Engineer II/III, Automation

Biogen; North Carolina; On-site; USD 77,000 - 100,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Fitness reimbursement

Paid vacation

Paid holidays

401(k) match

Employee stock purchase plan

Tuition reimbursement

Job summary

Biogen’s RTP Bio site seeks an Automation Engineer II/III to support DeltaV DCS and Syncade MES systems. You will craft software, validate changes, and ensure reliable integration with PI Historian, Oracle, CMMS, Veeva, and Labware (LIMS).

This role emphasizes continuous improvement and rigorous quality standards in a fast-paced biopharmaceutical environment. You will lead small to mid-sized projects, collaborate across functions, and contribute to the site’s automation strategy while

Qualifications

• Bachelor's degree in engineering from an accredited college.
• Engineer II requires 2+ years of experience in MES/DCS environments.
• Experience with MES validation, change controls, and troubleshooting.

Responsibilities

• Configure and maintain DeltaV DCS and Syncade MES software to support process improvements and new equipment implementations.
• Author, review, and approve MES and DeltaV DCS documentation and validation deliverables.
• Create and execute software testing scripts and support validation activities per GAMP 5.
• Execute and manage change controls while ensuring compliance with site procedures and quality requirements.
• Troubleshoot MES and DCS issues during testing and manufacturing operations; participate in on-call rotations.

Skills

MES recipe authoring

DeltaV DCS

Troubleshooting

Validation

Cross-functional collaboration

Education

Bachelor's degree in Engineering

Tools

Syncade MES

DeltaV DCS

PI Historian

Job description

About This RoleAs an Engineer II/III Automation, you will join the Automation & MES team at Biogen’s RTP Bio site, supporting both operational excellence and project-driven goals. This role provides technical solution development and hands-on support for DeltaV DCS and Syncade MES systems, partnering cross-functionally to design, implement, maintain, and continuously improve automation solutions that support biopharmaceutical manufacturing operations. You will be responsible for recipe authoring, software configuration, validation activities, change controls, troubleshooting, and ensuring seamless integration with systems such as PI Historian, Oracle, CMMS, Veeva, and Labware (LIMS). This position plays a critical role in optimizing manufacturing operations, enhancing system reliability, and supporting the site's long-term automation strategy.What You'll DoConfigure and maintain DeltaV DCS and Syncade MES software to support process improvements, new products, and new equipment implementations.Partner with Process Owners, Manufacturing, and cross-functional stakeholders to design and implement software that meet s operational and engineering requirements.Author, review, and approve MES and DeltaV DCS documentation, including lifecycle documents, project documents, procedures, work instructions, and validation deliverables.Create and execute software testing scripts and support software validation activities in accordance with established procedures and GAMP 5 principles.Define and support validation strategies in collaboration with Quality representatives and ensure consistency in execution across disciplines.Execute and manage change controls for DeltaV DCS and Syncade MES systems while maintaining compliance with site procedures and quality requirements.Troubleshoot MES and DCS system issues during testing and manufacturing operations, including participation in an on-call support rotation.Identify and implement opportunities for optimization in system design, programming, testing, integrations, and operational processes.Collaborate with automation, data systems, manufacturing, and engineering teams to ensure systems continue to meet evolving site needs.Support and lead small to medium engineering projects, ensuring timely execution and adherence to quality standards.Evaluate technical options and recommend optimal solutions for system enhancements and integrations.Support continuous improvement initiatives and drive operational excellence through automation solutions.Maintain training requirements, establish development goals, and support knowledge sharing across the team.Who You AreYou are a technically capable automation professional who thrives in a collaborative and fast-paced manufacturing environment. You are detail-oriented, proactive, and passionate about solving complex technical challenges. You leverage strong analytical and troubleshooting skills to identify effective solutions while working closely with cross-functional partners. You are committed to continuous improvement, system reliability, and delivering automation solutions that support safe, compliant, and efficient manufacturing operations.Required Skills for an Engineer IISalary Range: 65K-85KBachelor's degree in Engineering, or a related discipline from an accredited college or universityMinimum of 0-2 years of experience in a GMP manufacturing environmentStrong collaboration and communication skills with cross-functional teamsRequired Skills for an Engineer IIISalary Range: 77K-100KBachelor's degree in Engineering or a related discipline from an accredited college or universityMinimum of 2 years of experience with MES recipe authoring (preferably Syncade) and/or supporting DeltaV in an engineering related capacityStrong understanding of system validation, change controls, and troubleshooting within MES and DCS environmentsProven ability to develop and implement automation solutions that support manufacturing and operational objectivesAbility to evaluate technical options and drive optimal system enhancements across automation platformsExperience providing technical leadership and collaborating across functions to meet site goalsPreferred SkillsExperience supporting large-scale biotech or pharmaceutical manufacturing environmentsFamiliarity with integrations involving PI Historian, Oracle, CMMS, Veeva, and Labware (LIMS)Experience supporting investigations and implementing corrective and preventative actions (CAPAs)Ability to lead cross-functional meetings and coordinate change implementation activitiesFamiliarity with GAMP 5 principles and regulated system compliance requirementsExperience identifying and implementing process, design, and system optimization opportunitiesInterest in expanding expertise across automation platforms and integrated manufacturing systemsExperience serving as a subject matter expert for MES, DeltaV or other automation systems within a manufacturing environmentJob Level: ProfessionalAdditional InformationThe base compensation range for this role is: $77,000.00-$100,250.00Base 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 reimbursementShort- 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 Significance80 hours of sick time per calendar yearPaid Maternity and Parental Leave benefit401(k) program participation with company matched contributionsEmployee stock purchase planTuition reimbursement of up to $10,000 per calendar yearEmployee 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.