Quality Engineer (Contract)
Posted on Jun 2, 2026 by CV-Library
Cheap, City and County of the City of London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Contract/Project
- Remote
Your new company
You will be joining a leading global organisation within the life sciences sector, recognised for its commitment to quality, innovation, and improving global health outcomes. The company operates within a highly regulated environment and fosters a collaborative, high-performing culture focused on continuous improvement and operational excellence.
Your new role
As a Q&RA Engineer, you will play a key role in supporting quality and regulatory compliance across operations. You will work closely with cross-functional teams to maintain and improve quality systems, ensuring products and processes meet stringent regulatory standards.Key responsibilities include:
Supporting compliance with GMP/GxP and ISO standards
Leading and contributing to deviation investigations and root cause analysis
Managing change control and CAPA processes
Authoring and reviewing quality documentation (SOPs, reports, etc.)
Supporting internal and external audits and regulatory inspections
Analysing quality data and reporting on trends and metrics
Collaborating with manufacturing, QA, and engineering teams to drive improvementsThis is a primarily remote role with occasional on-site presence required.
What you'll need to succeed
To be successful in this position, you will have:
A degree in Life Sciences, Engineering, or a related discipline
Experience within a regulated industry (pharmaceutical, biotech, or medical devices)
Strong knowledge of GMP/GxP and ISO standards
Experience with quality systems, including deviations, CAPA, and change control
Familiarity with QMS platforms (e.g. MasterControl or similar)
Strong investigation and root cause analysis skills
Excellent technical writing and documentation skills
Strong communication skills and ability to work cross-functionally
The ability to work both independently and collaborativelyMust have Full Right to Work in the UK for duration of contract. No Sponsorship Provided
What you'll get in return
In return, you will receive:
Competitive hourly rate
Flexible, primarily remote working arrangement
Opportunity to work within a well-established and reputable organisation
Exposure to a fast-paced, quality-driven environment
Potential for contract extensionWhat you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now
You will be joining a leading global organisation within the life sciences sector, recognised for its commitment to quality, innovation, and improving global health outcomes. The company operates within a highly regulated environment and fosters a collaborative, high-performing culture focused on continuous improvement and operational excellence.
Your new role
As a Q&RA Engineer, you will play a key role in supporting quality and regulatory compliance across operations. You will work closely with cross-functional teams to maintain and improve quality systems, ensuring products and processes meet stringent regulatory standards.Key responsibilities include:
Supporting compliance with GMP/GxP and ISO standards
Leading and contributing to deviation investigations and root cause analysis
Managing change control and CAPA processes
Authoring and reviewing quality documentation (SOPs, reports, etc.)
Supporting internal and external audits and regulatory inspections
Analysing quality data and reporting on trends and metrics
Collaborating with manufacturing, QA, and engineering teams to drive improvementsThis is a primarily remote role with occasional on-site presence required.
What you'll need to succeed
To be successful in this position, you will have:
A degree in Life Sciences, Engineering, or a related discipline
Experience within a regulated industry (pharmaceutical, biotech, or medical devices)
Strong knowledge of GMP/GxP and ISO standards
Experience with quality systems, including deviations, CAPA, and change control
Familiarity with QMS platforms (e.g. MasterControl or similar)
Strong investigation and root cause analysis skills
Excellent technical writing and documentation skills
Strong communication skills and ability to work cross-functionally
The ability to work both independently and collaborativelyMust have Full Right to Work in the UK for duration of contract. No Sponsorship Provided
What you'll get in return
In return, you will receive:
Competitive hourly rate
Flexible, primarily remote working arrangement
Opportunity to work within a well-established and reputable organisation
Exposure to a fast-paced, quality-driven environment
Potential for contract extensionWhat you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now
Reference: 225190649
https://jobs.careeraddict.com/post/113340329
Quality Engineer (Contract)
Posted on Jun 2, 2026 by CV-Library
Cheap, City and County of the City of London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Contract/Project
- Remote
Your new company
You will be joining a leading global organisation within the life sciences sector, recognised for its commitment to quality, innovation, and improving global health outcomes. The company operates within a highly regulated environment and fosters a collaborative, high-performing culture focused on continuous improvement and operational excellence.
Your new role
As a Q&RA Engineer, you will play a key role in supporting quality and regulatory compliance across operations. You will work closely with cross-functional teams to maintain and improve quality systems, ensuring products and processes meet stringent regulatory standards.Key responsibilities include:
Supporting compliance with GMP/GxP and ISO standards
Leading and contributing to deviation investigations and root cause analysis
Managing change control and CAPA processes
Authoring and reviewing quality documentation (SOPs, reports, etc.)
Supporting internal and external audits and regulatory inspections
Analysing quality data and reporting on trends and metrics
Collaborating with manufacturing, QA, and engineering teams to drive improvementsThis is a primarily remote role with occasional on-site presence required.
What you'll need to succeed
To be successful in this position, you will have:
A degree in Life Sciences, Engineering, or a related discipline
Experience within a regulated industry (pharmaceutical, biotech, or medical devices)
Strong knowledge of GMP/GxP and ISO standards
Experience with quality systems, including deviations, CAPA, and change control
Familiarity with QMS platforms (e.g. MasterControl or similar)
Strong investigation and root cause analysis skills
Excellent technical writing and documentation skills
Strong communication skills and ability to work cross-functionally
The ability to work both independently and collaborativelyMust have Full Right to Work in the UK for duration of contract. No Sponsorship Provided
What you'll get in return
In return, you will receive:
Competitive hourly rate
Flexible, primarily remote working arrangement
Opportunity to work within a well-established and reputable organisation
Exposure to a fast-paced, quality-driven environment
Potential for contract extensionWhat you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now
You will be joining a leading global organisation within the life sciences sector, recognised for its commitment to quality, innovation, and improving global health outcomes. The company operates within a highly regulated environment and fosters a collaborative, high-performing culture focused on continuous improvement and operational excellence.
Your new role
As a Q&RA Engineer, you will play a key role in supporting quality and regulatory compliance across operations. You will work closely with cross-functional teams to maintain and improve quality systems, ensuring products and processes meet stringent regulatory standards.Key responsibilities include:
Supporting compliance with GMP/GxP and ISO standards
Leading and contributing to deviation investigations and root cause analysis
Managing change control and CAPA processes
Authoring and reviewing quality documentation (SOPs, reports, etc.)
Supporting internal and external audits and regulatory inspections
Analysing quality data and reporting on trends and metrics
Collaborating with manufacturing, QA, and engineering teams to drive improvementsThis is a primarily remote role with occasional on-site presence required.
What you'll need to succeed
To be successful in this position, you will have:
A degree in Life Sciences, Engineering, or a related discipline
Experience within a regulated industry (pharmaceutical, biotech, or medical devices)
Strong knowledge of GMP/GxP and ISO standards
Experience with quality systems, including deviations, CAPA, and change control
Familiarity with QMS platforms (e.g. MasterControl or similar)
Strong investigation and root cause analysis skills
Excellent technical writing and documentation skills
Strong communication skills and ability to work cross-functionally
The ability to work both independently and collaborativelyMust have Full Right to Work in the UK for duration of contract. No Sponsorship Provided
What you'll get in return
In return, you will receive:
Competitive hourly rate
Flexible, primarily remote working arrangement
Opportunity to work within a well-established and reputable organisation
Exposure to a fast-paced, quality-driven environment
Potential for contract extensionWhat you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now
Reference: 225190649
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