Validation Lead
Novartis
Validation Lead
Job Description
Summary
Summary Bring your expertise to a role where your decisions directly safeguard product quality, patient safety, and regulatory trust. As our Validation Lead in Indianapolis, you will shape and own the site’s end to end validation strategy—process, cleaning, primary packaging, and ongoing process verification—so manufacturing stays inspection ready and continuously compliant with current Good Manufacturing Practice. You’ll partner closely with Manufacturing Science and Technology, Engineering, Information Technology, Quality Control, and Analytical Science and Technology to orchestrate the Validation Master Plan, monitor meaningful performance indicators, and proactively manage risk. Your work will also enable smooth product transfers and launches by generating robust, data driven evidence for registration dossiers. If you thrive on building clear standards, coaching teams, and turning complex technical challenges into practical, reliable solutions, this role gives you the platform to make an impact that matters.#LI-Onsite
Location: Indianapolis, IN
Relocation Support: Yes
Locations
- USA
Salary
Estimated Salary Rangemedium confidence
80,000 - 135,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Validation strategy developmentintermediate
- Process validationintermediate
- Cleaning validationintermediate
- Primary packaging validationintermediate
- Ongoing process verificationintermediate
- Risk managementintermediate
- Performance indicator monitoringintermediate
- Data-driven evidence generationintermediate
- Cross-functional partnershipintermediate
- Coaching and standards buildingintermediate
Required Qualifications
- Expertise in cGMP compliance (experience)
- Validation experience in pharmaceutical manufacturing (experience)
- Technical knowledge in manufacturing sciences (experience)
- Relocation support available (experience)
Responsibilities
- Shape and own site’s end-to-end validation strategy
- Orchestrate Validation Master Plan
- Monitor meaningful performance indicators
- Proactively manage risk
- Partner with Manufacturing Science, Engineering, IT, QC, and Analytical teams
- Enable smooth product transfers and launches
- Generate robust data-driven evidence for registration dossiers
- Maintain inspection readiness and continuous compliance
Answer 10 quick questions to check your fit for Validation Lead @ Novartis.
10 Questions
~2 Minutes
Instant Score
Validation Lead
Novartis
Validation Lead
Job Description
Summary
Summary Bring your expertise to a role where your decisions directly safeguard product quality, patient safety, and regulatory trust. As our Validation Lead in Indianapolis, you will shape and own the site’s end to end validation strategy—process, cleaning, primary packaging, and ongoing process verification—so manufacturing stays inspection ready and continuously compliant with current Good Manufacturing Practice. You’ll partner closely with Manufacturing Science and Technology, Engineering, Information Technology, Quality Control, and Analytical Science and Technology to orchestrate the Validation Master Plan, monitor meaningful performance indicators, and proactively manage risk. Your work will also enable smooth product transfers and launches by generating robust, data driven evidence for registration dossiers. If you thrive on building clear standards, coaching teams, and turning complex technical challenges into practical, reliable solutions, this role gives you the platform to make an impact that matters.#LI-Onsite
Location: Indianapolis, IN
Relocation Support: Yes
Locations
- USA
Salary
Estimated Salary Rangemedium confidence
80,000 - 135,000 USD / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Validation strategy developmentintermediate
- Process validationintermediate
- Cleaning validationintermediate
- Primary packaging validationintermediate
- Ongoing process verificationintermediate
- Risk managementintermediate
- Performance indicator monitoringintermediate
- Data-driven evidence generationintermediate
- Cross-functional partnershipintermediate
- Coaching and standards buildingintermediate
Required Qualifications
- Expertise in cGMP compliance (experience)
- Validation experience in pharmaceutical manufacturing (experience)
- Technical knowledge in manufacturing sciences (experience)
- Relocation support available (experience)
Responsibilities
- Shape and own site’s end-to-end validation strategy
- Orchestrate Validation Master Plan
- Monitor meaningful performance indicators
- Proactively manage risk
- Partner with Manufacturing Science, Engineering, IT, QC, and Analytical teams
- Enable smooth product transfers and launches
- Generate robust data-driven evidence for registration dossiers
- Maintain inspection readiness and continuous compliance
Answer 10 quick questions to check your fit for Validation Lead @ Novartis.
10 Questions
~2 Minutes
Instant Score