Scientist - Process Development

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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.

The Scientist I position supports the efforts of the Process Development department within a fast-paced, expanding CDMO. This job will require extensive laboratory work, testing, and strategic client support of pharmaceutical development projects.

• Support Process Development projects, serving as a SME and collaborator for formulation and process design activities.
• Support senior scientists in performing experiments to achieve project milestones.
• Act as a Process Development representative on internal and client‑facing project calls, providing technical updates and strategic input.
• Support the formulation design, sterile filtration, lyophilization, and post‑processing for both small molecules and biologics, including antibody‑drug conjugates (ADCs) and other complex modalities.
• Support technology transfer activities and assist in scale‑up or manufacturing transitions.
• Executor of in‑process and finished product testing within the Process Development laboratory, utilizing methods such as HPLC/UPLC, UV‑Vis spectroscopy, Flowcam, Karl Fischer titration, DSC/FDM, and other related assays to confirm acceptance criteria.
• Ensure proper maintenance, calibration, and cleanliness of laboratory instruments and equipment.
• Perform or assist in routine facilities cleaning and equipment upkeep as required.
• Draft and review Process Development batch records, protocols, and reports to ensure technical accuracy and compliance with internal quality standards.
• Draft and maintain Standard Operating Procedures (SOPs) and related controlled documents for Process Development operations.
• Collaborate cross‑functionally with internal stakeholders including Quality Control (QC), Manufacturing Technical Services (MTS), and Operations, as well as external client teams, to ensure alignment and successful project execution.

• Requires proficient laboratory and wet chemistry skills.
• Knowledge of current Good Manufacturing Processes (cGMP), Regulatory Guidelines, Aseptic Manufacturing, as well as bulk intermediate and medical device manufacturing.
• Works independently with little direction; demonstrates a proven track record of leading tasks to completion.
• Must consistently exhibit positive, effective interpersonal skills with internal and external teams, including relationship management of clients.
• Ability to prioritize multiple ongoing projects and activities to meet customer and company timelines.
• Demonstrates excellent oral and written communication skills and can provide detailed project updates (PowerPoint) to clients and other internal departments efficiently and concisely.
• Requires excellent organizational and interpersonal skills, team‑player.

• BS/MS in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or other related fields with 0‑5 years' experience in pharmaceutical development or CDMO industry.
• A desire to work in clinical‑phase development and analytical characterization of drug products, including biologics.
• Experience with MS Office (Word/Excel/Teams/PowerPoint/SharePoint), Smart Sheets, LabX, and Empower.

• Detail oriented and a results driven team player.
• Ability to work in a dynamic, fast paced work environment.
• Honesty, integrity, respect and courtesy with all colleagues.
• Creative with the ability to work with minimal supervision and balanced with independent thinking.
• Resilient through operational and organizational change.

• Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes.
• Ability to gown and gain entry to controlled manufacturing areas.
• Ability to lift, pull or push equipment requiring up to 25‑50 lbs of force.
• Ability to stand for prolonged periods in a production suite and work extended hours.

• Works directly with Process Development personnel.
• Wo…