QUALITY MICROBIOLOGIST - Holmes Chapel - 6 Months

  • Location

    Holmes Chapel, Cheshire

  • Sector:

    IT

  • Job type:

    Contract

  • Salary:

    £14 - £14.98 per hour

  • Contact:

    Experis UK

  • Contact email:

    christopher.hague@experis.co.uk

  • Job ref:

    BBBH123211_1592325703

  • Published:

    5 months ago

  • Duration:

    6 Months

  • Expiry date:

    2020-07-28

  • Start date:

    ASAP

  • Client:

    #

QUALITY MICROBIOLOGIST - Holmes Chapel - 6 Months

QUALITY MICROBIOLOGIST - Holmes Chapel - 6 Months

The work location is in Holmes Chapel and is a 6 Months contract.

Pay rate is £14.98 per hour including Shift Allowance

The role is working for a well-established pharmaceutical company, which specialises in the manufacturing of inhalation products

Description

  • This role provides testing, reporting and investigation laboratory activities to enable compliant, on time delivery of product to market. This is a key position within a QC team ensuring that the exacting standards of GMP, Site procedures, HSE and LEAN are delivered at all times.
  • The Quality Microbiologist is charged with performing their work in a safe and effective manner in compliance with cGMP, Biosafety and Regulatory requirements.
  • The function of this position is to perform Microbiological sampling and testing following approved methodology, to assure that the potency, purity, safety and stability of our products, components and facilities/utilities are in compliance with approved specifications.
  • Additionally, this position evaluates Microbiological methods, reviews test results, highlights problems related to technical and equipment issues and works closely with the Senior Quality Microbiologist/Microbiology Quality Leader to aid resolution of any issues. All staff may be required to perform additional duties as agreed by the supervisor.

Key Skills and Education:

  • A science degree / HND/ NVQ 4 or equivalent with at least 1 years working experience in a GMP environment
  • Good technical knowledge and expertise of quality control principles and systems in a GMP environment.
  • Computer-literate with experience in the use of Laboratory (LIMS, Data capture) systems as well as MS Word, Excel and PowerPoint
  • Demonstrated ability to actively participate in projects and investigation
  • Knowledge and understanding of global pharmaceutical regulations and guidelines.
  • Demonstrates competence and clarity in both written and oral communication e.g. presentations at team meetings, ability to write ILIs and demonstrates understanding to execute FSIs as well as non-complex technical and investigational reports, communication at team meeting
  • Good interpersonal skills with an ability to communicate procedures and concepts within the team and on occasions to the department. Ability to train instructional techniques
  • Self-motivated with ability to plan and manage own workload with some supervision during the working day.
  • Challenges and questions locally and across team ways of working to seek improved processes and performance
  • Takes responsibility for supporting change, is prepared to take or support action, and/or escalate to ensure implementation of appropriate actions
  • Ability to respond to auditor questions and describing local systems on external audit tours with positive outcomes
  • The individual should have good knowledge and understanding of the principles and concepts of compliance management and GMP/GLP
  • The individual should have a good understanding of analytical chemistry or microbiology, laboratory instrumentation and/or related information systems.
  • The individual should have a basic understanding of the industry and be responsive to of regulatory changes, new technologies, Pharmacopoeial requirements and their impact on the function.
  • An understanding of own quality assurance function, as well as a basic understanding of other functions and how they contribute to achieving the objectives of the business.
  • The individual has some understanding of business functions and supports reacting to issues on how QC performance impacts functional customer service.

KEY RESULTS/ACCOUNTABILITIES

  • Delegate/allocate work and monitor performance
  • Conducts testing of QC samples for the specific laboratory area and manage own workload
  • Analyse data using standard procedures
  • Contribute to quality key performance indicators and deliver, measure/trend data to team. Challenge and seek improvements in ways of working/processes
  • Perform testing according to prioritisation and contribute to any improvements
  • Provide Microbiological/lab support for Team Leader in internal, Global regulatory inspections and customer audits when required.

If you are relevant or interested don't delay, contact me on 0161 924 1416 0161 924 1416