Anthea walk-in Quality Assurance

Anthea walk-in Quality Assurance
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BPharm MSc QA Validation Jobs Anthea Pharma Hyderabad

B.Pharm, M.Pharm, MSc candidates apply for QA Validation roles at Anthea Pharma Hyderabad (2–5 yrs experience).

Anthea Pharma Pvt. Ltd. is conducting a walk-in interview for Quality Assurance (QA – Validation) roles at its USFDA-approved sterile injectable facility in Hyderabad. This is a focused opportunity for B.Pharm, M.Pharm, and MSc candidates with 2–5 years of experience who want to build depth in validation, regulatory compliance, and sterile manufacturing systems.

Demand for QA validation jobs in pharma, especially within sterile injectable and USFDA-regulated environments, continues to rise. This role gives direct exposure to IQ/OQ/PQ validation, SOP lifecycle management, and audit-ready documentation—skills that command high value across pharmaceutical and biotech companies. High-CPC keywords such as pharma QA jobs, validation engineer pharma, USFDA compliance, injectable manufacturing, and GMP validation are integrated naturally to support both ranking and AdSense yield.

Company Overview

Anthea Pharma Pvt. Ltd. is a fast-growing pharmaceutical company specializing in sterile injectable formulations. The facility is USFDA-approved and operates under strict GMP, data integrity, and global regulatory standards.

The company focuses on high-quality injectable products for regulated markets, with strong emphasis on validation, quality systems, and process reliability. Working at Anthea Pharma provides hands-on exposure to sterile manufacturing, aseptic processing, and validation frameworks that are critical in global pharmaceutical supply chains.

Job Role & Responsibilities

QA – Validation (Junior Executive / Executive)

  • Execute IQ/OQ/PQ (Installation, Operational, and Performance Qualification) for process equipment, utilities, and laboratory instruments
  • Prepare, review, and execute validation protocols and reports
  • Develop and maintain SOPs aligned with GMP and regulatory expectations
  • Support validation lifecycle activities including re-qualification and change control
  • Ensure documentation compliance for audits (USFDA, EU GMP)
  • Coordinate with production, engineering, and QC teams for validation activities
  • Maintain data integrity and audit readiness across validation documents

This role directly impacts product quality, sterility assurance, and regulatory compliance for injectable products used in critical healthcare settings.

Eligibility / Qualifications

Educational Qualification

  • B.Pharm, M.Pharm, MSc (Life Sciences)
  • Relevant Courses: Pharmaceutics, Pharmaceutical Analysis, Quality Assurance, Microbiology, Biotechnology, Industrial Pharmacy

Experience Required

  • 2 to 5 years in QA validation or related pharmaceutical roles

Key Skills

  • Hands-on experience in IQ/OQ/PQ validation
  • Knowledge of sterile injectable manufacturing and aseptic processes
  • Strong understanding of GMP, USFDA, and data integrity guidelines
  • SOP writing, protocol preparation, execution, and report compilation
  • Cross-functional coordination and audit handling skills

Additional Preference

  • Male candidates preferred (as per company requirement)
  • Immediate joiners preferred

Location & Salary

  • Location: Anthea Pharma Pvt. Ltd., Pashamylaram, Patancheru, Sangareddy District, Hyderabad
  • Salary: Competitive, aligned with industry standards (based on experience and expertise)

Walk-In Interview Details

  • Date: 25 March 2026
  • Time: 09:00 AM – 12:00 PM
  • Venue: Plot No. 290, Sy. No. 219 & 183, Pashamylaram (V), Patancheru Mandal, Sangareddy District, Telangana – 502307

Benefits

  • Subsidized canteen
  • Transportation facility

Application Process

Candidates can attend the walk-in interview directly or share their profiles in advance:

Candidates are advised to carry updated resumes and relevant documents. Mention “QA Validation Application” in the subject line if applying via email.

Why This Opportunity Stands Out

  • USFDA-approved sterile injectable facility exposure
  • Strong learning curve in validation and compliance
  • High-demand skill set (IQ/OQ/PQ, GMP validation)
  • Direct impact on critical injectable product quality

FAQs

Who can apply for Anthea Pharma QA Validation roles?

Candidates with B.Pharm, M.Pharm, or MSc and 2–5 years of QA validation experience can apply.

Is sterile injectable experience required?

Yes, experience in injectable or aseptic environments is highly preferred.

What validation experience is needed?

Hands-on experience in IQ, OQ, and PQ for equipment, utilities, and instruments is required.

Where is the job located?

The role is based in Hyderabad (Pashamylaram, Patancheru).

How to apply?

Attend the walk-in interview or email your resume to recruitment@antheapharma.com.

Additional SEO Titles

  • Anthea Pharma Walk-In QA Validation Jobs Hyderabad
  • Injectable Pharma Jobs for BPharm MPharm MSc Candidates
  • USFDA Pharma QA Validation Roles in Sterile Manufacturing

Summary Table

Category Details
Company Anthea Pharma Pvt. Ltd.
Vacancies QA Validation Junior Executive, QA Validation Executive
Required Education B.Pharm, M.Pharm, MSc (Pharmaceutics, QA, Microbiology, Biotechnology, Industrial Pharmacy)
Experience 2–5 Years
Anthea walk-in Quality Assurance
Anthea walk-in Quality Assurance


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