{"id":2520970,"url":"https://alion.io/job/medpharm-scientist-analytical-medpharm","title":"Scientist, Analytical - MedPharm","company":{"id":2322662,"name":"MedPharm","domain":"medpharm.com","url":"https://alion.io/company/medpharm-com","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"JazzHR","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"junior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Guildford, United Kingdom"],"countries":["GB"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":39000,"max_usd":73000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":9},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GLP","optional":false},{"name":"HPLC","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-14T10:57:39Z","employer_posted_date":"2026-10-14","last_verified_at":"2026-10-21T18:03:26Z","board_verified":true,"closed_at":null,"days_open":7,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":7},"description":"Position Summary\nThe Scientist (Analytical) plays a key role in supporting research and development studies by performing analytical testing of pharmaceutical compound, drug substance and drug product. This role is integral to the development of new drug formulations, ensuring accurate data generation to guide formulation design and process development. Working independently with guidance from team leaders and senior scientists, the Scientist is responsible for executing analysis through HPLC and GC in compliance with internal protocols and industry standards. The position involves HPLC method development and optimisation to support early and late-stage pharmaceutical development. This role requires strong technical and organizational skills, attention to detail, and a commitment to scientific excellence in a fast-paced, collaborative R&D environment.\nEssential Functions\nResponsible for executing a variety of analytical techniques such as HPLC and GC to support the development of pharmaceutical drug products as well as assist in the day-to-day running of the laboratory in compliance with MedPharm’s QMS.\nPerforming and planning pre-defined experiments according to internal standard operating procedures (SOP) (e.g. forced degradation of substance and product, saturated solubility, excipient compatibility and formulation stability).\nSupport analytical method development and validation in accordance with ICH guidelines including contributions to formal update writing.\nAccurately document all experiments and results and have a good understanding and demonstration of good laboratory practice (GLP), data integrity and quality. \nAnalyze data using Empower and interpret results to support formulation development, stability studies and product release.\nTake active responsibility for your analytical work with respect to quality and compliance, particularly in the support of the analytical team.\nTo drive the progression of the study by collaborating with other departments, with oversight from your supervisor where appropriate. To attend meetings and contribute when appropriate. \nTo be involved in the department’s method development and continuous improvement strategies\nAdhere to Health and Safety and COSHH regulations and read relevant safety data sheets and risk assessments prior to undertaking work.\nTo maintain your training file (physical and MasterControl based) and to not use any equipment or handle any chemicals without following the appropriate health and safety guidance. \nTo undertake general waste disposal and contribute to the general tidiness and cleanliness of the laboratory environment\nTo conduct yourself in concordance with the MedPharm Ethos, professionalism and confidentiality.\nSupervisory responsibilities:\nN/A\n Key Relationships (examples: Depts or Individual positions that this position will be working closely with):R&D Laboratory staff\nAnalytical Team Leaders\nFD, PD and PT Study Managers\nProject Management team\nQC team\nQuality Assurance team\n3rd Party suppliers and vendors\nAuditory and Regulatory bodies\nTravel requirements:\nN/A\n Education and ExperienceBachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or related discipline.\nFamiliarity with common analytical equipment and instrumentation (e.g. analytical balance, pH meter, HPLC, GC)\n>2 years of relevant industry experience\nKnowledge, Skills, and Abilities\nComputer literate and knowledgeable in Microsoft Office Applications\nEffective oral and written communication\nGood observation skills and ability to document accurately\nStrong ability to work in teams and collaboration\nGood time management and organizational skills\nGood knowledge and practical experience in analytical laboratory\nPhysical Demands and Work Environment\nWhile performing the duties of this job, there may be certain physical demands required for the position.\nExample:\nOccasionally required to lift up to 20kg\nRequires standing for extended periods\nMay be exposed to loud noise levels\nMay be exposed to hot or cold temperatures\nOther Duties\nYou may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.\nLimitations and Disclaimer\nThe above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. 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