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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Scientist II PharmDev Formulations - **Company:** PCI Pharma Services - **Location:** Bedford, NH, United States - **Experience:** Starter - **Contract:** Permanent contract - **Skills:** Microsoft Word, Microsoft Excel, Data Analysis, Microsoft Office, Microsoft PowerPoint, Microsoft SharePoint - **Published:** August 10, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=d10b6d24d7e47dad ## About the Role * Advanced Degree in (PhD) in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or other related fields with 0-3 years' experience in pharmaceutical development or CDMO industry. * BS/MS in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or other related fields with 5+ years' experience in pharmaceutical development or CDMO industry * A strong foundation in clinical-phase development and analytical characterization of drug products, including biologics and other complex modalities * In-depth knowledge of biopharmaceutical and/or medical product regulation, formulation, filtration, filling, and lyophilization operations * Experience with MS Office (Word/Excel/Teams/PowerPoint/SharePoint), SmartSheets, LabX, and Empower QUALITIES: * 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 balance with independent thinking * Resilient through operational and organizational change ## Description * Leads Formulation Development projects for various modalities, serving as the technical lead and SME for formulation and process design activities. * Supports more complex Formulation Development projects as a collaborator, working with a senior scientist to achieve project milestones * Executes and analyze experiments to achieve project milestones without supervision. * Develops and implements phase-appropriate formulation development strategies aligned with program objectives and regulatory expectations. * Acts as a Formulation Development representative on internal and client-facing project calls, providing technical updates and strategic input. * Demonstrates proficiency in formulation design for both small molecules and biologics, analytical data interpretation and trending. * Develops and optimizes formulations for high-potency compounds, including antibody-drug conjugates (ADCs) and other complex modalities. * Supports technology transfer activities and assists in scale-up or manufacturing transitions as a formulation SME. * Performs analytical testing within Pharmaceutical Development laboratory to support formulation development, such as HPLC/UPLC, Capillary Electrophoresis, UV-Vis spectroscopy, FlowCam, Karl Fischer titration, DSC/FDM, and other related assays to confirm acceptance criteria as part of formulation development activities. * Troubleshoots formulation, analytical and process challenges and proposes scientifically sound corrective actions. * Responsible for proper maintenance, calibration, and cleanliness of laboratory instruments and equipment. * Performs or assists in routine facilities cleaning and equipment upkeep as required. * Authors and reviews Formulation Development records, protocols, and reports to ensure technical accuracy and compliance with quality standards and client demand. * Reviews executed documentation for accuracy and completeness prior to submission to management. * Drafts and maintains Standard Operating Procedures (SOPs) and related controlled documents for Pharmaceutical Development operations. * Provides training, technical guidance, and mentorship to junior scientists and laboratory staff. * Collaborates cross-functionally with internal stakeholders including Manufacturing Technical Services (MTS), and Operations, as well as external client teams, to ensure alignment and successful project execution. ## Related Videos - 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