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A career without limitsAs the nation’s flag carrier, we take great pride in connecting Britain with the world and the world with Britain.It’s something we’ve been doing for over 100 years, ever since we launched the world’s first international scheduled air service between London and Paris.This originality has been in our blood since day one. It’s the spirit we share with the people that fly with us, our partners, and our colleagues.So, whether you are a reassuring voice on the end of a phone, a smile at the door, under a wing keeping the turbines spinning or landing us gently in far-flung places, a job at British Airways is yours to make.We know great things can happen when you’re inspired to think big and bring your ambition to work every day, which is why, at British Airways the sky is never the limit.The role:We're looking for a Head of Occupational Health to lead the delivery of occupational health services across British Airways. Reporting into the Chief Medical Officer, you'll provide strategic leadership across occupational health operations, ensuring services remain clinically robust, compliant and aligned to business needs. Working closely with business leaders, regulators and clinical teams, you'll oversee service delivery, drive continuous improvement and support the development of policies, governance frameworks and innovative ways of working that enable the function to deliver excellent outcomes for both colleagues and the business. What You'll Do:Lead the delivery of occupational health services across British Airways. Provide leadership to Occupational Health Managers, Health Surveillance Managers and Musculoskeletal and Ergonomic Specialists. Oversee clinical governance, quality standards and regulatory compliance. Build strong relationships with internal business areas, external agencies and regulatory bodies. Provide specialist medical support and advice to physicians, nurses and managers. Lead the development of occupational health policies, service models and performance measures. Drive continuous improvement and transformation initiatives across occupational health services. Ensure occupational health services support business requirements and operational readiness. What You'll Bring to British Airways:Strong leadership and team development experience. Excellent stakeholder management and influencing skills. Strong organisational and project management capability. Strategic thinking and sound judgement. Excellent written and verbal communication skills. A collaborative approach and the ability to work effectively across a complex organisation. A data-led mindset with the ability to monitor performance and identify opportunities for improvement. Qualifications / Experience:Full registration with the General Medical Council (GMC) with a licence to practice in the UK (essential). Qualifications in Occupational Medicine (MFOM minimum with Specialist Registration in Occupational Medicine), and Aviation Medicine (DAvMed or equivalent desirable). Previous general practice or other general medical experience (essential). Occupational health experience with ability to understand, anticipate and implement occupational health requirements in a large and complex commercial organisation (essential). Experience of health issues associated with air travel (essential). UK CAA accredited AME (essential). What we offer:We believe that all the people who work with us should feel valued for the part they play. It’s one of the reasons our rewards go far beyond a competitive salary.From the day you join us, you’ll get access to brilliant staff travel benefits including unlimited basic and premium standby tickets on British Airways flights. You’ll also receive up to 30 discounted ‘Hotline’ airfares per year for yourself, friends, and family.At British Airways you’ll have the chance to take on new challenges and move forward in a way that feels right for you. We encourage all those who work for us to consider opportunities right across our business to help you develop and progress.We never stand still, and we don’t expect our people to either.Inclusion & DiversityAt British Airways we all have a part to play in creating an inclusive place to work. Diverse representation among our people is really important to us and we recognise that all our colleagues are uniquely different and bring their own originality, creativity and identity to work.Inclusion and diversity is a key driver of innovation and we’re committed to creating a culture where everyone feels that they can be themselves. We’re looking for people from all backgrounds and cultures to join us and be a part of our journey to become a Better BA as we continue to connect Britain with the world and the world with Britain.

We are currently supporting a leading pharmaceutical company with an opportunity for a Scientist - Antibody Formulation Development to join their team in Slough on a 12-month contract. \n \n This team plays a key role in supporting programmes from toxicology through to Phase III clinical studies. \n \n Responsibilities \n \n • Performing experiments/analyses and other enabling studies to support non-clinical and clinical studies \n • Supporting pre-formulation and formulation laboratory activities which include laboratory set-up and provision of technical resources \n • Authoring formulation protocols, reports and supporting documentation, based on a deep understanding of biochemical or physical degradation routes of antibody-derived molecules. \n • Presentation of results \n \n Skills and experience \n \n • Applicants should have a Masters (or equivalent) or PhD in Biotechnology, Biochemistry, Biology or similar, with a demonstrated minimum of 3 years' laboratory experience, knowledge and application of new and developing technologies \n • Applicants should have a good experience in protein/antibody analysis (HPLC /UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, MFI) with experience in formulation development and/or automation seen as an advantage. \n • High level of numeracy and the ability to critically evaluate data. \n • Ability to work in a busy team environment with changing priorities. \n • Excellent communication and organisational skills. \n • Excellent team player skills \n \n Candidates must have the right to work in the UK \n

Scientist, Antibody Formulation Development \n 📍 Slough, UK | 📅 12-Month Contract (Maternity Cover) \n \n We're recruiting for a Scientist to join a leading biopharmaceutical organisation's Injectable Formulation Development team. This is a hands-on laboratory role supporting the development of monoclonal antibody therapies from early-stage research through to late-stage clinical development. \n \n The successful candidate will be responsible for conducting protein and antibody characterisation studies, supporting formulation development activities, authoring technical documentation, and presenting scientific findings. You will work closely with cross-functional teams in a dynamic R&D environment. \n \n Key Responsibilities \n\n • Perform laboratory experiments and analytical studies to support pre-clinical and clinical development programmes.\n, • Support pre-formulation and formulation development activities.\n, • Author protocols, reports, and technical documentation.\n, • Analyse and interpret experimental data and communicate findings to stakeholders.\n, • Contribute to laboratory operations and continuous improvement activities.\n\n \n Requirements \n\n • MSc or PhD in Biotechnology, Biochemistry, Biology, Pharmaceutical Sciences, or a related discipline.\n, • Minimum 3 years of laboratory experience.\n, • Strong experience with protein/antibody analytical techniques such as HPLC, UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and particle analysis methods.\n, • Experience in formulation development and/or laboratory automation would be advantageous.\n, • Strong data analysis, communication, and organisational skills.\n, • Ability to work effectively in a fast-paced, collaborative environment.\n, • Must have the right to work in the UK/EU.\n\n \n This is an excellent opportunity to contribute to the development of innovative biologic therapies within a highly collaborative scientific team.

Scientist – Injectable Formulation Development (Biologics) \n Location: EU-based (right to work required) \n \n About the Opportunity \n Our client, a leading global biopharmaceutical organisation, is seeking a talented laboratory-based scientist to join their Injectable Formulation Development team. This group plays a pivotal role in advancing biologics programmes, providing robust formulations to support the full development lifecycle—from early toxicology studies through to late‑stage clinical trials. The team is also committed to innovating new formulation technologies to enhance the stability of both conventional and next‑generation antibody formats. \n This is an excellent opportunity to contribute to high‑impact therapeutic development within a collaborative, cross‑functional environment. \n \n Key Responsibilities \n\n • Conduct analytical experiments and enabling studies to support non‑clinical and clinical development.\n, • Contribute to pre‑formulation and formulation activities, including lab set‑up and maintenance of technical resources.\n, • Prepare scientific documentation such as protocols and reports, drawing on a strong understanding of biochemical and biophysical degradation pathways in antibody‑based molecules.\n, • Present experimental findings to project teams and stakeholders.\n\n \n Skills & Experience \n\n • Master’s degree (or equivalent) or PhD in Biotechnology, Biochemistry, Biology, or a related discipline.\n, • Minimum of 3 years’ hands‑on laboratory experience.\n, • Strong technical expertise in protein/antibody analytical methods such as HPLC/UPLC, iCE, UV spectroscopy, DLS, CGE, rheology, and sub‑visible particle analysis.\n, • Experience in formulation development and/or laboratory automation is advantageous.\n, • High level of numeracy with the ability to critically interpret data.\n, • Strong organisational and communication skills, with the ability to thrive in a dynamic environment with shifting priorities.\n, • Proven ability to work effectively within a team.\n\n

Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com . We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. This role reports to the Global Medical Lead, Global Medical Lead, Biopharma and Ophthalmology Development. This is a hybrid position and will require you to be onsite 1 day per quarter at Bourne office in London, UK. At Astellas we recognise the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimise the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines. As a Development Physician (Medical Director), you will play a key role in the design, execution, and oversight of global clinical studies. You will contribute to protocol and study design, develop and review key study documents, provide medical monitoring and safety oversight, interpret clinical and safety data, and support the training of investigators, site staff, and cross-functional study teams to ensure successful trial delivery. • In collaboration with the Medical Lead, responsible for designing and making recommendations in the clinical development plan that are aligned with the asset development strategy, after soliciting appropriate input and review from Medical and Clinical Operations colleagues as well as other contributing line functions (Regulatory Affairs, Statistics, Clinical Operations, Commercial)., • Be available to advise on assigned clinical trial(s) related medical questions or problems during the trial, including 24/7 emergency coverage for safety-related matters., • Reviews and analyzes the eligibility of participants per inclusion/exclusion requirements of a clinical trial., • Reviews all adverse events to look for trends or risks, reviews all serious adverse events (SAEs), including review of the narrative, investigators’ assessment on causality, and applicable regulatory reporting, with close collaboration with the study’s Product Responsible Person (PRP)., • Provides review of study protocols and ongoing medical oversight of clinical trials to ensure that safety concerns and/or adverse events are identified and appropriate responses to such concerns are developed and executed. Ensures activities related to Severe Adverse Events (SAEs) are conducted in accordance with applicable SOPs and regulations. Includes writing and/or reviewing Safety Narratives, Investigator Letters, and other safety documentation for site-reported safety events., • Consults with internal and external stakeholders in the development of clinical trial design and conduct, including drafting of protocols and amendments., • Develops and/or reviews operational, medical monitoring, and safety plans for studies., • Leads and/or participates in scientific and medical training of other team members and external clients, investigators, and other site staff as it pertains to assigned studies., • Generates safety-related documents, such as medical monitoring reports and the safety database, to ensure that the reporting of SAEs is current and complete., • In collaboration with the Medical Lead: Participate in Health Authorities communication: the Development Physician is responsible for clinical written feedback/response to deficiency letter, pre-IND/NDA communication meeting, or panel review meeting., • Investigators/KOL engagement: Development Physician is responsible for KOL/investigators scientific engagement., • Medical Degree (MD) or equivalent required. We also welcome applications from qualified Optometrists with relevant ophthalmology and clinical development experience., • Willingness to work across different ophthalmic indications., • Extensive relevant experience in drug development in a biotech/pharmaceutical company or equivalent experience in an academic clinical research institute (NCI, NIH, Academic Research groups, etc.)., • Proven record of being a successful medical leader and in study design., • Excellent writing skills with experience writing regulatory documents and attending Health Authority interactions., • Experience managing drug development programs., • Experience designing and planning clinical studies, to produce both timely and high-quality data., • Proven ability to get results in a matrixed management environment., • Proficiency with ICH/GCP guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, drug development, clinical trials, and clinical research., • Medical Degree (or Medically Qualified) with completion of residency in Ophthalmology with active or prior Board Certification., • Experience working in at least one other therapeutic area outside of ophthalmology., • Experience working in cell or gene therapy drug development. Careers | Astellas Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide. Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day. Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare. A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions. • Accountability, • Courage, • Impact, • Innovation, • Integrity, • One Astellas, • Outcome Focus, • Sense of Urgency Organizational Focus We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. #J-18808-Ljbffr

Astellas seeks a Development Physician (Medical Director) in Ophthalmology to lead global clinical studies, protocol design, and safety oversight, ensuring high-quality data and patient safety across programs. The role requires collaboration with Medical Lead, Regulatory, Statistics, and Clinical Operations, and involves a hybrid work arrangement with onsite presence in London/Bourne as needed. #J-18808-Ljbffr

Founded in Brazil in 1978, Silimed is a global manufacturer of silicone implants for aesthetic and reconstructive surgery. With more than four decades of experience, the company has developed one of the most comprehensive portfolios in the category, offering multiple surface technologies, shape formats, and projection options designed to support individualized surgical planning. Working in close collaboration with plastic surgeons, Silimed integrates clinical insight into product development, aligning design with real-world surgical needs. Its implants are manufactured under rigorous quality standards and comply with internationally recognized regulations, including European CE certification. Rooted in Brazilian-origin innovation, Silimed combines technical expertise with a structured and versatile design system, supporting a wide range of surgical approaches across global markets. Key Responsibilities • Support the development and execution of global Medical Affairs strategies and scientific initiatives, ensuring alignment with corporate objectives and regional needs., • Develop and maintain strategic scientific partnerships with Key Opinion Leaders (KOLs), investigators, and other healthcare stakeholders to foster scientific collaboration and generate actionable medical insights., • Lead scientific exchange with external experts, ensuring balanced, evidence-based communication of clinical data and product information., • Identify evidence gaps and support evidence generation initiatives, including investigator-initiated studies (IIS), real-world evidence (RWE), clinical publications, and scientific collaborations., • Gather, analyze, and communicate medical insights from healthcare professionals, KOLs, and international markets to inform medical strategy, product lifecycle management, and future evidence-generation activities., • Provide scientific leadership and medical support throughout the product lifecycle, including clinical evidence dissemination, scientific communications, and responses to medical information requests., • Review and approve scientific and promotional claims, marketing materials, educational content, and external communications to ensure scientific accuracy, clinical relevance, regulatory compliance, and consistency with approved product labeling., • Partner closely with Clinical Affairs, Regulatory Affairs, Quality, Marketing, Market Access, and Commercial teams to ensure cross-functional alignment while maintaining Medical Affairs independence and scientific integrity., • Contribute to the planning and execution of advisory boards, scientific congresses, expert meetings, and publication strategies to strengthen external scientific engagement., • Support the development, review, and approval of scientific publications, abstracts, manuscripts, medical presentations, and evidence summaries., • Monitor emerging scientific literature, clinical evidence, treatment guidelines, competitor activities, and healthcare trends to identify opportunities and support strategic medical planning., • Ensure all Medical Affairs activities are conducted in accordance with applicable regulations, ethical standards, industry codes of practice, and company compliance policies. Education • Bachelor's degree in Life Sciences, Pharmacy, Medicine, Biomedical Sciences, or a related healthcare discipline., • PhD or master’s in healthcare is considered mandatory if there is no previous experience in breast implants. Experience • Minimum 5 years of experience within the pharmaceutical, biotechnology, or medical device industry. Experience in breast implants will be considered a plus, • Previous exposure to Medical Affairs, Medical Education, scientific projects, or healthcare stakeholder engagement is preferred. Languages • Fluent English is required., • Fluent Spanish and basic Portuguese are highly desirable and would be considered an asset Key Competencies • Strong scientific acumen with the ability to critically evaluate, interpret, and communicate clinical evidence., • Excellence in scientific communication and medical storytelling for both internal and external stakeholders., • Proven ability to develop and maintain trusted scientific partnerships with Key Opinion Leaders (KOLs), investigators, and healthcare professionals., • Expertise in KOL engagement, medical insight generation, and translating field insights into actionable medical strategies., • Strong understanding of Medical Affairs principles, scientific exchange, evidence generation, and product lifecycle management., • Experience reviewing scientific claims and promotional materials to ensure scientific accuracy, regulatory compliance, and alignment with approved labeling., • Strategic thinking with the ability to identify evidence gaps, emerging clinical trends, and opportunities to strengthen the scientific value proposition., • Excellent cross-functional collaboration skills, with the ability to influence without authority while maintaining Medical Affairs independence., • Strong project management and organizational skills, with the ability to prioritize multiple initiatives in a fast-paced global environment., • High ethical standards, sound scientific judgment, and commitment to compliance with industry regulations and codes of practice. Adaptability and effectiveness in working within multicultural, cross-regional, and matrix organizations. #J-18808-Ljbffr

Your new company Join a global biopharmaceutical organisation dedicated to transforming patient outcomes across multiple disease areas. You'll be part of a science-driven environment that values innovation, collaboration, and meaningful impact and work with highly experienced colleagues. Your new role This is a long term contract role (initially 1 year but likely to extend) within a well-established team where you will be reporting into senior bioinformatics leadership.The company has a collaborative and innovative atmosphere, where you will be supporting multiple projects within translational and clinical development across several therapy areas. The role is hybrid, with c.3 days per week from home, though this can be negotiable for the right candidate. The role can be at either Senior Bioinformatician or Principal Bioinformatician grade and you will be working on drug development projects, playing a key role in generating biological insights from clinical stage omics data to support decision making across the therapeutic portfolio. Major responsibilities will include: • Processing, analysing, and interpreting multi-omic (RNAseq, NGS, proteomic, etc) datasets from clinical studies, • Deriving mechanistic, biological, and treatment related insights from patient-level data, • Developing and optimising analysis methods, pipelines, and computational workflows<...

Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren't afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact. • This role reports to the Global Medical Lead, Global Medical Lead, Biopharma and Ophthalmology Development. This is a hybrid position and will require you to be onsite 1 day per quarter at Bourne office in London, UK., • At Astellas we recognise the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimise the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines., • As a Development Physician (Medical Director), you will play a key role in the design, execution, and oversight of global clinical studies., • You will contribute to protocol and study design, develop and review key study documents, provide medical monitoring and safety oversight, interpret clinical and safety data, and support the training of investigators, site staff, and cross-functional study teams to ensure successful trial delivery., • In collaboration with the Medical Lead, responsible for designing and making recommendations in the clinical development plan that are aligned with the asset development strategy, after soliciting appropriate input and review from Medical and Clinical Operations colleagues as well as other contributing line functions (Regulatory Affairs, Statistics, Clinical Operations, Commercial)., • Be available to advise on assigned clinical trial(s) related medical questions or problems during the trial, including 24/7 emergency coverage for safety-related matters., • Reviews and analyzes the eligibility of participants per inclusion/exclusion requirements of a clinical trial., • Reviews all adverse events to look for trends or risks, reviews all serious adverse events (SAEs), including review of the narrative, investigators’ assessment on causality, and applicable regulatory reporting, with close collaboration with the study’s Product Responsible Person (PRP)., • Provides review of study protocols and ongoing medical oversight of clinical trials to ensure that safety concerns and/or adverse events are identified and appropriate responses to such concerns are developed and executed. Ensures activities related to Severe Adverse Events (SAEs) are conducted in accordance with applicable SOPs and regulations. Includes writing and/or reviewing Safety Narratives, Investigator Letters, and other safety documentation for site-reported safety events., • Consults with internal and external stakeholders in the development of clinical trial design and conduct, including drafting of protocols and amendments., • Develops and/or reviews operational, medical monitoring, and safety plans for studies., • Leads and/or participants in scientific and medical training of other team members and external clients, investigators, and other site staff as it pertains to assigned studies., • Generates safety-related documents, such as medical monitoring reports and the safety database, to ensure that the reporting of SAEs is current and complete., • In collaboration with the Medical Lead: Participate in Health Authorities communication: the Development Physician is responsible for clinical written feedback/response to deficiency letter, pre-IND/NDA communication meeting, or panel review meeting, • Investigators/KOL engagement: Development Physician is responsible for KOL/investigators scientific engagement., • Medical Degree (MD) or equivalent required. We also welcome applications from qualified Optometrists with relevant ophthalmology and clinical development experience., • Willingness to work across different ophthalmic indications, • Extensive relevant experience in drug development in a biotech/pharmaceutical company or equivalent experience in an academic clinical research institute (NCI, NIH, Academic Research groups, etc.), • Proven record of being a successful medical leader and in study design., • Excellent writing skills with experience writing regulatory documents and attending Health Authority interactions, • Experience managing drug development programs., • Experience designing and planning clinical studies, to produce both timely and high-quality data., • Proven ability to get results in a matrixed management environment., • Proficiency with ICH/GCP guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, drug development, clinical trials, and clinical research., • Medical Degree (or Medically Qualified) with completion of residency in Ophthalmology with active or prior Board Certification, • Experience working in at least one other therapeutic area outside of ophthalmology, • Experience working in cell or gene therapy drug development, • Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide., • Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day., • Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare., • A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions., • Impact, • Innovation, • Integrity, • One Astellas, • Accountability, • Courage, • Sense of Urgency, • Outcome Focus We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help. #J-18808-Ljbffr

You will collaborate across Real World Evidence, Medical Affairs, Clinical Development, and Market Access to deliver integrated RWE and data strategies.

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