- Location
- Hyderabad, IN · Telangana, India
- Department
- Product Development
- Seniority
- Senior
- Experience
- 8+ years
- Education
- Bachelor
- Source
- Greenhouse
Description
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
About the Role
We are seeking a highly motivated Project Manager to lead cross-functional pharmaceutical development programs from concept through commercialization. The role is responsible for planning, coordinating, and monitoring project activities, ensuring alignment between internal stakeholders and external partners (CMOs, CROs, and CDMOs). The Project Manager will drive execution against timelines, budgets, quality standards, and business objectives while proactively identifying and mitigating project risks. The person we select for this role will play a key part in Azurity’s scientific excellence, contribution to patient care and growth of business.
Key Responsibilities
- Develop and maintain integrated project plans, timelines, budgets, and resource plans.
- Coordinate cross-functional teams including R&D, Regulatory Affairs, Quality, Supply Chain, Commercial, and external partners.
- Manage project schedules through critical path analysis and identify opportunities to accelerate timelines.
- Track project progress, milestones, risks, dependencies, and action items, ensuring timely resolution of issues.
- Lead project governance meetings and provide status updates to senior leadership.
- Facilitate technology transfer, development, validation, registration, and launch activities.
- Coordinate external service providers, CMOs, CROs, and vendors to ensure project deliverables are met.
- Support budget planning, forecasting, and cost management for assigned projects.
- Ensure compliance with quality systems, regulatory requirements, and company procedures.
- Prepare project reports, management presentations, risk assessments, and executive summaries.
Required Skills and Experience
- Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Engineering, Life Sciences, or a related discipline with PMP and relevant project plaining certification.
- 8–15 years of experience in pharmaceutical product development, technical operations, project management, or related functions.
- Demonstrated experience managing multiple complex projects simultaneously.
- Experienced in developing complex ANDAs or NDA products for regulated markets.
- Strong project planning, scheduling, and risk management skills.
- Knowledge of pharmaceutical development, regulatory pathways, technology transfer, validation, and commercialization processes.
- Strong analytical thinking, problem-solving, and decision-making capabilities.
Preferred Qualifications
- Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Engineering, Life Sciences, or a related discipline with PMP and relevant project plaining certification.
By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
