caps, gloves, eye protection, heat-resistant wear, and hearing protection.
  • Dexterity and physical condition to perform repetitive-motion tasks.
  • Ability to wear a respirator when the product or task requires it.
  • Eyesight sufficient to inspect equipment and filled units; corrective lenses are acceptable.
  • Ability to use hands and fingers to manipulate office equipment.
  • Ability to qualify for gowning in Grade A/B filling areas.

Responsibilities

  • Understand, follow, coach, and lead teams to execute production activities in accordance with current Good Manufacturing Practices.
  • Provide guidance, support, direction, and leadership through positive interactions with personnel during daily operations.
  • Interview, hire, mentor, and develop staff; conduct annual performance reviews for direct reports; and assist in setting performance objectives and development plans.
  • Supervise day-to-day production, scheduling, staffing, material management, compliance, training, and auditing activities to meet customer deadlines and quality standards, with a high level of shop-floor presence.
  • Review, approve, and manage batch and system record documentation; assist with product release for distribution and meeting product release time goals.
  • Implement and support training programs so staff consistently carry out manufacturing processes in compliance with current Good Manufacturing Practices and environmental, health, and safety regulations.
  • Develop and implement performance measurement and internal auditing programs to evaluate operational efficiency and quality, and implement changes based on assessments.
  • Lead technical reviews, investigations, and process improvement projects; provide manufacturing input into integrating and validating new equipment and processes.
  • Resolve technical, material, and current Good Manufacturing Practice problems that may affect project deadlines.
  • Provide guidance and troubleshooting during process deviations, applying Root Cause Analysis tools when applicable.
  • Obtain qualification to perform selected critical operational processes.
  • Represent the company during audits and inspections.

Desired Qualifications

  • A bachelor's degree in a science, engineering, or business discipline is strongly preferred.

About the Company

Simtra BioPharma Solutions

Sterile injectable drug manufacturing

Simtra BioPharma Solutions is a contract development and manufacturing organization specializing in sterile injectable medicines. It supports pharmaceutical and biotechnology companies with formulation, process development, clinical and commercial manufacturing, filling, packaging and related technical services. Facilities and teams operate under regulated quality systems suited to complex parenteral products. Simtra is a business-to-business manufacturing partner rather than a consumer drug brand, helping sponsors move therapies from development into reliable supply through dedicated production expertise and capacity.

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