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Gmp Quality Control Jobs in Wisconsin (NOW HIRING)

Quality Control Lead Seneca Foods in Cumberland is currently seeking a Quality Control Lead to join ... Ensure that GMP's (General manufacturing Practices), safety rules, and regulations are being ...

Job Title: QC Laboratory Technician - Microbiology This entry-level QC Laboratory Technician role ... Carry out all tasks in compliance with GMP, FAMIqs, and FSMA requirements and internal quality ...

The Quality Control Technician is a vital position at Freshpack. The motivated, qualified candidate ... Proper GMP's are being followed * Inspect in-process and finished products for quality and ...

QC Technician

Janesville, WI · On-site

$17.25 - $22/hr

Seneca Foods in Janesville WI, is currently seeking a Full-Time QC Technician to join our night ... Required to follow all GMP rules and regulations. * Requires the ability to bend, lift, carry, push ...

QC Technician

Janesville, WI

$17.25 - $22/hr

Seneca Foods in Janesville WI, is currently seeking a Full-Time QC Technician to join our night ... Required to follow all GMP rules and regulations. * Requires the ability to bend, lift, carry, push ...

QC Technician

Janesville, WI

$18.50 - $23.50/hr

Seneca Foods in Janesville WI, is currently seeking a Full-Time QC Technician to join our night ... Required to follow all GMP rules and regulations. Requires the ability to bend, lift, carry, push ...

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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.

Is GMP Quality Control a good career path?

GMP Quality Control involves testing and inspecting pharmaceutical products to ensure they meet regulatory standards, making it a stable career with demand in the healthcare and biotech industries. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training or laboratory skills. The role offers opportunities for advancement into quality assurance, compliance, or management positions.

Is GMP Quality Control a good career?

GMP Quality Control is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It involves tasks such as testing, documentation, and compliance, often requiring knowledge of laboratory techniques and certifications like GMP training. The role offers opportunities for advancement and consistent employment due to industry regulation requirements.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and inspecting raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent defective or unsafe products from reaching consumers by verifying compliance with regulatory requirements and maintaining proper documentation. QC professionals often use analytical tools and follow strict protocols to support product safety and efficacy.

What are popular job titles related to Gmp Quality Control jobs in Wisconsin?

For Gmp Quality Control jobs in Wisconsin, the most frequently searched job titles are:

What cities in Wisconsin are hiring for Gmp Quality Control jobs?

Cities in Wisconsin with the most Gmp Quality Control job openings:

Quality Control Microbiology Specialist

eGenesis

Madison, WI • On-site

Full-time

Re-posted 6 days ago


Job description

About eGenesis
eGenesis is a clinical-stage biotechnology company developing human-compatible engineered organs to address the severe global organ shortage. The Company's proprietary genome engineering platform enables extensive, multiplex gene edits to remove key biological barriers, add protective human transgenes, and inactivate endogenous retroviruses. EGEN-2784, a genetically engineered porcine kidney, is the Company's lead program and is currently being evaluated in a multi-patient Expanded Access study at MGH. eGenesis is headquartered in Cambridge, MA. 

POSITION SUMMARY
eGenesis is seeking an innovative QC Microbiology Specialist to lead and provide the technical and strategic oversight of eGenesis's environmental monitoring program. In this position you will be responsible for hands-on environmental monitoring sampling, testing, reporting and trending of eGenesis GMP manufacturing facilities in Rensselaer, IN. You will ensure activities are executed in a cGMP compliant manner and have the opportunity to work collaboratively on implementation and maintenance of our contamination control program. The ideal candidate will be independently motivated, a strong communicator and demonstrate proficiency in regulatory compliance. This position will be in the Greater Madison Area in Wisconsin.
PRIMARY RESPONSIBILITIES
  • Coordinate the environmental monitoring (EM) program at both eGenesis manufacturing facilities ensuring the collection, transport and processing of air and surface samples.
  • Manage the schedule for all routine and non-routine monitoring activities internally and with external contract laboratory.
  • Perform environmental monitoring sample collection (nonviable, viable, and surface) as well as providing guidance and training on procedures to additional team members.
  • Keep complete and accurate documentation in electronic test methods.  
  • Review and trend environmental monitoring data.
  • Support EM and laboratory deviations. Identify and implement corrective actions to prevent reoccurrence.
  • Author, review, and/or approve data, SOPs, COAs, protocols, reports, deviations, and other quality records.
  • Work collaboratively with QC contamination control representative and work cross functionally to maintain and enhance cleaning/disinfection program, material/equipment and gowning programs as applicable.
  • This position will require some travel (~20% of time) between manufacturing sites in Wisconsin and Indiana, but primary location will be in Wisconsin.
BASIC QUALIFICATIONS
  • B.S./M.S. in Life Sciences or related field with 0-3 years of experience, in GMP QC Laboratory.
  • Proficient in microbiology methods (plate enumeration, growth promotion, microbial ID, etc.) and aseptic technique needed to perform EM in a GMP environment.
  • Strong knowledge of US and EU cGMP regulations/guidance.
  • The ability to work and lead in a fast-paced environment, manage priorities, and maintain timelines for multiple projects is essential.
  • Effective communication skills, both verbal and written, at all levels and across various functions.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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