Pharma R&D Technician – Process Development

Piramal Pharma Ltd; Sellersville (Bucks County); On-site; USD 42,000 - 66,000; Full time

Job summary

Piramal Pharma Solutions is seeking a Technician, Research and Development to support the R&D organization with hands-on batch support, registration, validation, technology transfer, and process scale-up for solid, semi-solid, and liquid dosage forms.

The role involves data compilation, in-process testing, and preparation of technical content, with collaboration across Manufacturing, QA, Regulatory Affairs, and Engineering.

Qualifications

• 2+ years in a cGMP manufacturing environment.
• Strong knowledge of cGMP guidelines, SOPs, and Batch Records.
• Experience with pharmaceutical manufacturing equipment.
• Experience in Technical Services, Process Engineering, Process Validation, Formulation R&D, Analytical R&D, or related pharmaceutical operations.
• Experience with sampling, in-process checks, batch record review, and data verification is preferred.
• Technical writing experience and ability to prepare clear, accurate protocols, reports, and summaries.

Responsibilities

• Operate and maintain pharmaceutical manufacturing equipment per SOPs and cGMP requirements.
• Support R&D/Technical Services projects including batches, technology transfer, and process scale-up.
• Prepare and review batch records, equipment logs, cleaning records, and GMP documentation.
• Perform in-process sampling, data entry, and support data verification and documentation.
• Assist with protocols, reports, investigations, and validation documentation.
• Prepare tables, charts, and summaries using Excel, JMP, or similar tools.

Skills

cGMP knowledge

Documentation

Data analysis

Attention to detail

Teamwork

Tools

Excel

JMP

Minitab

TrackWise

Job description

Piramal Pharma Solutions is seeking a Technician, Research and Development to support the R&D organization with hands-on batch support, registration, validation, technology transfer, and process scale-up for solid, semi-solid, and liquid dosage forms.

The role involves data compilation, in-process testing, and preparation of technical content, with collaboration across Manufacturing, QA, Regulatory Affairs, and Engineering.