Supervisor, Manufacturing-Filling 2nd Shift - 14024

Alkermes, Inc. • Wilmington, OH • 13h ago

Shift

Monday-Thursday, 3:00 pm to 1:30 am

Summary

This position will provide direct leadership across shifts in manufacturing clinical and commercial products. It will manage multi-disciplined teams of exempt and non-exempt members in a pharmaceutical production area to ensure that all manufacturing systems, production processes, equipment, and the final pharmaceutical product meet or exceed Alkermes' manufacturing standards, regulatory requirements, and business objectives.

Responsibilities

Essential Functions

Acts functionally as the operational leader on the floor during a shift with direct responsibility for Manufacturing Associates and operations executed by that shift

Provides effective, 'hands-on' leadership to the production team as a whole, including Team Leaders and Manufacturing Associates, across all shifts in the production of pharmaceutical drug product

Plans and supervises daily execution of tasks to support published production plan and supervises completion of work through the Team Leads

Supports the Line Manager in complying with identified responsibilities (RACI- Responsibility, Accountability, Consultation, and Information)

Ensures robust and timely communication of defined operational / planning activities associated with the execution of daily production

Provides Manufacturing Line Manager operational detail and planning as required to comply with production planning and to support Manager's initiatives

Drives / Writes / Approves new SOPs, batch records, and/or protocols in support of equipment and manufacturing processes associated with the assigned manufacturing area.

Directly interface with support groups, including facility and process maintenance, engineering, quality assurance, quality control, planning, warehousing, and process development, to ensure the operational status of the manufacturing area in support of the published production schedule.

Supports quality investigations, continuous improvement efforts, and engineering/maintenance/quality control/quality operations activities as they directly impact the functionality of the manufacturing area.

Initiate appropriate action when process deviations occur, authoring investigations when required, to ensure the timely release of product and/or continuity of operation of the manufacturing line

Ensures compliance with cGMP in the manufacture of products

Ensure maintenance and upkeep of the facility and process employed within the area of responsibility

Directly interfaces with Development and Engineering in the Technology Transfer of new products or processes to the manufacturing area, focusing on implementation, operation, and procedural execution.

In conjunction with manufacturing training support, ensure opportunities for training for new and current operators

Ensure qualification of operators, consistent with SOP, to support cGMP manufacturing of pharmaceutical product

Supervise, develop and evaluate Team Leader(s) and Manufacturing Associates

Works with Team Leads to ensure all their direct reports have clear goals and that the Team Leads are meeting regularly with their staff to review the goals and redirect work as needed.

Qualifications

Basic Requirements

High School Diploma or equivalent.

5 years' experience, preferably in pharmaceutical manufacturing or other regulated industry.

Preferred Requirements

Prefer BS in Engineering, Scientific Discipline or Business

3-5 years of supervisory experience

Competencies

Demonstrated experience leading/supervising exempt and non-exempt employees in a pharmaceutical manufacturing environment comparable to the proposed manufacturing area

Demonstrates advanced skills, particularly in operational

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