PCI Pharma Services Pharmaceutical Career Fair – July 15, 2026 | 3:00 PM–5:00 PM
Summary Of Positions Available
Formulation Technician III: 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 non-routine 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.
Manufacturing Technician I/II/III: 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.
Manufacturing Technician IV/Lead (First 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 non-routine 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.
Material Handler I/II/III (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.
QA Specialist I – Aseptic Core Monitoring (First and Second Shift): Provides real-time monitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas. Supports PCI’s commitment to aseptic integrity, product quality, and patient safety.
QA Specialist I – Operations (First Shift): Ensures product quality and compliance with internal procedures and external standards. Core responsibilities include Batch Record Review, Lot Disposition, and Quality System oversight. May also evaluate deviations, determine escalation needs, review and approve investigations, and manage associated CAPAs. This role provides the opportunity to strengthen GxP programs by delivering QA expertise for clinical and commercial manufacturing.
QC Microbiology Technician I (M-F 4PM to 12:30 AM): Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management.
QC Microbiologist I (M-F 4PM to 12:30 AM): Conducts environmental and clean-utility sampling and testing in accordance with approved procedures. Performs laboratory analyses and supports additional microbiology tasks as assigned by management.
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.
About the Role
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.
Responsibilities
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 non-routine 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.
Learns and performs 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.
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.
Solves non-routine 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.
Aids in inventory control functions supporting pharmaceutical fill/finish operations.
Provides real-time monitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas.
Ensures product quality and compliance with internal procedures and external standards.
Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures.
Conducts environmental and clean-utility sampling and testing in accordance with approved procedures.
Performs visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives.
Requirements
Education: Bachelor's degree in relevant field (e.g., Biotechnology, Chemistry, Engineering).
Experience: Minimum of 2 years of related experience in pharmaceutical manufacturing, quality assurance, or related fields.
Skills: Proficiency in GMP/ISO standards, strong problem-solving skills, ability to work independently and as part of a team, attention to detail, and excellent communication skills.
Qualifications
Education: Bachelor's degree in relevant field (e.g., Biotechnology, Chemistry, Engineering).
Experience: Minimum of 2 years of related experience in pharmaceutical manufacturing, quality assurance, or related fields.
Skills: Proficiency in GMP/ISO standards, strong problem-solving skills, ability to work independently and as part of a team, attention to detail, and excellent communication skills.
Skills
Proficiency in GMP/ISO standards.
Strong problem-solving skills.
Ability to work independently and as part of a team.
Attention to detail.
Excellent communication skills.
Benefits
Competitive compensation package.
Flexible work schedule.
Health insurance benefits.
Retirement savings plan.
Professional development opportunities.
Employee recognition program.
Pay
Competitive compensation package based on qualifications and experience.
Schedule
Various shifts available, including First Shift (First Shift), Second Shift (Second Shift), and Third Shift (Third Shift).