Process Development Scientist I — Innovate Biologics & ADCs

PCI TRGR Penn Pharmaceutical Services Ltd; Bedford (NH); On-site; USD 70,000 - 100,000; Full time

Job summary

PCI Pharma Services is seeking a Scientist I to support the Process Development department in a fast-paced CDMO environment. The role involves extensive laboratory work, testing, and collaboration with client teams to advance pharmaceutical development projects.

The ideal candidate will have a strong wet chemistry background, knowledge of cGMP, and experience documenting batch records and SOPs while coordinating with QC, MTS, and operations to meet project milestones.

Qualifications

• BS/MS in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemistry, or related field (0–5 years’ pharma development).
• Proficient laboratory and wet chemistry skills.
• Knowledge of cGMP and regulatory guidelines.
• Experience documenting batch records, SOPs, and reports.

Responsibilities

• Support Process Development projects as SME for formulation and process design.
• Assist senior scientists to perform experiments and meet milestones.
• Represent PD on internal/client calls with technical updates.
• Support formulation design, sterile filtration, lyophilization, and ADC-related work.
• Assist in technology transfer and scale-up activities.
• Execute in-process and finished product testing using HPLC/UPLC, UV-Vis, DSC, and related assays.
• Maintain equipment calibration, cleanliness, and facilities upkeep.
• Draft and review batch records, protocols, and reports for quality compliance.
• Collaborate with QC, MTS, Operations, and external client teams.

Skills

Laboratory skills

Wet chemistry

Written/oral communication

Project coordination

Education

BS/MS in Chemical Engineering / Pharma sciences

Tools

MS Office

SmartSheets

LabX

Empower

Job description

PCI Pharma Services is seeking a Scientist I to support the Process Development department in a fast-paced CDMO environment. The role involves extensive laboratory work, testing, and collaboration with client teams to advance pharmaceutical development projects.

The ideal candidate will have a strong wet chemistry background, knowledge of cGMP, and experience documenting batch records and SOPs while coordinating with QC, MTS, and operations to meet project milestones.