Job Description
Regulatory Assistant Manager – Regulatory Affairs | Rhydburg Pharma | Dehradun, Uttarakhand, India
Rhydburg Pharma is hiring experienced professionals for the role of Regulatory Assistant Manager at its pharmaceutical operations located in Dehradun, Uttarakhand, India. This full-time opportunity is suitable for candidates with 6 to 8 years of experience in regulatory affairs, pharmaceutical documentation, dossier preparation, compliance coordination, regulatory submissions, and healthcare manufacturing environments. The selected candidate will support regulatory operations, coordinate with quality and production departments, maintain compliance documentation, prepare regulatory submissions, and ensure adherence to pharmaceutical guidelines and international regulatory standards. Candidates having expertise in regulatory filing systems, pharmaceutical compliance procedures, documentation management, audit coordination, and GMP-regulated operations will be preferred. This role offers valuable exposure to advanced pharmaceutical compliance systems, global regulatory environments, healthcare documentation technologies, and quality-driven operational practices focused on regulatory accuracy, product compliance, operational excellence, and international pharmaceutical standards.
Location
Dehradun, Uttarakhand, India
Employment Type
Full-time
Experience Required
6 to 8
Compensation & Benefits
Competitive salary package with pharmaceutical regulatory exposure, compliance management opportunities, and long-term career growth.
About Rhydburg Pharma
Rhydburg Pharma operates in the pharmaceutical industry specializing in healthcare manufacturing, regulatory compliance systems, pharmaceutical documentation, and quality-focused operations.
Position Overview
The Regulatory Assistant Manager will oversee pharmaceutical compliance activities, regulatory documentation systems, and submission coordination operations.
Key Responsibilities
Manage pharmaceutical regulatory affairs activities.
Prepare and maintain regulatory documentation and dossiers.
Coordinate with quality assurance and production teams.
Support domestic and international regulatory submissions.
Ensure compliance with pharmaceutical regulatory standards.
Monitor changes in regulatory guidelines and requirements.
Participate in audit preparation and compliance inspections.
Maintain documentation accuracy and operational records.
Support product registration and approval activities.
Drive regulatory process improvement initiatives.
Required Skills & Competencies
Strong understanding of pharmaceutical regulatory systems.
Knowledge of compliance documentation and dossier preparation.
Communication and cross-functional coordination abilities.
Problem-solving and analytical thinking capabilities.
Awareness of GMP and pharmaceutical compliance standards.
Ability to manage regulatory workflows efficiently.
Attention to documentation quality and operational accuracy.
Strategic planning and reporting management skills.
Time management and multitasking capabilities.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
BPharma/MPharma
About the Project & Industry
The pharmaceutical regulatory industry depends on strong compliance systems, accurate documentation procedures, and global regulatory standards to support safe healthcare manufacturing and product approvals.
Why Join Rhydburg Pharma?
Rhydburg Pharma offers opportunities to work in advanced pharmaceutical regulatory environments with exposure to global compliance systems and 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.
Rhydburg Pharma is hiring experienced professionals for the role of Regulatory Assistant Manager at its pharmaceutical operations located in Dehradun, Uttarakhand, India. This full-time opportunity is suitable for candidates with 6 to 8 years of experience in regulatory affairs, pharmaceutical documentation, dossier preparation, compliance coordination, regulatory submissions, and healthcare manufacturing environments. The selected candidate will support regulatory operations, coordinate with quality and production departments, maintain compliance documentation, prepare regulatory submissions, and ensure adherence to pharmaceutical guidelines and international regulatory standards. Candidates having expertise in regulatory filing systems, pharmaceutical compliance procedures, documentation management, audit coordination, and GMP-regulated operations will be preferred. This role offers valuable exposure to advanced pharmaceutical compliance systems, global regulatory environments, healthcare documentation technologies, and quality-driven operational practices focused on regulatory accuracy, product compliance, operational excellence, and international pharmaceutical standards.
Location
Dehradun, Uttarakhand, India
Employment Type
Full-time
Experience Required
6 to 8
Compensation & Benefits
Competitive salary package with pharmaceutical regulatory exposure, compliance management opportunities, and long-term career growth.
About Rhydburg Pharma
Rhydburg Pharma operates in the pharmaceutical industry specializing in healthcare manufacturing, regulatory compliance systems, pharmaceutical documentation, and quality-focused operations.
Position Overview
The Regulatory Assistant Manager will oversee pharmaceutical compliance activities, regulatory documentation systems, and submission coordination operations.
Key Responsibilities
Manage pharmaceutical regulatory affairs activities.
Prepare and maintain regulatory documentation and dossiers.
Coordinate with quality assurance and production teams.
Support domestic and international regulatory submissions.
Ensure compliance with pharmaceutical regulatory standards.
Monitor changes in regulatory guidelines and requirements.
Participate in audit preparation and compliance inspections.
Maintain documentation accuracy and operational records.
Support product registration and approval activities.
Drive regulatory process improvement initiatives.
Required Skills & Competencies
Strong understanding of pharmaceutical regulatory systems.
Knowledge of compliance documentation and dossier preparation.
Communication and cross-functional coordination abilities.
Problem-solving and analytical thinking capabilities.
Awareness of GMP and pharmaceutical compliance standards.
Ability to manage regulatory workflows efficiently.
Attention to documentation quality and operational accuracy.
Strategic planning and reporting management skills.
Time management and multitasking capabilities.
Adaptability to regulated pharmaceutical environments.
Educational Qualification
BPharma/MPharma
About the Project & Industry
The pharmaceutical regulatory industry depends on strong compliance systems, accurate documentation procedures, and global regulatory standards to support safe healthcare manufacturing and product approvals.
Why Join Rhydburg Pharma?
Rhydburg Pharma offers opportunities to work in advanced pharmaceutical regulatory environments with exposure to global compliance systems and 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.