CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded graduate to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining hands-on experience with raw material data management.

The Role

As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data while collaborating with a skilled global regulatory team. You’ll play a key part in ensuring product compliance, analysing scientific information, and contributing to important business decisions.

Key Responsibilities

• Develop awareness of major chemical legislation including CLP, REACH, GPSR, and CSR.
• Communicate with raw material suppliers to request and obtain key data such as Safety Data Sheets (SDSs) and Technical Data Sheets (TDSs).
• Interpret scientific data from SDSs and external databases (e.g., ECHA) to identify substance and mixture classifications.
• Use your understanding of toxicology to process and analyse data that supports regulatory and business decision-making.
• Provide technical regulatory expertise on chemicals to support product assessments.
• Update and maintain chemical and raw material data within systems such as SAP.
• Monitor regulatory developments, including updates such as ATPs, and assess their impact on products.

Requirements

• A degree or equivalent in a relevant scientific discipline (e.g., Chemistry, Biology, Toxicology, or equivalent).
• Strong scientific literacy and an interest in chemical regulations and product safety.
• Ability to work in a hybrid role, with 3 days per week on-site.
• Strong communication skills and attention to detail.

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

📍 Australia | Visa Sponsorship | Bioanalysis | GLP | CRO | Pharma

Are you an experienced Study Director with a strong background in regulated immunoassay bioanalysis?

CY Partners is partnering with a leading global bioanalytical and toxicology organisation to recruit a Study Director – Immunoassay (IA). This is an exciting opportunity to join a highly respected laboratory business supporting pharmaceutical and biopharmaceutical drug development programs across APAC, Europe, and the USA.

The organisation is recognised for its scientific excellence, advanced bioanalytical capabilities, and strong regulatory reputation, supporting both large and small molecule development as well as emerging cell and gene therapy programs.

The Role

As Study Director, you will lead regulated immunoassay studies from initiation through to completion, ensuring scientific integrity, regulatory compliance, and successful client delivery.

You’ll work closely with operational, QA, and R&D teams while also mentoring junior team members and managing multiple client projects in a fast-paced GLP environment.

Key Responsibilities

✔ Lead GLP immunoassay studies as Study Director / Principal Investigator
✔ Manage study timelines, client expectations, and project delivery
✔ Ensure regulatory compliance and scientific quality standards
✔ Communicate scientific updates and resolve technical challenges with clients and internal teams
✔ Support validation activities and method transitions from R&D
✔ Mentor and support junior scientific staff
✔ Contribute to continuous improvement initiatives and SOP development

About You

🔹 Degree in Life Sciences or related discipline
🔹 Experience in regulated bioanalysis within Pharma or CRO environments
🔹 Experience operating as a Study Director in a regulated setting
🔹 Strong immunoassay development and validation experience
🔹 Experience with GLP studies and client-facing project management
🔹 Knowledge of LIMS systems (Watson preferred)
🔹 Excellent communication and stakeholder management skills

Why Apply?

⭐ Join a globally recognised scientific organisation
⭐ Work with cutting-edge bioanalytical technologies
⭐ Exposure to diverse therapeutic modalities including cell & gene therapy
⭐ Collaborative and high-performing scientific culture
⭐ Excellent opportunity for career progression within a growing global business

📩 Interested? Contact CY Partners for a confidential discussion or apply directly via LinkedIn.

#Bioanalysis #Immunoassay #StudyDirector #GLP #CRO #Pharmaceuticals #Biotechnology #LifeSciences #DrugDevelopment #CellAndGeneTherapy #Hiring #AustraliaJobs

CY Partners is acting as an Employment Agency in relation to this vacancy. Applicants must have the full right to work in the UK

As Study Director, you will be involved with bioanalysis, using immunoassay technologies. You'll be responsible for performing Study Director functions regarding immunoassay based validations and analysis.

In the role of Immunoassay Study Director, you will be:
* Performing the role of Study Director and/or Principal Investigator with overarching responsibility for assigned studies.
* Plan, coordinate and manage studies to ensure timelines set appropriately to be achieved.
* Communicate effectively, building relationships with internal and external stakeholders (i.e. R&D, QA and clients, Clinical Research Organisations (CROs), respectively).
* Ensure the scientific integrity and regulatory compliance of study data.
* Troubleshoot scientific issues by liaising with appropriate groups including Research & Development (R&D), operations, management.
* Coordinate with operations and, in particular, the Lead Analyst to ensure operational progression of studies.
* Liaise with R&D to ensure smooth transition of methods into validation.
In this role you will be project managing and leading studies, with responsibilities to external clients and internal teams for the delivery of key results and studies. With a strong background in bioanalysis, particularly immunoassay, you will be able to apply your knowledge to GLP related bioanalytical studies and be instrumental in the development of new drugs for use within ground breaking medicine and science.

This is an excellent opportunity to work within leading drug development studies, with a global leader and strong presence within the Asia pacific region.
Based within a picturesque and beautiful part of Australia, this is truly an opportunity which is exciting, and one which doesn't occur often. With Visa sponsorship taken care of and an attractive relocation package, this is a perfect opportunity to work in beautiful Australia in the heart of culture and natural beauty.
We look forward to receiving your application
 

CY Partners are excited to be supporting a global organisation in recruiting an enthusiastic, scientifically minded graduate to join their experienced regulatory team. This is an excellent opportunity to work in chemical regulatory affairs, working with innovative product solutions and gaining hands-on experience with raw material data management.

The Role

As a Scientific Data & Regulatory Associate, you will support the technical aspects of managing raw material data while collaborating with a skilled global regulatory team. You’ll play a key part in ensuring product compliance, analysing scientific information, and contributing to important business decisions.

Key Responsibilities

• Develop awareness of major chemical legislation including CLP, REACH, GPSR, and CSR.
• Communicate with raw material suppliers to request and obtain key data such as Safety Data Sheets (SDSs) and Technical Data Sheets (TDSs).
• Interpret scientific data from SDSs and external databases (e.g., ECHA) to identify substance and mixture classifications.
• Use your understanding of toxicology to process and analyse data that supports regulatory and business decision-making.
• Provide technical regulatory expertise on chemicals to support product assessments.
• Update and maintain chemical and raw material data within systems such as SAP.
• Monitor regulatory developments, including updates such as ATPs, and assess their impact on products.

Requirements

• A degree or equivalent in a relevant scientific discipline (e.g., Chemistry, Biology, Toxicology, or equivalent).
• Strong scientific literacy and an interest in chemical regulations and product safety.
• Ability to work in a hybrid role, with 3 days per week on-site.
• Strong communication skills and attention to detail.

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners is acting as an Employment Business / Agency in relation to this vacancy.

With your Life Sciences background, you will be responsible for supporting Tissue-culture production (TCP) related manufacturing in line with customer needs. Your responsibilities will include dilutions and material manufacturing, as well as performing ELISA assays, tissue culturing and more. This role requires a working knowledge of microbiological techniques and the ability to take on responsibilities related to safety and quality.

Your Responsibilities will include:

• Adhere to all health and safety regulations to ensure risk is minimised within the lab.
• Ensure all products make it through manufacturing process error free.
• Participate in process improvement activities to ensure products are released efficiently and safely.
• Use SAP system for some basic transactional work, for example confirmation of works orders and stock management.
• Ensure that all materials used are within specification and that all procedures are conducted in line with regulations.
• Actively maintain quality standards in line with the principles of cGMP.
• Actively participate in any business management systems training as well as QMS training.
• Listen and respond to customer needs with confidentiality.
• Use 5 whys and Non-conformance reporting.
• Be responsible for your own training files, ensuring they are up to standard.
• Maintain equipment used as part of normal daily tasks, as and when appropriate.
• Any other reasonable task assigned by line manager for which the individual is deemed suitability skilled.
• SME in a minimum of one process - creates and maintains standard work for the process.
• Take part in departmental projects as required.

You will have:

• A relevant scientific qualification (BSc/MSc) in a related subject.
• The ability to work well within a team of staff.
• Excellent communication skills.
• Effective time management skills.
• A competency within a laboratory environment and the use of microbiological techniques.
• A desire to exceed targets and excel within your team.

The recruiter has stated that all applicants for this job should be able to prove that they are legally entitled to work in the UK. CY Partners Recruitment Ltd, trading as CY Partners is an Employment Business/Agency.

Location: Adelaide, South Australia
Sector: Pharmaceutical / Biotechnology / CRO
Type: Permanent

The Opportunity

CY Partners are supporting a leading international Life Sciences organisation with the appointment of an experienced Study Director – Bioanalysis.

This is an excellent opportunity for a senior bioanalytical scientist with expertise in ligand binding assays (LBA) and immunoassays to join an established organisation supporting pharmaceutical and biopharmaceutical drug development programmes.

Visa sponsorship and relocation support are available, making this a particularly attractive opportunity for experienced professionals looking to relocate to Australia.

The Role

As Study Director, you will take scientific and operational ownership of multiple GLP bioanalytical studies, with a particular focus on ligand binding assays and immunoassay-based bioanalysis.

You will manage studies from initiation through to completion, working closely with clients and internal R&D, Operations and Quality teams to ensure projects are delivered on time, to a high scientific standard and in accordance with regulatory requirements.

Key Responsibilities

• Lead GLP bioanalytical studies as Study Director or Principal Investigator.
• Oversee ligand binding assay and immunoassay validation and analysis.
• Manage multiple studies, clients and project timelines.
• Ensure scientific integrity, data quality and GLP/regulatory compliance.
• Act as a senior scientific contact for clients and external partners.
• Work closely with R&D and Operations to support method development, transfer and validation.
• Troubleshoot complex bioanalytical, LBA and immunoassay issues.
• Coordinate analytical activities across multidisciplinary teams.
• Mentor and support junior scientists and study support personnel.
• Contribute to SOP development, process improvement and regulatory compliance.

About You

You will ideally have:

• A degree in a Life Sciences or a related discipline.
• Experience in regulated bioanalysis, ideally within a pharmaceutical, biotechnology or CRO environment.
• Experience as a Study Director within a regulated environment.
• Strong experience with ligand binding assays (LBA) and immunoassays, including development, validation and/or sample analysis.
• Experience with platforms such as ELISA, ECL/MSD or other immunoassay technologies.
• A strong understanding of GLP and regulated bioanalytical environments.
• Excellent scientific problem-solving, data interpretation and client-facing communication skills.
• Experience with LIMS; Watson experience would be advantageous.
• Previous team leadership, mentoring or management experience is desirable.

Why Apply?

• Visa sponsorship available
• Relocation support provided
• Join a highly established international CRO.
• Work on diverse pharmaceutical and biopharmaceutical programmes.
• Strong exposure to bioanalysis, ligand binding assays and immunoassay technologies.
• Senior scientific and client-facing position with significant study ownership.
• Opportunity to build your career while relocating to Australia.

Interested?

If you are an experienced Study Director with a strong background in bioanalysis, ligand binding assays and/or immunoassays, and you're considering a move to Australia, we look forward to receiving your application.

Location: London / Remote
Duration: 12 months
Commitment: 3–4 days per week
Sector: Pharmaceutical / Oncology
 

The Opportunity

CY Partners are working with a leading global pharmaceutical organisation seeking an experienced Pricing & Market Access Lead to support an exciting Access Acceleration Initiative within gastro-intestinal stromal tumours (GIST).

This is a high-impact opportunity to shape the pricing and market access strategy for an important emerging oncology technology, helping to maximise patient access while delivering value for healthcare systems and the organisation.

You will play a pivotal role in shaping the global Pricing & Access strategy, bringing together your expertise in market access, evidence generation, payer insights and competitive intelligence. Working across a highly collaborative, cross-functional environment, you will provide strategic leadership and ensure that access considerations are embedded throughout the asset's development.

Key Responsibilities

• Provide strategic advice and leadership to the global GIST cross-functional team on pricing and market access strategy.
• Lead the development of innovative and competitive Payer Value Propositions and Pricing Strategies.
• Coordinate the delivery of external strategic market access projects, including value proposition development and pricing research.
• Provide expert guidance on key strategic access issues in partnership with the senior GI Market Access leadership team.
• Act as the strategic “red thread” between external access projects and the wider GIST Market Access team.
• Input into evidence-generation planning, ensuring critical payer questions are appropriately addressed.
• Support the development and integration of the market access strategy within the wider brand plan.
• Identify gaps, risks and opportunities for additional access activities to maximise the probability of success.
• Collaborate closely with Health Outcomes, Commercial, Policy, Medical and other key functions to ensure the access strategy is effectively developed, aligned and communicated across the organisation.
• Influence and mobilise key stakeholders to support strategic decision-making and overcome barriers to access.

About You

We are looking for an experienced international Pricing & Market Access professional who can operate confidently at a senior strategic level and bring a strong understanding of global payer environments.

Essential experience

• Experience in international Pricing & Market Access strategy, with experience operating at Director level or equivalent.
• Strong understanding of international markets, including the US, Japan and China.
• Knowledge of pricing policy and regulations across key global markets, ideally with oncology-specific expertise.
• Proven experience leading the delivery of external strategic projects.
• Strong experience developing and implementing internal pricing and market access strategies.
• Excellent project management, prioritisation and problem-solving skills.
• Highly accountable, with the ability to work independently and take ownership of complex strategic deliverables.
• Exceptional communication and influencing skills, both internally and externally.
• Demonstrable ability to engage, align and mobilise senior stakeholders to influence decisions and remove barriers.
• A results-focused, customer-centric approach with a strong sense of urgency and resilience.

Desirable experience

• Previous experience within oncology, particularly gastro-intestinal tumours / GIST.
• Experience developing payer value propositions and conducting pricing research within oncology.
• Strong understanding of oncology market access and evidence requirements.

Why This Role?

This is an excellent opportunity to join a strategically important global initiative at a pivotal stage of asset development. You will have the opportunity to influence the global Pricing & Access strategy for an emerging oncology technology, working with senior stakeholders across multiple functions and international markets.

The assignment offers flexibility to work within the UK time zone, with access to the client's UK headquarters desirable but not essential.

If you're an experienced Pricing & Market Access leader looking for a strategic contract where your expertise can directly influence patient access and asset value, we'd love to hear from you.

We look forward to receiving your application.

Location: London / Hybrid
Sector: Pharmaceutical / Biotechnology
Function: Clinical Operations / Clinical Development

The Opportunity

CY Partners are supporting a leading global biopharmaceutical organisation in the search for an experienced Global Clinical Integration Lead.

This is a high-impact strategic role within Global Clinical Operations, supporting complex business development, licensing, partnership, integration and divestment activities.

You will work closely with senior stakeholders across Clinical Operations, Business Development and Clinical Development, ensuring clinical priorities are translated into clear transition plans, risks are effectively managed and programmes are delivered efficiently and to a high standard.

Key Responsibilities

• Lead clinical operations workstreams across integration, separation, divestment and partnership programmes.
• Provide senior leadership visibility of clinical priorities, risks, impacts and dependencies.
• Develop processes, standards and guidance to support business development and post-deal activities.
• Establish and coordinate Clinical Operations integration and separation working groups.
• Act as a Subject Matter Expert for study-level integration and separation.
• Partner with internal stakeholders, deal teams and external partners to develop effective transition strategies.
• Facilitate workshops, define roadmaps and ensure clear ownership and delivery.
• Identify, assess and mitigate operational risks across transition activities.
• Represent Clinical Operations within wider cross-functional integration forums.

About You

You will ideally have:

• A Bachelor's degree in a scientific, business or related discipline.
• Strong experience managing global clinical trials.
• Proven project/programme management experience within a matrix environment.
• Experience driving process improvement and organisational change.
• Exposure to business development, licensing, integration, separation or divestment activities.
• Experience working with CROs, vendors and external partners.
• Strong cross-functional stakeholder management skills.
• Excellent communication, judgement and problem-solving abilities.
• The ability to work at pace, manage ambiguity and deliver against demanding deadlines.

Why Apply?

This is an excellent opportunity to take on a highly visible global position at the intersection of Clinical Operations and strategic business development, with significant exposure to senior stakeholders and complex international programmes.

We look forward to receiving your application.

Teesside | Chemical | Pharmaceutical | Manufacturing

CY Partners are partnering with a specialist chemical manufacturing business to recruit an experienced QA Manager to lead the Quality Assurance function at their Teesside site.

Reporting to the Site Lead, you'll provide strategic and operational QA leadership, working closely with Operations, Technical, Engineering and SHEQ to drive quality standards, compliance and continuous improvement across the site.

This is an excellent opportunity for a quality professional who enjoys working close to manufacturing and wants genuine influence over quality culture and business performance.

Key Responsibilities

• Lead and develop the site QA function.
• Provide quality leadership as part of the senior site management team.
• Oversee quality systems, batch release, validation and qualification.
• Lead internal, customer and regulatory audits.
• Ensure compliance with GMP, speciality chemicals and wider regulatory requirements.
• Drive risk-based decision-making and continuous improvement.
• Coach and develop quality personnel.
• Build strong relationships with customers, suppliers and regulators.

About You

You'll be an established QA professional with significant experience in chemicals, pharmaceuticals or another highly regulated manufacturing environment.

You'll ideally have:

• A relevant scientific or engineering degree.
• Strong GMP knowledge and ideally experience within pharmaceuticals or speciality chemicals.
• Experience with validation, qualification, technical transfer and quality systems.
• Experience managing audits and regulatory relationships.
• Strong leadership and stakeholder management skills.
• A pragmatic, risk-based approach to quality.
• The ability to influence, challenge constructively and drive cultural change.

The Opportunity

This role offers the chance to lead and shape a QA function, influence quality culture across a complex manufacturing operation and deliver meaningful improvements.

If you're an experienced QA leader looking for a role where you can make a genuine impact, apply today through CY Partners to find out more.

We look forward to receiving your application.

Greater London, with a particular focus on West and South West London and the surrounding Home Counties.

Ready to take the next step in your field service career? CY Partners is supporting a leading life science organisation in the search for a Field Service Engineer who wants to make a real impact. This is a fantastic opportunity to join a business where your technical expertise, curiosity and customer focus will shape the experience of scientists across the region.

Your Role

As a Field Service Engineer, you’ll be the technical backbone of a growing Life Science operation. Your work will ensure customers receive exceptional service, seamless installations and reliable ongoing support. No two days will look the same and that’s exactly what makes this role exciting.

You’ll be involved in:

• Installation & commissioning: Installing and commissioning instrumentation, predominantly laboratory water purification systems across customer sites, ensuring outstanding performance from day one.
• Maintenance & servicing: Carrying out planned maintenance to maximise uptime and reliability.
• Repairs: Troubleshooting and resolving technical issues with speed, care and precision.
• Validation & calibration: Ensuring systems meet regulatory standards and customer specifications.
• Customer support & training: Empowering users to get the best from their equipment, delivering training with confidence and clarity.
• Regional Travel: A field-based role with regular travel across the West, South West of London, offering variety, autonomy and daily engagement with customers and teams.

Who You Are

• HNC (or equivalent) in an Engineering or Scientific discipline.
• Strong technical background, ideally from field service or alternatively demonstrable experience within a laboratory environment.
• Confident problem solver with the ability to diagnose and resolve issues quickly.
• Excellent communicator with a genuine customer-first mindset.
• Adaptable, organised and comfortable travelling across the region.
• A collaborative team player who can also work independently.
• Previous field service experience is beneficial, though full training and onboarding will be provided.
• Able to identify and generate leads for new hardware, consumables, accessories and service contracts through the CRM.
• Based within 30 minutes of the patch and within the M25. 
• Must hold a full UK driving licence.
• Must have full right to work in the UK (sponsorship is not available).

What’s on Offer

• You’ll be joining a company that values people for who they are and what they bring. You’ll have access to meaningful opportunities to grow, develop and carve your own path.
• If you’re motivated by autonomy, technical challenge and supporting scientific progress, this is a role where you can thrive.

CY Partners is acting as an Employment Agency in connection with this vacancy.

CY Partners are recruiting on behalf of a pharmaceutical company for a Dispensing Assistant to join a well established patient care pharmacy operation.

This is an excellent opportunity for a qualified dispensing professional who enjoys working in a patient focused environment where accuracy, quality and exceptional customer service are at the heart of everything they do.

Working within a busy pharmacy team, you will support the safe and efficient dispensing of prescription medicines while delivering an outstanding service.

Responsibilities will include:

• Processing patient prescriptions and customer orders accurately and efficiently.

• Dispensing and labelling prescription medicines in accordance with Standard Operating Procedures (SOPs).

• Answering enquiries from patients and healthcare professionals.

• Taking payments and coordinating medication deliveries.

• Maintaining accurate patient medication records (PMRs).

• Receiving and managing pharmaceutical stock.

• Ensuring medicines are stored safely and handled in line with regulatory requirements.

• Supporting regulatory inspections, audits and quality standards.

• Escalating clinical queries appropriately to the Pharmacist.

• Delivering a consistently high level of customer service.

We're looking for someone who has:

• A recognised pharmacy dispensing qualification (such as an NVQ Level 2 or BTEC in Pharmacy Services).

• Previous experience working within a UK pharmacy environment.

• Excellent communication and customer service skills.

• Strong IT skills and confidence using pharmacy systems.

• Excellent attention to detail and a methodical approach to your work.

• The ability to work effectively both independently and as part of a team.

• A proactive, professional and reliable attitude with a genuine commitment to patient care.

This is a permanent, full-time position (Mon-Fri, 9.00am - 5.30pm) offering the opportunity to join a supportive team environment, with ongoing training and professional development.

It is essential that applicants are already eligible to work in the UK. Unfortunately, sponsorship is not available for this position.

CY Partners is acting as an Employment Agency in relation to this vacancy.

A well-established and highly reputable company is looking to appoint a Facilities Technician to support ongoing maintenance and facilities operations across their site.

This is a hands-on role working closely with the Facilities Manager, covering both equipment and building services in a structured, regulated environment.

What you’ll be doing:

• Supporting planned and reactive maintenance across site equipment and facilities

• Working within strict quality standards, ensuring all work is compliant and documented

• Assisting with PAT testing, calibration and validation activities

• Liaising with contractors and internal teams to resolve maintenance issues

• Contributing to preventative maintenance programmes (TPM)

What they’re looking for:

• Some experience in facilities, maintenance, or engineering (mechanical or electrical)

• Basic electrical competency (17th/18th Edition ideal)

• Strong attention to detail and ability to work within structured processes

Why this role:

Permanent full-time opportunity, Monday – Friday (8:30am–5:00pm)

Opportunity to build experience in a regulated / manufacturing environment

Supportive company with a strong reputation for looking after their people

CY Partners are acting as an employment agency in relation to this vacancy. Applicants must have the right to work in the UK.

CY Partners are supporting an innovative and growing life sciences organisation in the North East in the search for a Laboratory Operations Scientist to join their team on an initial 12-month contract.

This is a great opportunity for a scientifically minded laboratory professional to join a regulated, quality-driven environment, where they will play an important role in supporting day-to-day laboratory operations and the delivery of key technical activities.

The successful candidate will contribute to a broad range of operational and laboratory-based responsibilities, helping to ensure work is delivered accurately, efficiently and in line with relevant quality standards. The role would suit someone who enjoys working in a structured environment, takes pride in high-quality laboratory practice, and is keen to be part of a collaborative technical team.

Key Responsibilities

• Support the delivery of routine laboratory activities 

• Carry out a range of sample handling and processing tasks, ensuring work is completed accurately and to agreed timelines

• Assist with quality control and stability study activities, including sample preparation, storage, scanning, shipping and archiving

• Maintain clear, accurate and traceable laboratory documentation to support compliance and data integrity

• Work in accordance with established procedures, quality requirements and regulated working practices

• Support laboratory readiness through routine maintenance, housekeeping and equipment checks

• Assist with stock control and internal or external ordering where required

• Contribute to continuous improvement activities and support wider technical or cross-functional projects where needed

Candidate Profile

We are looking for candidates with prior laboratory experience and a strong appreciation for quality, accuracy and teamwork. To be successful, you should be able to demonstrate:

• Previous experience working in a laboratory environment

• Good organisational skills and the ability to manage time effectively

• Strong attention to detail and a consistent approach to following processes

• The ability to work efficiently with a moderate level of supervision

• Experience working within a regulated environment would be highly advantageous

• A scientific degree in Biomedical Sciences or related subject

Candidates with additional experience in laboratory techniques, sample-based workflows or quality-led environments will be of particular interest.

The Opportunity

This is an excellent chance to join a forward-thinking life sciences organisation offering a varied laboratory role within a supportive and collaborative team. You will gain valuable experience in a highly regulated setting and play an important role in supporting laboratory operations across a range of business-critical activities.

For more information, or to discuss your suitability in confidence, please apply via CY Partners.

CY Partners are working with a growing and innovative life sciences organisation to recruit an Laboratory Scientist to support ongoing development programmes within their Research & Development function.

This is an excellent opportunity for a laboratory professional with experience in tissue culture and antibody based workflows to contribute to the development and optimisation of high quality diagnostic reagents within a regulated environment.

The Role

You will play a key role in supporting feasibility studies, reagent development and assay verification activities. The position will involve hands on laboratory work, maintaining robust documentation standards and contributing to continuous improvement initiatives.

Key responsibilities will include:

• Performing mammalian tissue culture and media preparation using aseptic techniques
• Supporting antibody purification workflows, including filtration, chromatography and buffer exchange
• Conducting assay testing on automated instrumentation, including slide preparation and troubleshooting
• Supporting analytical testing such as ELISA and protein quantification
• Maintaining accurate laboratory notebooks, batch records and electronic data systems
• Working in accordance with cGMP / ISO laboratory standards and safety procedures
• Contributing to assay development, optimisation and qualification activities
• Supporting general laboratory maintenance and equipment upkeep

About You

We are seeking a motivated and detail oriented scientist who enjoys working in a structured laboratory environment and contributing to collaborative R&D programmes.

Requirements:

• Degree (BSc or MSc) in a relevant life science discipline
• Practical experience in mammalian cell culture
• Experience with antibody purification techniques
• Ability to follow detailed SOPs and maintain high data integrity standards
• Previous experience working in a regulated laboratory environment is highly desirable

Why Apply?

• Opportunity to gain experience within an innovative R&D environment
• Exposure to diagnostic reagent development and automated assay platforms
• Collaborative team culture within a well-established scientific organisation
• Immediate impact role supporting key development projects

If you would like to find out more about this confidential opportunity, please apply via CY Partners or contact our scientific recruitment team for a discussion.

CY Partners are acting as an Employment Agency in relation to this vacancy.

Applicants must have the right to work in the UK.