Novartis Posted October 26, 2026

Direct Materials Life Cycle Manager

Hyderabad (Office), India FULL_TIME
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About this opportunity

#LI-HybridLocation: Hyderabad, IndiaRelocation Support: This role is based in Hyderabad, India. Novartis is unable to offer relocation support: please only apply if accessible.Take the lead in introducing new suppliers into our manufacturing network and help ensure a smooth, compliant transition from start to finish. As Direct Materials Life Cycle Manager, you will manage projects across the Small Molecules platform, focusing on excipients and chemicals while ensuring that quality and regulatory requirements are met. This is an individual contributor role with significant cross-functional impact, coordinating diverse project teams to deliver key direct materials initiatives successfully.

Key ResponsibilitiesPlan and deliver direct materials projects, coordinating activities across global and local functions.Define project goals, milestones and long-term plans to support successful outcome of the project.Establish clear project plans and objectives in collaboration with key stakeholders.Track project progress and communicate changes in strategy, priorities or timelines.Lead project communication and stakeholder engagement to strengthen alignment and support informed decisions.Identify, assess and manage project risks, escalating issues through established processes.Define and implement corrective actions to address project challenges and keep delivery on track.Maintain accurate project dashboards, documentation, status updates and key performance indicator tracking.Ensure compliance with internal policies, legislation, professional standards, Good Manufacturing Practice and regulatory requirements.Coordinate cross-functional project teams and support continuous improvement of life cycle management processes. Essential RequirementsUniversity degree in Science, Business Administration or another relevant field.At least 8 years of experience in a role of similar scope and complexity.Extensive project management experience, including coordinating cross-functional teams without direct reporting authority.Strong knowledge of supply chain life cycle management and product life cycle management processes.Knowledge of Good Manufacturing Practice, change management and relevant quality and regulatory requirements.Strong stakeholder, conflict management, negotiation and decision-making skills in complex, international environments.Fluent written and spoken English. Desirable RequirementsExperience with Chemicals, API and DP operations, supply chain or project managementCommitment to Diversity and InclusionNovartis is committed to building an outstanding, inclusive work environment and diverse team representative of the patients and communities we serve.Accessibility and AccommodationNovartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to diversityandincl.india@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Job details

Seniority
Manager
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Hyderabad (Office), India
Employment type
FULL_TIME

How this role compares

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

We currently track 596 comparable Manager Manufacturing & CMC roles across 98 biopharma companies.

596Comparable roles tracked
548Currently active
98Companies hiring similar roles
40Countries represented

Salary context

179 of 596 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 · Warehouse Associate I (M-F 11am-7:30pm) · AbbVie $16/hr – $29/hr (≈ $33,280–$60,320/yr)
Highest disclosed · Associate Director / Director - Biologics Drug Product Development · AbbVie $160,500/yr – $305,000/yr
Peer group range $46,800 – $232,750 (median $165,150)

Where these roles are based

Top locations among the 596 comparable roles

United States334
India49
Ireland24
Japan23
Netherlands19
China17

+ 34 more countries

Seniority mix

596 of 596 peers have a known seniority level

Manager350
Associate142
Associate Director104

Therapeutic area mix

6 of 596 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease3
Vaccines & Infectious Disease2
Immunology1

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Notify me about similar jobs

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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.

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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.