AstraZeneca is a global, science-led biopharmaceutical company focused on discovering, developing, and commercializing prescription medicines. With a strong commitment to innovation, AstraZeneca works across oncology, cardiovascular, renal & metabolism, respiratory & immunology, and rare disease areas. The company fosters a collaborative, inclusive work environment where employees can grow and contribute to life-changing medicines.
Current Job Openings at AstraZeneca Bangalore
1. Job Title: Documentation Specialist – Clinical Pharmacology & Safety Science
Location: Bangalore, India
Job Type: Full-time
Posted: June 9, 2025
Last Date to Apply: June 23, 2025
Job Requisition ID: R-228514
Job Description:
As a Documentation Specialist in Clinical Pharmacology & Safety Science (CPSS), you will play a key role in supporting regulatory submissions and ensuring compliance with global standards. You will work closely with project teams to prepare high-quality clinical and regulatory documents.
Key Responsibilities:
- Prepare and compile regulatory submissions (e.g., CTD, ICH-GCP compliant documents).
- Ensure compliance with AstraZeneca’s submission-ready standards and regulatory requirements.
- Format, edit, and cross-reference submission documents (Word, PDF).
- Manage documents in validated electronic document management systems (eDMS).
- Provide training and support for ERV (Electronic Regulatory View) and SharePoint.
- Collaborate with cross-functional teams to maintain submission templates.
Qualifications & Experience:
- Bachelor’s degree (Life Sciences, Pharmacy, or related field).
- 1-2 years of experience in regulatory documentation, eDMS, or clinical submissions.
- Knowledge of GxP, ICH guidelines, and CTD structure.
- Proficiency in Microsoft Office, Adobe Acrobat, and SharePoint.
- Strong attention to detail and excellent English communication skills.
Desirable Skills:
- Experience with ISI Toolbox or regulatory submission tools.
- Understanding of CFR 21 Part 11 compliance.
2. Job Title: Senior Scientist – In Vitro Secondary Pharmacology
Location: Bangalore, India
Job Type: Full-time
Posted: June 10, 2025
Last Date to Apply: June 24, 2025
Job Requisition ID: R-227428
Job Description:
As a Senior Scientist, you will contribute to drug safety assessments by conducting in vitro pharmacological profiling to identify off-target risks. Your work will support early drug discovery and clinical development.
Key Responsibilities:
- Design and execute in vitro pharmacological assays (kinase profiling, radioligand binding, enzyme activity).
- Analyze off-target risks and interpret data for safety assessments.
- Collaborate with CROs (Contract Research Organizations) for high-quality data.
- Translate in vitro findings into preclinical and clinical safety insights.
- Support regulatory submissions with scientific documentation.
Qualifications & Experience:
- PhD / Master’s degree in Pharmacology, Toxicology, Biochemistry, or related field.
- 4+ years of industry experience in drug safety, in vitro pharmacology, or kinase profiling.
- Expertise in assay development, high-throughput screening (HTS), and cell-based models.
- Strong problem-solving, data interpretation, and communication skills.
Desirable Skills:
- Experience in regulatory safety assessments.
- Knowledge of emerging trends in pharmacovigilance.
Why Join AstraZeneca?
- Innovative Science: Work on cutting-edge drug development in a global biopharma leader.
- Career Growth: Opportunities for lifelong learning and leadership development.
- Hybrid Work Model: Flexible 3-days office, 2-days remote policy.
- Inclusive Culture: A diverse workplace that fosters collaboration and bold thinking.
How to Apply?
Application Link for Documentation Specialist – Clinical Pharmacology & Safety Science
Application Link for Senior Scientist – In Vitro Secondary Pharmacology
