Senior Manufacturing Supervisor Visual Inspection

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.

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following, but other duties may be assigned.

• 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.

Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodation which may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties, the employee may be required to:

·         Constantly required to sit, and to reach to use computers and other office equipment.  

·         Constantly stand for extended periods of time, up to four (4) hours/time.

·         Frequently required to lift up to 50 pounds.   

·         Constantly required to view objects at close and distant ranges with hand and eye coordination. 

·         Frequently required to communicate with others. 

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

·         Employee will work with moderate noise level. 

·         Employee will perform tasks while experiencing numerous interruptions.

·         Employee may occasionally be exposed to fumes, airborne particles, toxic chemicals, vibration, and bio-hazardous materials.

·         The work environment is fast-paced and demanding.

·         This position has the utmost responsibility for compliance with the rules and regulations regarding a safe and healthy work environment relative to their actions and conduct.

·         Off-shift, weekend and overtime duties may be required.

Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• 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.

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future.

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.