R&D Technician: Process Development & Scale-Up

Piramal Pharma Limited; Northern (KY); Hybrid; USD 42,000 - 65,000; Full time

Job summary

Piramal Pharma Limited, a global CDMO, is seeking a Technician in Research and Development to support Technical Services activities, technology transfer, process scale-up, and GMP documentation. This role blends hands-on batch support with data compilation and protocol execution in solid, semi-solid, and liquid dosage forms.

The ideal candidate has 2+ years in cGMP manufacturing or laboratory settings, strong technical writing skills, and the ability to work across Manufacturing, QA, Regulatory

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, or related areas.
• Experience with solid, liquid, or semi-solid dosage forms is preferred.
• Technical writing skills for protocols, reports, and data charts.

Responsibilities

• Operate and maintain pharmaceutical manufacturing equipment.
• Support R&D/Technical Services projects and batches.
• Prepare batch records, logbooks, and GMP docs.
• Perform in-process sampling and data verification.
• Assist with data auditing and document reviews.
• Prepare tables and summaries using Excel or JMP.
• Analyze batch and process data for reports.
• Maintain cGMP documentation and ALCOA+ data integrity.

Skills

Attention to detail

Independent work style

Data handling

Verbal and written communication

Cross-functional collaboration

Tools

TrackWise

JMP

Minitab

StatGraphics

Microsoft Excel

Job description

Piramal Pharma Limited, a global CDMO, is seeking a Technician in Research and Development to support Technical Services activities, technology transfer, process scale-up, and GMP documentation. This role blends hands-on batch support with data compilation and protocol execution in solid, semi-solid, and liquid dosage forms.

The ideal candidate has 2+ years in cGMP manufacturing or laboratory settings, strong technical writing skills, and the ability to work across Manufacturing, QA, Regulatory