Senior Manager Site MSAT Advanced Therapies

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 https://www.jnj.com

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Job Description:

We are seeking a highly accomplished and results-oriented (Senior) Manager Site MSAT Adv Ther to lead the site MSAT Advanced Therapies group and represent the group on site and in the network. The successful candidate will be a proven leader with extensive experience in viral vector and/or biologics manufacturing and a deep understanding of technical operations within a pharmaceutical or biotechnology environment. This role requires a strong technical background, exceptional leadership skills, and a passion for driving operational excellence and continuous improvement.

Key Responsibilities:

• Leadership & Team Management:

  • Lead and mentor a team of (Senior) Associate Scientists and Scientists, fostering a collaborative and supportive environment that encourages professional growth and development.

  • Effectively delegate tasks and provide clear direction to ensure smooth and efficient project execution.

  • Promote a culture of scientific excellence and innovation within the team.

• Technical Leadership:

  • Lead and oversee all aspects of the Life Cycle Management (LCM) process for commercial products at the site. This includes ownership of the technical aspects of LCM, performing process validation impact assessments, leading tech transfers and driving process improvements.

  • Monitor technical process and product performance, identifying areas for improvement and implementing corrective actions. Develop and implement strategies to significantly increase performance, reliability and robustness.

  • Lead and oversee performance qualification in the validation process of equipment.

  • Support technology and product technical life cycle management by deployment of standards on site.

  • Ensure accurate and timely reporting of scientific data and findings to key stakeholders.

• Collaboration & Communication:

  • Collaborate effectively with local and global stakeholders, including project teams, site and global Leadership teams, ensuring seamless integration and communication of scientific findings.

  • Represent the Site MSAT group at internal and external meetings, effectively communicating scientific data and insights.

Minimum Qualifications and Requirements:

• Educational Background:

  • BSc in Biochemistry, Biotechnology, Chemical Engineering, or a related field. An Advanced degree (MSc/PhD) is considered a plus.

• Experience:

  • Minimum 8 years of experience in the pharmaceutical or biotechnology industry, with a focus on biologics drug substance development. Specific advanced therapies or lentiviral vector experience is considered a plus.

  • Proven track record of leading and mentoring scientific teams.

• Technical Skills:

  • Strong expertise in biological manufacturing processes, including upstream and downstream processing.

  • Familiarity with regulatory guidelines and good manufacturing practices (GMP).

  • Experience with process improvements, and technology transfer processes and CPV.

• Communication & Leadership:

  • Excellent communication and interpersonal skills, with the ability to build strong relationships with team members and stakeholders.

  • Proven ability to lead and inspire others, creating a positive and productive work environment.

• Problem-Solving & Analytical Skills:

  • Demonstrated ability to solve complex scientific and technical challenges independently and within a team setting.

  • Strong analytical skills, with the ability to critically evaluate data and draw sound conclusions.