La Chandra Pharma Lab Pvt. Ltd. is hiring for 2 positions of Executive / Senior Executive – Regulatory Affairs at its pharmaceutical manufacturing facility in Gujarat. This opportunity is suitable for candidates with an M.Sc. in Organic Chemistry and 1–4 years of experience in API Regulatory Affairs (RA). Applicants should have experience with regulatory documentation, CTD/eCTD dossiers, DMF and CEP submissions, customer and regulatory agency queries, post-approval changes, and regulatory compliance. Candidates must have API Regulatory Affairs experience in an organization with USFDA and/or EU-GMP approval.
La Chandra Pharma Lab Recruitment 2026 – Job Overview
| Job Detail | Information |
|---|---|
| Company Name | La Chandra Pharma Lab Pvt. Ltd. |
| Job Position | Executive / Senior Executive – Regulatory Affairs |
| Number of Vacancies | 2 |
| Department | Regulatory Affairs |
| Industry | Pharmaceutical / API Manufacturing |
| Qualification | M.Sc. in Organic Chemistry |
| Experience | 1–4 Years |
| Required Experience | API Regulatory Affairs |
| Job Location | Dantiwada, Banaskantha, Gujarat |
| Employment Type | Not specified |
| Salary | Not specified |
| Application Mode | |
| Email Address | regulatory@lachandra.in |
| Contact Number | +91 8879226604 |
| Company Website | www.lachandra.in |
About La Chandra Pharma Lab Pvt. Ltd.
La Chandra Pharma Lab Pvt. Ltd. is a pharmaceutical company based in Gujarat. According to the recruitment poster, the company emphasizes quality, integrity, innovation, and regulatory compliance in its operations.
The company highlights regulatory standards and certifications associated with USFDA, WHO-GMP, and EU-GMP (WC) compliance. The current recruitment is focused on strengthening its Regulatory Affairs team with professionals experienced in API regulatory submissions, documentation, licensing, and compliance activities.
Job Description – Executive / Senior Executive Regulatory Affairs
The selected candidates will support regulatory affairs activities related to active pharmaceutical ingredients (APIs), including preparation and compilation of regulatory dossiers, communication with customers and regulatory agencies, licensing activities, and maintenance of regulatory documentation.
Candidates should have practical knowledge of regulatory requirements and experience working in an API manufacturing organization with USFDA and/or EU-GMP approval.
Key Responsibilities
1. Regulatory Documentation and Dossier Preparation
- Compile and prepare CTD/eCTD regulatory documentation.
- Support the preparation and maintenance of Drug Master Files (DMF).
- Assist with Certificate of Suitability (CEP) documentation.
- Maintain accurate regulatory records and supporting documents.
2. Customer and Regulatory Agency Communication
- Handle customer queries related to regulatory documentation.
- Respond to queries from regulatory agencies.
- Coordinate with internal departments to obtain required technical information.
- Ensure regulatory responses are accurate and submitted within applicable timelines.
3. Post-Approval Changes and Customer Notifications
- Prepare submissions for post-approval changes.
- Coordinate customer notifications related to regulatory changes.
- Maintain appropriate documentation for changes affecting approved products or dossiers.
4. State FDA Licensing Activities
- Support State FDA licensing and related regulatory activities.
- Coordinate documentation required for licensing procedures.
- Maintain records associated with regulatory approvals and licences.
5. Audit and CAPA Documentation
- Maintain customer and regulatory agency audit records.
- Support the preparation and maintenance of Corrective and Preventive Action (CAPA) plans.
- Coordinate with relevant departments to track audit observations and corrective actions.
6. Regulatory Database Management
- Maintain regulatory databases and documentation trackers.
- Ensure regulatory information is updated and readily accessible.
- Support document control and compliance activities.
Eligibility Criteria
Candidates applying for La Chandra Pharma Lab Regulatory Affairs jobs should meet the following requirements.
| Requirement | Details |
|---|---|
| Educational Qualification | M.Sc. in Organic Chemistry |
| Work Experience | 1–4 Years |
| Functional Experience | API Regulatory Affairs |
| Regulatory Exposure | CTD/eCTD, DMF, CEP, licensing and regulatory submissions |
| Compliance Background | Experience in an organization with USFDA and/or EU-GMP approval |
| Communication Skills | Ability to handle customer and regulatory agency queries |
| Documentation Skills | Regulatory dossier preparation, database maintenance and audit documentation |
Important: The recruitment poster specifically states that applicants must have API Regulatory Affairs experience in an organization with USFDA and/or EU-GMP approval. Candidates should verify that their experience matches this requirement before applying.
Job Location
Work Location: La Chandra Pharma Lab Pvt. Ltd., Gujarat.
The address provided in the recruitment poster is:
Survey No. 64/2/2,
Village Vaghrol, Taluka Dantiwada,
District Banaskantha, Gujarat, India – 385510.
Candidates should confirm the exact reporting location and work arrangements with the recruitment team.
Salary and Benefits
The recruitment poster does not disclose the salary range for the Executive / Senior Executive Regulatory Affairs positions.
The company highlights the following workplace benefits and features:
- Regulatory-compliant facility.
- Exposure to pharmaceutical regulatory requirements.
- Growth-oriented work environment.
- Continuous learning and development.
- Employee well-being and engagement initiatives.
Salary, working hours, leave policy, and other employment terms should be confirmed directly with the company.
How to Apply for La Chandra Pharma Lab Recruitment 2026
Interested and eligible candidates can apply for the Executive / Senior Executive – Regulatory Affairs positions by sending an updated resume to the company’s recruitment email address.
Email: regulatory@lachandra.in
Contact Number: +91 8879226604
Website: www.lachandra.in
Candidates should mention their relevant API Regulatory Affairs experience, current designation, educational qualification, and familiarity with CTD/eCTD, DMF, CEP, and regulatory compliance in their application.

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