Location: Hybrid
Salary: Competitive + Bonus + Excellent Benefits

CY Partners are recruiting on behalf of a leading global pharmaceutical organisation for an experienced Clinical Project Manager looking to apply their clinical operations expertise in a strategic patient access role.

This is an exciting opportunity to move into the growing field of Expanded Access and Compassionate Use programmes, where you'll lead complex, global projects that enable patients with serious illnesses to access investigational oncology medicines before commercial approval.

If you have experience delivering global clinical studies, managing multiple stakeholders and vendors, and driving projects from planning through execution, this role offers the opportunity to broaden your career while continuing to make a meaningful impact on patient outcomes.

The Role

As Expanded Access Manager, you will lead the planning and operational delivery of global Expanded Access and Compassionate Use programmes. Working closely with Medical Affairs, Clinical Development, Regulatory Affairs and external partners, you will ensure programmes are delivered efficiently, compliantly and with a patient-first approach.

Key Responsibilities

• Lead the end-to-end delivery of global Expanded Access and Compassionate Use programmes.
• Develop project plans and oversee programme execution from initial physician request through to programme completion or transition.
• Coordinate cross-functional teams including Medical Affairs, Regulatory Affairs, Safety, Supply Chain and external vendors.
• Manage timelines, risks, budgets and programme milestones to ensure successful delivery.
• Oversee vendor selection, performance and ongoing relationships.
• Monitor programme utilisation and provide regular updates to senior stakeholders.
• Drive process improvements and operational excellence across patient access programmes.

About You

We're particularly interested in hearing from Clinical Project Managers or Clinical Operations professionals with experience leading complex clinical programmes.

You'll ideally have:

• A degree in Life Sciences or a related scientific discipline.
• Experience managing global or regional clinical trials within a pharmaceutical, biotech or CRO environment.
• Strong project management skills, including planning, risk management, budgeting and stakeholder coordination.
• Experience managing external vendors and cross-functional project teams.
• Oncology experience is highly desirable, although candidates with experience in other therapeutic areas are encouraged to apply.
• Knowledge of GCP and clinical development processes.
• Excellent organisational, communication and relationship-building skills.
• The ability to manage multiple priorities within a fast-paced global environment.

Why Apply?

This role offers an excellent opportunity for an experienced Clinical Project Manager to transition into a highly visible global position focused on patient access rather than traditional clinical trial delivery. You'll work with international teams, influence strategic programmes and help deliver innovative oncology treatments to patients who have limited treatment options.

If you're an experienced Clinical Project Manager looking for your next challenge and want to use your project leadership skills to help improve patient access to innovative medicines, we'd love to hear from you.

We look forward to receiving your application.

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 recruiting for a Regulatory Compliance Product Steward to join a well-established organisation within the chemical sector. This role is ideal for someone with experience in Safety Data Sheets (SDS), product labelling, and chemical regulations, looking to develop their career within regulatory compliance.

Key responsibilities include:

• Creating, reviewing, and maintaining SDSs and product labels
• Monitoring regulatory changes and ensuring ongoing compliance
• CLP/GHS classification and chemical label preparation
• Managing regulatory documentation and databases
• Liaising with suppliers and internal stakeholders
• Responding to customer and colleague regulatory queries

About you:

• Experience within the chemical industry
• Strong understanding of SDSs and hazard communication
• High attention to detail and excellent organisational skills
• Experience with SDS software (Lisam ExESS or similar preferred)
• Degree or equivalent in Toxicology, Ecotoxicology, Chemistry or related.

We look forward to receiving your application

Location: Tees Wear, Durham Region
Salary: c£45K
Job Type: Full-Time, 4 on, 4 off

Join a leading pharmaceutical manufacturing team as a Clean Room Microbiologist.

CY Partners is recruiting on behalf of an established pharmaceutical manufacturer seeking a Clean Room Microbiologist to support microbiological testing and environmental monitoring within GMP clean room facilities. This is an excellent opportunity for an experienced microbiologist who enjoys working in a regulated environment and is comfortable working a shift pattern.

The Role

As a Clean Room Microbiologist, you will play a key role in maintaining the microbiological integrity of manufacturing environments by carrying out routine environmental monitoring, testing, and investigation activities to ensure compliance with GMP and quality standards.

Key Responsibilities

• Perform environmental monitoring of clean rooms, including viable and non-viable sampling.
• Conduct microbiological testing of samples using standard laboratory techniques.
• Identify and report microbial isolates where required.
• Monitor environmental trends and support investigations into out-of-specification or out-of-trend results.
• Ensure all laboratory documentation is completed accurately and in compliance with GMP requirements.
• Support contamination control initiatives and continuous improvement activities.
• Maintain laboratory equipment and ensure adherence to health, safety, and quality procedures.
• Work collaboratively with Manufacturing, Quality Assurance, and other site departments.

About You

We're looking for candidates with:

• A degree (or equivalent qualification) in Microbiology, Biological Sciences, or a related discipline.
• Experience working within a GMP pharmaceutical, biotechnology, or similar regulated laboratory environment.
• Hands-on experience of clean room environmental monitoring.
• Knowledge of GMP and aseptic manufacturing principles.
• Strong attention to detail and excellent documentation skills.
• The ability to work effectively as part of a shift team.

What's on Offer?

• Comprehensive training and career development opportunities.
• Excellent benefits package.
• The opportunity to join a growing organisation committed to quality and innovation.
• A supportive and collaborative working environment.

If you're looking to take the next step in your microbiology career within a regulated pharmaceutical environment, we'd love to hear from you.

We look forward to receiving your application.

📍 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.

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.

The opportunity:

You’ll be involved in the manufacture of pharmaceutical products, working to clearly defined SOPs and GMP standards. The role offers exposure across multiple manufacturing areas, with structured training and clear expectations around quality, documentation and compliance.

It is particularly well suited to someone who enjoys working in a precise, structured environment, takes pride in producing high quality work and is keen to learn new skills and progress over time.

Key responsibilities

• Manufacturing products in line with GMP, SOPs and agreed timescaleCompleting all production and training documentation accurately
• Maintaining high standards of cleanliness to minimise cross contamination risk
• Cleaning and preparing glassware, equipment and manufacturing areas
• Rotating across manufacturing, staging and washroom areas as required
• Supporting stock control, material preparation and routine checks
• Accurately recording daily monitoring activities (e.g. balances, room pressures, water flushes)
• Working collaboratively to support a positive, professional production culture

What we’re looking for:

• Strong organisational skills with high attention to detail
• Comfortable working in structured, repetitive and regulated environments
• Able to manage fluctuating workloads and tight deadlines
• Proactive, reliable and quality-driven

Desirable (but not essential):

• Experience in pharmaceutical or GMP manufacturing
• Confidence using basic IT systems (e.g. MS Word, Excel, Outlook)

Additional information

Full on-the-job training will be provided. The business places real value on learning, development and long term progression for the right individuals.

Applicants must have the right to work in the UK.

CY Partners is acting as an employment agency in relation to this vacancy.

Location: Worthing

CY Partners are recruiting for a QA Scientist – Microbiology to join a leading pharmaceutical manufacturing company. This is an exciting opportunity for a microbiologist with GMP laboratory experience to become part of a collaborative Quality team responsible for ensuring products meet the highest quality standards before release.

You'll be involved in microbiological testing of non-sterile pharmaceutical products, environmental monitoring, water testing and laboratory investigations, while working in a regulated GMP environment.

What you'll be doing

• Perform microbiological testing of non-sterile pharmaceutical products, water samples and stability samples.
• Carry out environmental monitoring of manufacturing and laboratory areas.
• Perform microbial identification and accurately record laboratory data.
• Calibrate, maintain and troubleshoot microbiology laboratory equipment.
• Review analytical results and microbiological reports to ensure compliance with GMP requirements.
• Support Out of Specification (OOS) investigations and CAPA activities.
• Assist with equipment qualification and microbiological method validation.
• Ensure compliance with GMP, GLP and Standard Operating Procedures (SOPs).
• Participate in audits, continuous improvement initiatives and cross-functional projects.
• Support the training of colleagues on laboratory procedures where required.

What we're looking for

• Degree, HNC or HND in Microbiology, Biology or another Life Science discipline.
• Previous experience working in a GMP, pharmaceutical, healthcare or regulated laboratory environment.
• Hands-on experience of microbiological techniques and environmental monitoring.
• Understanding of GMP/GxP principles and laboratory documentation.
• Strong attention to detail with excellent record-keeping skills.
• Good communication and organisational skills.
• Comfortable working both independently and as part of a team.
• Competent with Microsoft Office and laboratory computer systems.

Desirable

• Experience of pharmaceutical microbiology testing.
• Experience supporting validation or qualification activities.
• Knowledge of microbial identification techniques.
• Experience participating in investigations and CAPA activities.

Why apply?

• Join a global pharmaceutical manufacturer with a strong commitment to quality.
• Be part of a supportive and experienced Quality team.
• Gain exposure to validation, investigations and continuous improvement projects.
• Competitive salary and comprehensive benefits package.
• Excellent training and career development opportunities.

If you're a QA Scientist, Microbiologist, QC Microbiologist or Microbiology Analyst looking for your next opportunity in the pharmaceutical industry, we'd love to hear from you.

We look forward to your application.

Location: London (Hybrid/Flexible)
 

CY Partners is partnering with a leading global pharmaceutical organisation to recruit a Research Manager, Global Health Outcomes (GHO).

This is an exciting opportunity to join a growing Global Health Outcomes team supporting an innovative HIV and infectious disease portfolio. You'll play a key role in generating high-quality health economics and outcomes research (HEOR) that demonstrates the value of medicines and supports patient access across global markets.

Working within a collaborative, cross-functional environment, you'll contribute to evidence generation across the product lifecycle, with a strong focus on Real World Evidence (RWE), Patient Reported Outcomes (PROs) and health economic analyses that support reimbursement and market access.

Key Responsibilities

As Research Manager, Global Health Outcomes, you will:

• Design and support non-interventional studies investigating disease burden, treatment patterns and patient experience.
• Deliver systematic literature reviews (SLRs), meta-analyses and indirect treatment comparisons (ITCs).
• Develop and contribute to health economic models and global value dossiers to support product launches.
• Manage multiple projects simultaneously, ensuring timelines, budgets and deliverables are achieved.
• Identify and proactively escalate project risks where appropriate.
• Conduct comprehensive literature reviews to support evidence generation strategies.
• Collaborate with Medical Affairs, Commercial, Market Access and other cross-functional teams.
• Present complex scientific findings clearly to both technical and non-technical stakeholders.
• Manage relationships with external research partners and vendors to ensure successful project delivery.

About You

We're looking for a motivated HEOR professional who enjoys working collaboratively and has experience delivering evidence generation projects within the pharmaceutical industry, academia or a specialist research organisation.

Essential Requirements

• Degree or higher qualification  in Health Economics, Health Outcomes Research, Epidemiology, Pharmacy, Health or Life Sciences, or a related discipline.
• Relevant experience within the pharmaceutical industry, academia or a research organisation.
• Experience supporting pharmaceutical drug development and/or product launch through value evidence generation.
• Hands-on experience in:
  • Systematic Literature Reviews (SLRs)
  • Meta-analyses
  • Indirect Treatment Comparisons (ITCs)
  • Health Economic Modelling
  • Clinical Outcome Assessments (COAs) and Patient Reported Outcomes (PROs)
• Experience managing external research vendors and delivering projects to agreed timelines.
• Excellent communication, presentation and stakeholder management skills.
• Strong organisational and project management capabilities.

Desirable Experience

• Experience within a pharmaceutical Global Health Outcomes, HEOR or Value Evidence team.
• Knowledge of infectious diseases, particularly HIV treatment and/or prevention.
• Experience generating Real World Evidence (RWE) and patient-centred outcomes research.

Why Join?

This is an opportunity to join an organisation at the forefront of HIV innovation, where your work will directly influence global healthcare decision-making and patient access to life-changing medicines.

You'll benefit from:

• Working on high-impact, global HEOR programmes.
• Collaboration with internationally recognised experts across Medical, Market Access and Commercial teams.
• Exposure to innovative evidence generation methodologies, including RWE and patient-centred research.
• A collaborative, supportive environment with opportunities for professional growth and career development.

Apply

If you're an experienced HEOR professional looking to make a meaningful impact within global health outcomes research, we'd love to hear from you.

We look forward to receiving your application.