{"id":2980065,"url":"https://alion.io/job/qrc-group-manufacturing-support-specialist-document-control","title":"Manufacturing Support Specialist - Document Control","company":{"id":4422706,"name":"QRC Group","domain":"qrcgroup.net","url":"https://alion.io/company/qrcgroup-2","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Zoho Recruit","truth_index":null},"role":"Customer Success","role_family":"Customer Success","seniority":"junior","employment_type":"contractor","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Cayey, Puerto Rico"],"countries":["PR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":26000,"max_usd":54000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":1966},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-10-14T00:00:00Z","employer_posted_date":"2026-10-14","last_verified_at":"2026-10-25T14:18:27Z","board_verified":true,"closed_at":null,"days_open":11,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":11},"description":"Manufacturing Support Specialist to support manufacturing operations by managing controlled documentation, coordinating Engineering Change Orders (ECOs), and assisting with continuous improvement initiatives in a highly regulated FDA and ISO environment.\nKey Responsibilities\nSupport manufacturing areas with the implementation of document changes through Engineering Change Order (ECO) systems.\n Ensure documentation updates related to Capital Projects, Validation activities, Quality Notifications, and CAPAs are completed on time.\nCreate, format, revise, and maintain SOPs, manufacturing batch records, and other GMP-required documentation.\nAssist in manufacturing data collection, reporting, and performance metrics tracking.\nParticipate in Continuous Improvement (CI) and Lean Manufacturing initiatives.\nSupport document control activities, including deviation records and periodic document reviews.\nPromote compliance with regulatory, quality, environmental health, and safety requirements.\nIdentify opportunities to improve product quality, process efficiency, and manufacturing performance.\nRequirements\nEducation & Experience\nAssociate Degree or equivalent required.\nMinimum of 2 years of experience working with documentation control systems in an FDA and ISO regulated environment. \nKnowledge & Skills\nExperience with Documentation Control Systems. \nStrong attention to detail and accuracy.\nExcellent organizational, planning, and time-management skills. \nEffective written and verbal communication skills. \nProficiency in Microsoft Office Suite (Word, Excel, and PowerPoint). \nAbility to work independently with minimal supervision. \nFully bilingual in English and Spanish.","description_format":"text","description_chars":1685,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"associate","optional":true},"security_clearance":false,"languages":[{"language":"Spanish","level":"Proficiency (C2)","optional":false},{"language":"English","level":"Proficiency (C2)","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biotechnology","Security Compliance","IT Consulting & Digital 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