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Quality Assurance Assistant, Pharmaceutical (open to Science graduates)

Russell Taylor Group Ltd
Posted 5 days ago, valid for 6 days
Location

Widnes, Halton WA8 8GP, England

Salary

£23,000 - £27,000 per annum

Contract type

Full Time

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Sonic Summary

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  • The Quality Assurance Assistant position is located in Widnes and is a permanent, onsite role with working hours from 9 AM to 5:30 PM, Monday to Friday.
  • The salary for this role ranges from £23,000 to £27,000, depending on the candidate's experience.
  • Candidates are expected to have a degree in a relevant scientific discipline and experience working in GMP settings, ideally with exposure to CAPA, deviations, and change controls.
  • The role involves supporting the QA team in batch release activities, maintaining QA documentation, assisting in quality investigations, and ensuring compliance with training records.
  • Additional benefits include 25 days of holiday plus bank holidays, a company bonus scheme based on performance, a pension plan, and onsite parking.

Quality Assurance Assistant, Pharmaceutical

Location: Widnes, (this is an onsite role and duties cannot be performed from home).

Type: Permanent

Hours:  Working 9-17.30 Monday to Friday

Salary: £23,000 - £27000 depending on experience

Additional:   25 days +BH hols, company bonus scheme (dependant on performance), company pension, onsite parking 

Russell Taylor is working with a leading pharmaceutical company, who are looking to appoint an QA Assistant – this is a fantastic opportunity for someone who is looking to move into a full time QA role in a Pharmaceutical setting.

To support the organising of market release batch packs in accordance with company procedures in collaboration with fellow QA associates to enable on time market release by the Qualified Person to meet business objectives.

Major Duties and Responsibilities

  • Support key Pillars of the QMS as and when required, e.g. Initiating DR’s, CC’s and CAPA’s.
  • Support the QA team in matters of batch releases activities required by the licensed Qualified Person.
  • Follow company procedures to ensure QA documentation is correctly archived, traceable, and retrievable.
  • Assist in Quality related Investigations, Market Complaints, and support updates of SOP’s, when necessary.
  • Support the business in site KPI’s, product quality and HSE standards to help meet targeted levels.
  • Ensure that your training record file is kept up to date at all times with a target of 95% training compliance.

The Person

  • Will hold a degree in a relevant scientific discipline
  • Experience working in GMP settings
  • Ideally will have exposure to CAPA, OOs, OOt, deviations , change controls etc  
  • We want people with strong attention to detail, who will work off instructions and follow the company guidelines (and QMS).

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By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.