 ##  [Validation Lead](/req-10083886-validation-lead "Validation Lead") 

  Job ID REQ-10083886 

 

 Sep 08, 2026 

 

 LOC_MY 

 

 

 

###  About the Role 

Key Responsibilities:

- Developing validation documentation to support compliant manufacturing processes and lifecycle management.
- Executing process and cleaning validation strategies aligned with regulatory and quality requirements.
- Coordinating validation activities with cross-functional teams to ensure timely and effective execution.
- Providing validation support for manufacturing processes serving global markets, including Singapore-related operations.
- Leading investigations and supporting resolution of validation deviations, observations, and technical issues.
- Reviewing and approving validation protocols, reports, risk assessments, and related technical documentation.
- Driving continuous improvement initiatives to enhance validation effectiveness, compliance, and operational performance.
- Managing validation projects and stakeholder engagement across multiple functions and sites.

Essential Requirements:

- Bachelor's or Master's degree in Chemistry, Biological Sciences, Pharmacy, Chemical Engineering, or a related field.
- Two to eight years of experience within a biopharmaceutical or pharmaceutical manufacturing environment.
- Strong understanding of manufacturing processes and associated production equipment.
- In-depth knowledge of quality systems and regulatory requirements across multiple health authorities.
- Experience executing process validation and/or cleaning validation activities in a regulated environment.
- Demonstrated expertise in technical report writing, document review, and cross-functional project management.

Desirable Requirements:

- Fundamental understanding of pharmaceutical analytical testing methods and laboratory practices.
- Fluency in Artificial Intelligence tools and technologies to support innovation and operational excellence.

Commitment to Diversity and Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.



 

###  Role Requirements 

 

**Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? [https://www.novartis.com/about/strategy/people-and-culture](https://www.novartis.com/about/strategy/people-and-culture "https://www.novartis.com/about/strategy/people-and-culture")

**Benefits and Rewards:** Learn about all the ways we’ll help you thrive personally and professionally.  
[Read our handbook (PDF 30 MB)](https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf)



 

 

 

 

 

 Division DIV_TO 

 

 Business Unit Production / Manufacturing 

 

 Location LOC_MY 

 

 Site Selangor 

 

 Company / Legal Entity MY01 (FCRS = MY001) Novartis Corporation (Malaysia) Sdn. Bhd. (197101000541) 

 

 Functional Area FCT_TO 

 

 Job Type Full time 

 

 Employment Type Regular 

 

 Shift Work No 

 

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 ![careers default image](https://prod1.jobapi.novartis.com.cn/themes/custom/cosmos/patterns/images/careers-default-image.webp "careers default image") 

 Job ID REQ-10083886 

 

 

###  Validation Lead 

 [Apply to Job](https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Selangor/Validation-Lead_REQ-10083886-2 "Apply to Job") <a class="link_button button_text" href=""></a>