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Manufacturing Technician (FTC) - Double Day Shift

Mundipharma
Job LocationCambridge
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Company DescriptionMundipharma is a global (ex-US) network of independent associated companies that research, develop and manufacture innovative pharmaceutical medicines and consumer healthcare products. We are an agile and fast-paced company seeking to increase access tohealth care through programmes and effective partnerships.We are forward-looking and dedicated to bringing innovative treatments to many of the worlds most challenging conditions and diseases including: Pain Management & Supportive Care, Consumer Health, Anti-Infectives, Biosimilars, CNS, Diabetes, Oncology, Ophthalmology,Respiratory and transplantation immunity.We make a difference to patient lives by delivering value to healthcare professionals in 120+ countries across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.Our guiding principles, centred around Integrity and Patient-Centricity, are at the heart of everything we do. We encourage our people to think differently and our inclusive culture of continuous learning and collaboration make Mundipharma a great placeto work.Job DescriptionJob PurposeResponsible for the Manufacturing of the pharmaceutical products within designated suites, accountable for the processes within an assigned manufacturing area, working closely with cross functional teams. Ensuring that production KPIs are delivered whilstmeeting the highest standards of cGMP and Health & Safety.Key Responsibilities

  • Personnel
To support the Cell Leads in ensuring that the Manufacturing targets are achieved within their respective area and working as a team to cover breaks and operational activities.Ensure that tasks for the oncoming shift are completed and prepared so they are starting from a good position. E.g. parts ready for change overs, materials are readily available, 5S and work place management is in good order.Take part in root cause analysis / problem solving as part of their development and gain process knowledge / understanding.Closely working alongside Engineering team and Quality team as required to overcome and resolve atypical events.
  • Performance
Understand & support KPIs, including but not limited to, Changeover times, run speed performance and downtime or performance losses.Being involved in Continuous Improvement initiatives and projects as required such as waste reduction and yield improvements.A champion of small Kaizen projects and actively involved in Autonomous Maintenance program.Supporting any validation activities including completion of Validation Protocols and sampling requirements.Ownership for working environment, delivering work place management processes (5S delivery, GMP of area, stock levels)Managing own workload and able to resolve issues. Supporting the Co-Ordinator and Shift Manager through inputting of operational data (Downtime reporting, maximo submission)
  • Good Manufacturing Practice (GMP)
Good knowledge of the pre-requisite quality requirements and documentation.Able to raise DCRs for Batch Record & procedure updates to maintain operational & regulatory complianceTo understand and comply to the security responsibilities of the operation.To ensure machinery is maintained in a safe, clean and tidy condition.Work areas to be maintained to a good standard at all times including embedding work place management.
  • Other
Carrying out any other reasonable task as requested to help ensure that the production operations maintain supporting demand and achieve improvements in performance, quality and safety.QualificationsEducation
  • Minimum of 4 GCSEs of grade C or above in Maths & English (or equivalent)
  • A level or above (or equivalent)
Experience
  • GMP background
  • Cleaning or servicing of production equipment
  • Process equipment maintenance
  • Pharmaceutical industry
Knowledge and Skills
  • 5S, GMP, Kaisen, work-place management, Process equipment TPM
  • Action and results oriented
  • Quality focused
  • Good time management
  • Positive attitude to work and an understanding of the need to change and improve
  • Sound understanding of regulatory and business compliance

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