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Sr Engineer I, Automation (Syncade MES)

Biogen

Sr Engineer I, Automation (Syncade MES)

full-timePosted: Aug 2, 2026Updated: Sep 1, 2026NC, Research Triangle Park

Job Description

About This RoleWe are seeking an experienced technical contributor to join our Automation Systems Engineering team at the Biogen RTP Bio site. The Senior Automation Engineer I will support Syncade (MES) system administration within a GMP-regulated manufacturing environment. This role operates with a high degree of independence and is accountable for ensuring system reliability, supporting manufacturing execution, and driving continuous improvement initiatives. The Senior Automation Engineer I will be a subject matter expert for Syncade, capable of leading small-to-moderate complexity initiatives to influence cross-functional outcomes.What You’ll DoAct as system administrator/SME for Syncade (MES), including configuration, maintenance, troubleshooting, and lifecycle managementOwn and support Syncade Application and the relevant infrastructure to enable electronic batch record (eBR) workflows, recipe configuration, and exception handlingEnsure system availability, performance, and data integrity to support GMP manufacturing operationsLead root cause investigations and implement corrective/preventive actions for MES-related deviationsManage user access, security roles, and audit trail reviews in compliance with GxP and cybersecurity requirementsExecute and support change controls, including system updates, enhancements, and validation deliverables (IQ/OQ/PQ)Drive continuous improvement efforts to enhance system usability, reliability, and operational efficiencySupport integration and data flow between Syncade and other automation and Enterprise systems, e.g. DeltaV, PI, and Infobatch, CMMS, Oracle, Veeva, LIMSProvide technical support during manufacturing operations, including off-hours support as requiredWho You AreYou are a meticulous professional with a strong foundation in automation / manufacturing systems engineering, particularly in biopharmaceutical settings. Your analytical mindset and problem-solving skills empower you to tackle complex challenges independently. You thrive in collaborative environments, easily engaging with diverse teams to achieve shared goals. Yourdedication to operational excellence and compliance ensures that systems run smoothly and efficiently.Required SkillsBachelor’s degree in Engineering5–8+ years of automation engineering experience in a regulated environment (GMP preferred)Minimum of 3 years of experience with Syncade/MES Infrastructure, workflows, eBR design, and manufacturing process supportStrong understanding of GxP compliance, data integrity, and change control processesProven ability to independently troubleshoot and resolve complex technical issuesPreferred SkillsExperience with Emerson DeltaV (DCS) integration and supportExperience with AVEVA PI System for data collection and analyticsFamiliarity with Infobatch for batch reportingParticipation in system upgrades, tech transfers, or manufacturing modernization initiatives Job Level: ProfessionalAdditional InformationThe base compensation range for this role is: $93,000.00-$121,000.00Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:Medical, Dental, Vision, & Life insurancesFitness & Wellness programs including a fitness reimbursement Short- and Long-Term Disability insuranceA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar yearPaid Maternity and Parental Leave benefit 401(k) program participation with company matched contributionsEmployee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year Employee Resource Groups participationWhy Biogen?We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our Biogen.All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Locations

  • NC, Research Triangle Park

Skills Required

  • regulated environmentintermediate
  • Syncade/MES Infrastructureintermediate
  • Emerson DeltaVintermediate
  • AVEVA PI System for data collectionintermediate
  • Infobatch for batch reportingintermediate

Required Qualifications

  • You are a meticulous professional with a strong foundation in automation / manufacturing systems engineering, particularly in biopharmaceutical settings. Your analytical mindset and problem-solving skills empower you to tackle complex challenges independently. You thrive in collaborative environments, easily engaging with diverse teams to achieve shared goals. Your (experience)
  • dedication to operational excellence and compliance ensures that systems run smoothly and efficiently. (experience)
  • Bachelor’s degree in Engineering (degree in engineering)
  • 5–8+ years of automation engineering experience in a regulated environment (GMP preferred) (experience, 8 years)
  • Minimum of 3 years of experience with Syncade/MES Infrastructure, workflows, eBR design, and manufacturing process support (experience, 3 years)
  • Strong understanding of GxP compliance, data integrity, and change control processes (experience)
  • Proven ability to independently troubleshoot and resolve complex technical issues (experience)
  • Bachelor’s degree in Engineering (degree in engineering)
  • 5–8+ years of automation engineering experience in a regulated environment (GMP preferred) (experience, 8 years)
  • Minimum of 3 years of experience with Syncade/MES Infrastructure, workflows, eBR design, and manufacturing process support (experience, 3 years)
  • Strong understanding of GxP compliance, data integrity, and change control processes (experience)
  • Proven ability to independently troubleshoot and resolve complex technical issues (experience)

Preferred Qualifications

  • Experience with Emerson DeltaV (DCS) integration and support (experience)
  • Experience with AVEVA PI System for data collection and analytics (experience)
  • Familiarity with Infobatch for batch reporting (experience)
  • Participation in system upgrades, tech transfers, or manufacturing modernization initiatives (experience)
  • Experience with Emerson DeltaV (DCS) integration and support (experience)
  • Experience with AVEVA PI System for data collection and analytics (experience)
  • Familiarity with Infobatch for batch reporting (experience)
  • Participation in system upgrades, tech transfers, or manufacturing modernization initiatives (experience)

Responsibilities

  • Act as system administrator/SME for Syncade (MES), including configuration, maintenance, troubleshooting, and lifecycle management
  • Own and support Syncade Application and the relevant infrastructure to enable electronic batch record (eBR) workflows, recipe configuration, and exception handling
  • Ensure system availability, performance, and data integrity to support GMP manufacturing operations
  • Lead root cause investigations and implement corrective/preventive actions for MES-related deviations
  • Manage user access, security roles, and audit trail reviews in compliance with GxP and cybersecurity requirements
  • Execute and support change controls, including system updates, enhancements, and validation deliverables (IQ/OQ/PQ)
  • Drive continuous improvement efforts to enhance system usability, reliability, and operational efficiency
  • Support integration and data flow between Syncade and other automation and Enterprise systems, e.g. DeltaV, PI, and Infobatch, CMMS, Oracle, Veeva, LIMS
  • Provide technical support during manufacturing operations, including off-hours support as required
  • Act as system administrator/SME for Syncade (MES), including configuration, maintenance, troubleshooting, and lifecycle management
  • Own and support Syncade Application and the relevant infrastructure to enable electronic batch record (eBR) workflows, recipe configuration, and exception handling
  • Ensure system availability, performance, and data integrity to support GMP manufacturing operations
  • Lead root cause investigations and implement corrective/preventive actions for MES-related deviations
  • Manage user access, security roles, and audit trail reviews in compliance with GxP and cybersecurity requirements
  • Execute and support change controls, including system updates, enhancements, and validation deliverables (IQ/OQ/PQ)
  • Drive continuous improvement efforts to enhance system usability, reliability, and operational efficiency
  • Support integration and data flow between Syncade and other automation and Enterprise systems, e.g. DeltaV, PI, and Infobatch, CMMS, Oracle, Veeva, LIMS
  • Provide technical support during manufacturing operations, including off-hours support as required

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