Job Description
Manager Regulatory Affairs – Regulatory Affairs | Indasi Lifescience Pvt Ltd | Daman, Daman and Diu, India
Indasi Lifescience Pvt Ltd is inviting applications for the role of Manager Regulatory Affairs at its pharmaceutical operations in Daman, Daman and Diu, India. This full-time opportunity is ideal for experienced professionals with 10 to 12 years of expertise in regulatory affairs, pharmaceutical compliance management, dossier preparation, product registration activities, regulatory submissions, documentation management, audit coordination, GMP compliance, international regulatory systems, and pharmaceutical operational support within regulated manufacturing environments. Male candidates will receive preference for this position.
The selected candidate will manage regulatory affairs operations across pharmaceutical business activities, coordinate product registration and submission processes, maintain regulatory documentation and compliance records, support audit and inspection activities, coordinate with quality assurance and manufacturing departments, ensure adherence to pharmaceutical regulatory guidelines, monitor submission timelines, participate in operational review meetings, support international compliance requirements, and maintain regulatory workflow efficiency across organizational systems. Candidates should possess strong knowledge of pharmaceutical compliance procedures and regulatory operational management.
This role offers valuable exposure to pharmaceutical regulatory systems, compliance management workflows, audit coordination activities, international documentation standards, and operational regulatory management within a growing pharmaceutical organization. Professionals interested in regulatory leadership and compliance operations can build strong technical and managerial expertise through this opportunity.
Location
Daman, Daman and Diu, India
Employment Type
Full-time
Experience Required
10 to 12
About Indasi Lifescience Pvt Ltd
Indasi Lifescience Pvt Ltd operates in the pharmaceutical industry specializing in regulated manufacturing systems, healthcare product development, pharmaceutical compliance operations, and quality-focused manufacturing environments.
Key Responsibilities
Manage pharmaceutical regulatory affairs operations.
Coordinate regulatory submissions and registration activities.
Maintain compliance documentation and regulatory records.
Support audits and inspection coordination activities.
Coordinate with manufacturing and quality departments.
Monitor regulatory timelines and operational workflows.
Ensure adherence to GMP and compliance standards.
Participate in regulatory reviews and compliance planning.
Support international regulatory documentation systems.
Maintain operational discipline within regulatory activities.
Required Skills
Strong understanding of pharmaceutical regulatory affairs systems.
Knowledge of GMP and international compliance procedures.
Documentation and regulatory reporting expertise.
Communication and coordination management skills.
Problem-solving and analytical thinking capabilities.
Time management and operational planning abilities.
Awareness of audit and inspection management systems.
Regulatory submission and workflow coordination expertise.
Attention to compliance accuracy and operational quality.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
BPharm
Industry
Pharmaceutical
Why Join Indasi Lifescience Pvt Ltd?
Indasi Lifescience Pvt Ltd offers professionals opportunities to work in regulated pharmaceutical environments with exposure to regulatory management systems and compliance operations.
How to Apply
Interested candidates can apply through ACKJOBS and complete the application process for this pharmaceutical regulatory affairs opportunity.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.
Indasi Lifescience Pvt Ltd is inviting applications for the role of Manager Regulatory Affairs at its pharmaceutical operations in Daman, Daman and Diu, India. This full-time opportunity is ideal for experienced professionals with 10 to 12 years of expertise in regulatory affairs, pharmaceutical compliance management, dossier preparation, product registration activities, regulatory submissions, documentation management, audit coordination, GMP compliance, international regulatory systems, and pharmaceutical operational support within regulated manufacturing environments. Male candidates will receive preference for this position.
The selected candidate will manage regulatory affairs operations across pharmaceutical business activities, coordinate product registration and submission processes, maintain regulatory documentation and compliance records, support audit and inspection activities, coordinate with quality assurance and manufacturing departments, ensure adherence to pharmaceutical regulatory guidelines, monitor submission timelines, participate in operational review meetings, support international compliance requirements, and maintain regulatory workflow efficiency across organizational systems. Candidates should possess strong knowledge of pharmaceutical compliance procedures and regulatory operational management.
This role offers valuable exposure to pharmaceutical regulatory systems, compliance management workflows, audit coordination activities, international documentation standards, and operational regulatory management within a growing pharmaceutical organization. Professionals interested in regulatory leadership and compliance operations can build strong technical and managerial expertise through this opportunity.
Location
Daman, Daman and Diu, India
Employment Type
Full-time
Experience Required
10 to 12
About Indasi Lifescience Pvt Ltd
Indasi Lifescience Pvt Ltd operates in the pharmaceutical industry specializing in regulated manufacturing systems, healthcare product development, pharmaceutical compliance operations, and quality-focused manufacturing environments.
Key Responsibilities
Manage pharmaceutical regulatory affairs operations.
Coordinate regulatory submissions and registration activities.
Maintain compliance documentation and regulatory records.
Support audits and inspection coordination activities.
Coordinate with manufacturing and quality departments.
Monitor regulatory timelines and operational workflows.
Ensure adherence to GMP and compliance standards.
Participate in regulatory reviews and compliance planning.
Support international regulatory documentation systems.
Maintain operational discipline within regulatory activities.
Required Skills
Strong understanding of pharmaceutical regulatory affairs systems.
Knowledge of GMP and international compliance procedures.
Documentation and regulatory reporting expertise.
Communication and coordination management skills.
Problem-solving and analytical thinking capabilities.
Time management and operational planning abilities.
Awareness of audit and inspection management systems.
Regulatory submission and workflow coordination expertise.
Attention to compliance accuracy and operational quality.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
BPharm
Industry
Pharmaceutical
Why Join Indasi Lifescience Pvt Ltd?
Indasi Lifescience Pvt Ltd offers professionals opportunities to work in regulated pharmaceutical environments with exposure to regulatory management systems and compliance operations.
How to Apply
Interested candidates can apply through ACKJOBS and complete the application process for this pharmaceutical regulatory affairs opportunity.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.