PCI Pharma Services Pharmaceutical Career Fair - August 5, 2026 | 11:30 AM -2:30 PM
 PCI Pharma Services | |
 United States, New Hampshire, Bedford | |
| 23 Commerce Drive (Show on map) | |
 Jul 23, 2026 | |
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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. PCI is hosting an onsite job fair for multiple positions. At PCI Pharma Services, we provide a comprehensive range of pharmaceutical services from the earliest stages of development through to commercial launch and ongoing supply. We have an uncompromising focus on providing quality and operational excellence and providing the industry with leading customer experience. PCI Pharma Services Pharmaceutical Career Fair
Summary of positions available: QA Specialist ll - Operations (First Shift) Ensures the quality of products and compliance to internal procedures and external standards. Primary responsibilities for this role include Batch Record Review, Lot Disposition, and Quality System review. may also be responsible for evaluating deviation incidences and determining which warrant escalation to an investigation, quality review and approval of investigations, and creating and monitoring the 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 that provide raw materials, components, contract test labs and services for GMP operations.Ensure all aspects of the Supplier Qualification program are successfully executed across all PCI facilities QA Specialist I - Raw Materials (First Shift) Provides QA oversight to the Materials Management workstream and associated tasks across the Bedford, NH site. Primarily responsible for supporting Materials Management and Quality Control in the receipt of raw materials, review of internal and external raw material documentation, and disposition of raw materials. Also assists with the initiation and review of raw material quality systems, material specifications creation and revisions, and ensures adherence to site procedures and material specification receipt, testing, and release requirements. QA Specialist II - Doc Control (First Shift) Manage, coordinate, and maintain cGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived: evaluate document needs and participate in the processing of Documents and Records, maintain databases and Quality Management System tools and supports personnel and functional areas as needed. The primary objective of the Document Control QA Specialist II will be to contribute to the maintenance and improvement of the Document Control program and its systems. The QA Doc Control group is dedicated to the continuous improvement of the Document Change Control Lifecycle and Quality Systems to meet current compliance standards and ensure proper processing and release of controlled documents QA Validation Specialist III Oversee and lead complex QAV validation projects, ensuring that all QAV validation activities meet stringent regulatory and industry standards. This role involves strategic planning, review, approval and continuous improvement of QAV validation processes. The QAV Specialist will work 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) Responsible for performing highly diversified duties like operating powered industrial trucks, installing, troubleshooting, repairing and maintaining utilities, production, and facility equipment in accordance with the site safety principles, predictive, and production maintenance systems and processes. Carry out a wide range of equipment repairs and maintenance program by performing assigned tasks (e.g. Mechanical; electrical, heating, ventilation, and air conditioning HVAC, plumbing, etc.) for GMP facilities, utilities equipment, laboratories, warehouse and buildings. Materials Handler (First Shift) Assists in the day-to-day activities relating to inventory control functions supporting pharmaceutical fill/finish operations. The main responsibility of this position is to assist with all aspects of logistics such as receiving, shipping, data entry, inventory control, labeling and maintaining all associated cGMP documentation as needed. Manufacturing Technician l/ll/lll Learn and perform a variety of tasks in accordance with the manufacturing GMP/ISO requirement and standards. Performs routine and critical manufacturing operations, including but not limited to work functions in equipment prep, formulation, aseptic compounding, and filling activities for biopharma and medical device products. Shifts available:
Manufacturing Technician IV/Lead (First Shift and Second Shift):Leads others in complex manufacturing tasks while ensuring compliance with GMP/ISO and PCI safety standards. Performs and oversees all operations, including equipment prep, dispensing, dissolution, formulation, purification, aseptic compounding, filling, and packaging. Resolves nonroutine issues using advanced technical expertise and escalates matters as needed. Reviews and updates MPRs and SOPs, monitors team behaviors, trains less experienced staff, and models Guardian values. Supervisor, Manufacturing (First Shift): Lead a manufacturing team in a variety of complex tasks in accordance with the FDA and other regulatory agencies while following all safety guidelines of PCI. Responsible for supervising an aseptic and medical device manufacturing team (ex. equipment preparation, filling and Lyophilization activities); ensure execution of production plans across multiple shifts and manage staff performance against department's 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 all formulation operations, including equipment prep, dispensing, dissolution, formulation, purification, and aseptic compounding. Addresses nonroutine issues using advanced technical knowledge and escalates matters as needed. Works with MPRs and SOPs, monitors team behaviors, and trains less experienced staff while modeling Guardian values. Visual Inspection Technician I (First Shift): Performing visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives. The primary job function will be to ensure finished drug product vials manufactured by PCI are free of visible defects which are culled through the visual inspection process to support patient safety and product quality. #LI-LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: 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. | |