Regulatory Affairs Manager, CMC - Mississauga

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance.You will work with cross-functional teams including R&D, Quality, Manufacturing and Commercial to build clear regulatory strategies and prepare submissions. · ...

+You will lead regulatory CMC (Chemistry, Manufacturing and Controls) activities in Canada to support product development and lifecycle maintenance. You will work with cross-functional teams including R&D, Quality, Manufacturing and Commercial to build clear regulatory strategies ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance. · Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada. · Prepare review and submit CMC sections for regulatory filings ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance. · - Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada.<- Prepare review and submit CMC sections for regulatory filing ...

We value people who are collaborative, curious, and focused on practical solutions. · Develop and execute CMC regulatory strategies for product development and lifecycle activities in Canada. · Prepare, review and submit CMC sections for regulatory filings, · ...

You will lead regulatory CMC activities in Canada to support product development and lifecycle maintenance. · This role will provide YOU the opportunity to lead key activities to progress YOUR career. · ...

The Manager CMC Regulatory Affairs will develop regulatory strategies to ensure timely approval of products. · Bachelor's degree in relevant scientific or regulatory discipline. · Minimum 8 years progressive experience drug regulatory affairs with 5 years CMC drug RA preferably p ...

The Manager CMC Regulatory Affairs develops regulatory strategies and provides guidance on compliance and ensures timely approval of products. · Bachelor's degree in relevant scientific or regulatory discipline. · Minimum 8 years of progressive experience in drug regulatory affai ...

Join the engine of Sanofi's mission — where deep immunoscience meets bold, AI-powered research. In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions. · ...

The Regulatory Submission Lead will support regulatory submission activities including authoring reviewing providing registration requirements and compiling dossiers in compliance with health authority regulations. · They will work with teams contacts Global Regulatory Strategy F ...

We are seeking an experienced SAP Business Objects (BO) Administrator to manage, optimize, and support the Business Objects reporting platform across multiple Banking applications. The ideal candidate will have strong hands-on experience with BO administration... · ...

+At Roche you can show up as yourself,+embraced for the unique qualities you bring.+Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professional ...

+This is a full-time Scientist - Drug Release Studies role at one of our portfolio companies. The responsibilities include designing and analyzing drug release experiments and developing protocols. · + · ...

In the position of Associate Regulatory Program Director you will be accountable for handling all Health Authority interactions pertaining to CMC Information as well as informational and pre-submission meetings with global Health Authorities partners and industry experts. · ...

We are SGS – the world's leading testing, inspection, and certification company... · We recruit, hire, train,... · ...

Inspirational, innovative and entrepreneurial - this is how we describe our empowered teams. · ...

As Global Technical Transfer Leader you are accountable for scoping planning and executing technical transfers of small and large molecules between clinical commercial manufacturing sites. · ...

Alex Systems searches for a R&D Senior Scientist in Mississauga, ON. The client is a Medical Device Manufacturer. · ...

at boston scientific we value collaboration and synergy this role follows a hybrid work model requiring employees to be in our local office at least three days per week · review complaint communications and assess complaints for regulatory reportability and potential impacts to p ...

We are hiring for the position of Regulatory Submission Lead to work in Mississauga with one of the biggest pharmaceutical manufacturing companies in the world. · Independently deliver assigned submissions as per agreed dossier strategy to the Submission teams by working collabor ...