Regulatory Affairs Associate Kuwait
at Johnson Johnson
Kuwait City, العاصمة, Kuwait -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 09 Oct, 2024 | Not Specified | 10 Jul, 2024 | 3 year(s) or above | Pharmaceutical Industry,English,Consideration,Life Sciences,Career Opportunities | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Welcome to an exceptional opportunity with Johnson & Johnson, a world-class leader in health and personal care. Join our ambitious team of over 125,000 employees across 60 countries as we work together to help billions of people live longer, healthier, and happier lives.
Johnson & Johnson Innovative Medicine is recruiting for a regulatory affairs associate in Kuwait. This position will support the GCC cluster.
EXPERIENCE AND SKILLS:
Required:
- University degree in pharmacy, life sciences, or another related field.
- Minimum of 3 Years of experience in the pharmaceutical industry in a similar role
- Strong knowledge of the pharma regulations in GCC
- Fluency in Arabic and English
At Johnson & Johnson, we are committed to being an equal-opportunity employer. We value diversity and inclusion in our workforce, and all qualified applicants will receive consideration for employment. We strive to create a supportive and inclusive work environment where everyone can thrive.
To learn more about the exceptional career opportunities and benefits we offer at Johnson & Johnson, visit our website at www.careers.jnj.com.
Join us in our mission to make a positive impact on the lives of billions of people worldwide. Apply now to become a Regulatory Affairs Associate in Kuwait with Johnson & Johnson
Responsibilities:
- Provide strategic and valuable regulatory input into the Business Unit discussions
- Be involved in all aspects of the application to take the product to market.
- Coordinate the preparations, review, submission, and follow-up of regulatory files to the health authorities for new registration, renewal, and variations and ensure that filing & submission meet local requirements & company objectives.
- Respond to inquiries from the Health Authorities,
- Communication with the Health Authority to overcome any obstacles that may affect product availability
- Implement regulatory plans, effectively managing timelines to achieve objectives
- Maintain accurate and organized archiving & tracking of regulatory activities and marketing authorizations.
- Maintain current knowledge of existing and new regulations, standards and guidance documents. And Ensure that relevant local regulations are properly communicated to the other functions
- Provide regulatory support to all company functions upon request.
- Strictly adhere to local laws & HCBI guidelines, the Foreign Corrupt Practices Act (FCPA), Policy on Business Conduct (PBC).
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Pharmacy life sciences or another related field
Proficient
1
Kuwait City, Kuwait