PCI Pharma Services - United States, Bedford

Seeking a Senior QA Specialist - Team Lead in Bedford to ensure GxP compliance and product quality. You will oversee QA Operations, including batch review, investigations, and CAPAs, while leading a team. Requires 7-9 years in pharma/biotech, with expertise in FDA regulations and commercial produ...

Seeking a Project Manager I to lead custom Drug Product projects in Bedford, USA. This role requires a Bachelor's degree, 3+ years in Biotech/Pharma, and 0-2 years of PM experience. You will develop timelines, manage budgets, and ensure on-time delivery while coordinating cross-functional teams a...

Lead QC Microbiology operations for a leading organization in Bedford, USA. This director role requires 10+ years' experience and a BS in Microbiology to oversee environmental monitoring and contamination control. You will provide strategic leadership, ensure regulatory compliance, and build a hi...

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 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...

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...

Join PCI as a Business Development Associate in Bedford, USA. You will craft high-quality, technical proposals for drug development and manufacturing. The role requires a Bachelor's in Pharmaceutical Sciences, strong business acumen, and excellent communication skills. Be part of a global team sh...

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...

Lead CSV validation for critical GxP systems in a cGMP environment. Apply your 5+ years of experience with GAMP, 21 CFR Part 11, and risk assessment to ensure compliance and patient safety. This Bedford-based role offers cross-functional collaboration and competitive benefits in a key quality pos...

Join our pharmaceutical operations team in Bedford as a Materials Handler I. You will manage key logistics including receiving, shipping, and inventory control while maintaining strict cGMP documentation. The role requires 1-2 years' experience, basic computer skills, and a commitment to safety a...