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Gmp Quality Control Jobs in Indiana (NOW HIRING)

Novartis

QC Chemist

Indianapolis, IN

$97K - $146K/yr

On-time and GMP-compliant release of dosage forms * Support Quality Control and AS&T as a valued business partner, with a culture of safety, quality, * delivery to patients, cost, compliance, and ...

INCOG

QC Microbiology Technician, 2nd Shift

Fishers, IN · On-site

$23.75 - $31.25/hr

Supports QC Microbiologists and QC leadership in establishing the new GMP QC Microbiology Laboratory. Maintains a constant state of safety and inspection-readiness in the QC microbiology laboratory.

Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

Develop/revise worksheets and system documentation Required Skills: * 8-10 years in Pharma/GMP environment * QC lab experience with LIMS/ELN (data admin or power user) * Strong understanding of data ...

INCOG

QC Scientist, Weekend Nights

Fishers, IN · On-site

Weekend QC Scientist Summary The Weekend QC Scientist supports GMP manufacturing and laboratory operations by performing routine microbiology and chemistry testing, sample handling, and laboratory ...

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Gmp Quality Control information

Is GMP quality control inspection a good career?

GMP quality control inspection is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The role offers opportunities for advancement and consistent employment in regulated environments.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and verifying raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent contaminated or substandard products from reaching consumers and maintains compliance with regulatory requirements through proper documentation and testing procedures.

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Is GMP Quality Control a good career?

GMP Quality Control is a vital role in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards through testing and documentation. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The career offers stability, opportunities for advancement, and the chance to work in regulated environments that prioritize quality and safety.
What are popular job titles related to Gmp Quality Control jobs in Indiana? For Gmp Quality Control jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Gmp Quality Control jobs in Indiana look for? The top searched job categories for Gmp Quality Control jobs in Indiana are:
What cities in Indiana are hiring for Gmp Quality Control jobs? Cities in Indiana with the most Gmp Quality Control job openings:
Gmp Quality Control jobs near you

QC Chemist

Novartis

Indianapolis, IN

$97K - $146K/yr

Full-time

Re-posted 29 days ago

Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 rated pharmaceutical

Job description

Job Description Summary

Location: Indianapolis, IN #LI-Onsite
About this role:
The QC Chemist is responsible for performing tasks associated with release testing and reviewing laboratory data. Communicating with and supporting internal & external partners of the Quality Control organization is also required.


Job Description

Major accountabilities:

  • Provide support to peers within the Quality Assurance, Quality Control and AS&T teams.
  • On-time and GMP-compliant release of dosage forms
  • Support Quality Control and AS&T as a valued business partner, with a culture of safety, quality,

  • delivery to patients, cost, compliance, and data integrity.

  • Author, review and support procedures, investigations, corrective and preventive actions, change

  • controls, complaints, and training as it relates to quality control testing.

  • Ensure that QC testing is properly conducted and documented for all performed activities, with

  • emphasis on Data Integrity. Evaluate and approve QC records as required.

  • Provide oversight and monitoring of quality control KPIs and programs.
  • Perform QC related validations, transfers, improvements, investigations related activities (deviations, OOS, OOE, OOT, CAPAs, trending), and Change Control systems.
  • Prepare and participate in health authorities’ inspections and internal audits of QC. Ensure quality control area is inspection ready.

Essential Requirements

  • BSc in Chemistry or relevant scientific
  • 3+ years of experience in a GMP quality control environment
  • Strong HPLC experience a must
  • General HSE Knowledge
  • Knowledge of GMP Manufacturing Process Execution
  • Quality Control (QC) Testing
  • Quality Control Sampling
  • Dealing With Ambiguity.
  • GMP Procedures
  • Quality Control (Qc) Testing.
  • Quality Standards.
  • Self Awareness.
  • Technological Expertise.
  • Technological Intelligence.


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

$97,600.00 - $146,400.00


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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Benefits

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