The vacancy you are looking for is no longer accepting applications and has been removed.
This resource is no longer available.
Customs & International Trade Regulations Analyst Homebased
Opportunity:
This is a great opportunity for a Customs & Trade Regulations Analyst to develop your career for a global pharmaceutical manufacturing company.
Do you have experience of import/export operations for a multinational company? Do you have experience with UK and Ireland customs related activities, incl. the management of specific authorizations (ex. EIDR, SDP) and local platforms (CHIEF, TSS and ROS)? Looking for a contract role with an exciting global pharmaceutical company? If yes then this is the role for you.
Your role as a Customs & International Trade Regulations Analyst will involve supporting the business across its EMEA sites for all Trade Compliance Processes and operations. You will be responsible for all import/export compliance with international trade, customs and other government agency laws and regulations to minimize the risk of penalty and fines due to non-compliance.
Essential Duties and Responsibilities include:
This is a 12 months contract role which will be reviewed for a possible extension or go permanent but this is all dependent on the individual and business performance. This is a role fully remote based home with travel to the company sites as and when required.
The PAYE rate is £32.20 per hour.
Skills:
To apply for role of Customs & International Trade Regulations Analyst you will have the following:
How to Apply:
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please do not hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Similar active jobs you might be interested in
Your new company
A leading commercial organisation is seeking a Procurement Specialist to join its growing procurement function. Initially available on a 3 month temporary basis with a view to then going permanent, the intention is to invest heavily in this role long-term once the initial 3 month period has been passed successfully. This is an excellent opportunity for an ambitious procurement professional looking to develop their career within a fast-paced, multi-site business, gaining exposure across a range of indirect spend categories while supporting strategic sourcing and supplier management initiatives.
Your new role
Reporting into the Procurement leadership team, you will support the delivery of procurement strategies, supplier management activities, and commercial projects across the business. Key responsibilities include:
What you'll need to succeedTo be successful in this role, you will have:
What you'll get in return
Apply now
If you're an analytical and commercially minded Procurement Specialist, Junior Procurement Manager, Procurement Analyst, or Purchasing Professional looking to accelerate your career, we'd love to hear from you. Apply today to join a forward-thinking procurement team and play a key role in delivering value, supplier excellence, and continuous improvement across the business.
Hays EA is a trading division of Hays Specialist Recruitment Limited and acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C's, Privacy Policy and Disclaimers which can be found at (url removed)
Evolve is partnering with a global healthcare organisation to recruit 2 SFE Analysts to join their Commercial Excellence team. This is a fantastic opportunity to work closely with Sales, Marketing, and Finance teams to deliver impactful Sales Force Effectiveness initiatives, commercial analytics, and data-driven reporting. Working with platforms including Salesforce, Veeva CRM, and Microsoft Power BI, you ll play a key role in driving commercial performance and supporting strategic business decisions within a global organisation.
These opportunities include both a permanent position and a -month contract role covering a secondment. The roles operate on a hybrid basis, with an expectation of three days per week in the office for those within commuting distance of our client's North West Head Office, or a minimum of two office days per month for candidates based further afield.
Why Apply?
Excellent Salary & Benefits - A competitive starting salary depending on experience, plus bonus, pension, and more!
Greater Impact - Work in a specialised team where your contributions visible and directly shape the company s success.
Job Stability Thrive in one of the industry s most resilient and future-proof organisations.
Ideal Requirements for the SFE Analyst
Role Responsibilities for the SFE Analyst
Recruitment Process
2 stage interview process
Connect with a hiring manager and team who are committed to guiding your career and helping you make an impact.
Excited to learn more? Click apply or reach out to the Pharmaceutical recruitment team for full details!
Application Process
Evolve Selection acts as a recruitment partner on behalf of our clients. All applications are reviewed by our specialist consultants and assessed against the specific requirements of the role. Suitable candidates will be contacted for an initial discussion before being introduced to the hiring client.
We appreciate every application; however, due to application volumes, we may not be able to respond to all candidates individually. If you have not heard from us within 3 working days, please consider your application unsuccessful for this particular role, however we may contact you regarding future opportunities that match your experience in line with our privacy policy.
Evolve is a leading recruitment and outsourcing organisation, operating within the Pharmaceutical, Healthcare, Medical Device and Life Science sectors.
Equal opportunities are important to us. We believe that diversity and inclusion are critical to our success as a company, We encourage applications from everyone, regardless of background, gender identity, sexual orientation, disability status, ethnicity, belief, age, family or parental status, and any other characteristic.
We are seeking a motivated and detail-oriented Junior QC Analyst to join an established pharmaceutical manufacturing team. This is an entry-level position ideal for recent graduates or individuals starting their career in Quality Control. You will support laboratory testing of raw materials, in-process samples, and finished products to ensure they meet required quality and regulatory standards.
If you receive suspicious outreach claiming to be from us, please contact us via the ManpowerGroup website.
Job Title: Quality Control Analyst
Location: Newmarket, England, United Kingdom.
About the Company
We are a leading UK manufacturer of fine chemicals and pharmaceutical intermediates, providing high-quality custom manufacturing and process development services to customers across the pharmaceutical, biotechnology, agrochemical, and specialty chemical industries. As part of our continued growth, we are seeking a motivated and detail-oriented QC Analyst to join our Quality Control team.
About the Role
As a QC Analyst, you will play a critical role in ensuring the quality and compliance of our products. Your key responsibilities will include:
Responsibilities
Qualifications
Essential:
Desirable:
Pay range and compensation package
Salary: 28,000 to 36,000 dependent on experience.
aJob Title: Behaviour Analyst
Location: Colchester, Essex
Contract Type: Permanent
Hours: Full-time
Salary: £41,000 - £43,000 (dependent on experience)
We are working on behalf of a well-established provider of adult social care, supporting people to lead active and fulfilling lives. They are looking for a Behaviour Analyst to join their team, working across services to deliver and embed positive behaviour support.
Key Responsibilities
Qualifications
Experience
Job Title: Behaviour Analyst
Location: Leicestershire & Nottinghamshire
Contract Type: Permanent
Hours: Full-time
Salary: £41,000 - £48,000 (dependent on experience)
We are working on behalf of a well-established provider of adult social care, supporting people to lead active and fulfilling lives. They are looking for a Behaviour Analyst to join their team, working across services to deliver and embed positive behaviour support.
Key Responsibilities
Qualifications
Experience
About Us
We are a leading national healthcare provider operating across both OFSTED-regulated Children's Services and CQC-registered Adult Services. With over 1,400 employees and a strong national presence, we are a fast-growing, innovative organisation committed to delivering outstanding care and support.
As we continue to invest in technology, data, and innovation, we are seeking a dynamic and forward-thinking Business Research Analyst to join our team and help shape the future direction of our organisation.
The Opportunity
This is an exciting opportunity for an ambitious graduate or early-career professional with a background in Technology, Artificial Intelligence, Business, Data Analytics, Research, or a related discipline. Working directly with the Senior Leadership Team, you will play a key role in supporting strategic decision-making through research, data analysis, and business intelligence.
You will be at the forefront of healthcare innovation, helping to identify opportunities, evaluate emerging technologies, analyse market trends, and support the development of operational and strategic plans that drive business growth and service excellence.
This is a highly autonomous role with genuine influence and decision-making responsibility, offering the opportunity to contribute to major business initiatives and long-term organisational development.
Key Responsibilities
What We're Looking For
What We Offer
Why Join Us?
This is more than a traditional analyst role. It is an opportunity to become a trusted partner to senior leaders and help shape the future of a national healthcare organisation. If you are passionate about research, technology, innovation, and making a meaningful impact in healthcare, we would love to hear from you.
Quality Control Laboratory Analyst GMP / GLP Kent
Opportunity:
Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!
Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards.
Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses.
You will also get involved in CAPA s, deviations and document control.
The hours of work are:
This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour.
Skills:
To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills:
How to Apply:
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Quality Control Laboratory Analyst GMP / GLP Kent
Opportunity:
Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!
Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards.
Testing techniques may include, but is not limited to, routine particle size analysis (Malvern Mastersizers, Sympatec), cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation (including particle size and cleanability assessments), DSC, Light microscopy, SEM, Moisture content (Karl Fisher), method optimisation and trouble-shooting, technology transfer and pharmacopoeia analyses.
You will also get involved in CAPA s, deviations and document control.
The hours of work are:
This is a 12 months contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour.
Skills:
To apply for the Quality Control Analytical Laboratory Analyst GMP / GLP role you will have the following skills:
How to Apply:
To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.
If this sounds like the role for you or a colleague then please don t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.
For a list of our current vacancies, please visit the Quality Start website.
If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.
Quality Start are acting as a specialist recruitment consultancy for this role.
Talent STEM are partnering with an established chemical manufacturer to recruit a Temporary QC Analyst to support their Quality Control laboratory during a busy production period.
This is an excellent opportunity for an experienced QC Analyst to join a busy manufacturing laboratory, carrying out routine analytical testing to support production and ensure products consistently meet quality standards.
The Opportunity
Working as part of the Quality Control team, you will perform routine analysis of raw materials, in-process samples and finished products using a range of analytical techniques. This is a hands-on laboratory role within a fast-paced manufacturing environment.
Key Responsibilities
- Perform analytical testing of raw materials, intermediates and finished products.
- Operate GC, HPLC, FTIR and Karl Fischer instrumentation.
- Carry out wet chemistry techniques including titrations.
- Prepare samples, standards and reagents.
- Record, review and report analytical results accurately.
- Support investigations into out-of-specification results.
- Maintain laboratory equipment and documentation.
- Ensure compliance with laboratory quality, HSE and COSHH procedures.
- Work closely with production and technical teams to support manufacturing.
About You
To be considered, you should have:
- A BSc (or equivalent) in Chemistry or a related scientific discipline.
- Previous experience within a QC or analytical laboratory.
- Essential: Hands-on industrial experience operating both GC and HPLC.
- Experience using FTIR and Karl Fischer would be advantageous.
- Wet chemistry experience, including titrations.
- Strong attention to detail and good laboratory documentation skills.
- A good understanding of laboratory safety and quality procedures.
- The ability to work effectively within a busy laboratory environment.
Why Apply?
- Immediate start available.
- Join an established chemical manufacturing business.
- Work with a wide range of analytical techniques.
For a confidential discussion, please contact Talent STEM directly.
Important: Applicants must have the unrestricted right to work in the UK. Unfortunately, this role is not eligible for visa sponsorship, and we are unable to consider applications from candidates who require sponsorship now or at any point in the future.
Talent STEM is a specialist recruitment consultancy supporting the scientific, engineering, chemical, pharmaceutical, environmental, waste, biotechnology, medical device and manufacturing sectors.
Create a job alert and we'll send you the latest matches straight to your inbox.
Our team is here to help you find the right role.
