Teva Pharmaceuticals Walk-In Drive for Quality Control and QA Roles in Indore

Career Opportunities in Quality Control and QA at Teva Pharmaceuticals

Teva Pharmaceuticals, a leader in Active Pharmaceutical Ingredients (APIs) and a trusted partner for global pharmaceutical companies, is conducting a Walk-In Drive for multiple Quality Control (QC) and Quality Assurance (QA) roles in Indore. This event is an excellent opportunity for experienced professionals to work with an organization that has over 80 years of expertise in the API industry.

Walk-In Drive Details

• Date: Saturday, December 7, 2024
• Time: 10:00 AM to 4:00 PM
• Venue: Hotel Lemon Tree, Indore, Madhya Pradesh

Job Roles and Responsibilities

1. Quality Control Technician II (HPLC)

• Location: Malanpur, Gwalior
• Experience: 3–10 years
• Qualification: BSc./MSc. in Chemistry
• Key Responsibilities:
  • Hands-on experience with HPLC systems.
  • Proficiency with Empower software.
  • Ensuring 24/7 audit readiness.
  • Investigation of OOS (Out of Specification) and OOT (Out of Trend) results.

2. Quality Control Technician II (Wet Labs)

• Location: Malanpur, Gwalior
• Experience: 3–10 years
• Qualification: BSc./MSc. in Chemistry
• Key Responsibilities:
  • Expertise in wet chemistry techniques.
  • Knowledge of PSD (Particle Size Distribution) and XRD (X-ray Diffraction) techniques.
  • Handling investigations related to OOS and OOT results.

3. Quality Control Analyst I (HPLC)

• Location: Indore
• Experience: 3–10 years
• Qualification: BSc./MSc. in Chemistry
• Key Responsibilities:
  • HPLC expertise with a focus on regulatory compliance.
  • Investigating OOS and OOT outcomes.
  • Participating in internal, external, and regulatory audits.
  • Overseeing CAPA (Corrective and Preventive Action) safety and instrument calibration.

4. Quality Assurance Specialist

• Location: Indore
• Experience: 3–10 years
• Qualification: BSc./MSc. in Chemistry or related disciplines
• Key Responsibilities:
  • Tracking CAPA activities triggered from audits or inspections.
  • Maintaining inspection readiness documentation.
  • Collaborating on product licensing applications for government bodies.
  • Supporting compliance initiatives, including GMP GEMBA and cGMP walks.

How to Apply

Interested candidates are encouraged to bring their updated resumes to the venue or email their CVs to:

• Snehal Mokashi: snehal.mokashi@teva.co.in
• Shweta Rattan: shweta.rattan@teva.co.in

Tagged as: Global Pharma Jobs, Pharmaceutical Careers, Pharmaceutical Jobs