Regulatory cmc in Medford, MA
Associate Director, Regulatory Affairs CMC
Company Overview Since its inception over a decade ago,CRISPR Therapeuticshas transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates...
Consultant Regulatoty CMC
Consultant Regulatory CMC- Permanent - Boston, MAProclinical is seeking a Senior Regulatory Affairs Associate or a Regulatory Affairs Consultant with a strong background in CMC post-approval. This permanent position is located in Boston, MA.Primary...
Microbiological/Environmental Monitoring Manager and Investigator
By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda...
Director, GRA CMC Pharmaceuticals, Oligonucleotides
By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda sPrivacy Noticeand Terms of Use. I further...
Vice President, Regulatory Affairs, CMC
Why Join Us?Be a hero for our rare disease patientsAt Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right thing to do. To achieve this goal, our vision is to lead...
Regulatory Affairs Specialist
Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care,...
Director, CMC Regulatory Affairs
Site Name: USA - Pennsylvania - Upper Providence, Durham Blackwell Street, GSK House, Rockville Biopharm, Stevenage, UK - Hertfordshire - Ware, Waltham, Zug House Posted Date: Feb 22 2024 Are you looking for a role where you will serve...
Microbiological/Environmental Monitoring Manager and Investigator
By clicking the Apply button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda...
Director, Regulatory CMC
Boston, MA (Remote)Development Global Regulatory and Access Solutions /RemoteCompany OverviewCerevel Therapeutics is dedicated to unraveling the mysteries of the brain to treat neuroscience diseases. We are tackling neuroscience diseases with a...
Director, Regulatory Affairs, CMC - Combination Products
Overview The Director, RA CMC Combination Products will work cross-functionally to lead development and implementation of global combination product/Medical Devices regulatory strategies across all applicable programs and lifecycle stages in...
Senior Director, Regulatory Affairs CMC
Reporting to theSVP of Global Regulatory Affairs, the Sr. Director, Regulatory Affairs CMC will be responsible for developing and implementing regulatory CMC strategy leading to successful registration and life-cycle management of unique products...
CMC Regulatory Affairs Program Manager
Responsibilities: ...
Senior Manager, Regulatory CMC Lead
About This Role This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products.
Director, Regulatory CMC
Summary of Position: The Director Regulatory CMC will be responsible for developing and delivering innovative regulatory CMC strategies for product development and approval. With limited guidance from the EVP Regulatory Affairs & Quality...
Director, Regulatory CMC
Overview Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: * developing...
Associate Director Global Regulatory Affairs CMC
Open for hire at one of the following locations - Cambridge Erie Street, Mainz K1. - Job ID: 7047 Become a member of the BioNTech Family! As a part of our team of more than 5.000 pioneers, you will play a key role in developing...
Director Regulatory Affairs-CMC
POSITION OVERVIEW: Disc Medicine is seeking a Director, Regulatory Affairs-CMC to serve as the Regulatory-CMC lead for Disc Medicine's small molecule program pipeline. This position will have close collaboration with the development teams...
Associate Director/Director, Regulatory CMC
Overview Be Seen and Heard at EyePoint Pharmaceuticals At EyePoint, leadership trusts our employees to get the job done. The patient-centric and award-winning approach we're taking in business fuels our success for: * developing...
Director, Regulatory Affairs CMC Small Molecule, Mature Products
Site Name: USA - North Carolina - Research Triangle Park, Bangalore, India - Maharashtra - Mumbai, Poznan Grunwaldzka, UK - London - Brentford, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence Posted Date: May 9...
Director, Regulatory CMC
At Editas, we're driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to...
Associate Director, Regulatory Affairs CMC
Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health Authority submissions, collaborating across the...
Regulatory Affairs Coordinator I
GENERAL SUMMARY/ OVERVIEW STATEMENT: The Alzheimer's Clinical and Translational Research Unit (ACTRU) is a unique group at Massachusetts General Hospital focused on early-stage interventional clinical trials for Alzheimer's disease and...
Associate Director, Regulatory Affairs CMC
The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health Authority submissions, collaborating across the business and with...
Director, Regulatory Affairs Vaccines CMC
About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted...
Regulatory CMC Director
Our client is developing and commercializing innovative ophthalmic products for the treatment of serious eye disorders. They are seeking a Regulatory CMC Director who can develop CMC regulatory strategies and prepare CMC submissions for their...
Associate Director, Regulatory Affairs CMC
Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team...
Director Regulatory CMC - Cell Therapy
Working with UsChallenging. Meaningful. Life-changing. Those aren t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From...
Director, CMC Regulatory Affairs
Job Description Overview: Great Science. Deep Compassion. Real Impact. Alkermes is offering exciting opportunities through our commitment to work together to help improve the lives of people...
Senior Manager, Regulatory CMC Lead
Company DescriptionJob Description About This Role This role is responsible for Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned...
Director, CMC Bioconjugation & External Manufacturing
Job Details 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...