S Kant Healthcare Ltd. is listed as hiring pharmacy professionals for Regulatory Affairs and In-Process Quality Assurance (IPQA) positions in Vapi, Gujarat. The opportunities are suitable for B.Pharm and M.Pharm candidates, with experience requirements varying by role.
The Regulatory Affairs opening is intended for candidates with experience in pharmaceutical dossiers, CMC documentation, stability data, and international regulatory submissions. The IPQA position may interest freshers and experienced candidates with knowledge of cGMP, in-process quality checks, pharmaceutical documentation, and quality systems.
According to the available third-party vacancy listing, applications can be submitted by email. Interested candidates should review the responsibilities and experience requirements for each position before applying.
S Kant Healthcare Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | S Kant Healthcare Ltd. |
| Job Location | Vapi, Gujarat |
| Job Openings | Regulatory Affairs and IPQA |
| Regulatory Affairs Designation | Officer / Executive |
| Regulatory Affairs Experience | 3–5 years |
| IPQA Designation | Officer – IPQA |
| IPQA Experience | 0–3 years |
| Qualification | B.Pharm / M.Pharm |
| Application Mode | |
| Application Email | latesh.nemade@skant.com |
| Salary | Not disclosed |
| Listing Date | October 26, 2026 |
About S Kant Healthcare Ltd.
S Kant Healthcare Ltd. operates in the pharmaceutical sector. The advertised positions cover two important functions in pharmaceutical manufacturing and product development: Regulatory Affairs and In-Process Quality Assurance.
Regulatory Affairs professionals support the preparation and submission of product documentation to regulatory agencies and customers. IPQA professionals help ensure that manufacturing activities, in-process checks, documentation, and quality systems follow applicable procedures and standards.
1. Officer / Executive – Regulatory Affairs
<text color=”secondary” size=”sm”>Location: Vapi, Gujarat | Experience: 3–5 years</text>
Job Description
The Regulatory Affairs Officer / Executive will support pharmaceutical regulatory documentation, dossier compilation, stability data evaluation, and submission activities for domestic and international requirements.
The role involves coordinating with Quality Assurance (QA), Quality Control (QC), and other departments to collect technical documents, address observations, maintain regulatory records, and prepare documentation for international agencies and customers.
Job Overview
| Particulars | Details |
|---|---|
| Position | Officer / Executive – Regulatory Affairs |
| Qualification | B.Pharm / M.Pharm |
| Experience | 3–5 years |
| Location | Vapi, Gujarat |
| Application Mode |
Key Responsibilities
- Coordinate the collection and review of dossier documents, including Chemistry, Manufacturing and Controls (CMC) information, from departments such as QA and QC.
- Coordinate with QA and QC heads regarding observations related to Out of Trend (OOT) and Out of Specification (OOS) results, where applicable.
- Review change control forms (CCFs) and provide monthly updates to the Regulatory Affairs team.
- Follow up with QA and QC teams for documents affected by change controls.
- Evaluate and extrapolate stability data in accordance with ICH Q1E guidance.
- Prepare Certificates of Pharmaceutical Products (COPPs).
- Compile documentation and product samples for tender submissions.
- Prepare and submit pharmaceutical product questionnaires and technical questionnaires for international agencies.
- Assist in responding to queries from ministries of health, international regulatory agencies, and customers.
- Coordinate order processing for international agency purchase orders according to their requirements.
- Manage regulatory samples and related documentation.
- Maintain housekeeping and laboratory discipline as required.
- Review, compile, and submit CMC documents to contract manufacturing or development partners for EU and MHRA submissions.
Eligibility Criteria
Educational qualification: B.Pharm or M.Pharm.
Experience required: 3–5 years of relevant experience.
Candidates with experience in pharmaceutical regulatory documentation, CMC dossiers, stability data, international submissions, and coordination with QA/QC teams may find this role relevant.
Required Skills
- Regulatory dossier preparation and compilation.
- CMC documentation.
- Stability data evaluation.
- Familiarity with ICH Q1E guidance.
- Pharmaceutical technical documentation.
- Regulatory query coordination.
- Change control documentation.
- Cross-functional communication and coordination.
These skills reflect the responsibilities in the supplied vacancy listing; the employer may specify additional requirements during recruitment.
How to Apply for Regulatory Affairs
Interested candidates can send their updated CV to the email address listed in the vacancy announcement.
Application Email: latesh.nemade@skant.com
Suggested email subject: Application for Officer / Executive – Regulatory Affairs
2. Officer – In-Process Quality Assurance (IPQA)
<text color=”secondary” size=”sm”>Location: Vapi, Gujarat | Experience: 0–3 years</text>
Job Description
S Kant Healthcare Ltd. is also listed as recruiting an Officer – IPQA for its Vapi location. This opportunity is suitable for B.Pharm and M.Pharm candidates interested in pharmaceutical manufacturing quality, in-process checks, documentation review, and quality system compliance.
The position involves monitoring IPQA activities, reviewing manufacturing and investigation records, coordinating with production and quality departments, and supporting compliance with standard operating procedures and current Good Manufacturing Practices (cGMP).
Job Overview
| Particulars | Details |
|---|---|
| Position | Officer – IPQA |
| Qualification | B.Pharm / M.Pharm |
| Experience | 0–3 years |
| Location | Vapi, Gujarat |
| Application Mode |
Key Responsibilities
- Monitor and review IPQA activities to ensure compliance with SOPs and cGMP guidelines.
- Review documentation related to in-process checks and finished products.
- Support the review of investigation records, including deviations, OOS results, change controls, and corrective and preventive actions (CAPA).
- Coordinate with Production, QA, QC, and other departments to support IPQA activities.
- Help maintain data integrity and accurate pharmaceutical documentation.
- Support regulatory compliance and the preparation of quality reports.
- Assist with audit-related activities.
- Contribute to continuous improvement initiatives within quality systems.
Eligibility Criteria
Educational qualification: B.Pharm or M.Pharm.
Experience required: 0–3 years of relevant experience.
The advertised experience range may make this position relevant to freshers and early-career pharmacy professionals, subject to the employer’s complete eligibility criteria.
Required Skills
- Basic understanding of pharmaceutical quality assurance.
- Knowledge of cGMP and SOP compliance.
- Familiarity with manufacturing documentation.
- Understanding of deviations, OOS, change controls, and CAPA.
- Attention to detail and data integrity.
- Communication and coordination with cross-functional teams.
- Interest in pharmaceutical quality systems and continuous improvement.
How to Apply for IPQA
Candidates interested in the Officer – IPQA position can send their updated CV to the email address provided in the listing.
Application Email: latesh.nemade@skant.com
Suggested email subject: Application for Officer – IPQA
Salary and Benefits
The salary for both positions has not been disclosed in the supplied vacancy listing. Information about allowances, insurance, transport, shifts, and other employee benefits is also unavailable.
Candidates should confirm compensation, working hours, and employment conditions with the recruiter during the application process.
How to Apply for S Kant Healthcare Recruitment 2026
Applicants should follow these steps:
- Update your resume with your educational qualifications, relevant experience, and technical skills.
- Select the position matching your background: Regulatory Affairs or IPQA.
- Mention the job title clearly in your email subject line.
- Send your CV to latesh.nemade@skant.com.
- Verify the vacancy and recruiter details before sharing personal documents.
Important: This recruitment information comes from a third-party vacancy listing, not a verified direct employer announcement. Confirm that the vacancies are still open before applying.
Frequently Asked Questions (FAQs)
1. Which positions are listed at S Kant Healthcare Ltd.?
The listing includes Officer / Executive – Regulatory Affairs and Officer – IPQA.
2. Where are these jobs located?
Both positions are listed in Vapi, Gujarat, India.
3. What qualifications are required?
B.Pharm and M.Pharm are the qualifications mentioned for both positions.
4. How much experience is required for Regulatory Affairs?
The Regulatory Affairs position requires 3–5 years of relevant experience.
5. Can freshers apply for the IPQA position?
The IPQA vacancy lists an experience range of 0–3 years, so freshers may be eligible, subject to the employer’s requirements.
6. What are the main responsibilities of the Regulatory Affairs role?
Responsibilities include dossier compilation, CMC documentation, stability data evaluation, regulatory submissions, technical questionnaires, and coordination with QA/QC teams.
7. What does the IPQA Officer do?
The IPQA Officer supports in-process quality activities, documentation review, cGMP compliance, deviation and CAPA records, and coordination with manufacturing and quality teams.
8. What is the salary for these positions?
Salary details have not been disclosed in the supplied listing.
9. How can candidates apply?
Candidates can email their CV to latesh.nemade@skant.com and specify the position in the subject line.
10. What is the last date to apply?
The supplied third-party listing does not specify an application deadline. Candidates should confirm current availability with the recruiter.
Disclaimer
This article is based on a third-party vacancy listing published on October 26, 2026. The job availability, eligibility criteria, recruiter contact details, salary, and employment terms have not been independently verified. Candidates should confirm the vacancy with S Kant Healthcare Ltd. or the listed recruiter before applying.