PCI Pharma Services Pharmaceutical Career Fair – August 5, 2026 | 11:30 AM –2:30 PM

PCI Pharma Services provides a comprehensive range of pharmaceutical services from the earliest stages of development through to commercial launch and ongoing supply, with an uncompromising focus on quality, operational excellence, and leading customer experience.

About the event

PCI is hosting an onsite job fair for multiple positions.

• Date: Wednesday, August 5, 2026
• Time: 11:30 AM to 2:30 PM
• Location: 29 Commerce Drive, Bedford, NH

Positions available

• QA Specialist II – Operations (First Shift)

  Ensures the quality of products and compliance to internal procedures and external standards. Responsibilities include Batch Record Review, Lot Disposition, and Quality System review. Evaluates deviation incidences, determines escalation needs, performs quality review and approval of investigations, and creates and monitors associated CAPAs.

• Sr. QA Specialist – Supplier Quality (First Shift)

  Part of PCI’s Quality Compliance team responsible for the quality aspects of supplier quality management for suppliers providing raw materials, components, contract test labs, and services for GMP operations. Ensures successful execution of the Supplier Qualification program across all PCI facilities.

• QA Specialist I - Raw Materials (First Shift)

  Provides QA oversight to the Materials Management workstream and associated tasks. Supports Materials Management and Quality Control in the receipt of raw materials, review of internal and external raw material documentation, and disposition of raw materials. Assists with initiation and review of raw material quality systems, material specifications creation and revisions, and ensures adherence to site procedures.

• QA Specialist II – Doc Control (First Shift)

  Manages, coordinates, and maintains cGMP documentation, procedures, and records to ensure controlled copies are reviewed, approved, issued, distributed, and archived. Evaluates document needs, processes Documents and Records, maintains databases and Quality Management System tools, and supports personnel and functional areas. Contributes to the maintenance and improvement of the Document Control program and its systems.

• QA Validation Specialist III

  Oversees and leads complex QAV validation projects, ensuring compliance with regulatory and industry standards. Involves strategic planning, review, approval, and continuous improvement of QAV validation processes. Works closely with senior management and cross-functional teams to drive quality initiatives and mentor junior team members.

• Maintenance Technician II/III (Sun to Wed 6AM to 4:30 PM)

  Performs diversified duties including operating powered industrial trucks, installing, troubleshooting, repairing, and maintaining utilities, production, and facility equipment. Carries out equipment repairs and maintenance tasks (e.g., mechanical, electrical, HVAC, plumbing) for GMP facilities, utilities, laboratories, warehouse, and buildings.

• Materials Handler (First Shift)

  Assists in day-to-day activities relating to inventory control functions supporting pharmaceutical fill/finish operations. Responsibilities include receiving, shipping, data entry, inventory control, labeling, and maintaining associated cGMP documentation.

• Manufacturing Technician I/II/III

  Learns and performs a variety of tasks in accordance with manufacturing GMP/ISO requirements and standards. Performs routine and critical manufacturing operations, including equipment prep, formulation, aseptic compounding, and filling activities for biopharma and medical device products.

  Shifts Available:

  • Sun to Wed 6AM to 4:30 PM
  • Sun to Wed 3:30 PM to 2AM
  • Wed to Sat 3:30 PM to 2AM
  • M-F 8:30 AM to 5PM
  • M-F 4PM to 12:30 AM
• Manufacturing Technician IV/Lead (First and Second Shift)

  Leads others in complex manufacturing tasks while ensuring compliance with GMP/ISO and PCI safety standards. Performs and oversees operations including equipment prep, dispensing, dissolution, formulation, purification, aseptic compounding, filling, and packaging. Resolves non-routine issues, reviews and updates MPRs and SOPs, monitors team behaviors, trains staff, and models Guardian values.

• Supervisor, Manufacturing (First Shift)

  Leads a manufacturing team in complex tasks in accordance with FDA and other regulatory agencies while following all safety guidelines. Supervises an aseptic and medical device manufacturing team, ensures execution of production plans across multiple shifts, and manages staff performance against operational goals.

• Formulation Technician III (Sun to Wed 6AM to 4:30 PM)

  Mentors others and performs complex formulation tasks under general guidance and in compliance with GMP/ISO and PCI safety standards. Executes formulation operations including equipment prep, dispensing, dissolution, formulation, purification, and aseptic compounding. Addresses non-routine issues, works with MPRs and SOPs, monitors team behaviors, and trains less experienced staff.

• Visual Inspection Technician I (First Shift)

  Performs visual inspection of sterile filled containers (vials) in accordance with applicable procedures, regulations, and safety directives. Ensures finished drug product vials are free of visible defects to support patient safety and product quality.