Regulatory Affairs Consultant Full-time Job

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.

In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.

Full Time Travel: Yes Glassdoor Reviews and Company Rating Success Profile

Check out the top traits we're looking for and see if you have the right mix.

Detail-Oriented Proactive Problem-Solver Results-Driven Organized Multi-Tasker Rewards Global Impact

We are one truly global team working together to propel each client´s journey ahead faster.

Balance

We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.

Collaboration

Work with industry leaders and subject matter experts.

Freedom

The ability to innovate, ask “what if†and try new solutions without fear of failure.

Variety

Opportunities to work on multiple accounts – never boring!

Management

Strong management with depth of experience working for global health authorities. Regulatory Affairs- CMC

6-12 years of experience

Supported the CMC activities related to Small molecules/Vaccine/Biologic manufacturing and control including authoring of submission dossiers related to:

new application, post approval variations Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation of data to appropriate standards & requirements Experienced in CTD update/authoring ( CTD Module 2&3) Handled and responded Health Authorities Request US & CA Annual reports, Renewals, PQVAR, APR Handled Labeling and safety variations in EU/ PSUR/DSUR Assessment of the Change Controls and associated technical dossiers Excellent individual project management and communication skills Veeva tool experience

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