QC Chemist

Novartis
$89,600 - $166,400 a year
Indianapolis, Indiana
Full time
3 days ago

Summary

About this role:

We are seeking a highly skilled and experienced QC Chemist to join our Quality Control team. The ideal candidate will have a strong background in analytical chemistry, wet chemistry techniques and knowledge in ICP analysis. The candidate will have a strong technical writing skill and experience with validation of analytical methods and qualification of analytical equipment. This position is crucial to ensure the quality, safety, and compliance of our products, contributing to the regulatory adherence and scientific integrity of our testing procedures. The QC Chemist is responsible for the quality control testing of the radioisotopes, incoming raw materials, and packaging components.

Location: Indianapolis, IN #LI-Onsite

Shift: This position involves shift work which will be defined through site start up and commercialization readiness.

About the Role

Key Responsibilities:

Demonstrates technical experience in aspects related to quality control testing, including QC method and instrument qualifications as well as technical transfers from third party laboratories or other Novartis sites. Supports and provides technical insight for QC testing, while ensuring documentation completion remains in full compliance with GMP regulations, Novartis procedures, and product specifications.

  • Executes testing for radioisotopes and incoming materials.
  • Execute testing associated to qualification and validation protocols.
  • Supports deviation investigations and OOS/OOT/OOE investigations with testing, if needed.
  • Responsible for successful on time completion of required training curricula comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications, Testing and specifications, and other relevant training including HSE for the specific role.
  • Prepares applicable documents, forms, and records, such as method or instrument qualification/validation records, and follows Good Documentation Practices.
  • Supports internal and external Audits and Inspections, if needed.

Essential Requirements:

  • Education: Bachelor’s degree in chemistry. Master's Degree is a plus.
  • A minimum of 2 years of experience in a cGMP or aseptic environment with prior Quality Control and analytical chemistry experience, expertise in method validation and instrument qualification is a plus.
  • In-depth knowledge of QC chemistry lab instrumentation (principles, operation, and troubleshooting) like, iTLC, and IPC. Experience with other analytical techniques (e.g., Wet Chemistry).
  • Proficiency in technical writing.
  • Experience with laboratory data management systems (LIMS) and electronic lab notebooks (ELN).
  • Adaptability to cross training in microbiology techniques such as bioburden and environmental monitoring.
  • Ability to interpret analytical data with high attention to detail focus on accuracy, quality, and compliance.
  • Strong analytical thinking with the ability to identify and resolve complex analytical chemistry challenges.

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $89,600 and $166,400/year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accessibility & Reasonable Accommodations

The Novartis Group of Companies are 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 application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Division
Operations
Business Unit
Innovative Medicines
Location
USA
State
Indiana
Site
Indianapolis
Company / Legal Entity
U469 (FCRS = US469) AAA USA Inc.
Functional Area
Quality
Job Type
Full time
Employment Type
Regular
Shift Work
No
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