Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
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.
JOB SUMMARY -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.JOB DUTIES -
- 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), SmartSheets, 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 prolong periods in a production suite and work extended hours.
- Works directly with Process Development personnel
- Works closely with QCAD, VAL, MTS, and Operations
- Will interact with Customers on a regular basis
- TRAVEL – < 10%
- Required to lead and train junior level Process Development Scientists positions.
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Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.
Skills Required
- BS/MS in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or related fields
- 0-5 years' experience in pharmaceutical development or CDMO industry
- Knowledge of Good Manufacturing Processes (cGMP) and Regulatory Guidelines
- Proficient laboratory and wet chemistry skills
- Experience with MS Office and lab software such as Empower
PCI Pharma Services Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about PCI Pharma Services and has not been reviewed or approved by PCI Pharma Services.
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Retirement Support — Feedback suggests the company provides a 401(k) with an employer match in the mid‑single‑digit range, with immediate vesting noted in certain cases. This is viewed as a solid component of the overall package.
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Leave & Time Off Breadth — PTO and paid holidays are commonly available, and some roles indicate vacation is accessible from early tenure. Availability of time off is frequently described as a positive element of the package.
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Affordable Benefits — Health insurance is sometimes described as reasonably priced depending on plan tier. Feedback suggests core medical, dental, and vision coverage is part of a standard offering.
PCI Pharma Services Insights
What We Do
PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.
