1

Gmp Quality Control Jobs in Indiana (NOW HIRING)

QC Chemist

Indianapolis, IN · On-site

$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 ...

QC Sample Management Technician

Fishers, IN

$17.50 - $22.50/hr

Position Summary The QC Sample Management Technician is a member of the Quality Control organization and is responsible for the endtoend lifecycle management of QC samples in a GMP-regulated ...

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 ...

... Quality Control Laboratory. The successful candidate will organize, execute, and complete their ... Reviews data packets for accuracy and compliance to GMP documentation practices and adherence to ...

The QC Supervisor is responsible for organizing and directing the daily activities of the Quality ... Experience in GMP-regulated environments required * Strong knowledge of laboratory concepts ...

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 ...

next page

Showing results 1-20

Gmp Quality Control information

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.

Which pays more, QA or QC?

In the context of GMP Quality Control, QA (Quality Assurance) roles typically pay more than QC (Quality Control) positions because QA involves broader responsibilities such as process audits and compliance oversight. QC roles focus on testing and inspection of products, often with more routine tasks. Salary differences can vary based on experience, certifications, and industry, but generally QA positions offer higher compensation.

Is QC a high paying job?

Quality Control (QC) roles in industries like pharmaceuticals and manufacturing can offer competitive salaries, especially with experience and relevant certifications. However, pay varies based on location, company size, and level of expertise, and QC positions are generally considered mid-range in terms of salary compared to other technical roles.

Is quality control part of GMP?

Yes, quality control is an essential component of Good Manufacturing Practice (GMP) standards. GMP requires quality control processes, including testing and validation, to ensure products meet safety and quality specifications. Quality control professionals in GMP environments perform inspections, sampling, and testing to maintain compliance and product integrity.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Quality or Director of Quality Control typically have the highest salaries, often exceeding six figures. These positions require extensive experience, leadership skills, and knowledge of Good Manufacturing Practices (GMP) and regulatory compliance.
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 cities in Indiana are hiring for Gmp Quality Control jobs? Cities in Indiana with the most Gmp Quality Control job openings:
QC Chemist

QC Chemist

Novartis

Indianapolis, IN • On-site

$97K - $146K/yr

Full-time

Re-posted 5 days ago


Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

55th of 74 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

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom