Aurobindo Hiring Formulation R&D OSD

M.Pharm Formulation R&D OSD Vacancy – Hyderabad

M.Pharm Formulation R&D OSD role at Aurobindo Pharma, Hyderabad. 5–7 years experience required. Apply now for regulated market projects.

Aurobindo Pharma is expanding its Formulation Research & Development team and invites experienced formulation scientists to join its Oral Solid Dosage (OSD) division in Hyderabad. This opportunity is ideal for professionals who want to work on complex dosage forms, global regulatory submissions, and large-scale product development programs for regulated markets such as the US and EU. The role offers direct exposure to end-to-end formulation development, from concept to commercialization, within a globally respected pharmaceutical organization.

Company Overview

Aurobindo Pharma is one of India’s leading global pharmaceutical companies with a strong presence across generic medicines, APIs, specialty formulations, and biosimilars. The company supplies high-quality pharmaceutical products to over 150 countries, with a significant footprint in regulated markets including the United States, Europe, and other advanced healthcare regions.

With state-of-the-art R&D infrastructure and a strong culture of scientific innovation, Aurobindo Pharma continues to invest heavily in formulation development, technology transfer, and lifecycle management of complex dosage forms. The organization is known for its compliance-driven approach, strong regulatory track record, and consistent delivery of affordable medicines that improve global healthcare outcomes.

Job Role & Responsibilities

As part of the Formulation R&D (OSD) team, the selected professional will be responsible for developing, optimizing, and transferring oral solid and liquid dosage forms for regulated markets. This role demands strong technical expertise, problem-solving ability, and hands-on execution across multiple formulation platforms.

Key responsibilities include:

• Leading and supporting development of oral solid dosage forms such as Immediate Release (IR), Extended Release (ER), Delayed Release (DR), Modified Release (MR), and pellet-based formulations
• Contributing to formulation development of oral liquid dosage forms where applicable
• Managing formulation development projects for regulated markets including US FDA and EU authorities
• Designing, executing, and evaluating formulation trials using Quality by Design (QbD) principles
• Performing scale-up, exhibit batch manufacturing, and technology transfer activities
• Coordinating with pilot plant, manufacturing, and analytical teams during scale-up and validation
• Investigating formulation challenges and implementing scientifically sound solutions
• Preparing formulation development reports and technical documentation
• Responding to formulation-related queries from regulatory agencies
• Conducting patent evaluations, freedom-to-operate assessments, and literature surveys
• Supporting ANDA and regulatory submission activities
• Ensuring compliance with cGMP, ICH guidelines, QbD frameworks, and global regulatory expectations

Eligibility / Qualifications

Educational Requirements

Candidates must possess a postgraduate qualification in pharmacy with specialization in pharmaceutics.

Relevant educational qualifications include:
M.Pharm (Pharmaceutics), M.Pharm Pharmaceutical Technology, M.Pharm Industrial Pharmacy

Experience Requirements

• 5 to 7 years of hands-on experience in formulation research and development
• Proven experience in Oral Solid Dosage formulation development
• Prior exposure to regulated market development projects is mandatory
• Experience with scale-up, exhibit batches, and technology transfer is essential

Technical & Professional Skills

• Strong understanding of formulation principles for IR, ER, DR, MR, and pellet-based dosage forms
• Practical experience with formulation trials, optimization, and troubleshooting
• Working knowledge of regulatory requirements for US and EU markets
• Familiarity with cGMP, ICH, QbD, and lifecycle management concepts
• Ability to interpret patents, scientific literature, and regulatory guidance documents
• Strong documentation, data analysis, and technical writing skills
• Ability to work collaboratively in cross-functional teams
• High attention to detail and compliance-driven mindset

Location & Salary

• Job Location: Hyderabad, Telangana
• Department: Formulation R&D – Oral Solid Dosage
• Employment Type: Full-time
• Salary: Competitive and commensurate with experience and technical expertise

Application Process

Interested and eligible candidates should apply by sharing their updated resume via email.

Email ID: Pooja.Uppalapati@aurobindo.com
Subject Line: Application for FRD

Shortlisted candidates will be contacted for further technical and HR discussions.

Why Join Aurobindo Pharma?

• Opportunity to work on complex and differentiated formulations
• Direct involvement in regulated market product development
• Exposure to global regulatory strategies and submissions
• Strong learning environment with experienced formulation scientists
• Career growth within a globally established pharmaceutical organization

Frequently Asked Questions (FAQs)

Is experience in regulated markets mandatory?
Yes. This role focuses on development for US and EU markets, and prior regulated market exposure is required.

Is this role limited to oral solid dosage only?
The primary focus is Oral Solid Dosage, with limited exposure to oral liquid formulations where applicable.

Does this role involve technology transfer?
Yes. Scale-up, exhibit batch manufacturing, and technology transfer are core responsibilities.

Is relocation to Hyderabad required?
Yes. This is an on-site role based in Hyderabad.

Are referrals accepted?
Yes. Referrals are welcome.

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Company	Aurobindo Pharma
Vacancies	Not Disclosed
Required Education	M.Pharm (Pharmaceutics)
Experience	5–7 Years