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PCI Pharma Services

Pharmaceutical packaging and contract services

Manufacturing Supervisor

Manufacturing & Production OperationsConfirmed live in the last 24 hours
Full-timeBedford, NH, USANo salary listedIn-person

About the Job

Requirements

  • A minimum high school diploma is required.
  • Five to seven years of experience in a Good Manufacturing Practices environment is required.
  • Experience with Good Manufacturing Practices, the Food and Drug Administration, and other regulated agency environments is required.
  • Experience making real-time decisions on safety, process, scheduling, and personnel-related issues is required.
  • Ability to prioritize and manage multiple resources in a production environment with flexibility to meet organizational needs is required.
  • Proven leadership, persuasiveness, initiative, and problem-solving skills are required.

Responsibilities

  • Lead a manufacturing team performing complex tasks in accordance with Food and Drug Administration and other regulatory requirements and PCI safety guidelines.
  • Supervise a 12-hour production shift for aseptic manufacturing, including equipment preparation, formulation, filtration, aseptic and non-aseptic compounding, isolator filling, and lyophilization activities.
  • Ensure execution of the production plan across multiple shifts and manage staff performance against departmental operational goals.
  • Ensure the safety of the manufacturing area and work practices under PCI’s Health, Safety and Environmental program.
  • Motivate, coach, support, inspire, retain, and develop high-performing teams.
  • Coordinate and supervise manufacturing personnel in current Good Manufacturing Practices operations to meet scheduled manufacturing work.
  • Guide and train employees to ensure Food and Drug Administration and other regulatory agency requirements are implemented and maintained.
  • Plan and execute manufacturing instructions for equipment preparation, compounding, filtration, formulation, and filling activities for aseptic and terminally non-aseptic products in accordance with Good Manufacturing Practices.
  • Provide leadership, guidance, and direction to staff in alignment with current Good Manufacturing Practices requirements, departmental goals, and corporate quality standards.
  • Partner with Planning to prioritize work, maintain schedule adherence, and meet capacity demands.
  • Collaborate with enabling groups to optimize processes.
  • Recruit and supervise staff, ensure effective resource utilization, and manage consistent performance.
  • Identify, assess, and mitigate operational and organizational risks, escalating key risks and issues to manufacturing senior management and cross-functional support teams.
  • Establish key performance indicators aligned with departmental goals and maintain and report applicable area or organizational metrics.
  • Collaborate with Training to design and execute the departmental training plan and ensure training materials are accurate and sufficiently detailed.
  • Complete investigations, deviations, and corrective and preventive actions on time; use quality metrics to measure, analyze, and improve team performance; ensure real-time batch review and right-first-time execution.
  • Enhance inspection readiness in assigned manufacturing areas and participate in inspections conducted by external regulators.
  • Identify continuous-improvement opportunities to improve processes and practices.

Desired Qualifications

  • Three to five years of experience leading direct reports or teams is preferred.

About the Company

PCI Pharma Services

Pharmaceutical packaging and contract services

PCI Pharma Services provides end-to-end pharmaceutical packaging and related services, including folding cartons, labels, contract packaging, clinical services, and brand protection, acting as a one-stop source for healthcare product development and commercialization. It handles packaging operations from cartons and labels to contract packaging and labeling, plus clinical packaging and brand protection, with processes built on cGMP and ISO compliance, lean manufacturing, and ongoing R&D, supported by mandatory training and strict security, hygiene, and inspections. It differentiates itself with eight decades of experience and a broad, integrated service suite under one roof, reducing risk and handoffs for clients. Its goal is to be a trusted packaging partner that delivers reliable, compliant, and scalable solutions so healthcare brands stay protected and clients can focus on their core business.

Company size
1-10
Company stage
Debt Financing
Total funding
$4B
Headquarters
Burlington, Canada
Founded
1971

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