Graduate Product Technologist
Monday to Friday - 9am to 5pm
The ideal candidate will possess -
Preferably a science-based qualification.
Experience working in a pharmaceutical, FMCG or other regulated production operations Demonstrated project skills, including the ability to deliver projects on schedule, within budget, and meeting the predefined quality requirements are required.
Strong analytical and problem-solving skills.
Experience of Process and Equipment (or at least awareness of) desirable.
Experience in batch processing in a cGMP pharmaceutical industry desirable.
Lean manufacturing and/or Lean Six-Sigma training and experience desirable.
Proficient in project work/tasks.
Support delivery of the weekly production plan and drive line performance to achieve agreed targets and measures of performance.
To provide support for Scale Up, Technical Transfers Scale Up, Technical Transfer and technology/equipment introduction for all current and future product introductions to the site. Manage and coordinate projects (process validation/equipment validation/material changes/continuous improvement).
Track project deliverables in terms of milestones and maintaining project timelines with forecasts; including escalation to line manager.
Protocol and report writing, execution of protocols.
Author, update and review batch documentation and SOPs.
Coordinate the timely closure of batch documentation (including all electronic transactions) utilising the resources within the lead operator population.
Monitor and report team performance to targets. Drive corrective and preventative actions where shortfall occurs. Support the introduction of new products, equipment and processes.
Identify staff training and development needs to assure competency (suitably qualified and experienced personnel) and support the achievement of objectives.
Manage and monitor non-conformance and deviation processes.
Lead and train team members in delivery/facilitation of RCA.
Through a presence in the workplace that allows staff member to be coached and mentored, ensure products are manufactured and documentation completed inaccordance with GMP, Standard Operating Procedures and other regulatory agency requirements.
Timely completion of relevant deviation and complaint investigations to identify true root cause. Along with timely closure of corrective/preventative actions for deviations, complaints and GMP audits that are assigned to them with a focus on improved processes, documentation, documentation completion and training
Understand and ensure implementation of emergency procedures and safe systems of work.
Ensure compliance with environment, health and safety rules, signage and instructions.
Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules.
PROMAN acts as an employment agency for permanent staff and an employment business for temporary workers. We recruit for roles based in Engineering, Technical, Warehousing, Manufacturing, Office, Logistics and Industrial.
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