QC Microbiologist

Posted 17 Days Ago
Be an Early Applicant
Indianapolis, IN
In-Office
81K-151K Annually
Mid level
Biotech • Pharmaceutical
The Role
The QC Microbiologist conducts quality control tests, manages samples, supports investigations, and prepares documentation in compliance with regulations.
Summary Generated by Built In

Job Description Summary

The QC Microbiologist supports all technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation and daily cleaning and maintenance activities, sample management and QC testing, and documentation completion and review in full compliance with GMP regulation, procedures, and product specifications.
Location: Indianapolis, IN #LI-Onsite
Shift: Sunday- Wednesday 2pm-12am


 

Job Description

Key Responsibilities:

  • Finished Product testing, Environmental Monitoring and Sterility QC testing, and reporting of the QC results.
  • Escalation in case of non-conformances and deviations and manage these quality incidents as per AAA procedures.
  • Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions.
  • Participation in assigned qualification/validation activities, as necessary.
  • 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 analytical batch records and follows Good Documentation Practices.
  • Support internal and external Audits and Inspections, as required.

Essential Requirements:

  • Education: Bachelors' degree required in relevant Scientific discipline (e.g Chemistry, Microbiology) strongly preferred.  In lieu of a degree, 3-5 years of relevant experience in similar role in Pharma/Manufacturing sector in analytical lab may be considered.
  • Minimum of 3-year experience in cGMP or aseptic environment required.
  • Knowledge of cGMP regulations and FDA guidance applicable to Quality Control for product and Environmental Monitoring testing, as well as Aseptic techniques.
  • Practical experience with Microbiology method verification and routine testing practices, EM Monitoring and basic knowledge of method/equipment validation principle and methodologies.
  • Ability to interpret analytical data and convert into technical documentation.
  • Basic knowledge and understanding of aseptic principles and techniques.

Novartis Compensation and Benefit Summary:  The salary for this position is expected to range between $81,200 and $150,800/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.


 

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 and 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.


 

Salary Range

$81,200.00 - $150,800.00


 

Skills Desired

Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence

Top Skills

Analytical Batch Records
Aseptic Techniques
Environmental Monitoring
Gmp Regulation
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The Company
HQ: Basel
110,000 Employees
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

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