This site uses cookies. By continuing to use this site you consent to our use of cookies. Close
MUJO Jobs
Sign In Register Advertise With Us
menu
  • clear
  • Home
  • About Us
  • Find a Job
  • Career Advice
  • Job Alerts
  • Contact Us
  • Sign In Register Advertise With Us
    • Login
    • Register
  • Home
  • Jobs
  • Job Alerts
  • News & Advice
Hiring?
More options
410 Gone

This job has expired

The vacancy you are looking for is no longer accepting applications and has been removed.

HTTP Status: 410 Gone

This resource is no longer available.

Browse Similar Jobs Create Job Alert
EXPIRED JOB

Operational Assurance Administrative Assistant

Lincolnshire, United Kingdom

Thera Trust has an exciting opportunity available for a Operational Assurance Admin Assistant to join our team homebased, with occasional travel when required. You will join us on a full time, 12 months fixed term basis until July 2027. In return, you will receive a competitive salary of £19,882.08 per annum pro rata.

Information: We operate flexi time and flexible working

Thera Trust

Thera Trust is the parent company of Thera Group; a charitable group of companies that supports people with a learning disability. Our unique leadership and structure includes people with a learning disability. Through this we can demonstrate that people with a learning disability can be leaders in society but we can t do this without you! Thera trust has a new opportunity for a Health and Safety Admin Assistant, to join our compliance on a part time basis.

About The Operational Assurance Admin Assistant Role

Working for the Operational Assurance Department for Thera group. You will be responsible for ensuring that all systems and processes are in place, updating, formatting and issuing information, assisting with queries and providing a range of information in respect of Operational Assurance.

Your Skills and Experience

Essential Skills:

  • Ability to work well under pressure
  • Demonstrates an excellent telephone manner
  • Remaining calm when dealing with demanding behaviour or circumstances
  • Excellent organisational skills
  • Ability to deal sensitively and diplomatically with a range of people
  • Good communication skills at all levels
  • Excellent telephone manner
  • Ability to multi-task
  • IT competency in a variety of software packages
  • Attention to detail and accuracy

This position requires full flexibility of working hours. The ability to work as part of a team to meet tight deadlines. It is essential that you maintain confidentiality at all times.

What are the Benefits?

  • 28 day holiday including bank holidays- pro rata
  • Contributory pension
  • Blue light card
  • Cycle to work scheme
  • Employee support line to support you
  • Continuous on the job training is provided

If you have a passion for making a difference to peoples lives, consider a career with Thera Group as a Operational Assurance Admin Assistant

We reserve the right to close this advert before the closing deadline if we interview and offer the right candidate

Expired on
02/09/2026
This position is no longer accepting applications.

Similar active jobs you might be interested in

View all jobs
NEW
QA Officer

Stoke-on-Trent

Permanent £38000.00 - £40000.00 Annual

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

  • Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
  • Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
  • Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
  • Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
  • Raising and overseeing the implementation of Change Controls and CAPA's when required
  • Participating in site inspections by Regulatory Authorities
  • Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
  • Writing, reviewing and contributing to Risk Assessments

Benefits:

  • Discretionary Bonus
  • Healthcare & More

About You:

  • Experience within a pharmaceutical environment
  • A strong Quality Assurance background (2 to 3 years experience)
  • Experience within sterile manufacturing environments (desirable)
  • Good working knowledge of GMP requirements and quality systems
  • Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
  • Strong communicator and team player
  • Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

View Details Apply Now
NEW
QA Officer

United Kingdom

Permanent £38000.00 - £40000.00 Annual

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

  • Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
  • Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
  • Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
  • Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
  • Raising and overseeing the implementation of Change Controls and CAPA's when required
  • Participating in site inspections by Regulatory Authorities
  • Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
  • Writing, reviewing and contributing to Risk Assessments

Benefits:

  • Discretionary Bonus
  • Healthcare & More

About You:

  • Experience within a pharmaceutical environment
  • A strong Quality Assurance background (2 to 3 years experience)
  • Experience within sterile manufacturing environments (desirable)
  • Good working knowledge of GMP requirements and quality systems
  • Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
  • Strong communicator and team player
  • Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

View Details Apply Now
NEW
Qa Officer

Liverpool

Permanent £27000.00 - £32000.00 Annual

Our client is a leading Pharmaceutical Manufacturer going through a period of successful expansion to cater for their ever growing production requirements.

They are a well regarded GMP site, producing products that fall under the "Liquids, Orals and Creams" definition of Pharmaceutical Products.

As part of their expansion, they are looking for a Quality Assurance Officer (x2) for their site near Liverpool.

This role is 100% site based, and is offering a competative salary and benefits package, and the opportunity to work within a very exciting Life Science company.

Requirements

- Previous experience as a QA officer (preferably in a GMP environent)

- A degree in Life Sciences

- The ability to be on site 5 days per week

- Strong communication skills and a high attention to detail

View Details Apply Now
NEW
Quality Assurance Officer

Sandwich

Permanent £29000.00 - £35000.00 Annual

We are working with an established pharmaceutical company who are looking to employ a QA Officer, permanently in the Sandwich area.

PLEASE DO NOT APPLY IF YOU DON'T LIVE LOCALLY TO SANDWICH, KENT AND HAVE A FULL RIGHT TO WORK WITH NO RESTRICTIONS (NO GRADUATE VISAS/SPONSORSHIP/RELOCATIONS PLEASE)

This is an exciting full-time permanent position with a salary of up to 35,000/annum and a host of great benefits.

Responsibilities:

  • To provide QA support to all departments.
  • Maintain and develop the Quality Management System.
  • Ensure all pre & post-production documentation is submitted to QA, checked and approved prior to use of any materials, and batch release.
  • Ensure all materials meet required specifications.
  • Complete QA review and approval of deviations, C.A.P.A's, change controls, complaints, out of specifications and other documentation such as SOP's and forms.
  • Assist with internal and external audits.
  • Assist with product recalls.
  • Ensure quality agreements and quality questionnaires are in place with external companies.
  • Manage and develop the company training matrix and complete quarterly reviews on employee training records.
  • Participate in weekly QA meetings.
  • Ensure investigations are carried out in a timely manner.
  • Develop and update logbooks as and when required.

About You:

  • Minimum 3 years' Quality Assurance experience within a GMP pharmaceutical manufacturing environment
  • Strong understanding of GMP and wider GxP requirements
  • Experience of QMS, CAPAs, Deviations, Change Controls and batch record review
  • Excellent investigation and problem-solving skills
  • Ability to write clear technical reports and quality documentation
  • Strong organisational skills with the ability to prioritise multiple activities
  • Excellent communication skills and confidence working across all departments

Local candidates need only apply and those with no restrictions on their right to work.

New Appointments Group, Expertly Matching Employers and Jobseekers since 1975.

If this role isn't for you, please check out our website for other opportunities that may be suitable, or send us your CV, we'd still like to hear from you. You can find us on our website or on LinkedIn, Facebook, Instagram and

We are committed to fostering a diverse and inclusive environment in line with the Equality Act 2010. All qualified applicants will be considered regardless of age, disability, gender reassignment, marriage or civil partnership, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. New Appointments Group acts as an Employment Agency for permanent roles and as an Employment Business for temporary roles.

View Details Apply Now
NEW
Sterility Assurance Specialist

Permanent £50000.00 - £60000.00 Annual

Sterility Assurance Specialist
Burton upon Trent On-site Pharmaceutical Manufacturing

Talentmark is partnering with an established pharmaceutical manufacturer to recruit a Sterility Assurance Specialist. This is an excellent opportunity for an experienced microbiologist or sterility assurance professional with aseptic production experience to play a key role in safeguarding product quality and patient safety within a GMP-regulated aseptic manufacturing environment.

Working as the site's sterility assurance expert, you'll help strengthen quality systems, lead microbiological initiatives, and support the development of a growing microbiology function.

Key Responsibilities

  • Lead and maintain sterility assurance and environmental monitoring programmes in line with GMP requirements.
  • Act as the site subject matter expert for microbiology and sterility assurance.
  • Investigate deviations, non-conformances, environmental monitoring excursions and complaints.
  • Analyse and trend microbiological and environmental monitoring data to identify risks and opportunities for improvement.
  • Support validation activities, including microbiological methods and sanitisation processes.
  • Manage external laboratory relationships and oversee testing programmes.
  • Develop and maintain quality documentation, SOPs and technical procedures.
  • Deliver microbiology and aseptic technique training across the business.
  • Drive continuous improvement initiatives to strengthen quality and compliance.
Your Background:

You'll bring experience from a sterile pharmaceutical, healthcare or aseptic manufacturing environment and be passionate about maintaining the highest standards of product quality.
  • A degree in Microbiology or a related scientific discipline (or equivalent experience).
  • Strong operational experience in sterility assurance within a GMP-regulated aseptic environment.
  • Strong knowledge of environmental monitoring programmes and microbiological quality systems.
  • Experience investigating deviations, out-of-specification or out-of-limit results.
  • A good understanding of GMP and pharmaceutical regulatory requirements.
Benefits
  • Private Healthcare cover.
  • Company Pension Scheme.
  • Life Assurance.
  • Gym Discount.
  • Access to Wellness platforms.
  • Yearly Pay Reviews
If you're looking for an opportunity where your expertise in sterility assurance and microbiology will make a real difference, we'd love to hear from you.

Apply:

It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence.
View Details Apply Now
NEW
QA Officer

Manchester

Permanent £38000.00 - £40000.00 Annual

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

  • Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
  • Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
  • Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
  • Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
  • Raising and overseeing the implementation of Change Controls and CAPA's when required
  • Participating in site inspections by Regulatory Authorities
  • Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
  • Writing, reviewing and contributing to Risk Assessments

Benefits:

  • Discretionary Bonus
  • Healthcare & More

About You:

  • Experience within a pharmaceutical environment
  • A strong Quality Assurance background (2 to 3 years experience)
  • Experience within sterile manufacturing environments (desirable)
  • Good working knowledge of GMP requirements and quality systems
  • Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
  • Strong communicator and team player
  • Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

View Details Apply Now
NEW
QA Officer

Guildford

Permanent £38000.00 - £40000.00 Annual

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

  • Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
  • Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
  • Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
  • Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
  • Raising and overseeing the implementation of Change Controls and CAPA's when required
  • Participating in site inspections by Regulatory Authorities
  • Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
  • Writing, reviewing and contributing to Risk Assessments

Benefits:

  • Discretionary Bonus
  • Healthcare & More

About You:

  • Experience within a pharmaceutical environment
  • A strong Quality Assurance background (2 to 3 years experience)
  • Experience within sterile manufacturing environments (desirable)
  • Good working knowledge of GMP requirements and quality systems
  • Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
  • Strong communicator and team player
  • Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

View Details Apply Now
NEW
QA Microbiologist

Permanent £27000.00 - £29000.00 Annual

QA Microbiologist Irvine, Ayrshire 27,000 - 29,000 + Benefits

Escape Recruitment is working with a well-established manufacturing business in Ayrshire that is investing heavily in its laboratory and quality capabilities. As part of this growth, they are looking to appoint a QA Microbiologist to support the introduction of in-house microbiological testing.

This is an excellent opportunity for someone with commercial microbiology laboratory experience who enjoys a varied, hands-on role within a manufacturing environment. Graduates with a relevant industrial placement are also encouraged to apply.



The Role

Reporting into the Quality team, you'll be responsible for carrying out microbiological testing across raw materials, environmental samples and finished products, helping to ensure products meet the highest quality and regulatory standards.

Duties will include:

  • Microbiological testing of raw materials, environmental and finished product samples
  • Identifying bacteria, yeast and mould contamination
  • Environmental monitoring and hygiene testing
  • Preparing media and laboratory reagents
  • Recording, analysing and reporting test results
  • Investigating out of specification results
  • Supporting laboratory validation activities
  • Maintaining laboratory equipment and consumable stocks
  • Working closely with the wider Quality and Laboratory teams
  • Supporting continuous improvement within the laboratory


About You

We're interested in candidates who have:

  • A degree in Microbiology, Biological Sciences or a related discipline
  • Commercial laboratory experience within a manufacturing environment
  • Experience of microbiological testing techniques
  • Good laboratory documentation and reporting skills
  • Strong attention to detail and organisational skills
  • The ability to work both independently and as part of a team
  • The right to work in the UK without sponsorship

Graduates who have completed a substantial industrial placement within a commercial laboratory are also encouraged to apply.



What's on Offer

  • Salary of 27,000 - 29,000
  • Opportunity to join a growing manufacturing business
  • Modern laboratory environment
  • Excellent opportunity to develop within Quality and Microbiology
  • Full-time permanent position based in Irvine

If you're looking for your next opportunity within microbiology and quality, we'd love to hear from you.

View Details Apply Now
NEW
Quality Assurance Officer

London

Permanent £30000.00 - £35000.00 Annual

Walker Cole International is supporting a growing pharmaceutical organisation in the search for a Quality Assurance Officer to join their Quality team on a 12-month fixed-term contract. This is an excellent opportunity to join a rapidly expanding business that has experienced significant growth in recent years, offering exposure to a diverse portfolio of pharmaceutical products and medical devices supplied across European markets.

Operating within a virtual pharmaceutical model, the company works closely with Contract Manufacturing Organisations (CMOs), providing broad exposure to external manufacturing and quality assurance activities. This role offers a hybrid working pattern and the opportunity to develop within a collaborative and supportive Quality team.

You will be responsible for:

  • Reviewing batch manufacturing and packaging records to ensure compliance with GMP requirements prior to product release.

  • Performing batch release activities, ensuring products meet the required quality standards before distribution.

  • Working closely with external manufacturing partners and internal stakeholders to support day-to-day quality assurance activities.

  • Maintaining accurate quality documentation while supporting compliance with GMP and the Quality Management System.

The successful candidate will have:

  • Previous Quality Assurance experience within a GMP-regulated pharmaceutical, biotechnology or medical device environment.

  • Experience reviewing batch records and/or supporting batch release activities.

  • A strong understanding of GMP principles and pharmaceutical quality systems.

  • Excellent attention to detail, communication skills and the ability to work effectively with both internal teams and external manufacturing partners.

Quality Assurance QA Quality Assurance Officer GMP Good Manufacturing Practice Batch Record Review Batch Release QMS Quality Management System Pharmaceutical Medical Devices CMO Contract Manufacturing Organisation Compliance GDP Hybrid

View Details Apply Now
NEW
QA Officer

Lancaster

Permanent £38000.00 - £40000.00 Annual

We have all known someone who has been affected by Cancer, whether that be a friend, family member, or colleague.

That is why, at ARx we are pleased to be working closely with a fantastic, highly regulated pharmaceutical company that plays a significant role supporting efforts to diagnose and treat advanced cancers more efficiently, and with less negative effect on the patient.

As a growing organisation, they are seeking an experienced Quality Assurance Officer to join their established Quality Team.

The Role: Full Time (Monday to Friday) On-site

  • Working with the Corporate Senior QA Manager & QA departments in the UK to ensure the Global Document / Quality Management System (QMS) is being administered compliantly to Good Manufacturing Processes (GMP), Company Procedures and Regulatory rules & guidelines
  • Contributing to the Global QA function in the UK and acting as a QA representative to support outsourced activities while working effectively with colleagues across multiple sites within the organisation
  • Supporting activities relating to Manufacturing Authorisations/ Product Licences and Marketing Authorisations
  • Reviewing and updating policies, Standard Operating Procedures (SOPs), forms, logbooks and templates
  • Raising and overseeing the implementation of Change Controls and CAPA's when required
  • Participating in site inspections by Regulatory Authorities
  • Preparing information and taking part in the Global Quality Management Meetings (QMM) and tracking performance against KPI's and specified standards
  • Writing, reviewing and contributing to Risk Assessments

Benefits:

  • Discretionary Bonus
  • Healthcare & More

About You:

  • Experience within a pharmaceutical environment
  • A strong Quality Assurance background (2 to 3 years experience)
  • Experience within sterile manufacturing environments (desirable)
  • Good working knowledge of GMP requirements and quality systems
  • Practical experience in the quantitative and qualitative analysis of active substances, including the necessary testing (ideally)
  • Strong communicator and team player
  • Confident using Microsoft Office products

If this sounds like a role that you have been looking for, click APPLY NOW

View Details Apply Now

Don't miss your perfect job

Create a job alert and we'll send you the latest matches straight to your inbox.

Need help?

Our team is here to help you find the right role.

Contact Us
close

Apply this job

Click OK to Apply Manage your account
close

Saved Successfully!!!.


close

You're about to be taken to the employer's website to complete your application.
Please either log in, or enter your name and email address before we re-direct you

We are now directing your application to one of our trusted partners to complete the application.

close

Registration

Registered Successfully!!!. We have sent you a confirmation email to your email address.
Apply
close

Verify Your Account

We've sent a verification code to

Time remaining:
Verifying...
Code expired. Please request a new one.
Verify & Register
Didn’t receive the code? 
close You must sign in / sign up to save or apply to job opportunities.
  • Sign In
  • Sign Up

Create an Account

Your Preferences

(word/pdf/rtf/textfiles)

Contact Preferences

In addition to providing our recruitment services to you, we may want to occasionally contact you to let you know about our recruitment services, industry insights, employment news and competitions. 

You will be able to update your preferences or delete your account/information at any time by logging into your account or making a request via email or phone.



Already registered?

Sign in with your account

Use your social media account to register (Don't worry we won't post anything)

LinkedIn
By connecting your social account, you are agreeing to our Terms & Conditions and Privacy Policy.

Login to your account


Forget your Password ?

click here to reset your password

- or sign in using -
Facebook
LinkedIn
By connecting your social account, you are agreeing to our Terms & Conditions and Privacy Policy
Not got an account? Please register here

mujo.com is brought to you by International Medical Information. For more details. visit http://www.medicalimi.com

Disclaimer: All information on this site has been collated by healthcare professionals from around the globe. Where every possible step has been taken to ensure its accu-racy, MedicalUpdateOnline cannot accept responsibility for the authenticity of the content matter.

Copyright: The copyright of the material on this site rests with the author unless otherwise indicated. It is a breach of copyright to use any material from this site without prior written consent.

Jobs
Jobs
  • Upload CV
  • Find a job
  • Job alerts
  • Career advice
  • Recruiter A-Z
Candidate
More Info
  • Sign in
  • Register
Recruiter
  • Advertise with us
  • Sign in
  • Register
More Info
Community
  • About us
  • Terms and Conditions
  • Privacy policy

Subscribe for job alerts

If you're a healthcare professional, you can sign up for our job alerts to receive high-quality opportunities in medicine, pharmaceuticals, and healthcare. Get the latest jobs and updates across a broad range of specialties delivered straight to your inbox.

Copyright © ICR (UK) Limited t/a International Medical Information (IMI). Registered in the UK Company no. 05894351

Powered by Talenetic Job Board Software

arrow_upward