About This role

We are seeking a dynamic and detail-oriented New Product Introduction (NPI) Specialist to join our RTP Bio Manufacturing team. This highly visible role sits within the Manufacturing organization and is responsible for ensuring new products are successfully introduced into the RTP Bio manufacturing facility. The NPI Specialist plays a critical role in driving timelines, coordinating cross-functional stakeholders, and enabling operational readiness to support on-time manufacturing start-up for new products.

What you’ll Do

Support cross-functional project teams responsible for introducing new products into manufacturing operations.Manage and execute detailed project plans, timelines, and deliverables for NPI initiatives, ensuring milestones are met on time and within budget.Track and drive completion of key deliverables required to ensure overall site readiness.Present project progress, operational status, and timeline-related risks at appropriate governance forums.Identify, assess, and mitigate risks related to operational readiness and new product launches.Drive continuous improvement initiatives to enhance NPI processes and reduce time-to-market.

Who You Are

A proactive and organized project leader who thrives in a fast-paced, cross-functional manufacturing environment, with the ability to clearly communicate complex information to a wide range of stakeholders. Highly detail-oriented with a strong problem-solving mindset, able to anticipate, assess, and manage risks effectively. Comfortable balancing multiple priorities while maintaining focus on timelines, deliverables, and overall project success.

Required Skills

Bachelor’s degree in engineering or related STEM field from an accredited college or universityAt minimum 5 years of experience in pharmaceutical manufacturing, process development, or related disciplineExperience with technology transfer, process validation, and equipment qualificationProven ability to work effectively in a deadline-driven, dynamic environment in support of a successful execution of site readiness planStrong knowledge of cGMP, regulatory requirements, and pharmaceutical manufacturing processesDemonstrated project management experience, including leading cross-functional teamsExcellent communication, organizational, and analytical problem-solving skills

Preferred Skills

Master’s degree in engineering or related STEM field from an accredited college or universityProject Management certification (PMP or equivalent)Familiarity with Lean Manufacturing and/or Six Sigma methodologiesProficiency with documentation systems and electronic batch record (EBR) platforms

 

Job Level: Management

Additional Information

The base compensation range for this role is: $133,000.00-$178,000.00

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 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 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 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.