Home
Communities
Companies
- Companies
  
  Discover best places to work
- Compare Companies
  
  Compare & find best workplace
- Add Office Photos
  
  Bring your workplace to life
- Add Company Benefits
  
  Highlight your company's perks
Reviews
- Company reviews
  
  Read reviews for 6L+ companies
- Write a review
  
  Rate your former or current company
Salaries
- Browse salaries
  
  Discover salaries for 6L+ companies
- Salary calculator
  
  Calculate your take home salary
- Are you paid fairly?
  
  Check your market value
- Share your salary
  
  Help other jobseekers
- Gratuity calculator
  
  Check your gratuity amount
- HRA calculator
  
  Check how much of your HRA is tax-free
- Salary hike calculator
  
  Check your salary hike
Interviews
- Company interviews
  
  Read interviews for 40K+ companies
- Campus placements
  
  Interviews questions for 2K+ colleges
- Share interview questions
  
  Contribute your interview questions
Jobs
Awards

WINNERS AWAITED!
- ABECA 2025
  
  WINNERS AWAITED!
  
  AmbitionBox Employee Choice Awards - 4th Edition
- ABECA 2024
  
  AmbitionBox Employee Choice Awards - 3rd Edition
- AmbitionBox Best Places to Work 2022
  
  2nd Edition
- AmbitionBox Best Places to Work 2021
  
  1st Edition

Premium Employer

Sandoz

Compare

4.0

based on 413 Reviews

399 Sandoz Jobs

Associate Manager - Quality Operations

Sandoz

4.0

based on 413 Reviews

4-8 years

Hyderabad / Secunderabad

1 vacancy

Associate Manager - Quality Operations

Sandoz

posted 4mon ago

Job Role Insights

Flexible timing

Key skills for the job

Analytical Chemistry Compliance SAP Quality Management GMP Data Integrity OPEX

+ 1 more

Job Description

-Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.

About the Role:

Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.

Key Responsibilities:

Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance.
Support exception investigations
Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person.
Implements batch release in compliance with registration
Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Essential Requirements:

Functional Breadth. QC/ QA in pharmaceutical ind./ biotech with environmental monitoring
Collaborating across boundaries. cleanliness zones.
Worked in Quality Control laboratory with experience on Finish product testing, handling of Analytical methods and Specifications, Method validation and transfer.

Desirable Requirements:

Bachelor Degree or equivalent experience with experience in Pharmaceutical Industry/ specifically GMP background.

Skills Desired

Continuous Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

Employment Type: Full Time, Permanent

Read full job description

Prepare for Associate Quality Manager roles with real interview advice