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Director, Analytical Sciences and Technology, MSAT

Location: London (Hybrid)

Reports to: Senior Director, Manufacturing & Analytical Sciences and Technology (MSAT)

 

Position Summary

We are seeking a dynamic and experienced leader to join our MSAT (Manufacturing Science and Technology) team as Director of Analytical Sciences and Technology. This individual will lead the late-phase Analytical Sciences team, overseeing the qualification, validation, and deployment of analytical methods while ensuring effective control strategies and ongoing method improvements. The role will be integral to the lifecycle management of Cell and Gene Therapy products, particularly focusing on viral vectors and cell therapies.

The Director will play a key role in developing and executing phase-appropriate strategies for test methods, partnering with internal and external stakeholders, and representing the organization during regulatory inspections.

This role provides an exciting opportunity to influence the advancement of transformative Cell and Gene Therapy products and develop a high-performing team in a fast-paced, innovative environment.

Key Responsibilities

Team Leadership:

•      Lead the Analytical Sciences team within the MSAT organization to develop, qualify, validate, and manage robust analytical methods.

•      Cultivate a culture of scientific excellence, collaboration, and continuous improvement.

Method Development and Compliance:

•      Ensure compliance with ICH guidelines, FDA/EMA, and global regulatory expectations for analytical methods.

•      Oversee drug product characterization and establish critical quality attributes (CQAs) to support clinical efficacy and safety.

Strategic Oversight:

•      Develop science-based, risk-informed analytical validation strategies for pivotal to commercial phases.

•      Chair the Orchard Specifications Committee, ensuring alignment with program goals and regulatory requirements.

Stakeholder Engagement:

•      Collaborate with cross-functional teams and external partners, including CDMOs and contract labs, to drive method improvements and control strategy optimization.

•      Actively engage with industry organizations to stay ahead of regulatory trends and incorporate them into control strategies.

 

Regulatory Support:

•      Serve as a subject matter expert during inspections and author high-quality CMC documentation for regulatory submissions and amendments.

•      Ensure inspection readiness and actively support health authority interactions.

Technology and Process Development:

•      Develop and execute an Analytical Sciences technology roadmap aligned with manufacturing strategy.

Performance Management:

•      Oversee the performance, development, and growth of the Analytical, MSAT team.

Required Knowledge & Experience

•      Extensive experience in qualification, validation, trending, and continuous improvement of analytical methods.

•      Proven ability to deliver high-quality documentation for regulatory submissions, including FDA/EMA inspections.

•      Direct experience of working for a company in the fieldCell and Gene Therapy, particularly lentiviral vectors, plasmids, cell banks, or related biologics and vaccine characterization.

•      Strong understanding of FDA, EMA, and ICH regulatory guidelines.

•      Demonstrated success in managing third-party laboratories for assay development and validation.

 

Skills & Competencies

•      Strong technical expertise with a history of scientific innovation and problem-solving.

•      Exceptional communication skills, capable of effectively presenting complex technical issues to diverse audiences.

•      Ability to prioritize and manage multiple projects under tight deadlines.

•      Proactive leadership style, fostering trust, collaboration, and team performance.

•      Skilled at building partnerships with internal teams and external stakeholders.

 

Education & Qualifications

•      PhD or MSc in a relevant scientific discipline (e.g., Chemistry, Biochemistry, Molecular Biology, Cell Biology, or Chemical Engineering).

•      Significant experience in life sciences, preferably in MSAT roles focusing on analytical methods.

What You Should Know About Director, Analytical Sciences and Technology, MSAT, Orchard Therapeutics

Are you ready to take your career to the next level? Join us as the Director of Analytical Sciences and Technology at MSAT in London! This is an exciting opportunity for a seasoned leader to make a significant impact in the dynamic field of Cell and Gene Therapy. In this pivotal role, you will lead the late-phase Analytical Sciences team, guiding the qualification and validation of analytical methods. Your expertise will ensure compliance with regulatory standards while driving continuous method improvements essential for the lifecycle management of innovative products, especially viral vectors and cell therapies. You will collaborate with cross-functional teams, internal and external stakeholders, and be an integral player during regulatory inspections. We are looking for someone who thrives in a fast-paced, innovative environment and is eager to cultivate a high-performing team committed to scientific excellence. If you have a passion for advancing transformative therapies and possess extensive experience in analytical methods, compliance, and leadership, we’d love to have you with us at MSAT. Join us in shaping the future of healthcare!

Frequently Asked Questions (FAQs) for Director, Analytical Sciences and Technology, MSAT Role at Orchard Therapeutics
What are the key responsibilities of the Director, Analytical Sciences and Technology at MSAT?

The Director of Analytical Sciences and Technology at MSAT is responsible for leading the analytical sciences team, ensuring compliance with regulatory guidelines, developing robust analytical methods, and overseeing their qualification and validation processes. This role also includes collaborating with both internal stakeholders and external partners while ensuring effective control strategies and continual method improvements.

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What qualifications are required for the Director, Analytical Sciences and Technology position at MSAT?

Candidates for the Director of Analytical Sciences and Technology position at MSAT should hold a PhD or MSc in a relevant scientific discipline such as Chemistry or Biochemistry. Significant experience in life sciences, particularly within the Cell and Gene Therapy field, is crucial, along with comprehensive knowledge of FDA, EMA, and ICH regulatory guidelines.

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How does the Director, Analytical Sciences and Technology contribute to regulatory compliance at MSAT?

The Director of Analytical Sciences and Technology at MSAT plays a critical role in regulatory compliance by serving as a subject matter expert during inspections, ensuring the preparation of high-quality CMC documentation for submissions, and actively supporting health authority interactions to maintain inspection readiness.

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What skills are essential for a successful Director, Analytical Sciences and Technology at MSAT?

Essential skills for the Director of Analytical Sciences and Technology include strong technical expertise, exceptional communication ability, a proactive leadership style, and demonstrated problem-solving capabilities. The role also requires the ability to manage multiple projects efficiently and foster collaborations with various stakeholders.

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What kind of team culture can one expect as the Director, Analytical Sciences and Technology at MSAT?

As the Director of Analytical Sciences and Technology at MSAT, you can expect a culture of scientific excellence, collaboration, and continuous improvement. The role emphasizes building a high-performing team in an innovative environment, where trust and proactive leadership are valued.

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Common Interview Questions for Director, Analytical Sciences and Technology, MSAT
What experience do you have with analytical method validation?

In responding to this question, focus on specific examples of analytical methods you have validated, detailing the processes you followed and any challenges you overcame. Highlight your familiarity with regulatory standards and how you ensured compliance throughout.

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How do you approach team leadership and development?

Discuss your leadership style, emphasizing collaboration and trust-building. Provide examples of how you've developed team members' skills and fostered an environment of scientific excellence and continuous improvement.

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Can you describe your experience with regulatory submissions?

When answering, outline your involvement in preparing CMC documentation for regulatory agencies like the FDA or EMA. Mention specific submissions you've led and the outcomes, showcasing your understanding of the regulatory landscape.

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What strategies do you employ for risk management in analytical methods?

Share your approach to developing science-based, risk-informed strategies for analytical validation. Mention any frameworks or methodologies you've found effective in assessing and managing risks during various project phases.

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How do you ensure compliance with ICH guidelines in your work?

Discuss your processes for staying updated on ICH guidelines and how you implement them into method development. Provide examples of how you've adapted protocols to remain compliant during inspections or audits.

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Describe a time you successfully engaged with external partners.

Provide a specific example where you collaborated with external labs or industry organizations, detailing the goals of the partnership and how your contributions led to success, specifically in the context of analytical methods or product development.

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What techniques do you use for continuous improvement in analytical methods?

Focus on specific methodologies you've implemented for continuous improvement, such as Lean Six Sigma or other quality management techniques. Discuss how you measure success and the impact on product quality.

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How do you prioritize multiple projects effectively?

Share your strategies for prioritizing tasks, such as using project management tools or methodologies. Showcase how you've managed competing deadlines while ensuring high-quality outcomes.

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Can you discuss your experience with assay development?

When answering, detail your experience overseeing the development of assays, including any specific types of assays you've worked with and challenges you encountered, demonstrating your technical expertise.

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What motivates you in a role like Director of Analytical Sciences and Technology?

Reflect on your passion for innovation in the field of Cell and Gene Therapy and your commitment to improving patient outcomes. Discuss how leading a team that pushes scientific boundaries inspires you.

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EMPLOYMENT TYPE
Full-time, hybrid
DATE POSTED
December 6, 2024

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