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Overnight Biotech Quality Control Jobs in Indiana

Novartis

QA Operations Specialist

Indianapolis, IN

$88K - $132K/yr

Functional Breadth * QA and QC experience in biotech pharmaceutical industry with environmental monitoring & cleanliness zones EEO Statement: The Novartis Group of Companies are Equal Opportunity ...

Novartis

QA Operations Specialist

Indianapolis, IN · On-site

$88K - $132K/yr

... QC experience in biotech pharmaceutical industry with environmental monitoring & cleanliness zones The pay range for this position at commencement of employment is expected to be between $88,000.00 ...

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Overnight Biotech Quality Control information

What is an overnight biotech quality control?

Overnight Biotech Quality Control jobs involve performing laboratory tests and inspections on biotechnology products during nighttime or overnight shifts. These professionals ensure that products such as pharmaceuticals, biologics, or laboratory samples meet quality and safety standards before they reach the market. Responsibilities often include running assays, documenting results, maintaining equipment, and following strict protocols and Good Manufacturing Practices (GMP). Working overnight helps maintain round-the-clock quality assurance in fast-paced biotech environments. Candidates typically need a background in biology, chemistry, or related fields and attention to detail.

What are the key skills and qualifications needed to thrive as an overnight biotech quality control professional?

To thrive as an Overnight Biotech Quality Control professional, you need a strong background in biology or chemistry, attention to detail, and familiarity with quality assurance practices, often supported by a relevant bachelor's degree. Proficiency in laboratory equipment, data analysis software, and compliance with regulatory standards like GMP or ISO is typically required. Strong problem-solving skills, reliability, and effective communication are important soft skills for this role. These skills are crucial to ensure consistent product quality, regulatory compliance, and effective issue resolution during overnight operations.

What are some common challenges faced by overnight biotech quality control professionals, and how can they be managed?

Overnight Biotech Quality Control professionals often encounter challenges such as working with limited onsite support, maintaining focus during late hours, and responding quickly to unexpected results or equipment issues. Effective communication with day-shift teams and thorough documentation are essential to ensure continuity and avoid errors. Establishing a consistent routine, prioritizing tasks, and utilizing available digital resources can help manage the unique demands of this role and ensure the accuracy and reliability of quality control results.

What is the difference between Overnight Biotech Quality Control vs Microbiologist?

AspectOvernight Biotech Quality ControlMicrobiologist
CredentialsBachelor's in biology, microbiology, or related field; GMP trainingBachelor's or higher in microbiology, biology, or related field; lab certifications
Work EnvironmentLaboratory setting, often overnight shifts, regulated biotech facilitiesLaboratory, research, or clinical settings; may include overnight or day shifts
Industry UsageBiotech, pharmaceutical manufacturing, quality assuranceHealthcare, research institutions, biotech, pharmaceuticals

Overnight Biotech Quality Control specialists focus on testing and ensuring product quality in biotech manufacturing, often working overnight shifts. Microbiologists conduct research, analyze microorganisms, and may work in various settings, including clinical labs. While both roles require microbiology knowledge and lab skills, Quality Control roles emphasize compliance and product safety in biotech environments, whereas Microbiologists may have broader research responsibilities.

What are the most commonly searched types of Biotech Quality Control jobs in Indiana?

The most popular types of Biotech Quality Control jobs in Indiana are:

What are popular job titles related to Overnight Biotech Quality Control jobs in Indiana?

For Overnight Biotech Quality Control jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Overnight Biotech Quality Control jobs in Indiana look for?

The top searched job categories for Overnight Biotech Quality Control jobs in Indiana are:

What cities in Indiana are hiring for Overnight Biotech Quality Control jobs?

Cities in Indiana with the most Overnight Biotech Quality Control job openings:

Overnight Biotech Quality Control jobs near you

QA Operations Specialist

Novartis

Indianapolis, IN

$88K - $132K/yr

Full-time

Re-posted 14 days ago

Novartis rating

7.8

Company rating: 7.8 out of 10

Based on 18 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

Job Description Summary

#LI-Onsite
This role is located on-site in Indianapolis, IN. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for experienced Quality Control professionals to help us reach our ambitious goals.
Our QA Operations Specialist manages Quality aspects and projects within area of responsibility as well as ensuring and supporting overall GxP conformity and Compliance with the Novartis Quality Management Systems.


Job Description

Major accountabilities:

  • Provide shopfloor quality oversight of all production, quality control and supply chain departments to ensure their practice fully adheres to cGMP, including data integrity. Ensure timely escalation to management of all applicable incidents.
  • Perform live review of manufacturing batch records in preparation for batch release and escalate any discrepancies immediately.
  • Assist functional areas with achieving timely and compliant final product disposition of the product.
  • Review, approve and support procedures and production/testing records as required and assist in the training of site associates.
  • Ensure compliance of site personnel and application of aseptic techniques and full compliance to sterile manufacturing regulations.
  • Support FDA/Regulatory interactions for the Indianapolis site activities and products to ensure successful regulatory submissions and inspections.
  • Support QA Operations as a valued business partner, with a culture of safety, quality, delivery to patients, cost, compliance and data integrity.
  • Other related duties as assigned.

Shift: This role will be Wednesday - Sunday, 6:00am - 4PM. This position may involve mandatory overtime as needed.

Essential Requirements:

  • Bachelor's Degree, preferably in Life Sciences, chemistry or related relevant degree.
  • 2+ years of experience in a GxP Biopharmaceutical manufacturing operations
  • 1+ years of experience in a quality assurance role
  • Collaborating across boundaries
  • Functional Breadth
  • QA and QC experience in biotech pharmaceutical industry with environmental monitoring & cleanliness zones


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. 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. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.


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 us.reasonableaccommodations@novartis.com 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

$88,000.00 - $132,000.00


Skills Desired

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

What Novartis employees say

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