Scientific Manager, Biologics Analytical Development

Johnson & Johnson Innovative Medicine • Malvern, PA

2d • Hybrid

About The Position

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine We are searching for the best talent for a Scientific Manager, Biologics Analytical Development to be located in Malvern, PA. Purpose: The Scientific Manager, Reference Material and Critical Reagents (RMCR), is part of the Analytical Development (AD) Proteins organization and is responsible for shaping strategy and delivering on reference materials and critical reagents to support analytical testing for the lifecycle of the biologics portfolio.

Requirements

• A minimum of a Bachelor's degree in Chemistry, Biology, Biochemistry or a related scientific field with 8+ years of relevant industrial experience is required.
• Prior managerial experience is required.
• Experience working in a GMP environment is required.
• Experience with analytical methods and understanding of the critical reagents associated with method execution is required.
• Strong matrix leadership skills is required.
• Strong technical writing experience (SOPs, protocols, and qualification reports) is required.
• Highly organized to independently plan, implement, and document work is required.
• Excellent interpersonal skills with the ability to adapt effectively to constantly evolving organization issues, structures, and dynamics is required.
• Strong written and verbal communication skills to collaborate with internal teams, external vendors, and partners is required.

Nice To Haves

• An advanced degree is preferred.
• Knowledge of automation systems and digital platforms (e.g., LIMS, Biovia) is highly preferred.
• Experience with authoring regulatory filings and responses (Reference Material focus) is preferred.
• Basic understanding of data trending and experience with statistical software applications is preferred.

Responsibilities

• Leading a team to efficiently deliver on supply of RMCRs without impact to analytical testing timelines.
• Managing storage and distribution of RMCRs globally
• Managing preparation of RMCRs per protocol.
• Driving qualification and requalification schedules for RMCRs, and work with analytical labs to acquire the data necessary to prepare qualification and requalification documents and issue Certificate of Analysis.
• Collaborating and coordinating with analytical testing labs to ensure testing is completed to support RMCR activities, meeting accelerated project timelines.
• Working with sites and statisticians to compile trending data as appropriate for reference materials.
• Authoring SOPs, protocols, and specifications to support project needs.
• Driving continuous improvement and shaping future strategies.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager
• Number of Employees: 5,001-10,000 employees