Ind Swift Hiring RA & FRD
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs (RA) – Officer to Executive
- Formulation Research & Development (FRD) – Tablets & Capsules
- Formulation Research & Development (FRD) – Ointments
- Eligibility / Qualifications
- Key Skills Required
- Location & Salary
- Application Process
- Why Consider This Opportunity?
- FAQs
- What is the qualification required for Ind Swift Labs hiring?
- Is prior USFDA experience mandatory?
- What is the experience range for these roles?
- How can I apply for this job?
- Are freshers eligible for this role?
- Additional SEO Title Ideas
- Summary Table
M.Pharm RA & FRD Jobs at Ind Swift Labs Panchkula
M.Pharm candidates apply for RA & FRD roles at Ind Swift Labs Panchkula with multiple vacancies and 3–10 years experience.
Ind Swift Laboratories Limited is actively hiring skilled professionals in Regulatory Affairs and Formulation Research & Development (FRD) for its Panchkula facility. This opportunity is ideal for M.Pharm graduates with hands-on experience in OSD formulations and exposure to regulated markets such as USFDA, MHRA, and EU guidelines. With increasing global demand for compliant pharmaceutical products, roles like these are critical in ensuring quality, safety, and regulatory adherence in drug development and manufacturing.
Professionals seeking high-growth pharma jobs in India, especially in regulatory affairs jobs, formulation development jobs, and USFDA pharma jobs, will find this opportunity aligned with long-term career advancement. Ind Swift Laboratories is known for its strong compliance culture and export-focused manufacturing, making it a reliable employer in the pharmaceutical industry.
Company Overview
Ind Swift Laboratories Limited is a well-established pharmaceutical company with a strong presence in API manufacturing and finished dosage formulations. The company operates with strict adherence to international regulatory standards including USFDA, MHRA, and EU GMP guidelines.
With a focus on innovation, compliance, and global healthcare delivery, Ind Swift plays a significant role in supplying high-quality pharmaceutical products across regulated and semi-regulated markets. The company’s commitment to quality assurance and regulatory excellence makes it a trusted name in the pharma industry.
Job Role & Responsibilities
Regulatory Affairs (RA) – Officer to Executive
- Prepare and review regulatory dossiers for global submissions
- Handle documentation for EU, MHRA, and USFDA markets
- Ensure compliance with international regulatory guidelines
- Coordinate with cross-functional teams for submission readiness
- Maintain updated knowledge of regulatory frameworks and changes
Formulation Research & Development (FRD) – Tablets & Capsules
- Develop and optimize OSD formulations (tablets and capsules)
- Conduct pre-formulation and compatibility studies
- Execute scale-up and technology transfer activities
- Maintain documentation as per regulatory requirements
- Ensure product stability and performance
Formulation Research & Development (FRD) – Ointments
- Develop topical formulations including ointments
- Conduct formulation trials and stability studies
- Optimize formulation processes for commercial production
- Ensure compliance with regulatory and quality standards
These roles are critical in ensuring the development of safe, effective, and compliant pharmaceutical products for global markets.
Eligibility / Qualifications
Candidates must meet the following criteria:
- Qualification: M.Pharm
- Relevant Courses: Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Analysis, Industrial Pharmacy, Regulatory Affairs
- Experience:
- RA: 3 to 6 years
- FRD Tablets/Capsules: 4 to 8 years
- FRD Ointments: 5 to 10 years
Key Skills Required
- Strong knowledge of OSD formulation development
- Experience in USFDA, EU GMP, and MHRA regulatory environments
- Hands-on experience in dossier preparation and submission
- Understanding of pharmaceutical quality systems and compliance
- Analytical and problem-solving skills
Location & Salary
- Location: Panchkula (Chandigarh)
- Salary: Competitive and aligned with industry standards (based on experience and expertise)
Application Process
Interested and eligible candidates can apply using the details below:
- Email: hrbp.rd@indswiftlabs.com
- WhatsApp: 8894599858
Candidates are advised to mention the applied department (RA/FRD) clearly in the subject line for faster processing.
Why Consider This Opportunity?
- Work in a USFDA-approved pharmaceutical company
- Exposure to global regulatory markets (EU, MHRA, USFDA)
- Strong career growth in regulatory affairs and formulation R&D
- Opportunity to work on export-oriented pharma projects
FAQs
What is the qualification required for Ind Swift Labs hiring?
M.Pharm in relevant specializations such as Pharmaceutics or Regulatory Affairs is required.
Is prior USFDA experience mandatory?
Yes, candidates must have experience working in USFDA, EU, or MHRA approved facilities.
What is the experience range for these roles?
The roles require 3 to 10 years of experience depending on the department.
How can I apply for this job?
You can send your resume to hrbp.rd@indswiftlabs.com or apply via WhatsApp at 8894599858.
Are freshers eligible for this role?
No, these roles require prior industry experience in regulatory or formulation development.
Additional SEO Title Ideas
- Ind Swift Labs Hiring M.Pharm RA & FRD Professionals
- Regulatory Affairs & Formulation Jobs in Panchkula Pharma Industry
- USFDA Pharma Jobs for M.Pharm Candidates at Ind Swift Labs
Summary Table
| Category | Details |
|---|---|
| Company | Ind Swift Laboratories Limited |
| Vacancies | RA Officer, RA Executive, FRD Research Scientist (Tablets/Capsules), FRD Ointments Specialist |
| Required Education | M.Pharm (Pharmaceutics, Pharmaceutical Chemistry, Pharmaceutical Analysis, Industrial Pharmacy, Regulatory Affairs) |
| Experience | 3–10 Years |
You must sign in to apply for this position.