Technical Training Specialist III – Pharma Manufacturing (ASO & OSD)

About this roleThe Technical Training Specialist III supports the development and execution of training programs within a regulated manufacturing environment. This role partners with functional leaders and subject matter experts (SMEs) to ensure employees are trained, qualified, and operating in compliance with regulatory and business requirements.The position focuses on training program administration, On-the-Job Training (OJT) facilitation, and continuous improvement of training effectiveness. As a senior team member, this individual operates with independence while supporting audits, quality events, and site performance initiatives.What you’ll doAdminister and maintain competency-based training programs, ensuring accurate assignment, tracking, and completionFacilitate OJT programs across 1:1, classroom, small group, and virtual training environmentsPartner with SMEs to develop and maintain training content aligned to regulatory and operational requirementsConduct training needs assessments and implement continuous improvement initiativesServe as a Training SME during quality events (investigations, CAPAs, root cause analysis)Support inspection readiness activities, audits, and regulatory compliance effortsDrive human performance and efficiency improvement initiatives focused on safety, quality, and waste reductionWho you areYou are a detail-oriented and collaborative training professional with strong facilitation skills and the ability to operate effectively within a regulated manufacturing environment. You bring a proactive mindset focused on continuous improvement, compliance, and operational excellence.Required skillsBachelor’s degree in scientific, technical, or relevant disciplineAt minimum 2 years of experience in training and/or instructional delivery in a manufacturing environmentExperience administering training programs, including OJT and certification processesFamiliarity with learning management systems (LMS) and training tools, preferably Veeva and ArticulateKnowledge of regulatory requirements (e.g., cGMP) and training compliance standardsStrong organizational skills and attention to detail in documentation and trackingDemonstrated ability to collaborate across cross-functional teamsProblem-solving skills with the ability to support and influence process improvementsPreferred skillsExperience in pharmaceutical or highly regulated manufacturing environmentsKnowledge of adult learning principles and instructional designExperience supporting audits, inspections, and quality eventsAbility to develop engaging training materials across multiple delivery formats Job 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. 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 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.