Quality Assurance Administrator
Job Location:
Job Location:
Birmingham - UK
Yearly Salary:
£ £ 27000 - 29000
Yearly Salary:
Posted on:
16 hours ago
Posted on:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Talentmark are recruiting for an QA Administrator to join a pharmaceutical company based in Birmingham on a permanent basis.
The salary is around per annum.
The Company:
Our client are a Pharma manufacturing company who produce import and distribute bespoke medicines (Specials) and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
Your Background (Essential):
Your Background (Desireable):
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 193744 in all correspondence.
If this position isnt suitable but you are looking for a new role or if you are interested in seeing what opportunities are out there head over to our LinkedIn page (Talentmark) and follow us to see our latest jobs and company news.
The salary is around per annum.
The Company:
Our client are a Pharma manufacturing company who produce import and distribute bespoke medicines (Specials) and CBPMs (Cannabis-Based Products for Medicinal Use).
Your main duties will be:
- Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs forms master documents batch records policies and specifications).
- Provide administrative support for deviations NCs CAPAs change controls complaints and incident reports.
- Ensure document activities comply with EU GMP (as applicable to Specials) MHRA expectations and internal quality procedures.
- Work closely with Production QC and QA teams to ensure correct and timely use of controlled documents.
- Design and execute method validation/verification method transfers and robustness studies as required.
Your Background (Essential):
- Degree in scientific pharmaceutical or quality-related discipline.
- Previous administration experience in an office or documentation-focused role.
- Strong command in Microsoft Excel.
Your Background (Desireable):
- Familiarity with core GMP documentation.
- Experience in a GMP pharmaceutical specials or other regulated environment.
- Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance.
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 193744 in all correspondence.
If this position isnt suitable but you are looking for a new role or if you are interested in seeing what opportunities are out there head over to our LinkedIn page (Talentmark) and follow us to see our latest jobs and company news.
About Company
Idibu
100 employees
Every business is now operating in an environment that’s susceptible to change. idibu has evolved against this changing backdrop. Whether driven by legislation, technology, customer demand or the economy, businesses now need to be agile and fleet of foot to ensure they can attr ... View more
