Rhydburg Biotech Senior Executive Regulatory Affairs Jobs

Rhydburg Biotech Senior Executive – Regulatory Affairs Jobs in Dehradun

Rhydburg Biotech Ltd. is hiring a Senior Executive – Regulatory Affairs (JB-1702) for its pharmaceutical regulatory team in Dehradun, Uttarakhand. Candidates with a B.Pharm or M.Pharm qualification and at least 3 years of experience in Quality Assurance or analytical validation roles are eligible to apply. The position involves regulatory dossier preparation, analytical method validation document review, regulatory submissions, quality documentation, and compliance with applicable regulatory guidelines. The company lists a salary range of ₹25,000–₹30,000 and mentions flexible working arrangements.

Company Overview

Rhydburg Biotech Ltd. manufactures, markets, and exports generic pharmaceutical products. The company focuses on research and development, regulatory capabilities, and supplying quality products through public and private drug distribution systems.

Job Details

• Company: Rhydburg Biotech Ltd.

• Designation: Senior Executive – Regulatory Affairs

• Job Code: JB-1702

• Location: Dehradun, Uttarakhand, India

• Employment Type: Full-time

• Experience: Minimum 3 years in Quality Assurance or analytical validation roles

• Salary: ₹25,000–₹30,000

• Date Posted: October 14, 2026

• Industry: Pharma, Biotechnology, Clinical Research

Job Role & Responsibilities

Regulatory Documentation & Submissions

• Prepare, review, and maintain regulatory documents and submissions in accordance with applicable guidelines and company procedures.

• Compile and coordinate regulatory dossiers, applications, renewals, variations, amendments, and other regulatory submissions.

• Maintain regulatory trackers, submission records, approvals, licenses, certificates, and related documentation.

• Prepare and coordinate responses to regulatory queries, deficiencies, observations, and requests for additional information.

Analytical Data & Technical Document Review

• Review technical documents, product specifications, analytical data, stability data, and manufacturing information for regulatory compliance.

• Review analytical method validation documentation.

• Assess technical information for accuracy, completeness, and compliance with applicable requirements.

Quality Assurance & Cross-Functional Coordination

• Coordinate with Quality Assurance, Research and Development, Production, and other departments to obtain regulatory information and supporting documentation.

• Review quality documents, including deviations, Corrective and Preventive Actions (CAPA), change controls, SOPs, and batch-related records, for regulatory requirements and impact.

• Support regulatory audits and inspections by preparing documents and coordinating responses with QA and relevant departments.

Regulatory Compliance & Data Integrity

• Monitor updates to regulatory guidelines and assess their impact on products, processes, documentation, and quality systems.

• Ensure regulatory activities are completed within required timelines.

• Maintain accurate documentation, regulatory compliance, and data integrity.

Eligibility & Qualifications

Candidates should meet the following requirements:

• Educational Qualification: B.Pharm or M.Pharm. A bachelor’s or master’s degree in Pharmacy is mandatory.

• Experience: Minimum 3 years of experience in Quality Assurance or analytical validation roles.

• Technical Skills: Hands-on experience reviewing analytical method validation documentation.

• Analytical Skills: Ability to interpret analytical data and review technical documentation.

• Regulatory Knowledge: Understanding of regulatory submissions, dossier preparation, quality documentation, and compliance requirements.

• Communication Skills: Good communication skills and the ability to coordinate with cross-functional departments.

Salary & Work Arrangements

• Salary Range: ₹25,000–₹30,000.

• Work Location: Dehradun, Uttarakhand.

• Employment Type: Full-time.

• Working Arrangements: The listing mentions a remote working option with defined review responsibilities and flexible working hours aligned with dossier and submission timelines.

• Role Focus: Technical documentation and regulatory responsibilities, without laboratory or shop-floor operations, as described in the listing.

Candidates should confirm the applicable remote or office arrangement with the employer before joining.

 

How to Apply

Interested and eligible candidates can apply through the official Rhydburg Biotech recruitment portal.

Apply Online: Rhydburg Biotech Senior Executive – Regulatory Affairs

Applicants should highlight their pharmaceutical qualifications, Quality Assurance or analytical validation experience, analytical method validation document review skills, and regulatory documentation expertise.

Job Summary