Regulatory Affairs Associate
Job Description
Job Description
Job Description
We have multiple openings for Life Science Quality Assurance Analysts, Regulatory Affairs Specialist, and Quality Control Analysts.
All of these roles will interface with clients on different projects to provide consulting services.
We are seeking entry-level experienced personnel or fresh graduate students willing to be trained as per our client's requirement and able to relocate.
Most of our openings require 3-4 days' onsite presence at the client site.
Minimum Qualification :
0-3 years of experience in life science (pharmaceutical, biology, chemistry, bioinformatics) or engineering industry with a focus on information technology, clinical research, quality, regulatory affairs, manufacturing, or supply chain.
Minimum bachelor’s degree in the above concentration.
Valid US work authorization.
Virtually able to participate in our training program.
Able to relocate anywhere in the US.
About
White Collar Technologies Inc. is one of the fastest-growing pharmaceutical and life science consulting companies. We specialize in providing Information Technology, Engineering, Quality Assurance, and Project Management services.
Our clients range from small Biotech and Gene Therapy companies to Large Biopharmaceutical companies.
Our white-glove project placement includes the following benefits
- State-of-the-art client interview preparations with industry experts
- Relocation Package including airfare and hotel stay
- Competitive salary packages with full benefits package that includes PTO, Sick Time Off, Health Insurance (Medical, Dental, Vision)
- 1x1 supervision and support during client project delivery
- No-stress immigration visa processing with reputed attorney firms (CPT, OPT, H1B, H4 EAD, TN, L1, Green Card)
Company Description
White Collar Technologies is a boutique human capital consultancy firm specializing in information technology and engineering consulting for life science sector.
Our consultants serve multitude of clients within Pharmaceutical, Biotech, Medical Device, Clinical Research and Healthcare verticals.
We offer our workers Medical Dental and Vision healthcare benefits.
Company Description
White Collar Technologies is a boutique human capital consultancy firm specializing in information technology and engineering consulting for life science sector.
Our consultants serve multitude of clients within Pharmaceutical, Biotech, Medical Device, Clinical Research and Healthcare verticals.
r nWe offer our workers Medical Dental and Vision healthcare benefits.
Associate Director, Global Regulatory Affairs CMC
Join Takeda as an Associate Director, Global Regulatory Affairs CMC where you will develop and lead the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products. Can apply and adapt this understanding to projects to enhance probability of regula...
Associate Director, Regulatory Affairs
Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Associate Director Regulatory Affairs. Responsible for integrating and applying knowledge of gl...
Associate Director, Global Regulatory Affairs Cmc
Join Takeda as an Associate Director, Global Regulatory Affairs CMC where you will develop and lead the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products. Can apply and adapt this understanding to projects to enhance probability of regula...
Associate Director, Global Regulatory Affairs CMC
Join Takeda as an Associate Director, Global Regulatory Affairs CMC where you will develop and lead the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products. Can apply and adapt this understanding to projects to enhance probability of regula...
Associate Director, Regulatory Affairs, CMC
Collaborates with other functional work teams , Preclinical, Clinical, Medical Affairs, Manufacturing and Quality Control, providing regulatory guidance to aid in preparing, reviewing, and approving of regulatory NDA/IND/CTA/IMPD submissions materials. Manages a range of concurrent regulatory projec...
Associate Director, Global Regulatory Affairs Marketed Products
As an Associate Director, Global Regulatory Affairs Marketed Products you will define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. Demonstrates acceptable skills with increasing independence ...
Associate Director, Commercial Regulatory Affairs, Labeling Lead
The call to action to extend and improve the lives of cancer patients is louder than ever before, and Syndax is seeking individuals who are committed to science, innovation, and excellence to join us on this mission.With offices in Waltham and NYC and experts employed around the world, you will have...
Associate Director, Global Regulatory Affairs CMC
Join Takeda as an Associate Director, Global Regulatory Affairs CMC where you will develop and lead the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products. Can apply and adapt this understanding to projects to enhance probability of regula...
Regulatory Affairs Associate
Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes. Provide regulatory input to product lifecycle planning. Understand and investigate regulatory history/background of class, disease/ therapeutic/diagnostic context in order to. Determine trade...
Associate Director, Global Regulatory Affairs Marketed Products
As an Associate Director, Global Regulatory Affairs Marketed Products you will define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. Demonstrates acceptable skills with increasing independence ...