Novartis
Healthcare
Analyst,QualityControl-PhysicalChemistry
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Analyst, Quality Control - Physical Chemistry at Novartis. Skills: Physical Chemistry, Quality Control, Analytical Testing. Execute routine and non-routine analysis for cGMP release. Perform analytical testing with a focus on HPLC”
Industry & Context.
Problem Solving Skills
What They're Looking For.
Must Have
Bachelor’s degree in Biochemistry, Biology, Microbiology, or related scientific discipline, Hands-on experience or exposure to HPLC and/or UPLC analytical techniques, Ability to learn and apply professional concepts in a laboratory environment, Understanding of and ability to follow company policies and procedures to resolve routine issues, Communication skills, Ability to work effectively within a team, Ability to follow detailed instructions and maintain accuracy in a structured work environment
Nice to Have
Experience with method validation activities in a regulated laboratory environment, Experience supporting or executing method transfers
What You'll Do.
Execute routine and non-routine analysis for cGMP release
Perform analytical testing with a focus on HPLC
and Western Blot testing
Conduct compendial assays including pH
Support method verifications and transfers for multiple projects
Perform sampling of incoming materials for use in
Initiate and maintain documentation including LIMS entries
Maintain laboratory equipment
and ensure compliance with
Initiate and support laboratory investigations and quality events
Assist in analytical and instrument troubleshooting through assay
Apply lean lab and six sigma concepts to
How You'll Work.
Team & Collaboration
High-performing team
Communication Scope
Communication skills
Process & Methodology
Project Management
Full Job Description
**Job Description Summary** Join Novartis and play a vital role in ensuring the quality and integrity of life-changing medicines. As an Analyst, Quality Control – Physical Chemistry, you will support critical compliance activities through the preparation, testing, and monitoring of products to ensure alignment with established quality standards in manufacturing and production. In this hands-on laboratory role, you will build your technical expertise while contributing to a high-performing team dedicated to delivering safe, effective therapies to patients around the world. **Job Description** **Location:** * This position will be located in Durham, NC and will be an onsite role. * Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. **Key Responsibilities:** * Execute routine and non-routine analysis for cGMP release and characterization testing * Perform analytical testing with a strong focus on HPLC and UPLC, alongside AUC, SEC, CE, and Western Blot * Conduct compendial assays including pH, conductivity, and osmolality testing * Support method verifications and transfers for multiple projects * Perform sampling of incoming materials for use in manufacturing and production * Initiate and maintain documentation including LIMS entries, SOPs, and assay forms * Maintain laboratory equipment, logbooks, and ensure compliance with safety standards * Initiate and support laboratory investigations and quality events with guidance * Assist in analytical and instrument troubleshooting through assay execution * Apply lean lab and six sigma concepts to support continuous improvement initiatives **Essential Requirements:** * Bachelor’s degree in Biochemistry, Biology, Microbiology, or a related scientific discipline * Hands-on experience or exposure to HPLC and/or UPLC analytical techniques * Ability to learn and apply professional concepts in a laboratory environment * Understanding of and ability to follow compa
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