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Process Technician Formulation

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

Job Description

To provide the production skills sets necessary to complete multi area vaccine processing operations to deliver the production schedule in a safe, cGMP compliant, and cost-effective manner.Responsibilities:

  • Carries out process operations such as formulation, buffers, MF59 bulk and MF59 sterile filtration using cGMP, MES, EBR as required, whilst in full compliance with local SOPs, HSE risk management systems & procedures. Thereby achieving the production scheduleand requirements of the F&B area .
  • Moves materials required in F&B (pallet trucks, mobile vessels, rigs, raw mats, etc.) using cGMP, MES, EBR systems as required, and in full compliance with local SOPs and HSE risk management systems & procedures. In order that the production schedule andrequirements of the F&B area are met.
  • Carries out basic area cleaning as required to maintain EM, cGMP and HSE standards in the F&B area.
  • Performs in Process Control checks and Environmental Monitoring so that process operations are maintained in control and products made in specification.
  • Completes documentation to the required standards of accuracy, timeliness, and cGMP compliance, including raising work orders and HSE incident reports. Might be able to provide first response on PCS, MES, SAP issues and exceptions.
Knowledge, Skills & Competencies
  • Aseptically qualified (e.g., sterile connections, sterility assurance)
  • Attention to detail and high personal standards of compliance with relevant site and area procedures. Proven knowledge of cGMP. Computer competent (e.g., PCS, GLIMS, SAP, MES…).
  • Documentation skills (based on literacy and numeracy) and capable of operating material moving equipment such as pallet trucks (manual & electronic)
Minimum Education Requirements
  • Numerate, literate, and competent in automated transaction skills (e.g., SAP & MES).
  • English language.
  • Competent in cGMP and sterile product production operations in Biotech or Pharma industry.
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.#LI-MS1Our BenefitsCSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus.About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn moreabout CSL Seqirus.We want Seqirus to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL Seqirus.Do work that matters at CSL Seqirus!Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

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