Formulation Development Jobs in Hyderabad: Azurity Pharmaceuticals is Hiring
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Azurity Pharmaceuticals is seeking a Formulation Development Scientist in Hyderabad to lead the development, scale-up, and optimization of innovative pharmaceutical products. This role focuses on oral dosage forms, process development, and global product development projects across markets including the US, EU, and China. Ideal for candidates who are looking for Formulation Development Jobs in Hyderabad with 3–6 years of industrial experience in pharmaceutical formulation and a strong commitment to delivering high-quality, patient-centric medications.
Job Details:
- Job Title: Formulation Development Scientist
- Location: Hyderabad
About the Company:
Azurity Pharmaceuticals is a privately held specialty pharmaceutical company focusing on innovative products for underserved patients. The company’s patient-centric portfolio spans cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, benefiting millions globally. Azurity combines integrated capabilities and a vast partner network to deliver high-quality medications and maintain a robust late-stage pipeline. The company promotes an inclusive work environment and is an Equal Opportunity Employer.
Education Requirements:
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M. Pharm or Ph.D. in Pharmacy with 3–6 years of industrial experience in pharmaceutical development and product scale-up.
Key Responsibilities:
- Design, conduct, and supervise formulation development, process optimization, scale-up, and manufacturing of products.
- Prepare and review documents including Batch Records, Product Development reports, SOPs, Stability protocols, Raw/Packaging material specifications, and labelling.
- Review test results, identify causes of variances, and recommend solutions to meet project goals.
- Schedule experiments and prioritize tasks to meet project objectives and deadlines.
- Maintain laboratory equipment and follow company safety standards.
- Conduct experiments, document results, and prepare reports with conclusions and recommendations.
- Develop new laboratory procedures or improve existing procedures to meet project objectives.
- Identify and manage potential risks within complex projects promptly.
- Record accurate experimental methods and results in compliance with good documentation practices (GDP).
- Act as the primary scientific contact for external collaborators.
- Manage inventory of supplies and raw materials.
- Ensure timely completion of all required training.
Skills:
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Expertise in oral dosage forms, including modified release, extended release, targeted release, immediate release, solid, suspensions, or solutions.
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Experience in global product development for US, EU, China, and ROW markets.
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Preferred experience in developing branded and differentiated products, especially 505(b)(2) category.
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Experience working with CROs/CDMOs preferred.
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Proficiency in Microsoft Office applications.
