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Senior Manager - Quality operations

Sandoz Private Limited

Full time
Experience
6+ years
Location
India
Work mode
Not stated
Posted 1 day ago Last checked 1 hr ago

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Role at a glance

You will
  • Conduct scientific literature and information searches.
  • Promote knowledge sharing within the organization.
  • Handle multiple activities simultaneously.
Experience
6+ years
Education
Master's degree or higher
Must-have skills
Good Manufacturing Practice (GMP)People ManagementProject ManagementQuality AssuranceQuality ControlStakeholder Management

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Job description

Location: India

**Job Description Summary**

Lead and manage scientific and operational project activities related to nitrosamine risk assessment and control, ensuring alignment with regulatory requirements, scientific standards, and business objectives and serve as a subject matter expert for N-Nitrosamines, mutagenic impurities, and other related impurity assessments across drug substances and drug products.

**Job Description**

**Major accountabilities:**

Scientific & Technical Expertise

  • Apply advanced scientific knowledge in **mutagenic impurities and N-nitrosamines**.
  • Perform complex risk assessments and develop mitigation/remediation strategies.
  • Troubleshoot scientific challenges using analytical and problem-solving skills.
  • Conduct scientific literature and information searches.
  • Promote knowledge sharing within the organization.

Execution & Delivery

  • Independently manage and complete projects within agreed timelines and quality standards.
  • Handle multiple activities simultaneously.
  • Demonstrate initiative, accountability, and innovative thinking.
  • Work proactively with minimal supervision.

Compliance

  • Ensure all activities comply with regulatory requirements.
  • Follow applicable quality standards, SOPs, and guidelines.

Collaboration & Communication

  • Work in alignment with the Sandoz culture and values.
  • Collaborate effectively with international cross-functional teams.
  • Build and maintain strong stakeholder relationships.
  • Communicate scientific findings clearly and effectively.

**Minimum Requirements:**

### Experience

  • Minimum 6 years of relevant pharmaceutical industry experience; or
  • Minimum 3 years of relevant experience with a PhD.
  • Proven experience in assessing mutagenic impurities and/or nitrosamines within a pharmaceutical environment.

Technical Competencies

  • Strong understanding of ICH M7 principles and regulatory expectations related to mutagenic impurities and nitrosamines.
  • Experience performing impurity risk assessments and developing control strategies.
  • Familiarity with pharmaceutical manufacturing processes, API synthesis, and impurity formation pathways.
  • Strong scientific writing and documentation skills.
  • Technical expertise in Organic Chemistry, API synthesis, and pharmaceutical manufacturing processes.
  • Experience in nitrosamine, mutagenic impurity, and quality risk assessments.
  • Strong regulatory compliance knowledge (ICH M7, FDA, EMA, MHRA requirements).
  • Excellent scientific writing, analytical thinking, and data interpretation skills.
  • Effective communication, project management, and cross-functional collaboration capabilities.
  • Hands on experience using Sci finder, Reaxys, Chem draw and other literature searching tools

**Skills:**

### Professional Skills

  • Excellent analytical thinking, problem-solving, and decision-making abilities.
  • Ability to work independently and manage multiple priorities effectively.
  • Strong stakeholder management and communication skills.
  • Demonstrated success working within global, cross-functional teams.
  • Fluent in English, both written and spoken.

**Skills Desired**

Continued Learning, Dealing With Ambiguity, Employee Performance Evaluations, Gmp Procedures, People Management, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

Our Purpose here at Sandoz is pioneering access for patients. As the global leader in 'off-patent' high quality medicines, we are able to make medicine more affordable and accessible.

Our broad global portfolio comprises of approximately 1,300 quality biosimilar and generic medicines, enabling us to provide more than 900 million patient treatments across 100+ countries per year, and while we are proud of this achievement, we have an ambition to do more!

Powered by our talented and ambitious colleagues, who, in return for dedication and skills, experience a flexible, collaborative & inclusive culture where diversity of thought is welcomed and where personal growth is nurtured!

Job data: Headcount Labs (headcountlabs.com), ODbL 1.0. The job description belongs to the employer. Location data © OpenStreetMap contributors and Overture Maps.

Key skills

Required

Good Manufacturing Practice (GMP)People ManagementProject ManagementQuality AssuranceQuality ControlStakeholder Management

Soft skills

Analytical ThinkingCommunicationDecision MakingProblem Solving

Job market insights

5active Good Manufacturing Practice (GMP) jobs in India
324active People Management jobs in India
1,332active Project Management jobs in India
6 more open jobs at Sandoz Private Limited

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From live job posts on CoreHRx, updated 6 Nov 2026. Skill figures count posts that list their skills; salary figures only posts that show a salary.

Questions about this job

How much experience does this job need?

The post asks for 6 Yrs experience.

What kind of job is this?

It is a full time job.

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