{"id":3879205,"url":"https://alion.io/job/merck-co-spclst-planning-scheduling","title":"Spclst, Planning & Scheduling","company":{"id":3768,"name":"Merck & Co.","domain":"msd.com","url":"https://alion.io/company/msd","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":97,"open_postings":212,"ghost_share":0.028,"stale_share":0.146,"repost_share":0.203,"time_to_fill_p50_days":16,"computed_at":"2026-11-11T05:49:22Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Lucerne, Switzerland"],"countries":["CH"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":1,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GCP","optional":false},{"name":"GMP","optional":false},{"name":"Veeva","optional":true}],"status":"live","first_seen_at":"2026-11-05T00:00:00Z","employer_posted_date":"2026-11-05","last_verified_at":"2026-11-11T09:15:54Z","board_verified":true,"closed_at":null,"days_open":6,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":6},"description":"Job Description\nThe Specialist, Planning & Scheduling, in Global Clinical Supply (GCS), Global Operations Planning is a technical professional responsible for executing and supporting GxP Quality System activities to ensure clinical supply operations are performed in a compliant, inspection-ready, and risk-based manner. GCS supports Phase I-IV trials across 60+ countries in alignment with applicable GxP regulations (GMP, GDP, and GCP) and Environmental Health & Safety requirements.\nThis role supports core GCS processes- primarily focused on deviations and CAPA, however, support of change control, documentation, training, audits/inspections, analytics, risk management, and safety-working under established procedures and governance structures are developmental opportunities should proficiency be demonstrated across multiple compliance domains.\nThe Specialist partners with GCS functional areas and stakeholders within Operations Planning, Distribution & Logistics, Clinical Supply, Quality, IT/Digital, and other cross-functional teams to support Quality Management System (QMS) execution, issue resolution, and continuous improvement across the GCS network.\nQualifications\nEducation & Experience:\nBachelor’s degree in a Scientific, Engineering, or related field with 1+ years of relevant experience in a regulated GxP environment.\nExperience supporting one or more GxP Quality System processes (e.g., deviations, CAPA, change control, documentation, training, audits/inspections, risk management, safety).\nExperience working within cross-functional teams in a regulated environment.\nSkill-based Qualifications: \nWith developing subject matter expertise, strong execution focus, and the ability to follow defined processes and procedures, candidates must demonstrate:\nAbility to execute compliance activities in alignment with established GxP procedures and Quality System expectations.\nFoundational understanding of GxP and ALCOA+ principles, with the ability to apply data integrity expectations to daily work.\nAbility to identify risks to compliance execution, timelines, or deliverables and escalate appropriately.\nAbility to support deviation investigations and CAPA activities with accurate documentation and attention to detail.\nAbility to collaborate effectively with stakeholders across organizations.\nAnalytical skills to review data, support trending, and contribute to performance monitoring.\nClear, professional communication skills for written documentation and routine stakeholder interactions.\n\nPreferred Experience and Skills:\nExperience supporting audits, inspections, or readiness activities.\nExperience with documentation lifecycle activities (authoring, reviewing, periodic updates).\nExperience working with GMP electronic systems (e.g., MEDs, Veeva, TrackWise, LMS).\nInterest in continuous improvement or Lean methodologies.\nAdditional location(s) Compensation Information:\nRequired Skills:\nAdaptability, Analytical Thinking, CAPA Investigations, Conducting Investigations, Cross-Functional Communications, Data Analysis, Driving Continuous ImprovementPreferred Skills:\nMRP Systems, Six SigmaCurrent Employees apply HERE\nCurrent Contingent Workers apply HERE\nSearch Firm Representatives Please Read Carefully\nMerck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.\nEmployee Status:\nRegularRelocation:\nNo relocationVISA Sponsorship:\nNoTravel Requirements:\nNo Travel RequiredFlexible Work Arrangements:\nNot ApplicableShift:\nNot IndicatedValid Driving License:\nNoHazardous Material(s):\nNoJob Posting End Date:\n11/20/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. 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