Hetero Hiring Executive – DQA (Formulation R&D)

M.Pharm Pharmaceutics – Executive DQA | Hyderabad

Apply for Executive – DQA (Formulation R&D) at Hetero, Hyderabad. Open for M.Pharm Pharmaceutics graduates with 2–5 years experience.

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Hetero, a leading pharmaceutical organization, is seeking a motivated Executive – DQA to join its Formulation R&D team in Hyderabad. This role offers an exciting opportunity for professionals with a background in pharmaceutics to actively contribute to the development, documentation, and quality assurance of innovative pharmaceutical formulations while ensuring compliance with global regulatory standards.

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Company Overview

Hetero Labs Ltd. is a globally recognized pharmaceutical company with a strong commitment to research, development, and manufacturing of high-quality formulations. Known for its innovation in generic medicines, APIs, and biologics, Hetero serves patients across multiple therapeutic areas worldwide. The organization prides itself on maintaining robust Quality Management Systems (QMS), GMP compliance, and fostering a culture of scientific excellence and ethical standards. Hetero’s Hyderabad R&D center plays a critical role in product innovation, process development, and lifecycle management.

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Job Role & Responsibilities

As an Executive – DQA (Formulation R&D), you will be responsible for ensuring the quality and compliance of formulation development activities. Key responsibilities include:

• Review and evaluation of Formulation Development Documents to ensure accuracy and compliance.

• Assess Master Formulation/Process Control (MFC/MPC), Product Development Reports (PDR), and scale-up documentation.

• Ensure that the Formulation Laboratory adheres to established GMP and SOP standards.

• Support Quality Management System (QMS) activities, including deviations, CAPAs, and audits.

• Collaborate with Formulation Scientists, Analytical Teams, and Production Units for smooth product development and approval processes.

• Maintain thorough documentation to support regulatory submissions and product lifecycle management.

• Actively contribute to continuous improvement initiatives in formulation processes and quality systems.

This role requires attention to detail, regulatory awareness, and proficiency in documentation review, ensuring that all R&D activities meet both internal and external compliance requirements.

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Eligibility / Qualifications

Educational Requirements:

• M.Pharm in Pharmaceutics

Experience:

• 2–5 years in pharmaceutical formulation development or quality assurance roles.

Skills & Competencies:

• Strong understanding of product development and formulation processes.

• Knowledge of GMP, QMS, and regulatory compliance for pharmaceutical R&D.

• Excellent documentation, review, and analytical skills.

• Effective communication and team collaboration abilities.

• Ability to work under tight deadlines and manage multiple documentation tasks simultaneously.

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Location & Work Type

Location: Hyderabad, India
Job Type: Full-time
Salary: Commensurate with experience and industry standards

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Application Process

Interested candidates are requested to share their updated resumes via email:

vijaybabu.r@hetero.com

Tip: Include a cover letter highlighting relevant experience in formulation development, quality assurance, and compliance. Immediate joiners will be preferred due to urgent requirements.

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Why Join Hetero?

• Work in a leading pharmaceutical R&D organization with global recognition.

• Gain exposure to formulation development, documentation, and QMS activities.

• Enhance your professional growth with hands-on experience in regulatory-compliant formulation processes.

• Collaborate with a dynamic team of experts in pharmaceutical R&D and quality assurance.

• Contribute to innovative drug development that impacts patient care worldwide.

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FAQs – Executive DQA (Formulation R&D) at Hetero

Q1. Who is eligible for this role?
Candidates with M.Pharm in Pharmaceutics and 2–5 years of relevant experience.

Q2. Is prior formulation R&D experience mandatory?
Yes, experience in formulation development, documentation, and QMS compliance is required.

Q3. How do I apply?
Submit your resume to vijaybabu.r@hetero.com with a brief cover letter highlighting your relevant experience.

Q4. What is the preferred joining timeline?
Immediate joiners are highly preferred due to urgent recruitment requirements.

Q5. What is the role’s primary focus?
Ensuring accuracy, compliance, and quality of formulation R&D documents while supporting product lifecycle management and QMS activities.

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