QC Technician Micro-1st shift, weekends
Novartis Pharma Schweiz, Indianapolis, IN, United States
Indianapolis, Indiana. Relocation Support: This role is based in Indianapolis, Indiana. Novartis is unable to offer relocation support: please only apply if accessible. Are you passionate about microbiology and feeling that your work directly protects patients? As a QC Technician at Novartis, you’ll play a vital role in ensuring the safety and integrity of our products through rigorous microbiological testing and documentation. Working in a regulated laboratory environment, you’ll apply standardized methods and procedures to support product release, stability programs, and quality investigations. This entry‑level role offers hands‑on laboratory experience, meaningful impact, and the opportunity to grow your quality expertise within a collaborative, compliance‑driven team.
Weekend 1st Shift: Wednesday – Saturday, 7 am – 5 pm.
Key Responsibilities
Perform microbiological testing of drug products, stability samples, and packaging materials in compliance with quality standards.
Manage sample receipt, storage, tracking, and disposition to ensure integrity and regulatory readiness.
Document microbiological and sterility testing results accurately using approved procedures and controlled systems.
Execute sterility testing activities while maintaining complete, inspection‑ready documentation.
Identify, document, and escale technical complaints or adverse events within required timelines.
Support audit and inspection readiness by consistently following Good Manufacturing Practices (GMPs) and internal procedures.
Contribute to continuous improvement initiatives that enhance laboratory efficiency, compliance, and data integrity.
Essential Requirements
High school diploma with at least one year of experience working in a laboratory or quality control environment, or bachelor’s degree in microbiology or another scientific discipline with no prior experience required.
Foundational understanding of microbiological laboratory principles.
Ability to follow Standard Operating Procedures and established laboratory methods in a regulated environment.
Basic knowledge of Good Manufacturing Practice expectations or willingness to learn and apply them on the job.
Ability to accurately document laboratory activities and results using controlled systems and procedures.
Strong attention to detail, reliability, and a willingness to learn in a team‑based laboratory setting.
Desirable Requirements
Experience working in a pharmaceutical, biotechnology, or regulated manufacturing laboratory environment.
Familiarity with microbiological aseptic techniques.
The salary for this position is expected to range between $32.12/hr and $59.62/hr. 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.
To learn more about the culture, rewards, and benefits we offer our people.
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Weekend 1st Shift: Wednesday – Saturday, 7 am – 5 pm.
Key Responsibilities
Perform microbiological testing of drug products, stability samples, and packaging materials in compliance with quality standards.
Manage sample receipt, storage, tracking, and disposition to ensure integrity and regulatory readiness.
Document microbiological and sterility testing results accurately using approved procedures and controlled systems.
Execute sterility testing activities while maintaining complete, inspection‑ready documentation.
Identify, document, and escale technical complaints or adverse events within required timelines.
Support audit and inspection readiness by consistently following Good Manufacturing Practices (GMPs) and internal procedures.
Contribute to continuous improvement initiatives that enhance laboratory efficiency, compliance, and data integrity.
Essential Requirements
High school diploma with at least one year of experience working in a laboratory or quality control environment, or bachelor’s degree in microbiology or another scientific discipline with no prior experience required.
Foundational understanding of microbiological laboratory principles.
Ability to follow Standard Operating Procedures and established laboratory methods in a regulated environment.
Basic knowledge of Good Manufacturing Practice expectations or willingness to learn and apply them on the job.
Ability to accurately document laboratory activities and results using controlled systems and procedures.
Strong attention to detail, reliability, and a willingness to learn in a team‑based laboratory setting.
Desirable Requirements
Experience working in a pharmaceutical, biotechnology, or regulated manufacturing laboratory environment.
Familiarity with microbiological aseptic techniques.
The salary for this position is expected to range between $32.12/hr and $59.62/hr. 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.
To learn more about the culture, rewards, and benefits we offer our people.
#J-18808-Ljbffr