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Quality Analyst

TN United Kingdom

Runcorn

On-site

GBP 60,000 - 80,000

Full time

17 days ago

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Job summary

An established industry player is seeking a Quality Analyst to join their dynamic team in Runcorn. This role offers an exciting opportunity to contribute to the pharmaceutical manufacturing sector, focusing on quality control and compliance. You will be responsible for authoring qualification documents, coordinating with various teams, and ensuring adherence to GMP standards. With a supportive work environment and a contract that allows for growth, this position is perfect for someone looking to make a significant impact in a vital industry. If you have a science degree and a passion for quality assurance, this could be the perfect fit for you!

Benefits

25 days annual leave pro rata
Bank holidays

Qualifications

  • Strong communication and planning skills are essential for this role.
  • Attention to detail and understanding of GMP and CFR21 regulations required.

Responsibilities

  • Author qualification documents for Quality Control equipment.
  • Coordinate with teams for execution of qualifications and write SOPs.

Skills

Good planning skills
Good organisational skills
Good communication skills
Understanding of GMP
Understanding of CFR21
Understanding of Data integrity
Attention to detail

Education

Science degree or equivalent

Job description

Job Description:

Kinetic Recruitment are looking to recruit a Quality Analyst with immediate starts to work for a busy Pharmaceutical Manufacturing Company based in Runcorn.

Salary: £21.31 per hour

Schedule: Monday - Friday 9-5 / 37.5 hours per week

Start Date: To begin ASAP

Contract Type: 70% on site, 30% off site, 12 months from start date / Temp to perm for right candidate.

Benefits: 25 days annual leave pro rata + bank holidays

Purpose of the role:

  1. Author of qualification documents for Quality control department equipment (Examples: CSV, VP, FDS, URS, etc).
  2. Writing the protocols required for qualification documents such as IOQP, etc.
  3. Coordinating with CSV, QA, IT team, and external vendors for execution of the qualifications.
  4. Writing user SOPs for the equipment within the Quality Control department.
  5. Project planning and attending regular meetings within the department.

Qualifications / qualities:

  1. Good planning skills
  2. Good organisational skills
  3. Good communication skills
  4. Understanding of GMP, CFR21, and Data integrity
  5. Good attention to detail
  6. Science degree or equivalent

If you feel you are suitable for the role and have the desired skills/experience, please apply with your CV for immediate consideration or email your CV direct to Kate.martin@kinetic-plc.co.uk.

Kinetic treats all applications with a high degree of care; we review all submissions and will attempt to contact applicants who match the job profile. Those that do not meet the specification will not be contacted, but their CV will be retained to be considered against future opportunities.

Kinetic Industrial is a division of Kinetic Recruitment Services Ltd, a consultancy with over 30 years of experience delivering staffing solutions to the engineering and manufacturing and affiliated sectors. Kinetic Recruitment Services Ltd operates as an Employment Business and Recruitment Agency as defined under the Employment Agencies Act 1973.

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Created on 02/04/2025 by TN United Kingdom

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