Manufacturing Engineer III - Solid Dose Manufacturing
About This RoleAs a Manufacturing Engineer III, you will serve as a key technical resource supporting manufacturing equipment within our production areas, with a focus on solid dose (OSD/ASO) operations. This role plays a critical part in maintaining reliable manufacturing processes, improving equipment performance, and driving continuous improvement initiatives. You will partner closely with manufacturing, maintenance, and cross-functional teams to troubleshoot issues, lead equipment-related projects, and ensure successful validation and implementation of new or modified systems.What You'll DoSupport manufacturing operations by troubleshooting equipment issues and driving root cause analysis, implementing sustainable solutions to improve uptime and reliabilityServe as the equipment SME for assigned manufacturing systems, providing hands-on technical support and guidanceLead and support continuous improvement (CI) initiatives to optimize equipment and manufacturing performanceDesign, specify, and support installation or modification of manufacturing equipment and systemsDevelop, execute, and support CQV (Commissioning, Qualification, and Validation) activities including protocol authoring, execution, and reportingPartner with process and maintenance teams to resolve equipment issues and enhance overall manufacturing capabilityLead or contribute to equipment-related projects, including capital projects, tech transfers, and system upgradesSupport onboarding, training, and drawing/documentation management for equipment and systemsParticipate in investigations (deviations, CAPAs) and change controls related to equipment and process improvementsProvide on-call support as needed, with a focus on parenteral fill (PF) or manufacturing support areasWho You AreYou're a hands-on, self-motivated engineer who takes initiative and enjoys working directly with equipment and manufacturing teams. You thrive in a fast-paced environment, proactively identifying opportunities for improvement and driving solutions from concept through implementation.You're also flexible and dependable, willing to support extended hours during critical project timelines and participate in an on-call rotation to ensure consistent manufacturing support.Required SkillsBachelor's and/or master's degree in engineering from an accredited college or university2+ years of experience supporting manufacturing equipmentExperience with some or all the below in a cGMP environment:Troubleshooting and root cause analysisContinuous improvement methodologies and equipment optimizationHands-on mechanical aptitude with manufacturing equipmentExperience supporting CQV activities, including protocol development and executionStrong ownership mindset with demonstrated initiative and accountabilityPreferred SkillsExperience with some or all the manufacturing equipment below:Solid dose manufacturing (OSD, OSM, or ASOS)Parenteral fill (PF) operationsHands-on experience with equipment such as:Chromatography skids or columnsTablet pressesEncapsulation machinesIsolatorsJob Level: ProfessionalAdditional InformationThe base compensation range for this role is: $77,000.00-$100,000.00Base 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.BenefitsIn 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 onto learn more about our DE&I efforts.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.VEVRAA Federal Contractor.We request Priority Protected Veteran & Disabled Referrals for all of our locations within the state.PDN-a1c64110-ca99-4560-8e6f-977302fe105d