{"id":1724380,"url":"https://alion.io/job/cdmo-drug-device-combination-kindeva-supervisor-production-operations-2","title":"Production Operations Supervisor - Second Shift","company":{"id":2177732,"name":"Kindeva Drug Delivery","domain":"kindevadd.com","url":"https://alion.io/company/kindevadd","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Dayforce","truth_index":{"grade":"A","score":85,"open_postings":15,"ghost_share":0,"stale_share":0.6,"repost_share":0,"time_to_fill_p50_days":45,"computed_at":"2026-11-05T05:54:30Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","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":["Bridgeton, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":50000,"max_usd":91000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":4038},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false},{"name":"Microsoft Office","optional":false},{"name":"Veeva","optional":false}],"status":"live","first_seen_at":"2026-07-08T04:00:00Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-05T19:32:14Z","board_verified":true,"closed_at":null,"days_open":120,"trust":{"level":"ok","repost_count":1,"flags":[],"days_open":120},"description":"Our Work Matters\nAt Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.\n\nWhy Kindeva?\nPurpose-driven work environment\nSignificant growth opportunities\nCollaborative, team-oriented culture\nDirect impact on patient care\nIndustry-leading pharmaceutical innovation\n\nThe Impact You Will Make\nLead the production of life-saving therapies.\nAs a Production Supervisor, you will provide leadership for our Sterile Production Manufacturing (SPM) operations, overseeing daily manufacturing activities while leading a team of production operators in a regulated pharmaceutical environment. You will ensure production schedules are achieved while maintaining the highest standards of quality, safety, and current Good Manufacturing Practices (cGMP).\nWorking closely with Quality, Engineering, Maintenance, Planning, and Supply Chain, you will help drive operational excellence, develop employees, and support the production of therapies that improve the lives of patients around the world.\n\nGrowth Opportunity\nOur St. Louis manufacturing operations continue to grow, creating exciting opportunities for Production Supervisors to lead high-performing teams in a fast-paced pharmaceutical manufacturing environment. Join us during this exciting period of growth and help build a culture focused on safety, quality, operational excellence, and continuous improvement.\nShift Schedule: This is a second shift position\n\nResponsibilities\n\nProduction Leadership & Team Development\nDirectly supervise production personnel and Lead Operators.\nManage staffing, scheduling, attendance, vacations, and overtime.\nInterview, hire, onboard, train, coach, mentor, and develop employees.\nConduct performance evaluations and administer corrective action when appropriate.\nEnsure employees maintain required qualifications, certifications, and training.\nLead daily production meetings while promoting accountability, teamwork, safety, quality, and continuous improvement.\nSupport employee relations and labor relations activities, including union environments when applicable.\n\nManufacturing Operations\nLead daily aseptic manufacturing operations and ensure production schedule attainment.\nSupervise Sterile Production Manufacturing (SPM) operations while ensuring production activities are completed safely, efficiently, and in compliance with established procedures.\nCoordinate manufacturing activities to support production goals and customer commitments.\nSupport operational readiness and timely execution of manufacturing activities.\nPerform other duties as assigned.\n\nQuality, Compliance & Documentation\nEnsure compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), site safety requirements, and applicable regulatory expectations.\nReview production documentation for accuracy and completeness.\nInvestigate deviations, quality events, and manufacturing issues while driving timely resolution.\nSupport audits of aseptic manufacturing processes and supporting operations.\nMaintain compliance with documentation requirements and regulatory expectations.\n\nContinuous Improvement & Operational Excellence\nDrive continuous improvement initiatives focused on safety, quality, productivity, and operational performance.\nIdentify opportunities to improve manufacturing processes and eliminate waste.\nSupport operational excellence initiatives and promote a culture of continuous improvement.\n\nCross-Functional Collaboration\nPartner closely with Quality, Engineering, Maintenance, Planning, and Supply Chain to support manufacturing operations.\nCollaborate with site leadership to resolve operational issues and achieve production objectives.\nFoster strong communication across departments to ensure safe, compliant, and efficient manufacturing operations.\n\nQualifications\nRequired: Associate degree in a scientific, technical, manufacturing, business, engineering, or related field and a minimum of two (2) years of supervisory experience in a manufacturing environment; OR a minimum of ten (10) years of supervisory experience in pharmaceutical operations in lieu of a degree.\nPreferred: Pharmaceutical and/or manufacturing experience, experience in regulated environments, and union leadership experience.\nEffective written and oral communication skills required.\nProficiency with Microsoft Office applications, Kronos, and Veeva.\nDemonstrated reading comprehension and writing proficiency with the ability to communicate effectively across a diverse workforce.\nSelf-starter with strong interpersonal, coaching, and leadership skills.\nProven problem-solving, decision-making, and process improvement abilities.\nPosition requires regular onsite attendance.\nAbility to manage multiple priorities across multiple functions in a fast-paced manufacturing environment.\nAbility to work effectively under strict production, quality, and performance deadlines.\nMust be willing and able to work beyond normal business hours, including weekends and holidays, as business needs require.\n\nPhysical Requirements\nAbility to stand for extended periods without medical restrictions that would prevent completion of essential job duties.\nAbility to bend, stoop, squat, carry, and lift up to 50 pounds.\nFrequent walking throughout production areas while supervising manufacturing operations.\nSpecific vision abilities include close vision, color vision, and the ability to adjust focus.\nAbility to work around moving machinery, varying temperatures, and while wearing required personal protective equipment (PPE).\n\nJoin our One Team mission of manufacturing more tomorrows. Your leadership will help ensure safe, compliant manufacturing operations while delivering life-saving therapies to patients around the world.\n\n#LI-Onsite #WH","description_format":"text","description_chars":5783,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"associate","optional":false},"security_clearance":false,"languages":[]},"benefits":["Growth opportunities"],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["CRO & CDMO Services","Infusion & Drug Delivery Devices"],"lifecycle":[{"event":"open","at":"2026-10-02T21:39:44Z"},{"event":"close","at":"2026-10-26T05:04:41Z"},{"event":"reopen","at":"2026-10-30T13:13:32Z"}],"visa":[{"country":"US","licensed_sponsor":true,"evidence":"H-1B filings in 12 months: 2 · green card filings: 1","filings_12m":2,"filings_prev_12m":1,"green_card_filings_12m":1,"median_offered_wage_usd":135833,"route":null,"cap_exempt":false,"checked_at":"2026-10-29T16:27:21+00:00","sources":["US Department of Labor: LCA disclosure data (H-1B, H-1B1, E-3)","US Department of Labor: PERM disclosure data (green cards)"],"filings_for_role_12m":0}],"liveness":{"score":8,"band":"cold","label":"Long shot","p_open":1,"p_active":0.3,"p_room":0.28,"age_days":120,"expected_fill_days":45,"reasons":["conf:2","stale_co","win:tail","crowd:junior"],"computed_at":"2026-11-05T05:54:30Z"},"pay":null,"html_url":"https://alion.io/job/cdmo-drug-device-combination-kindeva-supervisor-production-operations-2","json_url":"https://alion.io/job/cdmo-drug-device-combination-kindeva-supervisor-production-operations-2.json","meta":{"generated_at":"2026-11-05T23:24:43Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":4742,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-06T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":2177732},"rest":"https://alion.io/mcp/rest/get_company?id=2177732"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fcdmo-drug-device-combination-kindeva-supervisor-production-operations-2"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Fcdmo-drug-device-combination-kindeva-supervisor-production-operations-2"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Fcdmo-drug-device-combination-kindeva-supervisor-production-operations-2"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/cdmo-drug-device-combination-kindeva-supervisor-production-operations-2\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fcdmo-drug-device-combination-kindeva-supervisor-production-operations-2"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":1724380}},{"tool":"search_jobs","arguments":{"company":"kindevadd.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":1724380},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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