Dyne Therapeutics Inc
Director, Drug Product External Manufacturing
Dyne Therapeutics Inc, Watertown, Massachusetts, us, 02472
Company Overview:
Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases. With its proprietary FORCE™ platform, Dyne is developing modern oligonucleotide therapeutics that are designed to overcome limitations in delivery to muscle tissue. Dyne has a broad pipeline for serious muscle diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and a preclinical program for facioscapulohumeral muscular dystrophy (FSHD). For more information, please visit https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook.
Role Summary:
The Director, Drug Product External Manufacuring will be accountable for all Drug Product External Manufacturing operations activities globally for our products. This role will partner closely with colleagues across Dyne to ensure seamless supply of all Drug Product for clinical trials and will lead efforts for Drug Product commercial readiness
This role is based in Waltham, MA without the possibility of being fully remote
Primary Responsibilities Include: Collaborate with CMC, Quality Control, Quality Assurance, and Clinical Operations to esnusre continuity of drug supply Act as main point of contact for CDMO(s) including leading CDMO working teams and strategic business review chairperson Responsible for driving execution of the production plan at CDMO (PO through delivery) Working with CMC, Legal, and Strategic Sourcing take the lead in identification and resolution of business/contract issues and supply agreements Responsible for long term strategic supplier management and accountable for supplier relationship management Partners with CMC, Quality and Regulatory to champion a culture of quality with our CDMO's and to ensure that all activities and documentation comply with regulatory requirements Partner with Strategic Sourcing to develop and implement long term external manufacturing strategies that provide a reliable, robust, and cost-effective manufacturing network Champion a strong winning culture, fostering teamwork and commitment to excellent through transparent communication, engagement and collaboration Education and Skills Requirements:
Bachelor's Degree in Science, Supply Chain, Business or related field, or equivalent with 8-10 years of related work experience, or advanced degree and a minimum of 6 years of work experience Proven experience in clinical and commercial Drug Product manufacturing as well as understanding of analytical techniques that support manufacturing activities Demonstrated understanding of the principles and applications associated with external manufacturing operations Strong experience and knowledge of cGMP manufacturing requirements Strategic thinker with strong result-orientation and a sense of urgency to deliver quality results on time and in a highly ethical and professional manner. Experience managing complex schedules and priorities in dynamic pharmaceutical, biotech or related environments. Experience in PPQ planning and activities Ability to work, influence, and gain consensus across multiple functions (CMC, Quality and Regulatory Affairs) Experience in all phases of CMC regulatory submissions and interactions regarding CMC issues, including IND, BLA, and post-approval changes Strong analytical, problem solving and critical thinking skills. Expertise in use of MS Excel, as well as demonstrated proficiencies in Smartsheet, Visio, ERP systems and Power BI (or similar application) Collaborative work style to be part of a team to identify process gaps and develop solutions Excellent interpersonal, verbal, and written communication skills with the ability to work in strong cross-functional relationships and communicate complex issues enterprise-wide, from the executive team to the manufacturing floor. Resilient and able to work in a demanding, fast-paced environment and capable of supporting multiple programs and vendors
#LI-Onsite
The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.
This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned. All Employees are expected to adhere to all company policies and act as a role model for company values.
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.
Dyne Therapeutics is a clinical-stage muscle disease company focused on advancing innovative life-transforming therapeutics for people living with genetically driven diseases. With its proprietary FORCE™ platform, Dyne is developing modern oligonucleotide therapeutics that are designed to overcome limitations in delivery to muscle tissue. Dyne has a broad pipeline for serious muscle diseases, including clinical programs for myotonic dystrophy type 1 (DM1) and Duchenne muscular dystrophy (DMD), and a preclinical program for facioscapulohumeral muscular dystrophy (FSHD). For more information, please visit https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook.
Role Summary:
The Director, Drug Product External Manufacuring will be accountable for all Drug Product External Manufacturing operations activities globally for our products. This role will partner closely with colleagues across Dyne to ensure seamless supply of all Drug Product for clinical trials and will lead efforts for Drug Product commercial readiness
This role is based in Waltham, MA without the possibility of being fully remote
Primary Responsibilities Include: Collaborate with CMC, Quality Control, Quality Assurance, and Clinical Operations to esnusre continuity of drug supply Act as main point of contact for CDMO(s) including leading CDMO working teams and strategic business review chairperson Responsible for driving execution of the production plan at CDMO (PO through delivery) Working with CMC, Legal, and Strategic Sourcing take the lead in identification and resolution of business/contract issues and supply agreements Responsible for long term strategic supplier management and accountable for supplier relationship management Partners with CMC, Quality and Regulatory to champion a culture of quality with our CDMO's and to ensure that all activities and documentation comply with regulatory requirements Partner with Strategic Sourcing to develop and implement long term external manufacturing strategies that provide a reliable, robust, and cost-effective manufacturing network Champion a strong winning culture, fostering teamwork and commitment to excellent through transparent communication, engagement and collaboration Education and Skills Requirements:
Bachelor's Degree in Science, Supply Chain, Business or related field, or equivalent with 8-10 years of related work experience, or advanced degree and a minimum of 6 years of work experience Proven experience in clinical and commercial Drug Product manufacturing as well as understanding of analytical techniques that support manufacturing activities Demonstrated understanding of the principles and applications associated with external manufacturing operations Strong experience and knowledge of cGMP manufacturing requirements Strategic thinker with strong result-orientation and a sense of urgency to deliver quality results on time and in a highly ethical and professional manner. Experience managing complex schedules and priorities in dynamic pharmaceutical, biotech or related environments. Experience in PPQ planning and activities Ability to work, influence, and gain consensus across multiple functions (CMC, Quality and Regulatory Affairs) Experience in all phases of CMC regulatory submissions and interactions regarding CMC issues, including IND, BLA, and post-approval changes Strong analytical, problem solving and critical thinking skills. Expertise in use of MS Excel, as well as demonstrated proficiencies in Smartsheet, Visio, ERP systems and Power BI (or similar application) Collaborative work style to be part of a team to identify process gaps and develop solutions Excellent interpersonal, verbal, and written communication skills with the ability to work in strong cross-functional relationships and communicate complex issues enterprise-wide, from the executive team to the manufacturing floor. Resilient and able to work in a demanding, fast-paced environment and capable of supporting multiple programs and vendors
#LI-Onsite
The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an all-inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.
This description is not intended to be constructed as an exhaustive list of duties, responsibilities, or requirements for the position. This position may change or assume additional duties at any time. The employee may be requested to perform different or additional duties as assigned. All Employees are expected to adhere to all company policies and act as a role model for company values.
Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.