Pharma Production Tech II – Pilot Plant & cGMP

Piramal Pharma Limited; England; On-site; GBP 25,000 - 35,000; Full time

Job summary

Piramal Pharma Solutions is seeking a PRODUCTION TECH II to join our Division team in the UK. You will contribute to small-scale production of APIs and intermediates in a GMP environment, under supervision, and in line with SOPs.

Responsibilities cover loading/unloading vessels, transferring materials, monitoring parameters, documenting batch records, cleaning and setup, sampling, and adherence to cGMP and safety protocols.

Responsibilities

• Loading/unloading vessels
• Transferring liquids and solids between vessels
• Charging liquids and solids to a vessel
• Monitor parameters
• Complete production related documentation (e.g. batch sheet, log books)
• Dismantle, clean, assemble and set-up production equipment and complete cleaning logs as instructed by a senior level Technician
• Sample materials and products by reviewing and preparing documentation, preparing the sampling and protective equipment, obtaining the sample and submitting to Quality and Compliance function under the direction of a senior level Technicians
• Maintain cleanliness and order of work area to ensure cGMP and safety compliance
• Package, apply labels and lot numbers to identify batches under the guidance of a senior level Technician
• Actively train on SOP’s, Technical Manuals and safety procedures as required
• Participate in opportunities to develop industry relevant production knowledge
• Practice compliance with cGMP and safe operations (e.g. wearing Personal Protective Equipment including self contained breathing apparatus and cartridge respirators)
• Perform other duties as assigned

Job description

Piramal Pharma Solutions is seeking a PRODUCTION TECH II to join our Division team in the UK. You will contribute to small-scale production of APIs and intermediates in a GMP environment, under supervision, and in line with SOPs.

Responsibilities cover loading/unloading vessels, transferring materials, monitoring parameters, documenting batch records, cleaning and setup, sampling, and adherence to cGMP and safety protocols.