Life Sciences Jobs at Cencora | Regulatory Affairs Roles
Are you looking for Life Sciences Jobs in Regulatory Affairs? Cencora Careers has announced an exciting opportunity for a Specialist/Sr. Specialist – Regulatory Affairs in Noida. If you have a Life Science degree and experience in regulatory submissions, marketing authorisations, and client management, this Regulatory Affairs Jobs opening could be the perfect next step in your career. Explore the eligibility, responsibilities, qualifications, and application details below.
About Cencora
Cencora is a global healthcare company dedicated to creating healthier futures by improving access to pharmaceutical products and healthcare solutions worldwide. The company provides expertise across pharmaceutical distribution, commercialisation, consulting, and Regulatory Affairs, supporting healthcare providers, manufacturers, and patients through innovative solutions. Cencora is committed to delivering high-quality services while fostering professional growth, collaboration, and innovation for its employees.
Key Responsibilities
- Develop and maintain strong client relationships and identify opportunities for increased service support.
- Participate in regulatory processes to obtain and maintain marketing authorisations for human and veterinary medicinal products, including applications, renewals, and variations.
- Support regulatory activities related to medical devices, cosmetics, food supplements, and herbal products.
- Prepare, review, and compile documents for Regulatory Affairs projects.
- Communicate with clients and Health Authorities in coordination with the respective lead.
- Support planning and execution of client projects while meeting defined KPIs.
- Provide regulatory guidance to colleagues and clients on Regulatory Strategy and Procedure Management.
- Maintain up-to-date regulatory intelligence and share knowledge across teams.
- Support VDC strategy implementation and process optimisation.
- Ensure compliance with internal procedures and quality standards.
- Provide operational insights for commercial, marketing, and business development activities.
- Assist the respective lead in budget delivery, project reporting, and invoicing support.
- Provide on-site regulatory support to GCS clients when required.
- Perform additional responsibilities assigned by the Line Manager, Practice Area Lead, or Head of VDC REG.
Qualifications
- University degree in Life Science.
Experience Required
- Several years of experience or demonstrated capability in Regulatory Affairs or a similar field.
- Advanced knowledge of regulatory processes and the ability to independently manage responsibilities.
- Proven ability to handle more complex regulatory projects.
Skills Needed
- Strong project management and prioritisation skills.
- Ability to deliver customer and internal projects efficiently.
- Excellent analytical and problem-solving abilities.
- close attention to detail and a service-oriented mindset.
- Ability to work independently using a structured and systematic approach.
- Capability to train and support junior team members.
- Experience leading small projects with defined objectives.
- Strong relationship management skills with clients and internal stakeholders.
- Excellent written and verbal communication skills.
- Business-level fluency in English.
- Confident professional presentation and solution-oriented approach.
Why Join Cencora Careers?
Cencora offers professionals the opportunity to work on global Regulatory Affairs projects that contribute to healthier futures for people and animals worldwide. Employees collaborate with experienced regulatory experts, gain exposure to international compliance standards, and build rewarding careers in one of the leading healthcare organisations. If you’re searching for Life Sciences Jobs, Regulatory Affairs Jobs, or opportunities through Cencora Careers, this role provides excellent career growth and international project exposure.
