{"id":2170663,"url":"https://alion.io/job/perkinelmer-pharma-automation-controls-engineer-project-farma","title":"Pharma Automation & Controls Engineer - Project Farma","company":{"id":20344,"name":"PerkinElmer","domain":"perkinelmer.com","url":"https://alion.io/company/perkinelmer","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":76,"open_postings":25,"ghost_share":0,"stale_share":0.96,"repost_share":0,"time_to_fill_p50_days":26,"computed_at":"2026-11-04T06:34:25Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"junior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":{"min":60000,"max":180000,"currency":"USD","period":"year","gross":null,"usd_annual":180000},"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 11","optional":false},{"name":"Bioreactors","optional":false},{"name":"CAPA","optional":false},{"name":"Chromatography","optional":false},{"name":"GMP","optional":false},{"name":"LIMS","optional":false}],"status":"live","first_seen_at":"2026-09-29T00:00:00Z","employer_posted_date":"2026-09-29","last_verified_at":"2026-11-04T17:30:18Z","board_verified":true,"closed_at":null,"days_open":36,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":36},"description":"When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.\nJob Title\nPharma Automation & Controls Engineer - Project FarmaLocation(s)\nCustomer Site - AL, Customer Site - AL, Customer Site - AZ, Customer Site - CA, Customer Site - CO, Customer Site - DC, Customer Site - DE, Customer Site - FL, Customer Site - GA, Customer Site - IA, Customer Site - IL, Customer Site - IN, Customer Site - KS, Customer Site - KY, Customer Site - MA, Customer Site - MD, Customer Site - ME, Customer Site - MI, Customer Site - MN, Customer Site - MO, Customer Site - NC, Customer Site - NH, Customer Site - NJ, Customer Site - NY, Customer Site - OH {+ 7 more}Job Description\nProject Farma is growing our Digital Tranformation & Automation (DT&A) practice, and will consider candidates' ranging from 2 - 16+ years' relevant experience. The successful candidate will reside in one of Project Farma's primary markets and be willing to travel domestically, to meet client project requests.\nMarket locations include but are not limited to: Boston, Philadelphia, DMV, Northern New Jersey, Chicago, Indianapolis, Columbus, St Louis, Kansas City, Raleigh-Durham, Houston, Dallas, Boulder, Portland, San Francisco, San Diego, and Los Angeles.\nTheDigital Transformation & Automation (DT&A) Engineer provides subject matter expertise in the design, implementation, and lifecycle management of digital systems across biologics, pharmaceutical, and novel therapy manufacturing facilities. This is a fully billable role, requiring experience with various MES platforms, Data Repositories, Serialization and integration to manufacturing applications (ERP, LIMS, CMMS, etc) and the ability to author, interpret, and lead documentation such as URS, FRS, Functional Narratives, and detailed system architecture designs.\nIn addition to technical experience, the DT&A Engineer acts as client liaison during delivery of Project Farma service engagements. They are strategically responsible for client satisfaction through project delivery while maintaining and growing client relationships. Key\nResponsibilities\nAutomation Design & Architecture\nDevelop system architectures and data flows for biologics, pharmaceutical, and advanced therapy manufacturing (DCS, PLC/SCADA, MES, historians, network layers).\nDevelop product recipe strategies across the full application layer of ERP, MES and DCS Batch.\nDetailed knowledge of Master data and how to define and control Master Data.\nCreate ISA-88/ISA-95-aligned architecture diagrams, inc Application and Data Flow diagrams.\nEnsure architecture supports scalability, cybersecurity, data integrity, and multi-product flexibility.\nURS / FRS / Design Documentation\nLead the creation, review, and approval of: URS (User Requirements Specifications), FRS (Functional Requirements Specifications), DS / DDS (Design Specifications), Functional & Control Narratives, Recipe Design Documentation (ISA-88 compliant), Automation Standards & Engineering Guidelines\nWork cross functionally to translate process requirements into robust digital system design documents.\nDigital System Implementation\nConfigure, program, and deploy Digital System within the manufacturing environment.\nDevelop, modify, and test MES (eBR, RbE, eLogbooks, Equipment Tracking, Weigh & Dispense), LIMS, Serialization and CMMS application functionality.\nSupport integration of OEM skids: bioreactors, chromatography systems, filtration skids, CIP/SIP, and fill finish equipment.\nCommissioning, Validation & GMP Compliance\nDetailed knowledge of FAT, SAT, IQ/OQ, and PQ protocols in alignment with GAMP 5 and 21 CFR Part 11.\n2/2\nEnsure all changes meet data integrity requirements, change control processes, and validation lifecycle rules.\nLead deviation investigations, CAPAs, and risk assessments related to Digital systems.\nManufacturing & Operations Support\nServe as SME for troubleshooting, system optimization, batch failure analysis, and performance enhancements.\nSupport 24/7 operations through structured root cause analysis and resolution of Digital System issues.\nDevelop long-term lifecycle plans for upgrades, patches, and system expansions.\nCross Functional Leadership\nCollaborate with IT/OT, process engineering, MSAT, quality, and capital project teams to deliver integrated system solutions.\nManage vendors, system integrators, and OEMs; review design packages and ensure alignment with internal standards.\nMentor junior engineers and act as technical SME during audits and regulatory inspections.\nExperience Required\nBachelor’s degree in Engineering (Automation, Electrical, Chemical, Mechanical, or related).\nMinimum 2-16+ years in automation engineering within GMP life sciences (biotech, pharma, ATMP).\nExpert-level experience with various MES platforms, Data Repositories, Serialization and integration to manufacturing applications (ERP, LIMS, CMMS, etc).\nProven ability to author, interpret, and own URS/FRS/DS documentation.\nExperience designing system applications and data flows across the full spectrum of manufacturing applications.\nStrong understanding of ISA-88 batch control, ISA-95 manufacturing hierarchy, and GAMP 5.\nHands-on experience supporting biologics and sterile/aseptic manufacturing environments.\nUnderstanding multisite standards for global manufacturers\nOther Preferred\nStrong communicator and influencer across engineering, quality, IT/OT, and manufacturing.\nStructured thinker with advanced troubleshooting and problem solving skills.\nSkilled at managing multiple priorities in a high pressure, regulated environment.\nDemonstrated leadership and mentorship abilities.\nProject Farma is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce.\nApplicants must be authorized to work in the United States on a full-time basis. We will not sponsor applicants for current or future work visas for this position. This position may require significant travel to support project and business needs. We cannot employ anyone with an invalid driver's license.\nThe annual compensation range for this full-time position is $60,000 - $180,000. The final base pay offered to the successful candidate will be determined by factors including internal equity, work location, as well as individual qualifications, such as job-related skills, experience, and relevant education or training.\nPerkinElmer is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. 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