Job Description
API Regulatory Affairs Executive – Regulatory Affairs Department | MSN Laboratories Pvt. Ltd. | Hyderabad, Telangana, India
MSN Laboratories Pvt. Ltd. is hiring professionals for the role of API Regulatory Affairs Executive for its pharmaceutical regulatory operations located in Hyderabad, Telangana, India. This full-time opportunity is ideal for candidates with 1 to 7 years of experience in API regulatory affairs, pharmaceutical documentation workflows, DMF filing systems, regulatory compliance activities, dossier preparation operations, audit coordination workflows, quality documentation systems, regulatory submission activities, and regulated pharmaceutical industry environments.
The selected candidate will support API regulatory affairs and compliance activities associated with pharmaceutical manufacturing systems and global regulatory standards. Responsibilities include preparing and reviewing regulatory documentation and DMF submissions, maintaining regulatory records and compliance documentation, coordinating with QA, production, and R&D teams for operational support activities, monitoring regulatory workflows and submission timelines, ensuring adherence to GMP procedures and international regulatory standards, preparing audit reports and operational documentation, assisting in troubleshooting and regulatory coordination workflows, participating in regulatory review and compliance activities, supporting submission planning and documentation systems, and maintaining continuous improvement of regulatory operations and compliance workflows.
This role offers valuable exposure to pharmaceutical regulatory systems, API documentation workflows, global compliance operations, audit coordination activities, submission systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in regulatory affairs careers can strengthen their technical and operational expertise through this opportunity.
Location
Hyderabad, Telangana, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
1 to 7 Years
About MSN Laboratories Pvt. Ltd.
MSN Laboratories Pvt. Ltd. operates in the pharmaceutical industry specializing in API manufacturing systems, pharmaceutical regulatory operations, healthcare product development workflows, GMP-regulated production activities, and global pharmaceutical services.
Key Responsibilities
Support API regulatory affairs and compliance activities.
Prepare DMF submissions and regulatory documentation.
Maintain regulatory records and compliance systems.
Coordinate with QA, production, and R&D teams.
Monitor regulatory workflows and submission timelines.
Ensure adherence to GMP procedures and regulatory standards.
Prepare audit reports and operational documentation.
Support troubleshooting and regulatory coordination workflows.
Participate in compliance review and submission activities.
Assist in continuous improvement of regulatory systems.
Required Skills
Strong knowledge of API regulatory affairs operations.
Understanding of DMF filing and pharmaceutical compliance systems.
Knowledge of dossier preparation and regulatory documentation.
Experience in GMP workflows and audit coordination activities.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of international regulatory standards.
Ability to manage submission schedules and workflows.
Attention to documentation accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc Organic Chemistry
Industry
Pharmaceutical
Why Join MSN Laboratories Pvt. Ltd.?
MSN Laboratories Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to regulatory systems, API workflows, compliance operations, and global pharmaceutical activities.
How to Apply
Interested candidates can apply through ACKJOBS for this API Regulatory Affairs Executive opportunity by submitting their updated resume and relevant documents.
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.
MSN Laboratories Pvt. Ltd. is hiring professionals for the role of API Regulatory Affairs Executive for its pharmaceutical regulatory operations located in Hyderabad, Telangana, India. This full-time opportunity is ideal for candidates with 1 to 7 years of experience in API regulatory affairs, pharmaceutical documentation workflows, DMF filing systems, regulatory compliance activities, dossier preparation operations, audit coordination workflows, quality documentation systems, regulatory submission activities, and regulated pharmaceutical industry environments.
The selected candidate will support API regulatory affairs and compliance activities associated with pharmaceutical manufacturing systems and global regulatory standards. Responsibilities include preparing and reviewing regulatory documentation and DMF submissions, maintaining regulatory records and compliance documentation, coordinating with QA, production, and R&D teams for operational support activities, monitoring regulatory workflows and submission timelines, ensuring adherence to GMP procedures and international regulatory standards, preparing audit reports and operational documentation, assisting in troubleshooting and regulatory coordination workflows, participating in regulatory review and compliance activities, supporting submission planning and documentation systems, and maintaining continuous improvement of regulatory operations and compliance workflows.
This role offers valuable exposure to pharmaceutical regulatory systems, API documentation workflows, global compliance operations, audit coordination activities, submission systems, and industrial pharmaceutical environments within a reputed organization. Professionals interested in regulatory affairs careers can strengthen their technical and operational expertise through this opportunity.
Location
Hyderabad, Telangana, India
Employment Type
Full-time
Salary
Best in Industry
Experience Required
1 to 7 Years
About MSN Laboratories Pvt. Ltd.
MSN Laboratories Pvt. Ltd. operates in the pharmaceutical industry specializing in API manufacturing systems, pharmaceutical regulatory operations, healthcare product development workflows, GMP-regulated production activities, and global pharmaceutical services.
Key Responsibilities
Support API regulatory affairs and compliance activities.
Prepare DMF submissions and regulatory documentation.
Maintain regulatory records and compliance systems.
Coordinate with QA, production, and R&D teams.
Monitor regulatory workflows and submission timelines.
Ensure adherence to GMP procedures and regulatory standards.
Prepare audit reports and operational documentation.
Support troubleshooting and regulatory coordination workflows.
Participate in compliance review and submission activities.
Assist in continuous improvement of regulatory systems.
Required Skills
Strong knowledge of API regulatory affairs operations.
Understanding of DMF filing and pharmaceutical compliance systems.
Knowledge of dossier preparation and regulatory documentation.
Experience in GMP workflows and audit coordination activities.
Good analytical and problem-solving abilities.
Strong communication and teamwork skills.
Knowledge of international regulatory standards.
Ability to manage submission schedules and workflows.
Attention to documentation accuracy and compliance standards.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
M.Sc Organic Chemistry
Industry
Pharmaceutical
Why Join MSN Laboratories Pvt. Ltd.?
MSN Laboratories Pvt. Ltd. offers professionals opportunities to work in advanced pharmaceutical environments with exposure to regulatory systems, API workflows, compliance operations, and global pharmaceutical activities.
How to Apply
Interested candidates can apply through ACKJOBS for this API Regulatory Affairs Executive opportunity by submitting their updated resume and relevant documents.
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.