Utility Operations Supervisor

2 weeks ago

Indianapolis, United States Ives & associates inc Full time

Join an industry leader


Our client is currently constructing an advanced manufacturing facility for production of pharmaceutical ingredients located in Central Indiana area. This facility is the company's largest investment in manufacturing capacity and is intended to provide raw materials for current and future products. This is a unique opportunity to be a part of the leadership team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

The Supervisor Utility Operations is directly responsible for managing the utility operations for their respective area and shift. The Supervisor Utility Operations is responsible for ensuring that the generation and distribution of the utility services is provided without interruption of service to support the needs of the facility. The Supervisor Utility Operations for Plant Utilities will be responsible for gray, clean, and plant utilities, and the Supervisor Utility Operations for Environmental Control Utilities (ECU) will be responsible for tank farm operations, air emissions systems, and solvent recovery systems. The Supervisor is the management representative on shift. The role is responsible for the supervision of operators (5-10) involved in the direct execution of utility operations (per SOPs and operational execution instructions) in order to safely and compliantly support the manufacturing of high-quality product.

The Supervisor Utility Operations provides leadership and ensures that appropriate staffing is in place. The role will ensure equipment is maintained in a state of compliance and processes in a validated state for their respective area and shift.

In the project delivery phase and startup phase of the project (startup expected 2025 to 2027), leadership roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.

Responsibilities:

  • Build and promote a strong Safety and Quality culture. Maintain a safe working environment and conduct operations activities in a manner that protects safety, environment and quality
  • Ensure utility operations maintain compliance with all regulatory requirements at all times.
  • Ensure utility areas appropriately support the execution of the production plan for the site.
  • Ensure consistency of operations on designated shift through active engagement on the floor.
  • Ensure audit action items assigned to operations are completed in a timely manner.
  • Set objectives and development plans for operators. Respond to employee relations issues with operators on shift and escalate to management where necessary.
  • Manage events as required, ensuring appropriate communication within the team and with external teams. Provide input to investigations.
  • Build and develop a team, creating clear common purpose and promoting good team spirit.
  • Ensure that operators are appropriately trained, and that operating procedures and training material are available and current.
  • Communicate appropriately with operators regarding site objectives and team business.
  • Ensure the team is adequately resourced to meet the business objectives appropriately managing overtime as necessary.
  • pecifically, during the startup phase of the site (2025 to 2027) leadership will be expected to be collaborative, inclusive, and support the broader team to: Build the organization with the necessary capability, capacity and culture to operate this facility to the highest standards of operational excellence.
  • Develop and implement the systems and processes needed to run the site, leveraging existing company knowledge and practices where necessary, but also incorporating external experiences and learning.
  • Ensure regulatory compliance and operational excellence by supporting lean principles in their respective area.
  • Support the project team as they deliver the facility to the site team, by providing feedback and support.

Requirements:

  • High School Diploma or equivalent Bachelor’s or Associate Degree in science, engineering, or technical field preferred
  • Previous experience in facility/area start-up environments preferred
  • Experience in utility operations or directly supporting a pharmaceutical manufacturing operation.
  • Demonstrated leadership experience.
  • Skills in providing/receiving feedback and creating employee development plans.
  • Basic computer skills (desktop software) are required.
  • Solid understanding of FDA guidelines and cGMP requirements.
  • Strong organizational and training skills with ability to handle and prioritize multiple requests.
  • Knowledge of lean manufacturing principles
  • Ability to work with a team, make independent decisions, and influence diverse groups.
  • Must be US citizen or green card holder unable provide sponsorship at this time.
  • Ability to communicate verbally and in writing to various audiences, particularly one-on-one coaching, and feedback with direct reports.
  • Ability to work rotating 12-hour shifts with overtime if required

TOP HOURLY RATE-(including shift diff pay)- OT- BONUS- GREAT BENEFITS Full Relocation

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