{"id":1807613,"url":"https://alion.io/job/capgemini-site-conformance-expert-life-science","title":"Site Conformance Expert | Life Science","company":{"id":145,"name":"Capgemini","domain":"capgemini.com","url":"https://alion.io/company/capgemini","size_band":"5000+","is_staffing_agency":false,"employer_type":"services","is_intermediary":false,"listed_via":null,"ats_vendor":"Career site","truth_index":{"grade":"B","score":79,"open_postings":1705,"ghost_share":0.002,"stale_share":0.828,"repost_share":0.012,"time_to_fill_p50_days":30,"computed_at":"2026-11-02T06:13:15Z"}},"role":"Biotech","role_family":"Biotech","seniority":"senior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Diegem, Belgium"],"countries":["BE"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":50000,"max":null,"currency":"EUR","period":"year","gross":true,"usd_annual":56084},"salary_estimate":null,"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-08-14T22:35:54Z","employer_posted_date":"2026-08-14","last_verified_at":"2026-11-02T11:22:49Z","board_verified":true,"closed_at":null,"days_open":79,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":79},"description":"Your Role\nAs a Site Conformance Expert within our Quality Assurance team, you will be the vital link between operations and regulatory affairs, ensuring compliance across multiple production streams including Primary, Secondary, Quality Control, and Incoming Materials.\nIn this role you will play a key role in:\nEnsuring compliance with regulatory dossiers for activities related to Manufacturing Performance Units and Quality Control Departments, through variations and timely responses to health authority questions.\nProviding regulatory oversight within Manufacturing Performance Units and Quality Control Departments to maintain consistent alignment with evolving regulatory requirements.\nAnalysing potential compliance gaps and developing effective mitigation strategies to prevent supply issues, delays, or recalls due to misalignment with regulatory files.\nCollaborating with cross-functional teams to implement and maintain quality systems that meet global regulatory standards across all production streams.\nSupporting continuous improvement initiatives to enhance compliance processes, documentation systems, and overall quality assurance performance.\nYour Profile\nWe are looking for a motivated and detail-oriented professional who thrives in a regulated environment and is passionate about quality and compliance.\nYou hold a Master's degree in Pharmaceutical Sciences, Chemistry, Biology, or a related field, and bring a minimum of 3 years of experience in a quality assurance role within the pharmaceutical or life sciences industry.\nYou have strong knowledge of GMP regulations, quality systems, and regulatory compliance requirements, with hands-on experience in regulatory documentation including eCTD format and normative documents.\nYou are fluent in both English and French, with strong communication skills that allow you to effectively engage and collaborate with diverse stakeholders across departments.\nYou are a proactive team player with the ability to manage multiple priorities, work independently, and contribute meaningfully to a high-performing, cross-functional environment.\nWhat you'll love about working here\nCareer acceleration programs - From associate to leaders and beyond, get support in your career at every stage with award-winning programs such as our leadership development program, Connected Manager, to accelerate your growth and develop your expertise.\nContinuous feedback - We take a human-centric approach to foster growth and performance. Our performance management tool GetSuccess enables continuous feedback, quarterly check-ins with managers, and ongoing performance discussions.\n FlexAbroad - Employees in 20+ countries can work abroad for up to 45 days in a 12-month period.\nFor this role, the gross annual starting base salary is 50.000 euro (full-time). This covers base pay only; any bonuses, incentives, and benefits will be discussed later in the recruitment process. Candidates with additional experience or qualifications may receive a higher offer, determined by objective, gender-neutral criteria and consistent with our pay principles. If a collective labour agreement applies, we will explain the relevant pay terms at the interview stage. 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