About the JobSkillsRegulatoryRegulatory complianceRegulatory AffairsRegulatory DocumentationRegulatory SubmissionsRegulatory ReportingICHGood Clinical Practice (GCP)
Job Overview:
MidLevel: 4 to 6 years of experience FullTime position in Ahmedabad
Qualifications and Skills:
- Experience in regulatory affairs within the pharmaceutical sector
- Knowledge of regulatory frameworks and guidelines
- Strong understanding of regulatory documentation and submissions
- Excellent communication and problemsolving skills
- Ability to work collaboratively and adapt to regulatory changes
Roles and Responsibilities:
- Ensure compliance with regulatory requirements in the pharmaceutical industry
- Prepare and submit regulatory documents and dossiers
- Monitor changes in regulations and update internal policies accordingly
- Collaborate with crossfunctional teams to ensure regulatory compliance
- Handle regulatory reporting and maintain accurate records
Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains.
Please use the below Lifelancer link for job application and quicker response.
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Remote Work :
No