Ind Swift Laboratories Hiring FRD, RA, DQA

M.Pharm & B.Pharm Roles | Ind Swift Labs Panchkula

Ind Swift Laboratories invites M.Pharm/B.Pharm professionals for FRD, RA, DQA roles in Panchkula. EU/USFDA/MHRA experience required.

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Ind Swift Laboratories Limited, a pioneer in pharmaceutical innovation, is inviting qualified professionals to apply for multiple key roles in its Panchkula facility. Candidates with strong formulation, regulatory, and quality assurance experience in OSD manufacturing at EU, USFDA, or MHRA-approved facilities are encouraged to apply.

Company Overview

Ind Swift Laboratories is a research-driven pharmaceutical company, committed to delivering high-quality, affordable medicines globally. Operating across Formulation Research Development (FRD), Regulatory Affairs (RA), and Drug Quality Assurance (DQA), the organization fosters a culture of innovation, compliance, and scientific excellence. Employees gain exposure to cutting-edge research, international regulatory standards, and a dynamic work environment.

Job Role & Responsibilities

FRD (Formulation Research Development) – Technology Transfer

Designation: Executive/Scientist
Qualifications: M.Pharm
Experience: 3–8 years

Responsibilities:

• Transfer formulations from R&D to production scale.
• Optimize manufacturing processes and resolve technical issues.
• Prepare technical documentation and reports for regulatory compliance.
• Collaborate with cross-functional teams for smooth technology transfer.

FRD – Research Associate/Research Scientist

Designation: Research Associate/Research Scientist
Qualifications: M.Pharm
Experience: 4–10 years

Responsibilities:

• Design, execute, and analyze formulation experiments.
• Develop and optimize OSD formulations for commercial manufacturing.
• Maintain detailed lab records and technical documentation.
• Ensure adherence to quality and regulatory standards.

RA (Regulatory Affairs)

Designation: Executive
Qualifications: M.Pharm
Experience: 3–6 years

Responsibilities:

• Prepare and submit regulatory documents for approvals.
• Ensure compliance with EU, USFDA, and MHRA regulations.
• Maintain updated knowledge of post-approval guidelines.
• Coordinate with internal teams to support regulatory submissions.

DQA (Drug Quality Assurance)

Designation: Executive/Senior Officer
Qualifications: B.Pharm
Experience: 5–8 years

Responsibilities:

• Conduct quality audits and ensure compliance with GMP.
• Prepare and review SOPs, formats, and schedules.
• Manage documentation and reporting for regulatory inspections.
• Support continuous improvement initiatives in quality systems.

Eligibility / Qualifications

• Educational Background: M.Pharm (FRD, RA), B.Pharm (DQA)
• Experience: 3–10 years in relevant roles
• Special Requirements: Hands-on experience in OSD formulation, exposure to EU, USFDA, or MHRA-approved facilities

Location & Salary

• Location: Panchkula, Chandigarh
• Salary: Competitive, based on experience and role

Application Process

Interested candidates should submit their resumes to hrbp.rd@indswiftlabs.com or via WhatsApp at 8894599858. Ensure all relevant certifications, experience documents, and contact information are included.

Urgent CTA: Apply now to secure your position in a globally recognized pharmaceutical organization.

FAQs

Q1: Can freshers apply for these positions?
No, candidates must have 3–10 years of relevant experience.

Q2: Is prior regulatory exposure mandatory?
Yes, experience in EU, USFDA, or MHRA-approved facilities is required.

Q3: What are the key skills required for FRD roles?
Formulation development, technology transfer, OSD manufacturing, documentation, and process optimization.

Q4: Can candidates apply via WhatsApp?
Yes, resumes can be sent to 8894599858 for quick consideration.

Q5: Are there multiple openings across departments?
Yes, positions are available in FRD, RA, and DQA departments.

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Job Summary Table

Category	Details
Company	Ind Swift Laboratories Limited
Vacancies	FRD, RA, DQA positions
Required Education	M.Pharm, B.Pharm
Experience	3–10 years

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