Cleanroom Production Supervisor

4 weeks ago

Manchester, United States Merrimack Manufacturing Full time
Job DescriptionJob DescriptionMerrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing start up manufacturing company that will play a crucial part in bringing innovative and life changing products to life.

The Manufacturing Supervisor is responsible to oversee all areas of production under current Good Manufacturing Practice (cGMP) conditions. The Supervisor is expected to plan and prepare for production, schedule tasks, and assign duties to technicians to meet the production schedule, assess production records and meet release timelines to deliver quality product to our customers. The Supervisor is expected to set the example of safety and compliance for their teams, and demonstrate expertise and breadth of knowledge in executing production activities. The Supervisor is expected to train and coach their team members, review and manage performance, and support career development for employees. They are expected to demonstrate expertise and technical leadership in cGMP compliance and an in-depth understanding of process flow and be able to make decisions based on that experience.

How you will make an impact:
  • Assists manager in forecasting staffing needs necessary to meet customer demand including but not limited to vacation approvals, time card approval, daily and weekly overtime, hiring, and training.
  • Interfaces with internal departments, reports conflicts in production priorities and assists in the resolution.
  • Reports problems and makes recommendations to eliminate variances, facilitate workflow, change processes and improve efficiency.
  • Maintains department discipline and ensures that the employees produce acceptable quality, and quantity of work.
  • Recommends employee hires, terminations, promotions and wage adjustments.
  • Track and maintain employee attendance records & address performance problems.
  • Interfaces with manufacturing and engineering departments to introduce new or improved tools, fixtures and methods.
  • Supervise production line setup including ensuring production lines start on schedule.
  • Supervises all production activities performed by employees including shift change; maintains a high degree of visibility and access to employees throughout the shift and is responsible for the entire shift in the absence of the operations manager
  • Interfaces with materials management to coordinate materials for production.
  • Responsible for training technicians at all levels on equipment and processes.
  • Maintains standards for productivity, reliability, and accuracy.
  • Monitors and reports daily production results, material usage, yield and downtime.
  • Reports equipment issues to appropriate departments and operations manager.
  • Coordinates with quality control to maintain quality standards; takes appropriate corrective measures to resolve deficiencies.
  • Leads/participates in timely resolution of activities related to non-conformances.
  • Maintains a working knowledge of all operating systems pertaining to the work area.
  • Help promote a safe work environment within the organization.
  • Participates in continuous improvement activities as part of a cross-functional team.
  • Maintains good employee communication and relations.
  • Attends and participates in meetings when required and completes assignments.
  • Other production related duties as required.
To be successful in this role, you will need the following skills and experience:
  • High School Diploma or Equivalent minimum; AS/BS preferred.
  • Preferred area of study: Operations Management, Engineering, or other technical discipline.
  • Minimum four years leadership experience in a manufacturing environment, two of which must be direct supervisory experience, preferably in a regulated environment.
  • Demonstrated proficiency in supervision and motivating team members.
  • Proven logic and decision making abilities, critical thinking skills.
  • Knowledge of production practices and procedures in a cGMP & GDP environment.
  • Exceptional written and verbal communication abilities.
  • Willingness to undertake various tasks and adapt to unexpected situations within dynamic company environment.
  • Experience in the implementation and sustainability of lean manufacturing concepts.
  • Medical device manufacturing experience preferred.
  • Working knowledge of Microsoft Office applications.

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