Entry Level Life Science Jobs at Azurity Pharmaceuticals
Looking to begin your career in the pharmaceutical industry? This entry-level life science job opportunity at Azurity Pharmaceuticals Careers is an excellent choice for fresh graduates and early-career professionals. The Associate, Drug Safety – Quality, Standards & Training position in Hyderabad offers candidates the opportunity to work in pharmacovigilance, quality systems, and drug safety while building a rewarding career in the life sciences sector. If you are searching for Drug Safety Jobs with a globally recognized pharmaceutical company, this opportunity deserves your attention.
About the Company
Azurity Pharmaceuticals is a specialty pharmaceutical company dedicated to developing innovative medicines that address unmet patient needs. The organization focuses on creating high-quality pharmaceutical products while maintaining the highest standards of safety, regulatory compliance, and patient care. With a strong commitment to innovation and employee development, Azurity offers excellent career opportunities for professionals looking to build successful careers in life sciences and healthcare.
Job Details:
- Job Title: Associate, Drug Safety – Quality, Standards & Training
- Company: Azurity Pharmaceuticals
- Location: Hyderabad, Telangana, India
Role Overview
The Associate, Drug Safety – Quality, Standards & Training position at Azurity Pharmaceuticals supports the Global Drug Safety organization by maintaining quality systems, standards, audits, and training activities. The role plays a key part in ensuring inspection readiness, supporting compliance with global pharmacovigilance (PV) regulations, and promoting the consistent execution of drug safety processes through effective documentation, quality management, and training coordination.
Reporting to the Manager, Drug Safety Compliance, the Associate collaborates with Drug Safety Operations, Compliance, Quality, Regulatory Affairs, Clinical teams, and other cross-functional stakeholders to support quality and compliance initiatives across the organization.
Key Responsibilities
- Supports the maintenance and administration of Drug Safety Standard Operating Procedures (SOPs), work instructions, and quality standards, including document updates and version control.
- Coordinates Drug Safety training programs, including onboarding and periodic refresher training for team members.
- Tracks training completion, maintains training records, and prepares reports on training compliance metrics.
- Assists in preparing for regulatory inspections and internal or external pharmacovigilance audits.
- Organizes and maintains inspection-ready documentation and training records to ensure regulatory compliance.
- Collaborates with Drug Safety Operations, Compliance, Quality, Regulatory Affairs, and Clinical teams to ensure consistent implementation of standards and training requirements.
- Serves as a coordination point for quality- and training-related communications within the Drug Safety function.
- Supports global Drug Safety initiatives requiring standardized processes, documentation, and training support.
- Contributes to continuous improvement initiatives that enhance quality systems and operational efficiency within the Global Drug Safety organization.
Educational Requirements
- Bachelor’s degree in one of the following disciplines: Life Sciences & Related fields
Required Qualifications
- 1–3 years of experience in Pharmacovigilance, Quality, Compliance, Training, or related roles within pharmaceutical, biotechnology, or regulated healthcare environments.
- Experience supporting quality systems, SOP management, document control, and/or training coordination is preferred.
- Strong understanding of pharmacovigilance principles and regulated quality environments.
- Ability to maintain accurate documentation and ensure compliance with global regulatory requirements.
- Strong organizational, communication, and coordination skills with the ability to work effectively across cross-functional teams.
- Detail-oriented with a commitment to quality, compliance, and continuous improvement.
