Vaibhav Drugs Hiring QA Officers

B.Pharm, M.Pharm, MSc QA Officer Vacancies in Hyderabad

Vaibhav Drugs Pvt. Ltd hiring QA Officers in Hyderabad. B.Pharm, M.Pharm, MSc eligible. Freshers & experienced candidates can apply.

Vaibhav Drugs Pvt. Ltd has opened new hiring for Quality Assurance professionals at its Hyderabad facility. This opportunity is suitable for both fresh graduates and experienced candidates who want to build or strengthen a long-term career in pharmaceutical quality systems. The company is expanding its QA team to support regulated manufacturing operations and maintain compliance with national and international quality standards. Candidates with a strong understanding of GMP documentation, pharmaceutical quality control processes, and regulatory compliance will find this role aligned with industry expectations and future growth.

Company Overview

Vaibhav Drugs Pvt. Ltd is a growing pharmaceutical manufacturing company engaged in the development and production of quality pharmaceutical products for domestic and export markets. The organization follows strict quality management systems aligned with WHO-GMP and other regulatory guidelines. With a focus on patient safety, data integrity, and continuous improvement, Vaibhav Drugs has built a reputation for consistent product quality and regulatory compliance.

The company invests in skilled professionals, structured SOPs, and validated processes to ensure reliable manufacturing outcomes. Working at Vaibhav Drugs provides exposure to real-time quality assurance operations, audits, documentation control, and cross-functional collaboration with production, QC, and regulatory teams. This makes it an ideal workplace for candidates looking to grow within pharmaceutical quality assurance careers.

Job Role & Responsibilities

The Quality Assurance Officer / Senior Officer will be responsible for supporting and maintaining the pharmaceutical quality management system across manufacturing operations. The role requires hands-on involvement in documentation, compliance activities, and GMP implementation.

Key Responsibilities

• Preparation, review, and control of QA documentation including SOPs, BMRs, BPRs, protocols, and reports
• Ensuring compliance with GMP, GLP, and regulatory guidelines
• Review of batch manufacturing and packaging records before product release
• Handling deviations, change controls, CAPA, and risk assessments
• Supporting internal audits, external audits, and regulatory inspections
• Monitoring documentation control systems and data integrity practices
• Coordinating with production and quality control teams for issue resolution
• Assisting in training programs related to GMP and quality systems

This role plays a critical part in safeguarding product quality and regulatory compliance, directly impacting patient safety and company credibility.

Eligibility / Qualifications

Candidates applying for this position must meet the following educational and professional requirements.

Required Education

B.Pharmacy, M.Pharmacy, M.Sc (Pharmaceutical Sciences, Chemistry, Biotechnology, Microbiology, Biochemistry or other relevant life sciences disciplines)

Experience

• Minimum 2 years of experience in pharmaceutical quality assurance preferred
• Freshers with strong academic knowledge and GMP exposure can also apply

Preferred Skills

• Knowledge of QA documentation and pharmaceutical quality systems
• Understanding of GMP guidelines and regulatory compliance
• Attention to detail and documentation accuracy
• Ability to work in a regulated manufacturing environment

Location & Salary

• Job Location: Hyderabad, Telangana
• Salary: As per industry standards and based on qualification and experience

Candidates must be residents of Hyderabad, Telangana, or Andhra Pradesh, as per company hiring criteria.

Application Process

Interested and eligible candidates should apply by sharing their updated CV directly with the hiring team.

How to Apply:

• Send your updated resume via direct message (DM) as instructed by the company
• Shortlisted candidates will be contacted for further interview rounds

Early applications are encouraged due to limited vacancies and ongoing shortlisting.

Why Consider This Opportunity

• Entry-level and experienced QA roles available
• Exposure to real pharmaceutical GMP operations
• Career growth in pharmaceutical quality assurance and compliance
• Opportunity to work with an expanding pharma manufacturing company
• Strong learning environment for freshers entering the pharma industry

This role is especially suitable for candidates searching for pharma QA jobs in Hyderabad, quality assurance officer vacancies, pharmaceutical GMP documentation roles, and freshers QA jobs in pharma companies.

Frequently Asked Questions (FAQs)

Who can apply for this QA position?

Candidates with B.Pharm, M.Pharm, or M.Sc qualifications in relevant life sciences disciplines can apply. Both freshers and experienced professionals are eligible.

Is prior experience mandatory?

A minimum of 2 years of QA experience is preferred, but freshers with strong knowledge of GMP and documentation can also be considered.

What is the job location?

The position is based in Hyderabad, Telangana.

What skills are important for this role?

Key skills include GMP knowledge, QA documentation handling, attention to detail, and understanding of pharmaceutical quality systems.

How do I apply?

Interested candidates should send their updated CV via direct message as mentioned in the job notification.

Summary Table

Company                               Vaibhav Drugs Pvt. Ltd

Vacancies                               Multiple

Required Education               B.Pharmacy, M.Pharmacy, M.Sc (Relevant Disciplines)

Experience                             Freshers & Minimum 2 Years Experienced Candidates