Senior Medical Writer at Celegence: Apply Now!
About Celegence
Celegence provides services and solutions to support the life sciences industry with regulatory affairs operations and strategy. As regulatory specialists, Celegence works across all phases of the product lifecycle, offering regulatory strategy, authoring, and management services. With a global team of consultants, Celegence delivers local regulatory insights and intelligence to ensure regulatory compliance and efficiency for its clients.
About the Job
Celegence is hiring a Senior Medical Writer.
Eligibility
- Bachelor’s Degree/Post Graduation in any relevant Life Sciences field. Master’s Degree is preferred.
- Minimum 3 years of experience in Medical Device Regulatory documentation.
- Familiarity with the Life Sciences Industry, preferably Regulatory Services.
- Experience in handling projects independently and engaging with multiple clients.
Work Profile
The Senior Medical Writer will ensure timely development and delivery of high-quality regulatory documents compliant with MEDDEV 2.7/1 Rev. 4 and MDR for Medical Devices across various therapeutic areas. They will collaborate with internal stakeholders and client teams to deliver customised solutions aligned with client requirements.
Mode
Full Time, On-Site
Salary
To be discussed during the interview process.
Location
Bengaluru, India
Application Procedure
Interested candidates should email their updated resume to [email protected].
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