Regulatory Affairs Expert for MHRA Submissions

Product reference: · I sell a silicone heel cup/orthotic device marketed for plantar fasciitis, heel pain relief and similar conditions. I need an experienced regulatory consultant to prepare a full UK-compliant Medical Device Technical File and to assist with MHRA registration, ...

Reference product: · I am seeking an experienced medical device regulatory consultant to prepare a fully compliant UK Technical File for a sterile hydrocolloid wound dressing roll, and to assist with MHRA registration. The Technical File must be prepared under my company's name a ...

The Regulatory and Compliance Specialist is responsible for supporting the development, implementation, and maintenance of regulatory and quality assurance activity to ensure that the CellChem pharmaceutical meets applicable global regulatory requirements and internal quality sta ...

The Clinical Trial Submissions Operations role supports Clinical Trial Application (CTA) activities across EU and UK regions. · The position is responsible for preparation, submission, quality control, · and lifecycle management of CTA submissions through Health Authority portals ...

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 ...

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 are hiring a CMC Regulatory Consultant for one of our radiopharmaceutical clients based in Hamilton, Ontario. The CMC Regulatory Consultant will support global regulatory interactions by leading the coordination, review and regulatory alignment of Health Authority Questions (H ...

We are hiring a CMC Regulatory Consultant for one of our radiopharmaceutical clients based in Hamilton, Ontario. · ...

The Senior Associate Quality is responsible for supporting and executing quality assurance activities to ensure compliance with regulatory requirements. · Maintain and support key elements of the Quality Management System (QMS). · Assist with creation review revision of SOPs poli ...

The Senior Associate Quality is responsible for supporting and executing quality assurance activities to ensure compliance with regulatory requirements and internal quality standards. · This role plays a key part in maintaining and improving the Quality Management System QMS part ...

The Senior Associate, Quality is responsible for supporting and executing quality assurance activities to ensure compliance with regulatory requirements and internal quality standards. · Maintain and support key elements of the Quality Management System (QMS), including document ...

WE'RE HIRING · Let's help you launch your career with Alberta Veterinary Laboratories ("AVL/Solvet") We are looking for an energetic and dedicated Regulatory Affairs Analyst to join our team on-site in our Calgary facility working 40 hours/week (Monday - Friday). · THE ROLE · The ...

Job Description: · The Senior Associate, Quality is responsible for supporting and executing quality assurance activities to ensure compliance with regulatory requirements and internal quality standards. This role plays a key part in maintaining and improving the Quality Manageme ...