12 jobs in Nexus Life Sciences

Job Advertisement: Senior Scientist - Mass Spectrometry

We are hiring a senior scientist with expertise in advanced mass spectrometry (LC-MS/MS or GC-MS/MS) to join our growing team.

Salary: £40,000 - £50,000

• Develop and optimize methods using LC-MS/MS and GC-MS/MS.
• Handle complex sample types (e.g., lipids, oils, botanical materials).
• Contribute to method validation under ICH and GMP guidelines.
• Ensure analytical quality and data integrity.
• Act as a technical specialist in mass spectrometry and troubleshoot challenges.
• Support laboratory processes and improve best practices.
• Build proficiency in GMP requirements over time.

• Essential:
  • BSc/MSc/PhD in Analytical Chemistry or a related field.
  • Strong hands‑on experience with LC-MS/MS or GC-MS/MS.
  • Proven expertise in method development and problem‑solving.
  • Familiarity with analysing complex matrices.
  • Commitment to high analytical standards.
• Desirable:
  • GMP or regulated environment experience.
  • ICP-MS or complementary analytical techniques.
  • Understanding of data integrity (e.g., ALCOA+).

• Generous Leave: Up to 40.5 days annually, including Christmas closures.
• Pension: 15% employer contribution to a personal pension plan.
• Employee Support: Access to a confidential Employee Assistance Programme (EAP).
• Flexible Work Options: Self‑managed hours and work‑life balance flexibility.
• Career Growth: Opportunities to advance skills in mass spectrometry and GMP.
• Collaborative Team: Join a technically driven team in a growing pharmaceutical sector.

Join us to leverage your mass spectrometry expertise while contributing to innovative pharmaceutical solutions. This is an opportunity to work in a supportive, inclusive environment at the forefront of analytical development in a growing sector.

We are working with a specialty chemical manufacturing business operating within a highly regulated, safety-critical environment. Due to continued investment and growth, they are looking to appoint an experienced Maintenance Engineer with ATEX exposure and strong mechanical and electrical capability to join their site-based engineering team. This role offers the opportunity to work on equipment supporting the manufacture of materials used in pharmaceutical and advanced technology applications.

The Maintenance Engineer will play a key role in ensuring the safe, reliable, and efficient operation of site assets. Reporting into the site maintenance function, you will support planned and reactive maintenance activities while ensuring full compliance with health, safety, environmental, and quality standards.

• Maintenance & Engineering
• Carry out planned and reactive mechanical and electrical maintenance across production and facility equipment.
• Perform fault-finding, repairs, servicing, and installation work to minimise downtime.
• Support maintenance records, documentation, and compliance requirements.
• ATEX & Safety
• Work within ATEX / potentially explosive atmospheres, ensuring strict adherence to safety procedures.
• Complete task-based risk assessments and method statements.
• Maintain high standards of health, safety, and environmental compliance at all times.
• Electrical & Mechanical Duties
• Undertake electrical tasks including wiring, fault diagnosis, and basic control systems support.
• Use tool-craft equipment such as grinding and welding tools where required.
• Provide hands-on support across both mechanical and electrical disciplines.
• Work closely with production and engineering colleagues to prioritise maintenance activity.
• Liaise with contractors and suppliers to ensure maintenance tasks are delivered safely and on schedule.
• Build strong working relationships across the site.
• Support ongoing reliability and improvement initiatives.
• Assist with root cause analysis and non-routine problem solving.
• Carry out additional duties as required to support site operations.

• Mechanical and electrical maintenance experience within an industrial or manufacturing environment.
• Experience working with hazardous chemicals and/or ATEX-regulated environments.
• Understanding of relevant health and safety legislation, including:
• Explosive atmospheres (ATEX)
• Working at height
• Electrical experience including wiring and fault-finding.
• Basic IT competence and ability to complete maintenance documentation.
• Practical experience using general maintenance tools (e.g. grinding, welding).

• Background in chemical, pharmaceutical, or process manufacturing environments.
• Ability to interpret technical drawings and electrical schematics.
• Exposure to AutoCAD.

Salary: Up to £50,000 (dependent on experience)

What’s On Offer:

• Employee Assistance Programme
• Life assurance
• Income protection and critical illness cover
• Health cash plan

We are committed to diversity and inclusivity.

Nexus Life Sciences in Dundee is seeking a Senior Scientist with expertise in advanced mass spectrometry (LC-MS/MS or GC-MS/MS) to join our growing team.

You will develop and optimize methods, handle complex matrices, contribute to method validation under ICH and GMP guidelines, and support data integrity.

The role offers a collaborative environment, opportunities to advance skills in GMP and analytical development, and a focus on delivering high-quality pharmaceutical analytics.

Job Advertisement: Senior Scientist - Mass Spectrometry

Overview

We are hiring a senior scientist with expertise in advanced mass spectrometry (LC-MS/MS or GC-MS/MS) to join our growing team.

Salary: 40,000 - 50,000

Key Responsibilities

• Develop and optimize methods using LC-MS/MS and GC-MS/MS.
• Handle complex sample types (e.g., lipids, oils, botanical materials).
• Contribute to method validation under ICH and GMP guidelines.
• Ensure analytical quality and data integrity.
• Act as a technical specialist in mass spectrometry and troubleshoot challenges.
• Support laboratory processes and improve best practices.
• Build proficiency in GMP requirements over time.

Qualifications

• Essential:
  • BSc/MSc/PhD in Analytical Chemistry or a related field.
  • Strong hands-on experience with LC-MS/MS or GC-MS/MS.
  • Proven expertise in method development and problem-solving.
  • Familiarity with analyzing complex matrices.
  • Commitment to high analytical standards.
• Desirable:
  • GMP or regulated environment experience.
  • ICP-MS or complementary analytical techniques.
  • Understanding of data integrity (e.g., ALCOA+).

Benefits

• Generous Leave: Up to 40.5 days annually, including Christmas closures.
• Pension: 15% employer contribution to a personal pension plan.
• Employee Support: Access to a confidential Employee Assistance Programme (EAP).
• Flexible Work Options: Self-managed hours and work-life balance flexibility.
• Career Growth: Opportunities to advance skills in mass spectrometry and GMP.
• Collaborative Team: Join a technically driven team in a growing pharmaceutical sector.

Why Apply?

Join us to leverage your mass spectrometry expertise while contributing to innovative pharmaceutical solutions. This is an opportunity to work in a supportive, inclusive environment at the forefront of analytical development in a growing sector.

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

• Performing routine and non-routine analysis of raw materials, intermediates, and finished products.
• Operating and maintaining analytical instrumentation, including HPLC, GC, UV-Vis, FTIR, Karl Fischer, and wet chemistry techniques.
• Reviewing analytical data to ensure compliance with specifications.
• Preparing analytical reports and laboratory documentation in accordance with GMP and company procedures.
• Investigating Out of Specification (OOS), Out of Trend (OOT), and laboratory deviations as required.
• Supporting analytical method verification, validation, and method transfers.
• Assisting with stability studies and environmental monitoring activities.
• Performing instrument calibration, routine maintenance, and troubleshooting.
• Maintaining laboratory housekeeping and ensuring compliance with Health & Safety procedures.
• Participating in continuous improvement initiatives to enhance laboratory efficiency and quality.
• Collaborating with Production, QA, and Process Development teams.

Qualifications

Essential:

• Degree (or equivalent) in Chemistry, Analytical Chemistry, Pharmaceutical Science, or a related scientific discipline.
• Previous laboratory experience within a pharmaceutical, chemical, CDMO, or GMP-regulated environment.
• Hands-on experience using HPLC and/or GC.
• Good understanding of GMP and laboratory documentation practices.
• Strong attention to detail and excellent organisational skills.
• Ability to work independently and as part of a team.
• Strong written and verbal communication skills.

Desirable:

• Experience working within a pharmaceutical manufacturing environment.
• Knowledge of analytical method validation and transfer.
• Experience investigating OOS/OOT results.
• Familiarity with LIMS, Empower, Chromeleon, or similar chromatography software.
• Understanding of ICH guidelines and data integrity principles (ALCOA+)

Pay range and compensation package

Salary: 28,000 to 36,000 dependent on experience.

Job Advertisement: Senior Scientist - Mass Spectrometry

We are hiring a senior scientist with expertise in advanced mass spectrometry (LC-MS/MS or GC-MS/MS) to join our growing team.

• Develop and optimize methods using LC‑MS/MS and GC‑MS/MS.
• Handle complex sample types (e.g., lipids, oils, botanical materials).
• Contribute to method validation under ICH and GMP guidelines.
• Ensure analytical quality and data integrity.
• Act as a technical specialist in mass spectrometry and troubleshoot challenges.
• Support laboratory processes and improve best practices.
• Build proficiency in GMP requirements over time.

• BSc/MSc/PhD in Analytical Chemistry or a related field.
• Strong hands‑on experience with LC‑MS/MS or GC‑MS/MS.
• Proven expertise in method development and problem‑solving.
• Familiarity with analyzing complex matrices.
• Commitment to high analytical standards.

• Generous Leave: Up to 40.5 days annually, including Christmas closures.
• Pension: 15% employer contribution to a personal pension plan.
• Employee Support: Access to a confidential Employee Assistance Programme (EAP).
• Flexible Work Options: Self‑managed hours and work‑life balance flexibility.
• Career Growth: Opportunities to advance skills in mass spectrometry and GMP.
• Collaborative Team: Join a technically driven team in a growing pharmaceutical sector.

Join us to leverage your mass spectrometry expertise while contributing to innovative pharmaceutical solutions. This is an opportunity to work in a supportive, inclusive environment at the forefront of analytical development in a growing sector.

Overview

Senior QA Officer - Contract Role (DOE). Location: Cheshire. Sector: Pharmaceutical Manufacturing. Contract: Full-time, on-site.

Our client is seeking an experienced Senior QA Officer to join the Quality team on a contract basis, offering a highly attractive day rate for the right candidate. This role is ideal for a quality professional who thrives in a fast-paced GMP environment and has proven experience managing project-based work. This position plays a key role in supporting ongoing validation activities across the site. You will be responsible for ensuring that all data generated from validation work is accurately collated, assessed, and entered into the Pharmaceutical Quality Management System (QMS). Working closely with the QA Section Leader and wider Quality team, you will help maintain compliance, support continuous improvement, and ensure the smooth running of departmental operations.

• Support ongoing validation projects, ensuring data is collected, reviewed, and entered into the QMS in a timely and compliant manner.
• Work collaboratively with cross-functional teams to uphold GMP standards and maintain the Pharmaceutical Quality System.
• Review, approve, and manage quality documentation, ensuring accuracy and compliance with internal procedures.
• Assist with internal audits, risk management activities, investigations, and root cause analysis.
• Maintain logs and records relating to Quality Events, CAPA, Supplier Non-Conformances, IARs, and change controls.
• Support supplier management activities, ensuring documentation is kept up to date.
• Provide administrative support including filing, archiving, and document control.
• Monitor quality KPIs and highlight emerging trends.
• Deputise for the QA Section Leader when required.
• Promote a strong quality culture and adherence to site health & safety standards.

Essential:

• Strong experience in QA within a regulated environment, ideally pharmaceuticals or life sciences.
• Demonstrable experience managing project work and coordinating cross-functional activities.
• Excellent attention to detail and organisational skills.
• Strong communication skills, both written and verbal.
• Computer literate (Word, Excel, MS Office).
• Previous QA administrative or documentation experience.

Desirable:

• Knowledge of GMP and associated regulatory guidance.
• Experience within pharmaceutical manufacturing.
• Exposure to MHRA inspections or customer audits.

Essential:

• Excellent literacy skills to GCSE standard or equivalent industry experience.

Desirable:

• HNC or Degree in Life Sciences or equivalent industry experience.

Nexus Life Sciences in Cheshire is seeking a Senior QA Officer to join the Quality team on a contract basis. You will support validation activities, ensuring data is accurate and entered into the Pharmaceutical Quality Management System (QMS), while maintaining compliance in a fast-paced GMP environment.

Working closely with the QA Section Leader and cross-functional teams, you will review documentation, manage internal audits and CAPA, and help drive continuous improvement in site quality