Thermo Fisher Scientific
Director, Manufacturing Science and Technology
Thermo Fisher Scientific, Greenville, North Carolina, United States, 27834
Overview
Director, Manufacturing Science and Technology (MSAT) at Thermo Fisher Scientific. Location: Greenville, NC. Schedule: Standard (Mon-Fri). Reports To: Site Vice President and General Manager. What will you do?
The MSAT Director provides scientific leadership to ensure compliance, resilience, and competitiveness of Thermo Fisher's commercialized Grow, Value Optimization and Late Lifecycle portfolio. The successful candidate is a Subject Matter Expert (SME) in Large and Small Molecule Drug Products and directs a team of Molecular Biologists, Chemical & Process Engineers, and Scientists. This team leads strategic, tactical and operational technical projects for the commercialized product portfolio, working closely with operations, QA, QC, and various supply chain and development functions. This role builds strong partnerships with functions such as Sales, Business Marketing, Quality, Planning, Regulatory, and Procurement. This leader has a strong scientific background and drives successful commercialization of the current and future portfolio. They ensure successful New Product Introduction by prioritizing resources. The team manages Life Cycle Management projects, such as supply chain resilience, process optimization, and innovative improvements for efficiency, competitiveness, compliance, and health authority advocacy. The Director possesses a strong approach for people leadership and talent development resulting in the continuous uplift in team technical capability and project delivery excellence. Responsibilities
Own the site's technical continuous improvement strategy in collaboration with Site Leadership. Encourage a team supporting projects at all stages of the product life cycle, delivering the following aspects: Budget responsibility for team and related activities Define and own lab experiments Post PPQ, full ownership of all continuous process validation activities Lead and coordinate large-scale technical projects from initiation to completion, defining scope, objectives, actions, timelines, and budget, and collaborating with cross-functional teams for successful execution. Prioritize projects to support supply chain and the value optimization targets. Lead strategic change management initiatives, engaging and influencing key partners at all levels of the organization. Develop and implement communication plans for successful adoption and implementation. Qualifications
Master’s degree in engineering, science, or a related field, or PhD. 10 years of expertise in pharmaceutical processes, including DP characterization, stability profile understanding, and linking DP characteristics with bio-pharmaceutical performance. Minimum of 5 years people leadership experience, including technical and non-technical coaching and mentoring. Knowledge and experience with both current and new technologies in chemical synthesis, biologics, and new modalities. Strong experience and track record in technical transfer activities in commercial and clinical space to favor agility and fast time to market in a high VUCA environment. Track record of translating innovative ideas into practical solutions and timely project advancement. Applied critical thinking and vision for the future with ability to analyze complex situations and provide clear direction. Effective communicator with experience in teamwork and relationship-building with customers, including connections to academic and industry networks. About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. We support customers across life sciences research, analytical challenges, laboratory efficiency, diagnostics, and therapies. Our distributed team of over 130,000 colleagues collaborates across brands like Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. For more information, visit www.thermofisher.com. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Seniority level
Not Applicable Employment type
Full-time Job function
Production, Supply Chain, and Manufacturing Industries
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Director, Manufacturing Science and Technology (MSAT) at Thermo Fisher Scientific. Location: Greenville, NC. Schedule: Standard (Mon-Fri). Reports To: Site Vice President and General Manager. What will you do?
The MSAT Director provides scientific leadership to ensure compliance, resilience, and competitiveness of Thermo Fisher's commercialized Grow, Value Optimization and Late Lifecycle portfolio. The successful candidate is a Subject Matter Expert (SME) in Large and Small Molecule Drug Products and directs a team of Molecular Biologists, Chemical & Process Engineers, and Scientists. This team leads strategic, tactical and operational technical projects for the commercialized product portfolio, working closely with operations, QA, QC, and various supply chain and development functions. This role builds strong partnerships with functions such as Sales, Business Marketing, Quality, Planning, Regulatory, and Procurement. This leader has a strong scientific background and drives successful commercialization of the current and future portfolio. They ensure successful New Product Introduction by prioritizing resources. The team manages Life Cycle Management projects, such as supply chain resilience, process optimization, and innovative improvements for efficiency, competitiveness, compliance, and health authority advocacy. The Director possesses a strong approach for people leadership and talent development resulting in the continuous uplift in team technical capability and project delivery excellence. Responsibilities
Own the site's technical continuous improvement strategy in collaboration with Site Leadership. Encourage a team supporting projects at all stages of the product life cycle, delivering the following aspects: Budget responsibility for team and related activities Define and own lab experiments Post PPQ, full ownership of all continuous process validation activities Lead and coordinate large-scale technical projects from initiation to completion, defining scope, objectives, actions, timelines, and budget, and collaborating with cross-functional teams for successful execution. Prioritize projects to support supply chain and the value optimization targets. Lead strategic change management initiatives, engaging and influencing key partners at all levels of the organization. Develop and implement communication plans for successful adoption and implementation. Qualifications
Master’s degree in engineering, science, or a related field, or PhD. 10 years of expertise in pharmaceutical processes, including DP characterization, stability profile understanding, and linking DP characteristics with bio-pharmaceutical performance. Minimum of 5 years people leadership experience, including technical and non-technical coaching and mentoring. Knowledge and experience with both current and new technologies in chemical synthesis, biologics, and new modalities. Strong experience and track record in technical transfer activities in commercial and clinical space to favor agility and fast time to market in a high VUCA environment. Track record of translating innovative ideas into practical solutions and timely project advancement. Applied critical thinking and vision for the future with ability to analyze complex situations and provide clear direction. Effective communicator with experience in teamwork and relationship-building with customers, including connections to academic and industry networks. About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. We support customers across life sciences research, analytical challenges, laboratory efficiency, diagnostics, and therapies. Our distributed team of over 130,000 colleagues collaborates across brands like Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. For more information, visit www.thermofisher.com. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance. Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Seniority level
Not Applicable Employment type
Full-time Job function
Production, Supply Chain, and Manufacturing Industries
Pharmaceutical Manufacturing and Biotechnology Research Referrals increase your chances of interviewing at Thermo Fisher Scientific. Get notified about new Director of Manufacturing jobs in Greenville, NC.
#J-18808-Ljbffr