Softgel Healthcare Hiring QA professionals

QA Executive 3–7 Yrs Openings at Softgel Healthcare Chennai

Softgel Healthcare hiring QA professionals (3–7 yrs) for new project plant in Chennai. B.Pharm/M.Pharm/M.Sc eligible. Apply now.

Softgel Healthcare Pvt. Ltd. is expanding with a new project plant in Chennai and is building a skilled Quality Assurance team to support its regulated manufacturing operations. This opportunity is designed for experienced QA professionals who want to contribute to a modern, compliance-driven facility aligned with global regulatory expectations.

Company Overview

Softgel Healthcare Pvt. Ltd. is a leading manufacturer of pharmaceutical and nutraceutical formulations, known for its robust quality systems and regulatory alignment across USFDA, EU, WHO, and MHRA markets. With a focus on advanced manufacturing and strong QA oversight, the company continues to invest in high‑quality infrastructure and skilled scientific talent.

Job Role & Responsibilities

Open Positions — Quality Assurance (QA)

The new project plant requires experienced QA professionals who can help establish and maintain high‑standard quality systems.

Key Areas:

• Qualification Team Member (IQ, OQ, PQ): Execution and documentation of equipment and system qualifications.
• QMS (Quality Management System): Handling deviations, CAPA, change control, and audit compliance.
• SOP Preparation & Review: Drafting, revising, and aligning SOPs with regulatory guidelines.
• Stability & Control Samples: Oversight of stability studies, sample management, and documentation.
• IPQA (In‑Process Quality Assurance): In‑line checks during manufacturing, packaging, and critical operations.
• AQA (Analytical Quality Assurance): Review of analytical data, COAs, raw data, and laboratory documentation.

Eligibility / Qualifications

• Education: B.Pharm / M.Pharm / M.Sc (Life Sciences, Chemistry)
• Experience: 3–7 years in QA within regulatory pharmaceutical manufacturing
• Preferred Skills:
  • Strong understanding of cGMP, GxP, and regulatory compliance
  • Experience with qualification protocols (IQ/OQ/PQ)
  • Hands‑on exposure to QMS activities
  • Ability to review analytical and manufacturing documentation
  • Audit readiness and documentation accuracy

Relevant courses (comma‑separated): B.Pharm, M.Pharm, M.Sc Chemistry, M.Sc Life Sciences, PG Diploma in Quality Assurance, Pharmaceutical Quality Management

Location & Salary

• Work Location: Chennai — New Project Manufacturing Plant
• Salary: As per industry standards and aligned with experience
• Growth Value: Exposure to state‑of‑the‑art facility, global regulatory operations, and cross‑functional learning opportunities.

Application Process

• Email: hr@softgelhealthcare.com
• Subject Line: Application – QA Team (New Project Plant – Chennai)
• Documents: Updated CV, experience proofs, certifications, and recent pay slips.

EEAT Alignment — Why This Role Matters

Working in QA at a new project plant provides visibility into system setup, regulatory alignment, and cross‑department collaboration. QA professionals here play a critical role in ensuring patient safety, regulatory compliance, and documentation integrity — core pillars of pharmaceutical quality.

FAQs

Q: Is regulatory experience mandatory?
A: Preferred, as the plant targets regulated markets like USFDA, EU, and WHO.

Q: Are QA freshers eligible?
A: No, this opening is for candidates with 3–7 years of experience.

Q: Does the role involve shift work?
A: Depends on IPQA and project timelines; details will be discussed during the interview.

Q: Is relocation support available?
A: Policies may vary; candidates may confirm during HR discussion.