PCI Pharma Services Pharmaceutical Career Fair – July 15, 2026 | 3:00 PM–5:00 PM

Summary Of Positions Available

• Formulation Technician III (M-F 4PM to 12:30 AM): 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 (M-F 4PM to 12:30 AM): 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

PCI Pharma Services is dedicated to providing a comprehensive range of pharmaceutical services from the earliest stages of development through to commercial launch and ongoing supply. Our mission is to deliver quality and operational excellence, and to provide unparalleled customer experience to the industry.

Responsibilities

• Mentor and perform complex formulation tasks under GMP/ISO and PCI safety standards.
• Execute all formulation operations, including equipment prep, dispensing, dissolution, formulation, purification, and aseptic compounding.
• Address non-routine issues using advanced technical knowledge and escalate as needed.
• Work with MPRs and SOPs, monitor team behaviors, train less experienced staff, and model Guardian values.
• Perform and oversee all manufacturing operations, including equipment prep, formulation, aseptic compounding, filling, and packaging.
• Resolve non-routine issues using advanced technical expertise and escalate as needed.
• Review and update MPRs and SOPs, monitor team behaviors, train less experienced staff, and model Guardian values.
• Assist with logistics such as receiving, shipping, data entry, inventory control, labeling, and maintain cGMP documentation.
• Provide real-time monitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas.
• Evaluate deviations, determine escalation needs, review and approve investigations, and manage associated CAPAs.
• Conduct sampling and testing of production environments, and/or facility clean utilities, as per approved procedures.
• Perform lab work and other tasks as assigned by management.
• Conduct environmental and clean-utility sampling and testing in accordance with approved procedures.
• Perform laboratory analyses and support additional microbiology tasks as assigned by management.
• Perform visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives.

Requirements

• Formulation Technician III: Advanced technical knowledge, ability to mentor and train less experienced staff, and adherence to GMP/ISO and PCI safety standards.
• Manufacturing Technician I/II/III: Ability to learn and perform a variety of tasks in accordance with GMP/ISO and PCI safety standards.
• Manufacturing Technician IV/Lead: Advanced technical expertise, ability to resolve non-routine issues, and adherence to GMP/ISO and PCI safety standards.
• Material Handler I/II/III: Inventory control functions, logistics, and cGMP documentation.
• QA Specialist I – Aseptic Core Monitoring: Real-time monitoring of aseptic behaviors, gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas.
• QA Specialist I – Operations: Batch Record Review, Lot Disposition, Quality System oversight, deviation evaluation, investigation review, and CAPA management.
• QC Microbiology Technician I: Sampling and testing of production environments, and/or facility clean utilities, as per approved procedures.
• QC Microbiologist I: Environmental and clean-utility sampling and testing in accordance with approved procedures.
• Visual Inspection Technician I: Visual inspection of sterile filled containers (vials), ensuring product quality and safety.

Qualifications

• Formulation Technician III: Bachelor's degree in related field, relevant certifications, and experience in formulation operations.
• Manufacturing Technician I/II/III: High school diploma or equivalent, relevant certifications, and experience in manufacturing operations.
• Manufacturing Technician IV/Lead: Bachelor's degree in related field, relevant certifications, and experience in manufacturing leadership.
• Material Handler I/II/III: High school diploma or equivalent, relevant certifications, and experience in inventory control and logistics.
• QA Specialist I – Aseptic Core Monitoring: Bachelor's degree in related field, relevant certifications, and experience in aseptic manufacturing.
• QA Specialist I – Operations: Bachelor's degree in related field, relevant certifications, and experience in quality assurance.
• QC Microbiology Technician I: Bachelor's degree in related field, relevant certifications, and experience in microbiology.
• QC Microbiologist I: Bachelor's degree in related field, relevant certifications, and experience in microbiology.
• Visual Inspection Technician I: High school diploma or equivalent, relevant certifications, and experience in visual inspection.

Skills

• Formulation Technician III: Technical knowledge, mentoring skills, GMP/ISO compliance, and adherence to safety standards.
• Manufacturing Technician I/II/III: Learning and performing tasks, GMP/ISO compliance, and adherence to safety standards.
• Manufacturing Technician IV/Lead: Advanced technical expertise, issue resolution, GMP/ISO compliance, and adherence to safety standards.
• Material Handler I/II/III: Inventory control, logistics, and cGMP documentation.
• QA Specialist I – Aseptic Core Monitoring: Real-time monitoring, gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas.
• QA Specialist I – Operations: Batch Record Review, Lot Disposition, Quality System oversight, deviation evaluation, investigation review, and CAPA management.
• QC Microbiology Technician I: Sampling and testing, production environment sampling, and clean utility sampling.
• QC Microbiologist I: Environmental and clean-utility sampling and testing in accordance with approved procedures.
• Visual Inspection Technician I: Visual inspection, product quality, and safety.

Benefits

• Competitive compensation package.
• Flexible work schedule.
• Professional development opportunities.
• Health and wellness programs.
• Employee recognition and rewards.
• Comprehensive benefits package.

Pay

Compensation for these roles is competitive and commensurate with experience and qualifications.

Schedule

Shifts vary based on the specific role, typically M-F 4PM to 12:30 AM or First Shift.