Medical Affairs Scientist

OGT

OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. An opportunity has arisen in our Medical Affairs team for a Medical Affairs QC Analyst. This role offers a varied mix of hands‑on laboratory work and quality-focused administrative responsibilities, supporting key FISH and NGS processing activities. What you’ll be doing for us: * Responsible for an assigned proportion of FISH and NGS product testing * Act as a subject expert in microscopy and NGS process for the purposes of product testing * Adhering to documented procedures for all aspects of laboratory work, ensuring that all relevant information is recorded, products and samples are handled correctly, and that all necessary records and quality data are maintained. * Responsible for an appropriate proportion of the quality management system, including procedures and audits. * Oversee the smooth and efficient functioning of the laboratory, together with the other MA team members, including consumables, reagents, microscopes, equipment, and software. * Contribute to the documentation and infrastructure of the department by providing input into internal protocols and implementation of CAPAs and improvements. * Assist with investigations of product, process and equipment nonconformities, validations and process -efficiency initiatives. * To comply with all site quality management systems, regulations and health and safety procedures (ISO 9001:2015, ISO 13485:2016, ISO 27001:2022, (EU) 2017/746 (IVDR), GCLP and Human Tissue Act (2004)) * To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you Essential * A bachelor’s degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required, with a minimum of one-year laboratory experience * Experience of working in a GLP/GMP environment * Basic knowledge of FISH * Basic Knowledge of NGS * Good document practice * High accuracy and attention to detail * Familiarity with working to defined protocols or standard operating procedures (SOPs) * Able to work accurately and efficiently in a high-volume, process-driven, and protocol-driven environment * Strong team work ethic and commitment to successfully deliver to tight deadlines are essential. Desirable * Previous experience with FISH analysis is highly advantageous * Experience in microscopy is advantageous * Proficiency in molecular biology techniques is highly advantageous * Experience in NGS based analysis is advantageous. In return you will receive:  * Competitive salary * Pension Scheme (10% non-contributory) * Private Health Insurance * Private Dental Insurance * Group Income Protection * Group Life Assurance * 25 days holiday plus UK bank holidays * High Street Discount Scheme. Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period. Please note that we will need to establish your right to work during the recruitment process.

Cyted Health

ABOUT US We’re Cyted, a pioneering gastrointestinal diagnostics company transforming earlier detection for oesophageal cancer and Barrett’s oesophagus. Our EndoSign test combines a swallowable capsule with advanced biomarkers and analytics to detect disease earlier, improving patient outcomes while reducing pressures on healthcare systems. What started as an idea between a health-tech entrepreneur and leading clinical scientists in Cambridge UK, has quickly grown internationally, backed by EQT Life Sciences and a $44M Series B investment. But we still work like a startup - because we are one. Things move quickly and we’re building as we go. Some days you’ll solve brand new problems and others you’ll roll your sleeves up and get things done. We’re a collaborative team, so your work matters. We have our investors trust, but you won’t disappear into layers of hierarchy, waiting months for decisions. If you've got a good idea, we want to hear it - whatever your role. We like curious, adaptable people who are always willing to learn. This isn’t a polished corporate - we’re building as we go.  If you're excited to help build something ambitious from the ground up that makes a real difference to patients' lives - we'd love to hear from you. Our four-stage process runs on a rolling basis, with each stage serving a clear purpose. Shaped by candidate feedback, we've designed it to give you honest insights into Cyted, whatever the role. 1. Initial conversation – A relaxed online conversation with Maddie from our People team to get to know you, talk through your experience and answer any questions you have about Cyted. 2. Line manager interview – An online discussion exploring the role in more detail through scenario-based and role-specific questions. 3. Team interview & assessment – Meet the wider team in person and see how we work. You'll complete a presentation or practical assessment so we can hear your ideas and see how you approach challenges at Cyted. 4. Final Interview – Marcel, our CEO, still meets every potential new joiner. It's an opportunity to discuss your ambitions and how they align with Cyted's journey and future vision. ROLE SUMMARY We're looking for a Medical Science Liaison who's excited to learn, grow and help bring the clinical value of our technology to life. As we expand and commercialise in the US, you'll work alongside gastroenterologists, pathologists and healthcare teams, delivering clinical education, answering scientific questions and gathering field insights that help drive adoption in real-world practice. Joining a small Medical Affairs team, you'll work closely with Commercial, Clinical Operations and Product, where your ideas and initiative will have a genuine impact. Rather than stepping into an established function, you'll help shape how we work, ensuring customer feedback influences our evidence, product and future direction. We're looking for someone who's built early experience in Medical Affairs or a scientific field role and is hungry to learn, grow and make their mark. This role is for someone who enjoys building rather than maintaining, takes initiative and wants the opportunity to have an influence far beyond their job title. If you're motivated by innovation, excited by the pace of a growing company and want to play a meaningful role in bringing a first-of-its-kind diagnostic to patients across the US from the start, we'd love to hear from you. WORKING PATTERN AND LOCATION The role is a full-time position with a standard 40 hour working week. The role holder will need to visit other company sites frequently and may be required to work flexibly. IN THIS ROLE YOU WILL BE ACCOUNTABLE FOR: Building Clinical Partnerships * Building trusted relationships with gastroenterologists, pathologists, advanced practice providers and key healthcare stakeholders across your territory. * Communicating the scientific and clinical value of Cyted's technology, tailoring discussions to each audience and stage of adoption. * Delivering engaging clinical education, training and scientific presentations that build confidence and support successful adoption. * Becoming a reliable scientific partner, providing credible, evidence-based support throughout the customer journey. Driving Clinical Adoption and Insight * Partnering with Commercial and Clinical Operations to support customer onboarding, implementation and ongoing utilisation. * Gathering real-world clinical insights, customer feedback and market intelligence to help shape products, evidence generation and commercial strategy. * Identifying opportunities for clinical collaborations, investigator-initiated studies and real-world evidence generation. Helping Shape Medical Affairs at Cyted * Taking ownership of cross-functional projects, proactively solving problems and collaborating across Medical Affairs, Commercial, Product and Clinical teams to help shape Medical Affairs and deliver an exceptional customer experience. * Staying informed on developments in gastroenterology, oncology, diagnostics and the evolving US healthcare landscape, bringing valuable insights back to the business. * Contributing beyond defined responsibilities, embracing opportunities to improve processes, support colleagues and help Cyted grow. TO THRIVE IN THIS ROLE, YOU WILL HAVE: Qualifications & Experience * A degree in life sciences, healthcare or a related discipline, or equivalent scientific or clinical experience. * Early experience within Medical Affairs, diagnostics, biotechnology, medical devices or another scientific customer-facing role. * Experience communicating scientific or clinical information, with the confidence to explain evidence clearly and answer questions thoughtfully. Skills & Knowledge * Ability to build trusted relationships by listening first and adapting communication to different audiences. * Curiosity about science and enjoys turning complex information into practical clinical conversations. * Proactive organisation skills to manage your own territory while working closely with colleagues across the business. Personal Attributes * Enjoys learning, asking questions and taking on new challenges. * Takes ownership, follows through and looks for ways to improve. * Thrives in a collaborative team where ideas are shared, feedback is welcomed and everyone helps build something better. SUCCESS IN THIS ROLE WILL LOOK LIKE: Within your first 30 days * Building strong internal relationships, developing a deep understanding of Cyted's technology and confidently representing our scientific and clinical value. Within your first 60 days * Establishing trusted customer relationships, delivering clinical education and contributing to successful adoption across your territory. Within your first 90 days * Driving scientific engagement, identifying opportunities to strengthen adoption and making a visible contribution to the growth and evolution of Medical Affairs at Cyted. BENEFITS  Financial & Retirement Benefits: * 401(k) Safe Harbor Plan with employer match: * Dollar-for-dollar match on the first 1% * 50 cents on the dollar up to 6% * Automatic enrolment after 2 months * Equity Participation: Share grants subject to board approval, giving you a stake in our mission and long-term growth. Health & Insurance Coverage: * Access to the company's medical insurance with company contributions of up to $1000/month * Access to self-pay vision and dental insurance options * Life Insurance: 3x your annual base earnings, employer-paid * Long-Term Disability (LTD): 60% of base salary up to $10,000/month * Short-Term Disability (STD): 60% of salary up to $2,500/week for up to 13 weeks * Employee Assistance Program (EAP): Full access to our EAP platform including courses and resources to support your wellbeing. Leave & Time Off: * 20 vacation days per year * 9 paid sick days * 8 paid holidays * 3 floating holiday days * 2 personal holiday days * Parental Leave: * 6 weeks fully paid primary caregiver leave * 2 weeks fully paid secondary caregiver leave * Holiday Purchase Scheme: Buy up to 5 extra vacation days per year. Learning, Development & Culture: * Annual CPD Allowance: $1,000 per year for professional development activities relevant to your role. * Regular Company Events: Including summer and holiday parties, team socials, and more.

SallyQ AB

Immedica Pharma has experienced remarkable growth in recent years and is now strengthening their Manufacturing/CMC organization with an experienced analytical expert. The Manufacturing/CMC team is responsible for overseeing all aspects of the production of Immedicas’s products, all of which are manufactured externally. This includes defining CMC strategy, ensuring regulatory compliance, and coordinating activities with CLOs and CMOs. As Senior Scientist Analytical Technology, you will play a key role in securing the quality, compliance, and lifecycle performance of analytical methods across Immedicas’s product portfolio. You will take the lead on analytical method transfers, validation activities, and continuous improvement initiatives, ensuring that our methods remain robust, efficient, and fit for purpose. This is a new role created to gather all ASAT activities; hence it gives an exceptional opportunity for someone who wants to take lead and grow with the role. You will collaborate cross‑functionally and act as a central analytical resource supporting product quality, life cycle management projects such as manufacturing tech transfers, regulatory submissions, and ongoing development needs. Since all laboratory work is conducted externally at CMOs and partner laboratories, success in this role requires strong collaboration skills, excellent communication, and the ability to build productive relationships with external partners. Main responsibilities: Act as analytical subject matter expert (SME) for Immedica’s products Own and oversee analytical method performance, including trending of analytical release and stability data Identify and drive improvements in analytical methods and control strategies Coordinate stability studies, ensuring product stability and shelf life Manage reference standards Act as analytical SME in supporting investigations, changes, CAPAs and life cycle management activities Act as analytical SME in regulatory submissions, including ownership of specifications Lead analytical method transfers, method development activities and comparability studies Collaborate closely with internal product teams and external manufacturing & laboratory partners (CMO/CLO) to ensure quality and timelines Why join? Immedica Pharma offers an innovative, dynamic workplace with short decision paths and a high degree of ownership. Being a part of the Manufacturing/CMC team means you will work with engaged colleagues in a specialist role with high visibility and influence. You will have opportunities for professional development and continuous learning in a highly competent CMC environment. Your profile You are a self‑driven analytical expert with strong pharma experience and broad scientific knowledge. You take clear ownership of your responsibilities and communicate effectively with both internal and external stakeholders. You act confidently as an SME, and are structured, quality‑focused, and improvement‑oriented. You thrive in fast-paced, hands-on environment and combine strong analytical expertise with a collaborative, business-oriented mindset. Qualifications: MSc or PhD in analytical chemistry, biotechnology, or a related field 5-10 years of experience in pharmaceutical development or manufacturing of biologics or small molecules, including GMP Experience in analytical validation, tech transfer activities and stability study setup Experience in performing a broad range of analytical methods in the laboratory, e.g. HPLC, spectroscopy, ELISA, bioassay Good understanding of statistical methods for establishing specifications and evaluating analytical outcomes Ability to interpret and implement regulatory requirements (ICH/FDA/EMA etc.) in method transfer and comparability Experience of working with external labs/CMOs Fluency in Swedish and English, both written and spoken It is a strong advantage if you also bring: Previous leadership experience, such as project management or team management Previous experience of working with QC operations Appealing? Send in an application as soon as possible. In this recruitment, Immedica are collaborating with SallyQ. For questions, contact Ellinor Crafoord, Senior Recruitment Consultant, +46793554257 or ellinor.crafoord@sallyq.se. About Immedica Immedica is a pharmaceutical company, headquartered in Stockholm, Sweden, focused on the commercialization of medicines for rare diseases within metabolic, neurology, hematology & oncology, endocrinology and specialty care. Immedica’s capabilities cover marketing and sales, compliance, pharmacovigilance, quality assurance, external manufacturing, regulatory and medical affairs as well as market access. Serving patients in more than 50 countries, Immedica is fully dedicated to helping those living with diseases which have a large unmet medical need. Immedica was founded in 2018 by investment company Impilo and buy-in management and currently employs more than 180 people across Europe, the Middle East and the US. Of these, approximately 80 are based in the headquarters in Life City, Hagastaden, Stockholm. At Immedica, our core values are the foundation of our culture and the driving force behind how we operate, innovate, and collaborate. These values guide every decision we make, shaping our commitment to patients, partners, and colleagues. Open & Honest: We foster transparency, integrity, and trust through open communication. Effective: Focused on delivering excellence, we prioritize impact and quality to make a real difference in the rare disease landscape. Empowered: We encourage collaboration and ownership, creating a supportive workplace where all team members’ contributions drive innovation and growth.