QA Releaser Job at Baxter (Thetford)

QA Releaser

We are recruiting for QA Releasers to join our Compounding team in Thetford, ens...

Location

United Kingdom , Thetford

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree or BTEC (or equivalent) in Pharmaceutical or Science related subject preferable but not essential
At least 2 years experience in a GMP environment
Strong work ethic and able to work flexibly to meet the needs of the business
Uncompromising commitment to Quality
Ability to communicate effectively to all levels of the organisation
Committed and supportive teammate
Accurate worker with strong attention to detail

Job Responsibility

Support manufacture of aseptically products by making QA decisions during batch manufacturing and ensuring GMP is adhered to at all times
Complete documentation and batch reviews as required
Inspect and release final products as per Company policies
Support Production in the review and post compounding check operations
Support delivery of product release targets, including ensuring timely batch review activities and batch disposition of any deviations with impact to product release
Proactively identify and support implementation of continuous improvement opportunities in QA and Operations
Ensure timely completion of all GMP commitments
Ensure timely communication of significant GMP and product quality issues to QA Management
Align with EHS/GMP/GDP/Company and Corporate policies and external regulatory requirements
Ensure facility and process compliance through attendance of Gemba activities, identifying actions and facilitate implementation

What we offer

25 days annual leave + bank holidays
Employee discount scheme
Blue light card
Fantastic internal progression opportunities
Subsided canteen
Westfield healthcare
Up to 8% pension contribution
Employee assistance programme

Fulltime

QA Releaser

The QA Releaser will report to the Compounding QA Supervisor ensuring continuous...

Location

United Kingdom , Thetford

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree or BTEC (or equivalent) in Pharmaceutical or Science related subject preferable but not essential
At least 2 years experience in a GMP environment
Strong work ethic and able to work flexibly to meet the needs of the business
Uncompromising commitment to Quality
Ability to communicate effectively to all levels of the organisation
Committed and supportive teammate
Accurate worker with strong attention to detail

Job Responsibility

Support manufacture of aseptically products by making QA decisions during batch manufacturing and ensuring GMP is adhered to at all times
Complete documentation and batch reviews as required
Inspect and release final products as per Company policies
Support Production in the review and post compounding check operations
Support delivery of product release targets, including ensuring timely batch review activities and batch disposition of any deviations with impact to product release
Proactively identify and support implementation of continuous improvement opportunities in QA and Operations
Ensure timely completion of all GMP commitments
Ensure timely communication of significant GMP and product quality issues to QA Management
Align with EHS/GMP/GDP/Company and Corporate policies and external regulatory requirements
Ensure facility and process compliance through attendance of Gemba activities, identifying actions and facilitate implementation

What we offer

25 days annual leave + bank holidays
Employee discount scheme
Blue light card
Fantastic internal progression opportunities
Subsided canteen
Westfield healthcare
Up to 8% pension contribution
Employee assistance programme

Fulltime

QA Releaser

The QA Releaser will ensure continuous compliance of the Compounding Unit to cGM...

Location

United Kingdom , Thetford

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree or BTEC (or equivalent) in Pharmaceutical or Science related subject preferable but not essential
at least 2 years experience in a GMP environment
strong work ethic and able to work flexibly to meet the needs of the business
uncompromising commitment to Quality
ability to communicate effectively to all levels of the organisation
committed and supportive teammate
accurate worker with strong attention to detail

Job Responsibility

Support manufacture of aseptically products by making QA decisions during batch manufacturing and ensuring GMP is adhered to at all times
complete documentation and batch reviews as required
inspect and release final products as per Company policies
support Production in the review and post compounding check operations
support delivery of product release targets, including ensuring timely batch review activities and batch disposition of any deviations with impact to product release
proactively identify and support implementation of continuous improvement opportunities in QA and Operations
ensure timely completion of all GMP commitments
ensure timely communication of significant GMP and product quality issues to QA Management
align with EHS/GMP/GDP/Company and Corporate policies and external regulatory requirements
ensure facility and process compliance through attendance of Gemba activities, identifying actions and facilitate implementation

What we offer

25 days annual leave + bank holidays
employee discount scheme
blue light card
fantastic internal progression opportunities
subsidized canteen
Westfield healthcare
up to 8% pension contribution
employee assistance programme

Fulltime

Senior Quality Assurance Engineer

LoadUp is a fast-growing company offering consumers a modern alternative to pick...

Location

United States

Salary:

90000.00 - 100000.00 USD / Year

LoadUp

Expiration Date

Until further notice

Requirements

8+ years designing and developing test automation frameworks from scratch using tools like Playwright, Selenium, Cucumber, JavaScript/TypeScript, Java, or similar
4+ years hands-on software testing and writing automation code in at least one language (JavaScript, TypeScript, Java, C#, Python) and mentoring team members technically
4+ years creating and executing automated tests for REST APIs, including intercepting and mocking complex HTTP calls
4+ years leading complex end-to-end test automation projects
4+ years using test management and defect tracking tools to drive defect strategy (priority, traceability, root cause analysis, reporting)
2+ years implementing automated test suites across testing types (unit, component, API, UI, UAT, E2E)
Experience signing off engineering tickets through automated and manual smoke testing
Deep understanding of QA methodologies, defect tracking, and risk-based testing
Proficient with automated testing tools (RSpec, Capybara, Cypress, Playwright, Selenium) and maintaining robust test suites for frontend and backend
Skilled in API testing using Postman, Insomnia, or Karate

Job Responsibility

Ensure high-quality software at scale—test web, mobile, and APIs, collaborate with top engineers and product managers, and help deliver a transformational platform
Play a crucial role in scaling our platform and delivering cutting-edge capabilities to our customers across our web application, multiple mobile apps, and publicly consumed APIs
Collaborate with a phenomenal group of software engineers and product managers and be directly involved with the growth of our product organization to deliver and scale a transformational software product

What we offer

Competitive Compensation
Comprehensive Health & Wellness Benefits – Medical, Dental, Vision, and Life Insurance coverage
Flexible Spending & Savings Options – Tailor your healthcare planning with FSA or HSA accounts
401(k) with 5% Company Match
Employee Recognition Program
Monthly Lifestyle Stipends
Referral Rewards Program
Growth with Purpose
PTO, Sick Days & Parental Leave

Fulltime

QA Testing Intern – Hospitality Digital Products

We are seeking a detail-oriented and motivated QA Testing Intern to support the ...

Location

United States , Fort Lauderdale

Salary:

Not provided

Tambourine

Expiration Date

Until further notice

Requirements

Currently pursuing (or recently completed) a degree in Computer Science, Information Systems, Digital Media, Marketing Technology, Hospitality, or a related field
Strong attention to detail and ability to follow structured testing procedures
Basic understanding of how websites work (pages, links, forms, browsers, responsiveness)
Comfort working with digital tools (ticketing systems, documentation, spreadsheets)
Strong written communication skills and ability to document issues clearly
High accountability, curiosity, and willingness to learn in a fast-paced environment

Job Responsibility

Execute manual testing for hotel websites, booking flows, and marketing technology tools
Validate functionality across desktop, tablet, and mobile—including browser and device compatibility
Test enhancements, bug fixes, new modules, and template updates prior to release
Perform regression testing to confirm updates do not break existing functionality
Follow established QA checklists and contribute to expanding test coverage over time
Identify bugs, inconsistencies, broken UI elements, and usability issues
Document issues clearly using reproduction steps, screenshots, recordings, and environment details
Log and track issues in a ticketing system and support validation through resolution
Work closely with QA and engineering teams to verify fixes
Participate in QA reviews and release validation checkpoints

What we offer

Mentorship from seasoned professionals who are experts in their field
A supportive and inclusive environment where your ideas are valued and your growth is encouraged
Paid internship

Fulltime

Quality Assurance Release Supervisor

As a QA Release Supervisor, you lead and develop a team responsible for the rele...

Location

Belgium , Lessines

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree in Science or Engineering
an advanced degree is preferred
Proven experience in a similar QA Release or QA leadership role
Demonstrated experience in people management
Experience with GMP requirements (EU GMP, EudraLex Volume 4) and medical device regulations
Strong knowledge of quality systems, compliance expectations and release processes
QP delegate experience/training is an asset
Strong analytical mindset and structured problem‑solving approach
Excellent communication, presentation and stakeholder‑management skills
Ability to work under pressure and adapt to change

Job Responsibility

Lead, supervise, coach and support a QA Release team of ~10 employees
Plan, coordinate and monitor batch file review activities
Ensure engagement, development and well‑being within the team
Manage and control finished product release for sterile drugs and medical devices
Review and approve deviations/events linked to the manufacturing process
Monitor and continuously improve release performance and associated KPIs
Prepare and present KPI results to site leadership, regional and global Quality teams
Serve as the QA Release representative for interactions with Manufacturing, Supply Chain, CMOs/3rd parties, Product Development, Corporate QA
Ensure efficient and compliant communication across departments
Ensure updates of quality documentation, SOPs and quality agreements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Quality Assurance Release Supervisor

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Belgium , Lessines

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree in Science or Engineering
an advanced degree is preferred
Proven experience in a similar QA Release or QA leadership role
Demonstrated experience in people management
Experience with GMP requirements (EU GMP, EudraLex Volume 4) and medical device regulations
Strong knowledge of quality systems, compliance expectations and release processes
QP delegate experience/training is an asset
Strong analytical mindset and structured problem‑solving approach
Excellent communication, presentation and stakeholder‑management skills
Ability to work under pressure and adapt to change

Job Responsibility

Lead, supervise, coach and support a QA Release team of ~10 employees
Plan, coordinate and monitor batch file review activities
Ensure engagement, development and well‑being within the team
Manage and control finished product release for sterile drugs and medical devices
Review and approve deviations/events linked to the manufacturing process
Monitor and continuously improve release performance and associated KPIs
Prepare and present KPI results to site leadership, regional and global Quality teams
Serve as the QA Release representative for interactions with Manufacturing, Supply Chain, CMOs/3rd parties, Product Development, Corporate QA
Ensure efficient and compliant communication across departments
Ensure updates of quality documentation, SOPs and quality agreements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Quality Assurance Release Supervisor

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Belgium , Lessines

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Degree in Science or Engineering
an advanced degree is preferred
Proven experience in a similar QA Release or QA leadership role
Demonstrated experience in people management
Experience with GMP requirements (EU GMP, EudraLex Volume 4) and medical device regulations
Strong knowledge of quality systems, compliance expectations and release processes
QP delegate experience/training is an asset
Strong analytical mindset and structured problem‑solving approach
Excellent communication, presentation and stakeholder‑management skills
Ability to work under pressure and adapt to change

Job Responsibility

Lead, supervise, coach and support a QA Release team of ~10 employees
Plan, coordinate and monitor batch file review activities
Ensure engagement, development and well‑being within the team
Manage and control finished product release for sterile drugs and medical devices
Review and approve deviations/events linked to the manufacturing process
Monitor and continuously improve release performance and associated KPIs
Prepare and present KPI results to site leadership, regional and global Quality teams
Serve as the QA Release representative for interactions with Manufacturing, Supply Chain, CMOs/3rd parties, Product Development, Corporate QA
Ensure efficient and compliant communication across departments
Ensure updates of quality documentation, SOPs and quality agreements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

QA Releaser

Baxter

Location:
United Kingdom , Thetford

Category:
Quality Control

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 20, 2025

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