PCI Pharma Services - Manufacturing

Lead our packaging team in Mississauga as a Line Leader. This supervisory role requires 3+ years of GMP packaging experience and strong attention to detail. You will ensure efficient, high-quality production with minimal waste in a pharmaceutical environment. We offer extended health benefits, RR...

Lead a high-performing packaging team in a fast-paced, GMP-regulated CDMO environment in Dundalk. Drive operational excellence, safety, and efficiency across multiple packaging lines. Requires 5+ years of packaging experience and proven leadership in a pharmaceutical or high-volume manufacturing ...

Lead production operations at our Dundalk facility, ensuring GMP compliance and product quality. You will supervise line leaders, optimize shift output, and coordinate with warehouse and engineering teams. This role is key to delivering life-changing therapies to patients globally. Join PCI to dr...

Join our team in Dundalk as a Production Operator - Level 2. You will be responsible for shift output, quality, and yield, ensuring strict compliance with GMP standards. Key duties include material documentation, quality sampling, and visual inspections. We seek a goal-oriented individual with fl...

Join our team in Dundalk as a Production Operator - Level 2. You will be responsible for shift output, quality, and yield, ensuring strict compliance with GMP standards. Key duties include material documentation, quality sampling, and visual inspections. We seek a goal-oriented individual with fl...

Lead our Quality Control Analytical team in Bedford, USA. This supervisory role requires 5+ years of pharmaceutical QC experience, deep cGMP knowledge, and expertise in HPLC and other analytical methods. You will oversee lab operations, conduct investigations, and ensure compliance. Ideal candida...

Join our Bedford team as a Visual Inspection Technician I in a critical GMP environment. Your primary role is to ensure patient safety by meticulously inspecting sterile vials for defects. This position requires strong attention to detail, the ability to follow SOPs, and visual acuity qualificati...

Lead Engineering, Maintenance, and Facilities for pharmaceutical and medical device manufacturing at our NH campuses. This senior director role requires 10+ years in cGMP/biopharma engineering and 8+ years managing technical staff. You will ensure quality, drive continuous improvement, and provid...

Lead complex engineering projects for sterile drug product fill-finish in Bedford, USA. This hands-on principal role requires 10+ years in pharma/biotech, with deep expertise in GMP, aseptic processes, and capital projects. Optimize state-of-the-art equipment, mentor engineers, and ensure world-c...