Senior Manufacturing Supervisor Visual Inspection

PCI Pharma Services•Bedford, NH

1d•Onsite

About The Position

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Job Title: Sr. Supervisor, Visual Inspection Location: Bedford, NH Business Type: D&M Department/Function: Operations Reports to: Senior Manager, VI FLSA Status: Exempt Prepared By: Hiring Manager Approved By: Human Resources Date 03OCT2025 Summary of Objective: The Sr. Supervisor, Visual Inspection (VI), manages direct reports responsible for all aspects related to finishing team and operations. This position is responsible for implementation of all procedures as they relate to finishing operations to comply with regulatory requirements and also to coordinate the planning, scheduling, and execution of operations with other departments. It is expected the Sr. Supervisor will participate in regulatory and client interactions.

Requirements

Bachelor's Degree strongly preferred in a Life Sciences discipline, or equivalent training and experience required.
Minimum of five (5) years of relevant experience in a manufacturing, laboratory, or other applicable regulated environment preferred.
Minimum of two (2) years of strong leadership/supervisory experience required.
Experience with cGMP, manufacturing, machine operations, and data entry preferred.
Detail oriented with strong verbal and written communication skills.
Demonstrated ability to follow detailed directions in a manufacturing GMP environment.
Ability to work independently, within prescribed guidelines, or as a team member.
Proficiency with Microsoft Office applications.

Responsibilities

Supervises department Group Leads and/or Supervisors, and is responsible for employee feedback, development, and engagement.
Oversees the employee training program.
Oversees and schedules production operations and employees within cGMP guidelines.
Oversees Drug Product Finishing related deviations, investigations, and CAPAs.
Manages and facilitates interactions and communications with internal and external client stakeholders regarding production.
Manages and facilitates interactions and communications with internal and external client stakeholders regarding production.
Interacts with potential clients, client auditors, and regulatory bodies as a VI, Packaging, and cGMP subject matter expert.
Manages Drug Product Finishing activities including document production and review, internal continuous improvement projects, and assurance of cGMP compliance.
Provides technical support to manufacturing and investigations staff within areas of specialty.
Employs high level technical expertise to develop new processes and creatively solve problems.
Oversees, reviews, and approves required protocols, SOPs, forms, and study reports.
Oversees research and implementation of new methods and technologies to enhance operations.
Suggests improvements to existing methods and procedures.
Regular and reliable attendance on a full-time basis or in accordance with posted schedule.
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Suggests improvements to existing methods and procedures.
Suggests improvements to existing methods and procedures.