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.

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.

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
 

📍 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

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.

Location: Remote
Sector: Pharmaceutical & Biotechnology

CY Partners are partnering with a global biopharmaceutical organisation to recruit a Medical Director – Oncology Clinical Development. This is an exciting opportunity for an experienced physician to lead the clinical development of innovative oncology therapies, helping to bring life-changing medicines from early development through to regulatory approval and commercial launch.

Working within a global, cross-functional team, you'll provide medical leadership across Phase I–III clinical trials, shape clinical development strategy and collaborate with leading scientific experts to advance a growing oncology portfolio.

Key Responsibilities

• Lead the design, execution and medical oversight of global Phase I–III oncology clinical trials.
• Develop clinical protocols and contribute to overall clinical development strategy.
• Review and interpret clinical efficacy and safety data to support key development decisions.
• Work closely with Regulatory Affairs, Biostatistics, Pharmacovigilance, Research and Medical Affairs teams.
• Contribute to regulatory submissions, clinical study reports and scientific publications.
• Build strong relationships with Key Opinion Leaders, investigators and external experts.
• Represent Clinical Development within cross-functional programme teams and strategic initiatives.

About You

We're looking for a medically qualified professional with a strong background in oncology clinical development and a passion for advancing innovative treatments.

You'll bring:

• MD (or international equivalent).
• Board certification or eligibility in Medical Oncology, Haematology, Radiation Oncology or Internal Medicine with relevant oncology experience.
• Experience within the pharmaceutical, biotechnology or clinical research sector.
• Experience leading or supporting oncology clinical trials.
• Strong knowledge of clinical drug development, regulatory requirements and Good Clinical Practice (GCP).
• Excellent communication and stakeholder management skills within global, matrix organisations.

Desirable:

• MD/PhD or an additional postgraduate qualification (PhD, MBA, MPH).
• Strong industry experience.
• Experience leading oncology development programmes through regulatory submission.
• Strong understanding of the evolving oncology landscape, clinical practice and treatment guidelines.

Why Apply?

This is an opportunity to join an organisation at the forefront of oncology innovation, where you'll have the chance to influence the development of transformational therapies while working alongside internationally recognised experts in the field.

We look forward to receiving your application.

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.

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.

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.

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.