Regulatory Affairs Associate – Injectable Submissions - Oakville - SteriMax Inc.

The Associate Regulatory Affairs will prepare regulatory submissions for complex injectable products. · Coordinates the assembly of documents to support submissions including complex generics and biosimilars per established business processes. · ...

The Regulatory Affairs Associate will prepare regulatory submissions for complex injectable products · Cordinates the assembly of documents to support submissions including complex generics and biosimilars per established business processes · Fulfills lifecycle management activ ...

This Administrative Coordinator position supports coordination of assessments and treatments for interdisciplinary care for patients with work-related injuries in Specialty Clinics. · ...

The Administrative Coordinator, Specialty Clinics supports coordination of assessments and treatments for interdisciplinary care for patients with work-related injuries including coordination of schedule and collaboration with physicians and registered health professionals. · The ...

We are seeking a highly motivated and detail-oriented Design Engineer to join our dynamic R&D team. · In this role, you will be responsible for the end-to-end design, development, · and validation of implantable and non-implantable medical fasteners, · including screws, pins, sta ...

We are seeking a Regulatory Affairs/Product Registration Manager to join our team. · As a key member of our regulatory affairs group, · You will be responsible for managing and coordinating · the registration activities required for pharmaceutical products locally with Health Ca ...

We are seeking an experienced Net developer to join our team in Mississauga. The successful candidate will have experience with .NET and C# as well as strong skills in SQL and experience with Microsoft SQL Server. · ...

The Net Developer will design develop test and maintain backend services APIs using C# .NET/ .NET Core collaborate with the team modernize improve system architecture code quality performance work MS SQL Server databases schema design stored procedures query optimization work clo ...

++We are currently seeking an experienced Intermediate Mechanical Designer to join our team. · +Manage the Mechanical Design Cycle from inception through prototyping up to production to meet the project schedule and budget constraints. · Coordinate full life cycle of mechanical a ...

We are currently seeking a highly motivated Senior Protection and Control Testing Engineer to join our team on a full-time basis. · Testing and commissioning of power system protection & control schemes in the utility, power generation, and oil & gas industry. · Testing of micro ...

This individual will manage regulatory activities needed to register pharmaceutical products locally with Health Canada & globally. They must have technical expertise & strong organizational skills to meet deadlines. · ...

We are seeking a Regulatory Affairs/ Product Registrations Manager to manage regulatory activities for drug product registration locally with Health Canada and globally. · Prepare submissions to Health Canada & FDA · Maintain approved product monographs · ...

The Net Developer will design, develop, test, and maintain backend services and APIs using C# and .NET/.NET Core. · ...

We are seeking a skilled Software Developer to join our team on a permanent basis. The successful candidate will have experience with .NET and C#, as well as strong skills in SQL and Azure. · ...

We are currently seeking a highly motivated Senior Protection and Control Testing Engineer to join our team on a full-time basis. If you are an excellent communicator and skilled problem-solver with strong attention to detail, we offer a dynamic work environment where you will be ...

This position involves preparing and filing drug product submissions to regulatory agencies. The successful candidate will maintain approved product monographs and assist in global drug product registrations. · Prepare and file drug product submissions to regulatory agencies. · M ...

The Senior Regulatory Affairs Associate is responsible for planning, coordinating and filing drug product submissions in eCTD format to Canada & US.They will also support the preparation of regulatory filings to EU, UK & Australia. · Additional responsibilities include reporting ...

The Senior Associate Regulatory Affairs will prepare regulatory submissions for complex injectable generic products and biosimilars. · ...

Prepare and file drug product submissions to the US FDA · Prepare and/or review submissions to Health Canada and FDA for a variety of dosage forms. · ...

We have the capability to produce an extensive variety of products with our state-of-the-art in-house injection mold design and build capabilities, coupled with the latest injection molding process technologies. · We are looking for a dynamic individual to join our team as a Dime ...

An exciting Regular Full-Time Technologist CT opportunity exists in our Medical Imaging Department. · Medical Radiation Sciences Diploma/Degree in Radiography/Radiological Technology from a recognized program · Post diploma education and/or Certification in Computed Tomography pr ...