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Gxp Jobs in Minnesota (NOW HIRING)

DivIHN Integration Inc

R&D IT Site Lead

Plymouth, MN · On-site

Manage asset management, including laboratory tools and applications, and ensure compliance with IT controls. Support GxP workstations and IT QA activities, including IQ/OQ and computer system ...

Wischermann Partners Inc.

Room Attendant

Owatonna, MN · On-site

$15 - $16/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners

Room Attendant

Owatonna, MN · On-site

$15 - $16/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners

Room Attendant

Minneapolis, MN

$18.70/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners Inc.

Room Attendant

Edina, MN · On-site

$17/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners

Room Attendant

Edina, MN · On-site

$17/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners

Room Attendant

Edina, MN · On-site

$18.50/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners Inc.

Room Attendant

Minneapolis, MN · On-site

$18.70/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Wischermann Partners Inc.

Room Attendant

Edina, MN · On-site

$18.50/hr

Collaborate with all departments and communicate through GXP. * Resolve guest complaints to ensure guest satisfaction. * Monitor and maintain cleanliness, sanitation, and organization of assigned ...

Elliot Park Hotel

Maintenance Engineer

Minneapolis, MN · On-site

$21 - $23/hr

Collaborate with all departments and communicate through GXP. * Work with team to assess requests and provide a solution through, but not limited to, repair, maintenance, alteration, and new install.

DARCEO Inc

Automation Controls Engineer

Minneapolis, MN · On-site

$85K - $125K/yr

Capable of adhering to Good Manufacturing Practices (GxP) - Compliance, Change Control, Quality Oversight, Validation. Additional duties as assigned/required System Technical Skills Allen Bradley PLC ...

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Gxp information

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How much do gxp jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for gxp in Minnesota is $14.36, according to ZipRecruiter salary data. Most workers in this role earn between $12.69 and $15.05 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a GxP compliance specialist, and why are they important?

To thrive as a GxP Compliance Specialist, you need a solid understanding of regulatory standards (such as GMP, GLP, and GCP), quality management systems, and often a degree in life sciences or a related field. Familiarity with audit management tools, electronic quality management systems (eQMS), and relevant certification (like RAC or ASQ CQA) is highly valued. Strong attention to detail, analytical mindset, and effective communication skills help ensure regulatory adherence and facilitate cross-functional collaboration. These competencies are crucial for maintaining product quality, patient safety, and compliance with industry regulations.

What is a GxP job?

GxP jobs refer to roles that operate under 'Good Practice' guidelines in the life sciences and pharmaceutical industries, where 'GxP' stands for 'Good [x] Practice' (such as Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), or Good Clinical Practice (GCP)). These jobs are responsible for ensuring that products are developed, tested, manufactured, and distributed in compliance with regulatory standards to guarantee safety, quality, and integrity. GxP professionals may work in areas like quality assurance, laboratory management, clinical trials, and manufacturing. Their work is critical for meeting regulatory requirements set by agencies like the FDA or EMA. Adherence to GxP standards helps protect patient safety and product quality throughout the product lifecycle.

What is the difference between Gxp vs Quality Assurance Specialist?

AspectGxpQuality Assurance Specialist
Required CredentialsGxp compliance training, industry-specific certificationsQuality assurance certifications, such as CQE or CQA
Work EnvironmentRegulated industries like pharmaceuticals, biotech, and medical devicesManufacturing, healthcare, or software industries
Employer & Industry UsageUsed in industries with strict regulatory standardsCommon in quality-focused roles across various sectors
Comparison Search IntentUnderstanding Gxp compliance rolesComparing quality assurance roles with Gxp responsibilities

Gxp professionals focus on ensuring compliance with Good Practice standards in regulated industries, while Quality Assurance Specialists oversee quality processes across various sectors. Both roles require quality-related certifications, but Gxp roles emphasize regulatory compliance specific to industries like pharmaceuticals and biotech. Understanding these differences helps job seekers identify the right career path based on industry and certification requirements.

How does a GxP professional typically collaborate with cross-functional teams to ensure regulatory compliance?

GxP professionals regularly work alongside teams such as quality assurance, manufacturing, research and development, and regulatory affairs to ensure all processes and documentation meet regulatory standards. This collaboration often involves facilitating audits, reviewing protocols, and providing training on compliance requirements. Effective communication and a proactive approach are key, as GxP professionals must ensure that all stakeholders understand and adhere to the relevant guidelines throughout the product lifecycle.
What are popular job titles related to Gxp jobs in Minnesota? For Gxp jobs in Minnesota, the most frequently searched job titles are:
What job categories do people searching Gxp jobs in Minnesota look for? The top searched job categories for Gxp jobs in Minnesota are:
Gxp jobs near you
Infographic showing various Gxp job openings in Minnesota as of August 2026, with employment types broken down into 88% Full Time, 1% Part Time, 10% Contract, and 1% Nights. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $29,870 per year, or $14.4 per hour.

Validation Systems Administrator

Kindeva Drug Delivery

Woodbury, MN • On-site

$64K - $84K/yr

Full-time

Re-posted 27 days ago

Job description

Our Work Matters
At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
This role is responsible for the day-to-day administration and configuration of the Kneat eValidation system across all Kindeva sites. The Validation Systems Administrator creates, updates, and maintains templates, workspaces, disciplines, and document types within Kneat to support site validation activities. Working under the direction of the leader, this role ensures the system is configured correctly, users are supported, and records are maintained in compliance with GxP requirements and internal SOPs.
Role Responsibilities
Kneat System Administration:
  • Create, update, and modify Kneat templates, document types, and document packs for all Kindeva sites, ensuring they reflect current SOPs and validation requirements.
  • Set up and maintain workspaces and disciplines in Kneat for all Kindeva sites, configuring site-specific settings and ensuring correct workspace structure for each location.
  • Perform user management activities including account creation, role assignments, access modifications, and periodic access reviews for all Kindeva site users.
  • Execute and document validation lifecycle activities (IQ/OQ/PQ, protocol execution, discrepancy management, and summary reports) using Kneat workflows under guidance from the validation team.
  • Provide day-to-day end-user support and troubleshooting for Kneat configuration issues, document routing problems, and execution queries across all Kindeva sites.
  • Support Kneat system release updates by reviewing release notes, assisting with validation impact assessments, executing regression testing, and documenting results.
  • Collaborate with Quality, IT, Engineering, and Manufacturing teams to ensure compliant system use and alignment with SOPs and validation requirements.
  • Assist in training and onboarding users in Kneat functionality and best practices for compliant use.
  • CDMO experience is a plus, with exposure to supporting multiple clients, projects, or validation strategies within Kneat-supported environments.

Quality Assurance & Compliance
  • Support inspection readiness activities by ensuring Kneat records, audit trails, and system documentation are complete and accurate.
  • Ensure system compliance with GxP, 21 CFR Part 11, EU Annex 11, and other applicable regulations.
  • Collaborate with cross-functional teams to understand requirements and translate them into system solutions.

Business Process Support
  • Collaborate with cross-functional teams to understand requirements and translate them into system solutions.
  • Support quality processes such as Change Control, CAPA, Deviations, Complaints, and Document Management.
  • Ensure alignment with GMP and other regulatory requirements.

Global Governance & Standards
  • Establish and maintain Kneat procedures, and templates.
  • Participate in cross-functional governance meetings and harmonization initiatives as directed.
  • Stay informed on Kneat system updates, new features, and relevant regulatory guidance under the direction of the Kneat Administrator.
  • Assist in the delivery of Kneat user training and onboarding for new users across Kindeva sites

System Maintenance & Upgrades
  • Coordinate, draft test cases and test Kneat releases and updates including owning the associated change controls.
  • Monitor system performance and troubleshoot issues.
  • Maintain documentation for system configuration and validation activities.

Data & Security Management
  • Ensure data integrity, backup, and disaster recovery protocols are in place.
  • Monitor system logs and security alerts; implement corrective actions as needed.

BASIC QUALIFICATIONS
  • Bachelor's or Master's degree in Engineering, Life Sciences, Pharmacy, or related field preferred.
  • 2+ years of experience in validation, quality systems in the pharmaceutical, medical device or biotechnology industry
  • Hands-on experience with the Kneat eValidation platform, including template creation, workspace configuration, and user management.
  • Excellent problem-solving, communication, and organizational skills.
  • Ability to work independently and in a global, cross-functional team environment.
  • Hands on experience with GMP computerized systems, including system validation and regulatory compliance.
  • Working knowledge of GMP computerized systems, 21 CFR Part 11, and EU Annex 11 requirements in a regulated manufacturing environment.
  • Kneat admin certification preferred (or willingness to obtain upon hire)
  • Familiarity with GMP regulatory requirements and the importance of data integrity in a validated system.

#LI-remote #BM1-LI
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
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