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Allwin Medical Devices Regulatory Affairs Jobs 2026
Published on: September 26, 2026
Allwin Medical Devices has a Regulatory Affairs opening in Kandivali, Mumbai, Maharashtra. The position is open to freshers as well as candidates with 2–5 years of experience.
The company has listed B.Pharm, M.Pharm and Mechanical Engineering among the eligible qualifications.
The role covers regulatory compliance along with quality-system activities such as QMS documentation, validation, calibration, CAPA, audits and quality control. For pharmacy graduates, this can be an opportunity to gain experience in the medical-device industry.
Job Status: Check the official Allwin Medical Devices career page for the latest vacancy status. You can also explore our Regulatory Affairs Jobs page for related openings and career guidance.
1. Allwin Medical Devices Regulatory Affairs Jobs 2026 – Job Details
| Particular | Details |
|---|---|
| Company | Allwin Medical Devices |
| Position | Regulatory Affairs |
| Industry | Medical Devices |
| Location | Kandivali, Mumbai, Maharashtra |
| Experience | Fresher or 2–5 years |
| Qualification | B.Pharm, M.Pharm, Mechanical Engineering |
| Salary | Not specified |
| Application Mode | Official Career Page / Email |
| hr@allwinmedical.com | |
| Contact | +91 93138 07505 |
| Application Status | Check the official career page for the current status |
2. Who Can Apply?
The vacancy is open to candidates with:
- B.Pharm
- M.Pharm
- Mechanical Engineering
The experience requirement is fresher or 2–5 years.
For B.Pharm and M.Pharm graduates, the position is relevant if you are interested in Regulatory Affairs, Quality Assurance, QMS or medical-device compliance.
3. What Will You Work On?
This is a broader regulatory and quality role rather than a position limited to regulatory submissions.
| Area | Main Work |
|---|---|
| Quality Management System | Documentation, implementation and improvement of the quality system |
| Regulatory Compliance | Maintaining compliance with applicable medical-device requirements |
| Quality Documentation | Managing procedures, records and other quality documents |
| Validation | Handling validation and manufacturing-process verification |
| Calibration | Managing the calibration programme |
| CAPA | Coordinating corrective and preventive actions |
| Audits | Maintaining internal and external audit records |
| Customer Complaints | Handling complaints and related feedback |
| Quality Control | Supporting QC activities in laboratory and sterilization areas |
| Management Review | Coordinating management reviews and reporting quality-system performance |
So, despite the Regulatory Affairs title, the role also has a significant quality-system and compliance component.
4. Skills Required
The company has mentioned the following skills and qualities:
- Good communication and interpersonal skills
- Relationship-building ability
- Computer knowledge
- Good Excel skills
- Negotiation and influencing skills
- Ability to work effectively
- Creative thinking
- Immediate availability
Freshers preparing for this type of role should be comfortable with the basics of QMS, SOPs, CAPA, validation, calibration, documentation and audits.
Only mention skills on your CV that you actually understand and can explain during an interview.
5. What Should Freshers Highlight in Their CV?
If you don’t have full-time industry experience, your internship and academic work can still demonstrate relevant knowledge.
| CV Section | What to Include |
|---|---|
| Education | B.Pharm/M.Pharm, college and graduation year |
| Internship | QA, RA, QC or other relevant industry exposure |
| Academic Project | Quality, regulatory, compliance or medical-device-related project |
| Technical Skills | Excel, documentation and relevant regulatory/quality knowledge |
| Certifications | Relevant quality or regulatory courses, if completed |
| Contact Details | Active phone number and professional email |
Keep the CV focused on the position. There is no need to add unrelated skills simply because they appear in the vacancy description.
6. Why This Role May Interest B.Pharm Graduates
This vacancy is in the medical-device sector, rather than a conventional pharmaceutical Regulatory Affairs role.
The responsibilities provide exposure to areas such as:
- Quality Management Systems
- Regulatory compliance
- Validation
- CAPA
- Audits
- Quality documentation
- Manufacturing-process verification
This type of experience can be relevant to future roles in Regulatory Affairs, Quality Assurance, QMS, validation and medical-device quality.
If you are new to Regulatory Affairs, our Career in Regulatory Affairs After B.Pharm guide covers the field, important skills and common entry-level roles.
7. How to Apply
Allwin Medical Devices has provided two ways to apply.
Option 1: Official Career Page
Visit the official Allwin Medical Devices career page and check the current Regulatory Affairs vacancy before applying.
Option 2: Send Your CV by Email
Send your updated CV to hr@allwinmedical.com.
Contact: +91 93138 07505
A suitable email subject line would be:
Application for Regulatory Affairs Position – B.Pharm/M.Pharm
Before sending your application, make sure your CV clearly shows your qualification, relevant internship or project experience, phone number and email address.
Before Applying
The available vacancy information does not specify a salary. Candidates should confirm the latest vacancy status, salary, selection process, joining requirements and other employment terms directly with the company.
8. Frequently Asked Questions
| Question | Answer |
|---|---|
| Is the Allwin Medical Devices Regulatory Affairs job open to freshers? | Yes. The company has specified Fresher or 2–5 years as the experience requirement. |
| Can B.Pharm candidates apply? | Yes. B.Pharm is listed among the eligible qualifications. |
| Can M.Pharm candidates apply? | Yes. M.Pharm is also listed. |
| Where is the job located? | The position is based in Kandivali, Mumbai, Maharashtra. |
| What is the salary? | The available vacancy information does not specify a salary. Candidates should confirm the compensation directly with the company. |
| Is this a pharmaceutical Regulatory Affairs job? | No. The position is in the medical-device industry and combines regulatory work with quality-system responsibilities. |
| What does the role involve? | The position includes regulatory compliance, QMS documentation, validation, calibration, CAPA, audits, customer complaints, and quality-control activities. |
| How can I apply? | You can apply through the official Allwin Medical Devices career page or send your CV to hr@allwinmedical.com. |
9. Related Opportunity
If you are also looking for government pharmacy opportunities, you can check our RRB Paramedical Recruitment 2026 update.
10. Important Note
This article is based on the Regulatory Affairs vacancy information provided by Allwin Medical Devices. The company has specified that the position is open to freshers and candidates with 2–5 years of experience.
The available vacancy information does not specify a salary. Candidates should verify the current vacancy and confirm employment terms directly with the company before accepting an offer.
PharmaCareerUpdates.com is an independent career-information website and is not affiliated with or officially associated with Allwin Medical Devices.
