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Gmp Quality Control Jobs in Indiana (NOW HIRING)

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 ...

Quality Control Chemist Summary: INCOG is seeking a Quality Control (QC) Chemist with a passion for ... GMP) testing is performed. Excellent written and oral communication skills with the ability to ...

Execute and supervise QC testing for batch release within hours of production Routine Functions ... Experience in a GMP-regulated environment supporting clinical or commercial manufacturing. * Hands ...

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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 cities in Indiana are hiring for Gmp Quality Control jobs? Cities in Indiana with the most Gmp Quality Control job openings:

Quality Control Supervisor

Evonik Industries

Lafayette, IN โ€ข On-site

Full-time

Re-posted 17 days ago


Job description

What we offer
You will work on exciting and challenging topics together with a team in an ultra-modern, innovative and creative environment. Intensive on-the-job training with expert colleagues guarantees you will quickly become familiar with your duties and perform them independently. Performance related pay and the opportunity for personal and professional development are of course part of the package. Since 2009 Evonik Industries AG has been certified as a family-friendly company by the German Hertie Foundation.
Click on the link to learn more about Evonik from our employees:
https://careers.evonik.com/en/about/meet-the-team/
The QC Supervisor is responsible for organizing and directing the daily activities of the Quality Control laboratory to ensure safe, compliant, and efficient operations. This role ensures all laboratory methods, procedures, and activities are performed in accordance with cGMP and ESHS requirements while delivering high-quality products and services on time and within budget. The supervisor provides leadership across multiple shifts, drives continuous improvement initiatives, supports audit readiness, and collaborates cross-functionally to meet both internal and external customer needs.
The QC Supervisor is responsible for organizing and directing the daily activities of the Quality Control laboratory to ensure safe, compliant, and efficient operations. This role ensures all laboratory methods, procedures, and activities are performed in accordance with cGMP and ESHS requirements while delivering high-quality products and services on time and within budget. The supervisor provides leadership across multiple shifts, drives continuous improvement initiatives, supports audit readiness, and collaborates cross-functionally to meet both internal and external customer needs.
RESPONSIBILITIES
  • Manage QC Laboratory Operations: Organize daily activities, ensuring efficient workflows and adherence to cGMP and ESHS standards.
  • Safety & Compliance: Enforce safety protocols, proper documentation practices, and compliance with regulatory requirements.
  • Method Development & Support: Participate in method transfers, development, troubleshooting, and procedure writing/review.
  • Investigations & Audits: Write and coordinate deviation investigations, ensure audit readiness, and actively engage in audits.
  • Team Supervision: Manage 10-15 direct reports across shifts, ensuring proper staffing, training, and performance reviews.
  • Training & Development: Train new hires, contractors, and interns while ensuring ongoing procedural compliance for all analysts.
  • Continuous Improvement: Lead initiatives to enhance processes, methods, and documentation efficiency.
  • Process Oversight: Align QC operations with site priorities while managing quality, safety, and environmental processes.
  • Quality & ESHS Leadership: Promote product security, enforce safety standards, report hazards, and actively participate in ESHS systems.

REQUIREMENTS
  • Bachelor's degree in a scientific field preferred.
  • 3-5 years of leadership experience preferred.
  • Significant laboratory and leadership experience may substitute for degree requirement.
  • Experience in GMP-regulated environments required
  • Strong knowledge of laboratory concepts, practices, and procedures.
  • Experience with deviation management and investigation processes.
  • Computer proficiency required (MS Word, Excel; SAP preferred).
  • Strong analytical and problem-solving skills
  • Proven ability to lead teams toward common objectives.
  • Excellent communication and conflict resolution skills.
  • Self-directed, reliable, and capable of working with minimal supervision.
  • Strong interpersonal skills with the ability to provide excellent customer service internally and externally
  • Demonstrated commitment to continuous improvement and operational excellence.

The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations.
Your Application
To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at www.evonik.com/en/careers.html.
Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.
Your Talent Acquisition Manager:
Brittney Compton [C]
Company is
Evonik Corporation