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Gmp Quality Control Jobs in Indiana (NOW HIRING)

QC Equipment Coordinator

Fishers, IN

$18.50 - $25.50/hr

Quality Control Equipment Coordinator Summary The Quality Control Equipment Coordinator is ... GMP-regulated laboratory environment Familiarity with CMMS system Strong organizational ...

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 ...

QC Equipment Coordinator

Fishers, IN · On-site

$18.50 - $25.50/hr

Description Quality Control Equipment Coordinator Summary The Quality Control Equipment Coordinator ... GMP-regulated laboratory environment • Familiarity with CMMS system • Strong organizational ...

Quality Control Technician

Tipton, IN

$18 - $23/hr

... GMP). • Keep assigned area clean. • Perform other duties as assigned. Experience & Skills • 3 months of on the job training.Benefits This role is eligible for overtime pay for hours worked ...

Showing results 41-60

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:

QC Equipment Coordinator

INCOG

Fishers, IN

$18.50 - $25.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 29 days ago


Job description


Quality Control Equipment Coordinator Summary

The Quality Control Equipment Coordinator is essential in assisting the QC team with qualifying, calibrating, and maintaining quality control instruments and other assets. This position coordinates the annual requalification process for QC assets, communicates with vendors to arrange scheduled and unscheduled instrument repairs, helps with laboratory expansion projects, and supports updates for instrumentation software by managing related change actions as needed.


Essential Job Functions:

Supports laboratory operations by managing equipment documentation, coordinating with vendor services (annual visits), maintaining CMMS accuracy.

CMMS

Maintain and update equipment records with Blue Mountain CMMS

Coordinate PM and Calibration Schedules

Review, upload, close service documentation and work orders

Vendor Coordination

Schedule and coordinate on-site visits for implemented systems needing annual services

Primary point of contact for onsite visits when it's annual calibration services

Ensure completion and collection of required service documentation

Instrument Support

Track service contracts and spare part inventory

Assist with record updates, management of PM schedules, decommissioning activities


Special Job Requirements

Diploma/Certification

Experience in GMP-regulated laboratory environment

Familiarity with CMMS system

Strong organizational, documentation, communication skills

Ability to manage multiple priorities and vendor interactions


INCOG's Benefits:

Paid time off, based on tenure.

11 observed holidays + 1 floating holiday.

Choice to elect pet insurance.

401(k) plan with company match up to 3.5% of salary, vested immediately.

Choice of health & wellness plans.

FSA and HSA programs.

Dental & vision care.


Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.


If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.


INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.


By submitting your resume and details, you are declaring that the information is correct and accurate.

Employment Type: Full-Time

INCOG logo

About INCOG

Sourced by ZipRecruiter

Industry

Public administration

Company size

51 - 200 Employees

Headquarters location

Tulsa, OK, US

Year founded

1967