Job Description
Teva Pharmaceuticals
Teva Pharmaceuticals Hiring Manager – Regulatory Affairs (Sterile/Injectables) | Bangalore
Teva Pharmaceuticals • Bengaluru, Karnataka • via Pharma Jobs Post
9 hours ago
Full–time
Apply on Pharma Jobs Post
Apply directly on Pharma Stuff
Job description
Teva Pharmaceuticals, a global leader in generic and specialty medicines, is inviting applications from skilled professionals for a key role in Regulatory Affairs at its Bangalore location.
📍 Position: Manager – Regulatory Affairs (Complex Drugs – Sterile/Injectables, USFDA)
🏢 Location: Bangalore
💼 Work Mode: Hybrid (3 days Work from Office)
About the Role
Are you an experienced Regulatory Affairs professional ready to take on challenging and impactful responsibilities?
Join Teva’s dynamic team and contribute to global health by driving regulatory submissions and compliance for sterile and injectable products in the US market.
Key Requirements
• Experience: 10+ years in the pharmaceutical industry, with at least 8 years in Regulatory Affairs for sterile products (pre- and post-approval).
• Expertise: Strong knowledge of USFDA regulatory processes for complex sterile/injectable drugs.
• Qualification: M. Pharm or Pharm D.
• Skills:
• Regulatory submission strategy and lifecycle management.
• Familiarity with eCTD submissions and regulatory databases.
• Excellent communication and cross-functional collaboration abilities.
Why Join Teva?
At Teva, we’re dedicated to enhancing the quality of life for patients worldwide through science, innovation, and commitment. Join a global team that values excellence, integrity, and impact.
📩 Interested Candidates:
Send your updated CV to Apeksha.Shinde01@teva.co.in
Please send your updated CV to me Email ID: Apeksha.Shinde01@teva.co.in
Teva Pharmaceuticals Hiring Manager – Regulatory Affairs (Sterile/Injectables) | Bangalore
Teva Pharmaceuticals • Bengaluru, Karnataka • via Pharma Jobs Post
9 hours ago
Full–time
Apply on Pharma Jobs Post
Apply directly on Pharma Stuff
Job description
Teva Pharmaceuticals, a global leader in generic and specialty medicines, is inviting applications from skilled professionals for a key role in Regulatory Affairs at its Bangalore location.
📍 Position: Manager – Regulatory Affairs (Complex Drugs – Sterile/Injectables, USFDA)
🏢 Location: Bangalore
💼 Work Mode: Hybrid (3 days Work from Office)
About the Role
Are you an experienced Regulatory Affairs professional ready to take on challenging and impactful responsibilities?
Join Teva’s dynamic team and contribute to global health by driving regulatory submissions and compliance for sterile and injectable products in the US market.
Key Requirements
• Experience: 10+ years in the pharmaceutical industry, with at least 8 years in Regulatory Affairs for sterile products (pre- and post-approval).
• Expertise: Strong knowledge of USFDA regulatory processes for complex sterile/injectable drugs.
• Qualification: M. Pharm or Pharm D.
• Skills:
• Regulatory submission strategy and lifecycle management.
• Familiarity with eCTD submissions and regulatory databases.
• Excellent communication and cross-functional collaboration abilities.
Why Join Teva?
At Teva, we’re dedicated to enhancing the quality of life for patients worldwide through science, innovation, and commitment. Join a global team that values excellence, integrity, and impact.
📩 Interested Candidates:
Send your updated CV to Apeksha.Shinde01@teva.co.in
Please send your updated CV to me Email ID: Apeksha.Shinde01@teva.co.in
💡 Quick Summary
Seeking a career-building opportunity? The Teva Pharmaceuticals Hiring Manager – Regulatory Affairs position is now open for candidates interested in the Lab Technician / Pharmacist Jobs sector. This role in Bangalore offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Lab Technician / Pharmacist Jobs is a plus.
