Sandoz Posted August 10, 2026

Project Quality Manager - Specialist

Telangana, India Full time
Quality Manager

Sandoz is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description Summary

Coordinate and support quality, validation, and IT security control activities within projects, ensuring compliance with standards, effective execution, and continuous improvement under defined governance.

Job Description

Project Quality Manager - Specialist

Sandoz is going through an exciting and transformative period as a global leader and pioneering provider of sustainable Generic and Biosimilar medicines.

This is an exciting time in our history, and by creating a new and ambitious path, it will provide a unique opportunity for us all, both professionally and personally.

Summary

The Project Quality Manager - Specialist is responsible for coordination and support quality, validation, and IT security control activities within projects, ensuring compliance with standards, effective execution, and continuous improvement under defined governance.

Major accountabilities: 

Support end-to-end quality, validation, and IT security control activities across assigned projects, ensuring adherence to GAMP5, CSV SOPs, SDZ standards, IMF, and regulatory requirements.

Contribute to the development and execution of the quality & validation strategy, ensuring alignment with defined governance, deliverables, and project objectives.

Support oversight and assurance activities through execution of risk-based reviews, validation checks, and security control verification to ensure completeness and compliance.

Coordinate and monitor validation and quality execution, ensuring planned qualification/validation activities are tracked, performed, and documented appropriately.

Ensure documentation quality and compliance, supporting the creation, review, and maintenance of validation and system deliverables in line with required standards.

Maintain audit readiness for assigned projects, ensuring documentation is complete, traceable, and audit expectations are met.

Provide input to project teams on quality and compliance topics, highlighting risks and supporting issue resolution.

Collaborate with project managers and stakeholders to support quality outcomes, track escalations, and align on compliance requirements.

Prepare and review system and validation documentation, ensuring alignment with policies, standards, and regulatory expectations.

Support capability building by guiding teams on validation practices, documentation standards, and system lifecycle processes.

Contribute to continuous improvement initiatives, applying fit-for-purpose and lean approaches in quality and validation processes.

Engage with stakeholders, vendors, and suppliers to ensure consistent understanding and application of quality requirements.

Experience and Skills:

3-5 Years of relevant experience in BioPharma IT Quality & Compliance departments

Skills:

ITSQM skills

Has successfully managed quality during multiple international and/or cross- functional IT projects and/or operations and has a minimum of 3 years hands-on quality management.

Expert Knowledge and hands-on working experience of Quality and Security Management in the following areas / disciplines GxP, CSV and GAMP·

Good understanding of pharmaceutical validation requirements driven by health authorities like FDA etc.

IT System Lifecycle (Requirement Management, Design, Testing, Deployment)·

Adequate project management skills to plan quality and information security tasks and monitor their implementation during assigned projects.

Software Development Methodologies: Agile (must have), Dev / SecOPs (good to have)

Quality and Process Management (CMMI, Six Sigma, good to have)

Performs a range of work, sometimes complex and non-routine, in a variety of environments.

Applies methodical approach to issue definition and resolution.

Has a sound generic, domain and specialist knowledge necessary to perform effectively in the organization typically gained from recognized bodies of knowledge and organizational information

Other skills

Demonstrates effective application of knowledge.

Has an appreciation of the wider business context

Plans, schedules, and monitors own work (and that of others where applicable) competently within limited deadlines and according to relevant legislation, standards, and procedures.

Contributes fully to the work of teams.

Demonstrates an analytical and systematic approach to issue resolution.

Takes the initiative in identifying and negotiating appropriate personal development opportunities.

Understands how own role impacts security and demonstrates routine security practice and knowledge required for own work.

Communicates effectively, fluently both orally and in writing.

Can present complex information to both technical and non-technical audiences.

Open to resolving conflicts, provide/receive feedback(s), and maintain positive work relationships.

Education:

Bachelor's Degree (or equivalent) in Computer Science, Information Systems Management, Mathematics, Informatics, or other related fields.

Certification or accreditation in Information Security (CISM, CISA, CISSP etc.) is a plus.

Languages:

English.

Why Sandoz?

Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!

With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!

The future is ours to shape!

#sandoz

Skills Desired

Communication Skills, Compliance Audits, Compliance Management, Compliance Risk Assessment, Compliance Training, Influencing Skills, Quality Assurance

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Telangana, India
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 181 comparable Manager Quality roles across 52 biopharma companies.

181Comparable roles tracked
176Currently active
52Companies hiring similar roles
24Countries represented

Salary context

54 of 181 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Associate Scientist Overnight Shift · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Peer group range $75,920 – $219,500 (median $166,200)

Where these roles are based

Top locations among the 181 comparable roles

United States86
Ireland17
China17
Japan12
India11
Singapore7

+ 18 more countries

Seniority mix

181 of 181 peers have a known seniority level

Manager123
Associate Director37
Associate21

Therapeutic area mix

0 of 181 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Pfizer Healthcare India Private Limited Vizag, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country
60%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Manager (Quality Assurance – Operations/ Compliance/ Investigations)
Pfizer Healthcare India Private Limited · Vizag, India · Manager
Function Therapeutic area Seniority Country
60%
Manager IDQ Affiliates & Global Distribution Quality
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
60%
Manager - Quality Compliance
Pfizer Healthcare India Private Limited · Vizag, India · Manager
Function Therapeutic area Seniority Country
50%
Associate (Quality Assurance – Operations/ Compliance/ Investigations)
Pfizer Healthcare India Private Limited · Vizag, India · Associate
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.