Sr Engineer I, Automation (Syncade MES)

Posted 9 Hours Ago
Be an Early Applicant
Triangle Trailer Park, Township of Jacksonville, NC, USA
In-Office
93K-121K Annually
Senior level
Biotech
The Role
Serve as Syncade MES system administrator and SME in a GMP manufacturing site: ensure availability, support eBR workflows, manage access and validations (IQ/OQ/PQ), lead investigations, integrate MES with DeltaV/PI/Infobatch/enterprise systems, and drive continuous improvement including off-hours support as needed.
Summary Generated by Built In

About This Role

We 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 Do

  • 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

Who You Are

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

dedication to operational excellence and compliance ensures that systems run smoothly and efficiently.

Required Skills

  • Bachelor’s degree in Engineering

  • 5–8+ 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 support

  • Strong understanding of GxP compliance, data integrity, and change control processes

  • Proven ability to independently troubleshoot and resolve complex technical issues

Preferred Skills

  • Experience with Emerson DeltaV (DCS) integration and support

  • Experience with AVEVA PI System for data collection and analytics

  • Familiarity with Infobatch for batch reporting

  • Participation in system upgrades, tech transfers, or manufacturing modernization initiatives


 

Job Level: Professional


Additional Information

The base compensation range for this role is: $93,000.00-$121,000.00


Base 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 insurances
  • Fitness & Wellness programs including a fitness reimbursement 
  • Short- and Long-Term Disability insurance
  • A 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 year
  • Paid Maternity and Parental Leave benefit 
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan 
  • Tuition reimbursement of up to $10,000 per calendar year 
  • Employee Resource Groups participation

Why 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.



Skills Required

  • Bachelor's degree in Engineering
  • 5-8+ years of automation engineering experience in a regulated environment
  • Minimum of 3 years of experience with Syncade/MES infrastructure, workflows, eBR design, and manufacturing process support
  • Strong understanding of GxP compliance, data integrity, and change control processes
  • Proven ability to independently troubleshoot and resolve complex technical issues
  • Experience with Emerson DeltaV integration and support
  • Experience with AVEVA PI System for data collection and analytics
  • Familiarity with Infobatch for batch reporting
  • Participation in system upgrades, tech transfers, or manufacturing modernization initiatives

Biogen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.

  • Fair & Transparent Compensation Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
  • Equity Value & Accessibility Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
  • Leave & Time Off Breadth Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.

Biogen Insights

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The Company
HQ: Cambridge, MA
9,575 Employees
Year Founded: 1978

What We Do

Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.

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