Job Description
Dy Manager Regulatory Affairs – Regulatory Affairs | Mepro Pharmaceuticals Pvt Ltd | Vadodara, Gujarat, India
Mepro Pharmaceuticals Pvt Ltd is inviting experienced professionals to apply for the position of Dy Manager Regulatory Affairs at its pharmaceutical operations in Vadodara, Gujarat, India. This full-time opportunity is ideal for candidates with 10 to 15 years of experience in pharmaceutical regulatory affairs, dossier preparation, compliance management, product registrations, documentation systems, and coordination with international and domestic regulatory authorities. The selected candidate will manage regulatory submissions, oversee documentation compliance, coordinate with quality assurance and production departments, support audit readiness, and ensure timely execution of regulatory processes in accordance with pharmaceutical industry standards. Candidates with expertise in CTD submissions, regulatory documentation, market authorization procedures, and global pharmaceutical compliance requirements will be preferred. This role offers excellent exposure to advanced pharmaceutical regulatory systems, international compliance operations, healthcare product registrations, and strategic regulatory management focused on product approvals, compliance excellence, operational efficiency, and global market support.
Location
Vadodara, Gujarat, India
Employment Type
Full-time
Experience Required
10 to 15
Compensation & Benefits
Competitive salary package with leadership exposure, regulatory operations experience, and long-term pharmaceutical career growth opportunities.
About Mepro Pharmaceuticals Pvt Ltd
Mepro Pharmaceuticals Pvt Ltd operates in the pharmaceutical industry specializing in healthcare manufacturing, regulatory compliance systems, product registrations, and quality-focused pharmaceutical operations.
Position Overview
The Dy Manager Regulatory Affairs will oversee pharmaceutical regulatory activities, compliance documentation systems, and product registration processes.
Key Responsibilities
Manage pharmaceutical regulatory submission activities.
Prepare and review regulatory documentation and dossiers.
Coordinate with quality assurance and production departments.
Ensure compliance with pharmaceutical regulatory standards.
Support domestic and international product registration processes.
Maintain regulatory databases and compliance records.
Participate in audits and regulatory inspections.
Monitor changes in pharmaceutical regulatory guidelines.
Support strategic compliance and operational planning activities.
Assist in continuous improvement of regulatory systems.
Required Skills & Competencies
Strong understanding of pharmaceutical regulatory affairs.
Knowledge of dossier preparation and compliance systems.
Documentation and submission management expertise.
Communication and coordination abilities.
Problem-solving and analytical thinking skills.
Awareness of international pharmaceutical regulations.
Ability to manage regulatory operations efficiently.
Attention to compliance accuracy and documentation quality.
Leadership and workflow management capabilities.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B Pharm/M Pharm
About the Project & Industry
The pharmaceutical regulatory affairs industry plays a critical role in product approvals, compliance management, global registrations, and healthcare manufacturing operations across domestic and international markets.
Why Join Mepro Pharmaceuticals Pvt Ltd?
Mepro Pharmaceuticals Pvt Ltd offers opportunities to work in advanced pharmaceutical regulatory environments with exposure to global compliance systems and strategic healthcare operations.
How to Apply
Apply via AckJobs by clicking the Apply button. New candidates must complete a quick registration to access application details, while registered users can log in and apply instantly. Your profile is shared with hiring employers for relevant current and future opportunities.
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.
Mepro Pharmaceuticals Pvt Ltd is inviting experienced professionals to apply for the position of Dy Manager Regulatory Affairs at its pharmaceutical operations in Vadodara, Gujarat, India. This full-time opportunity is ideal for candidates with 10 to 15 years of experience in pharmaceutical regulatory affairs, dossier preparation, compliance management, product registrations, documentation systems, and coordination with international and domestic regulatory authorities. The selected candidate will manage regulatory submissions, oversee documentation compliance, coordinate with quality assurance and production departments, support audit readiness, and ensure timely execution of regulatory processes in accordance with pharmaceutical industry standards. Candidates with expertise in CTD submissions, regulatory documentation, market authorization procedures, and global pharmaceutical compliance requirements will be preferred. This role offers excellent exposure to advanced pharmaceutical regulatory systems, international compliance operations, healthcare product registrations, and strategic regulatory management focused on product approvals, compliance excellence, operational efficiency, and global market support.
Location
Vadodara, Gujarat, India
Employment Type
Full-time
Experience Required
10 to 15
Compensation & Benefits
Competitive salary package with leadership exposure, regulatory operations experience, and long-term pharmaceutical career growth opportunities.
About Mepro Pharmaceuticals Pvt Ltd
Mepro Pharmaceuticals Pvt Ltd operates in the pharmaceutical industry specializing in healthcare manufacturing, regulatory compliance systems, product registrations, and quality-focused pharmaceutical operations.
Position Overview
The Dy Manager Regulatory Affairs will oversee pharmaceutical regulatory activities, compliance documentation systems, and product registration processes.
Key Responsibilities
Manage pharmaceutical regulatory submission activities.
Prepare and review regulatory documentation and dossiers.
Coordinate with quality assurance and production departments.
Ensure compliance with pharmaceutical regulatory standards.
Support domestic and international product registration processes.
Maintain regulatory databases and compliance records.
Participate in audits and regulatory inspections.
Monitor changes in pharmaceutical regulatory guidelines.
Support strategic compliance and operational planning activities.
Assist in continuous improvement of regulatory systems.
Required Skills & Competencies
Strong understanding of pharmaceutical regulatory affairs.
Knowledge of dossier preparation and compliance systems.
Documentation and submission management expertise.
Communication and coordination abilities.
Problem-solving and analytical thinking skills.
Awareness of international pharmaceutical regulations.
Ability to manage regulatory operations efficiently.
Attention to compliance accuracy and documentation quality.
Leadership and workflow management capabilities.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
B Pharm/M Pharm
About the Project & Industry
The pharmaceutical regulatory affairs industry plays a critical role in product approvals, compliance management, global registrations, and healthcare manufacturing operations across domestic and international markets.
Why Join Mepro Pharmaceuticals Pvt Ltd?
Mepro Pharmaceuticals Pvt Ltd offers opportunities to work in advanced pharmaceutical regulatory environments with exposure to global compliance systems and strategic healthcare operations.
How to Apply
Apply via AckJobs by clicking the Apply button. New candidates must complete a quick registration to access application details, while registered users can log in and apply instantly. Your profile is shared with hiring employers for relevant current and future opportunities.
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.