Site Services Lead – RTP Pharma

Job Description

About This Role

The Site Services Lead has the responsibility to maintain the entirety of the RTP Pharma site including the interior and exterior of all buildings, structures, leased spaces and all other campus grounds. Responsibilities include managing the Pharma Site services team and contractors supporting work including remediation of GMP and plant equipment (exterior) cleaning, paining, caulking and rouge remediation. Maintains condition and appearance of facilities and equipment including cleaning of common spaces, landscaping, and facilities maintenance including plumbing and handyman services. Responsible for execution, review, and closure of work orders. This role will work with and provide direction to contractors and participate in and lead multi-functional teams to execute facility maintenance and make improvements on existing processes.

As a representative of the Site Services organization, your role carries the weight of GMP compliance and general appearance of the site. Your commitment lies in delivering quality and timely results and includes the ability to self-direct to ensure efficient results.

What You Will Do

• Management of Pharma Site services team
• Manage equipment exterior cleaning and remediation to ensure GMP compliance, and documenting and closing associated work orders.
• Review and manage vendor contracts, issue purchase orders and directing contracted staff to meet desired outcomes.
• Management of soft services including oversite of handymen, painting, caulking & drywall repair services.
• Management of plumbing services & building maintenance.
• Management of sustainability programs including trash & recycling programs.
• Management of disaster recovery including water damage remediation.
• Ensures compliance with GMP cleaning and safety procedures and updates documents as needed.

Who You Are

You are an experienced facilities and site services leader with a passion for maintaining all facility and manufacturing area appearance and upkeep. You understand GMP principles of oral solid dose, small molecule, and sterile filling manufacturing and are able to direct cleaning and maintenance contractors to execute their duties efficiently and compliantly. You are accountable for achieving timelines and quality of work for scheduled and unscheduled work orders. You have excellent communication skills and can easily identify stakeholders.

Qualifications

• Associates degree and 8 years of experience or a minimum of 10 years of experience in a related field, preferably in a GMP manufacturing supporting oral solid dose, small molecule and sterile filling environment.
• People management experience and experience onboarding, training and management of contract staff including facility cleaning, plumbing, groundskeeping and other related site services scope.
• Practical knowledge and application of GMP regulations and guidelines including GMP training and change control processes.
• Excellent organization, time management, oral and written communication skills.
• Ability to work on-site.

Additional Information

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.

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