1 to 25 of 41 Permanent Pharmaceutical Jobs in the South East

specifications, acceptance criteria, testing, validation, and success measures. Strong business acumen, data fluency, systems thinking, problem-solving, stakeholder influence, and facilitation skills. Experience in pharmaceutical, healthcare, or life sciences environments is preferred, with a collaborative and accountable approach across organizational boundaries. Are you ready to 'go beyond' to create value ...

with the ability to identify practical business applicationsExperience supporting laboratory, engineering, development sciences, manufacturing, or industrial environments is considered a strong plusExperience in the pharmaceutical industry or another regulated environment is considered a plusFluent in English. French and/or Dutch is considered an advantageAre you ready to 'go beyond ...

required, preferably in Health, Science, Information Technology or another relevant field. Minimum of 5 years of relevant experience in clinical trial execution with a Pharmaceutical, Medical Device company and/or a Clinical Research Organization (CRO) is required. Proficiency supporting IT systems and related processes that support clinical development, reporting ...

colleagues. Education and Experience Requirements Advanced degree in a scientific, technology, healthcare, or business discipline, or equivalent experience. At least 10 years of relevant pharmaceutical, healthcare, technology, or scientific experience, including substantial leadership of large, complex, cross‐functional programs! Demonstrated ability to set program direction, establish governance, lead execution ...

further! Education and Experience Requirements Advanced degree in a scientific, technology, data, or healthcare discipline, or equivalent experience. At least 8 years of relevant pharmaceutical, healthcare, scientific, or data experience in a related discipline, such as data management, data standards, data governance, biostatistics, clinical programming, or clinical data transparency! Expertise ...

between commercial business owners and technical teams. What You Bring Supply Chain & Regulated Expertise: Strong operational experience within 3PL, logistics, or highly regulated environments (pharmaceutical experience is a major plus). Data & Integration Capabilities: Hands-on exposure to Databricks, Power BI, and external-facing B2B portals. Experience with B2B/ ...

identify people at risk of a heart attack before symptoms appear allowing for proactive disease management. Working with leading hospitals, research institutions, and pharmaceutical partners, Caristo aims to save lives through early detection and personalized prevention. The company was named a 2026 Technology Pioneer by the World Economic Forum ...

through activities such as people management and mentoring• Working on projects in the Public Sector or other legislative driven sectors such Utilities, Energy or Pharmaceutical• Incorporating a sustainability mindset into solutionsAnd the ability to:• Influence strategy and leadership direction within complex engagements• Become a domain expert in the field ...

about embedding care into everything we do to make a difference every day for those that need it most. We’re an inclusive pharmaceutical company that takes time to understand what really matters to our patients, their families, and their healthcare professionals, helping our people to take bold actions that ...

train business users on the new processes. Self-sufficient, flexible, and motivated team player capable of managing several activities simultaneously. Experience in the healthcare, pharma or medical device industry a plus. Excellent communication skills are critical. Positive, results driven, rational, logical, team player. Ability to rapidly learn and take advantage ...

Biometrics requirements. You understand CDISC standards, including SDTM and ADaM, and have worked with Tables, Figures, and Listings. You have worked in regulated pharmaceutical environments and understand SDLC, validation, audit readiness, and compliant configuration expectations. You can communicate clearly with technical teams and business stakeholders, while tracking setup processes across ...

governance and data modelling Experience applying AI-driven approaches to data or metadata management Strong understanding of structured and unstructured data management Understanding of pharmaceutical and biotechnological research, ability to bridge research and technology with clear communication towards scientific and IT-technical stakeholders Curious and innovative mindset with a positive ...

into clinically useful measures such as cough counts, breathing rate and heart rate. Our technology is already deployed internationally in clinical trials, primarily with pharmaceutical companies, and its use is growing rapidly. The Role We are looking for a Principal Systems Test & Automation Engineer to take significant technical ownership ...

improvements Take on ad hoc analytical work regulatory query responses, exploratory analyses, publication support as studies require it Experience Required Experience of programming in pharmaceutical, biotech, CRO, or clinical research settings Strong SAS proficiency (Base/Macro/Stat/Graph); familiarity with R or other languages is a plus ...

technical documentation. Support design verification and validation activities. To be successful in this role, you will need: Early career experience in a medical device, pharmaceutical, or laboratory environment. Strong attention to detail and data integrity. Willingness to learn regulatory and quality system requirements. Good written and verbal communication skills Interpretation ...

companies that operate in the following industries: Defence Equipment, Food and Drink Manufacturers, FMCG, Packaging, Engineering, Automotive, Aerospace, Warehousing, Logistics, Waste Management, Petro Chemical, Pharmaceutical, Power & Renewable Energy. Our commitment: Equal opportunities are important to us. We believe that diversity and inclusion at Morgan Ryder Associates are critical ...

deliver a range of services from IT Consultancy, Software Project Development and Infrastructure/Application Support Services for our corporate clients covering Insurance, Banking, Pharma, Retail, FMCG, Automotive, Logistics & Leasing, Publishing and Charity domains (including UN organisations). The Technical Team Lead role will be based 2 days per week ...

deliver a range of services from IT Consultancy, Software Project Development and Infrastructure/Application Support Services for our corporate clients covering Insurance, Banking, Pharma, Retail, FMCG, Automotive, Logistics & Leasing, Publishing and Charity domains (including UN organisations). The Technical .NET Architect role will be initially based 2 days ...

Role Overview: Takes technical leadership for the end-to-end delivery of control and automation solutions across multi-industry projects (Nuclear, Energy, Oil & Gas, Pharma, Utilities). Manages technical scope, supervises engineering teams, and ensures projects meet safety, timeline, and budget targets. Key Responsibilities Technical Delivery: Lead control system design ...

specifications through to commissioning and handover. The business is known for delivering turnkey engineering and automation solutions across sectors such as food & beverage, pharmaceutical, personal care and chemical manufacturing, with a practical, safety-led culture and close collaboration across multidisciplinary teams. Due to continued growth and project demand, they ...

support of Cencora's third party logistics service in Europe operating through our Alloga business. Our 3PL division provides specialised logistics services to pharmaceutical and healthcare clients, managing complex supply chains that demand the highest levels of compliance, precision, and innovation. We are accelerating our digital transformation agenda, embedding … Finance.* Specific technology experience with Microsoft Dynamics 365 Suite.* Operational experience within a logistics environment, preferably 3PL environment.* Experience within a regulated environment, preferably pharmaceutical sector.* Demonstrable experience identifying and implementing AI, automation, or digital transformation initiatives in an operational environment.* Familiarity with Agile/Scrum delivery methodologies and tools ...

Planet Pharma in the Slough area is seeking a Safety Systems & Innovation Specialist to bridge pharmacovigilance operations, IT, and external suppliers. You will support and enhance safety systems, including Veeva Vault Safety, and lead upgrades and validation activities. This hybrid role (2-3 days onsite) offers exposure to AI opportunities ...

methods, protocols, and quality documentation (SOPs, WIs) to a consistently high standard Generating and recording accurate test data Working safely with hazardous chemicals and pharmaceutical formulations, following strict health and safety procedures Occasionally supporting electronic test and build work You'll work within a multi-disciplinary project team, under supervision ...

with programming and application development using Python or R is preferredPreferred Experience/Skills: Master/Doctor's degree in quantitative area Knowledge of pharmaceutical industry, ideally specialty pharma and biologic treatmentsDeep expertise in leveraging data science methodologies within the Research and Development and Clinical trials sphere of the pharmaceutical ...

global pharmaceutical client based in Milton Keynes is seeking a skilled IT/OT Automation Engineer to support the delivery of critical automation and infrastructure projects within a regulated pharmaceutical manufacturing environment. The role focuses on implementing and upgrading validated systems, ensuring compliance with GxP standards, and supporting the full … maintain automation solutions for IT and OT systems Administer and support Windows Server environments (2022 or later) Support and integrate automated systems used in pharmaceutical manufacturing Ensure systems comply with GxP regulations, including validation and documentation Create and maintain GxP documentation (IQ/OQ/PQ, SOPs, risk assessments, validation ...