...facilities for:
a) Approvals related to import, development, manufacture, storage and export of drug substance and drug product (human and animal), as well as,
b) Other associated approvals, namely: biosafety,...
...industry? If so, we have the perfect role for you as a Regulatory Professional responsible for Vault RIM in our Regulatory Affairs department... ...Knowledge of the overall RA business proces...
...Clinical Research Associate
Job Requirements Techno Endura Is Offering Internship, For Pharmacy Medical & LifeScience Grads On Live Projects & Clinical Software and Will support Job In Clinica...
...Job duties of a Regulatory Affairs Specialist include:
Developing and implementing regulatory strategies for new and existing products
Preparing and submitting regulatory documentation to regulatory authoritie...
...preferably in the pharmaceutical, biotechnology, or medical device industry.
Strong understanding of relevant regulatory guidelines (e.g., FDA, EMA, etc.).
Excellent written and verbal communication skills.
...
...people and our customers. We are embracing an approach wherein we spend more time together than apart – which for full-time employees translates to an average of at least 3 days working from the office and up to 2 d...
...Job Title: QARA Specialist
Job Role :
The Quality and Regulatory Affairs (QARA) Specialist will provide leadership in the quality and regulatory affairs function to understand regulatory requirements of medic...
...In cooperation with affiliate / Area Medical teams, Marketing, RA, Clinical and other functional areas, provides leadership, oversight and support for assigned products/projects.
Establishes and approves scientif...
...Medical Device Regulatory Affairs Job duties of a Regulatory Affairs Specialist include:
Developing and implementing regulatory strategies for new and existing products
Preparing and submitting regulatory documentation t...
