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Lims Manager Jobs in Minnesota (NOW HIRING)

PLS QA Document Control Specialist

Oakdale, MN · On-site

$21 - $24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience using laboratory information management system (LIMS) * Experience working in an FDA regulated environment or familiarity with FDA cGMP regulations PHYSICAL/MENTAL REQUIREMENTS The ...

PLS QA Document Control Specialist

Oakdale, MN

$21 - $24/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience using laboratory information management system (LIMS) * Experience working in an FDA regulated environment or familiarity with FDA cGMPregulations PHYSICAL/MENTAL REQUIREMENTS The physical ...

PLS Associate Scientist II

Oakdale, MN · On-site

$25 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Provides routine analysis, interpretation and counsel to clients, staff, management, and functional ... LIMS * UV -Vis * GC * HPLC * GMP * ALCOA+ * Root Cause Analysis PHYSICAL/MENTAL REQUIREMENTS: The ...

PLS Associate Scientist II

Oakdale, MN

$25 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Provides routine analysis, interpretation and counsel to clients, staff, management, and functional ... LIMS * UV -Vis * GC * HPLC * GMP * ALCOA+ * Root Cause Analysis PHYSICAL/MENTAL REQUIREMENTS: The ...

PLS GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and LIMS data/reports. Data and records may be in the form of electronic or paper records or ... Provides intermediate to complex analysis, interpretation and counsel to staff, management, and ...

GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and LIMS data/reports. Data and records may be in the form of electronic or paper records or ... Provides intermediate to complex analysis, interpretation and counsel to staff, management, and ...

PLS Associate Scientist II

Oakdale, MN · On-site

$25 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Provides routine analysis, interpretation and counsel to clients, staff, management, and functional ... LIMS * UV-Vis * GC * HPLC * GMP * ALCOA+ * Root Cause Analysis PHYSICAL/MENTAL REQUIREMENTS: The ...

CCI Technology Lead

Eden Prairie, MN · On-site

$120K - $140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Demonstrated leadership experience managing technical teams * Other Skills Required (computer, language, etc.): Microsoft Office, LIMS, QMS System * Ability to travel up to 20% WHAT WILL SET YOU ...

PLS GMP Data Reviewer (Pharma)

Oakdale, MN · On-site

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and LIMS data/reports. Data and records may be in the form of electronic or paper records or ... Provides intermediate to complex analysis, interpretation and counsel to staff, management, and ...

New

GMP Data Reviewer (Pharma)

Oakdale, MN

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and LIMS data/reports. Data and records may be in the form of electronic or paper records or ... Provides intermediate to complex analysis, interpretation and counsel to staff, management, and ...

GMP Data Reviewer (Pharma)

Oakdale, MN

$55K - $65K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... and LIMS data/reports. Data and records may be in the form of electronic or paper records or ... Provides intermediate to complex analysis, interpretation and counsel to staff, management, and ...

Quality Control Technician

Rochester, MN · On-site

$20 - $33/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience with laboratory information management systems (LIMS), chromatography software (e.g., Empower), and other QC data systems preferred. * Adaptable to quickly changing priorities and ...

Quality Assurance (QA) Technician

Randolph, MN · On-site

$23/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Review, support and verify the Laboratory Information System (LIMS) by conducting and evaluating ... Product Release Management: Verify product compliance to FSQR standards and coordinate the release ...

Showing results 41-60

Lims Manager information

See Minnesota salary details

$22.5K

$60.1K

$100.4K

How much do lims manager jobs pay per year?

As of Aug 17, 2026, the average yearly pay for lims manager in Minnesota is $60,088.00, according to ZipRecruiter salary data. Most workers in this role earn between $43,100.00 and $67,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the lims manager position, and why are they important?

To thrive as a Lims Manager, a strong background in laboratory science, data management, and experience with Laboratory Information Management Systems (LIMS) is essential, often supported by a relevant bachelor’s degree. Familiarity with LIMS software such as LabWare, STARLIMS, or Thermo Fisher, as well as certifications in data integrity or system administration, are highly valued. Excellent problem-solving, communication, and leadership skills help manage teams and facilitate collaboration across laboratory and IT departments. These competencies are crucial for ensuring accurate information flow, regulatory compliance, and efficient laboratory operations.

What is a lims manager?

A LIMS (Laboratory Information Management System) Manager is responsible for overseeing the implementation, maintenance, and optimization of a laboratory's data management system. They ensure that the LIMS software supports lab workflows, regulatory compliance, and data integrity. Their role involves coordinating with IT teams, lab staff, and external vendors to enhance system functionality and troubleshoot issues. Additionally, they may train users, manage system upgrades, and develop reports to improve operational efficiency.

What are the typical daily responsibilities of a lims manager?

As a Lims Manager, your daily responsibilities often include overseeing the configuration and maintenance of the LIMS to ensure it meets laboratory needs, managing user access, and providing technical support to lab staff. You may also coordinate with IT teams and laboratory personnel to implement system updates, ensure data integrity, and troubleshoot any system-related issues. Regular tasks can involve training users, generating reports for regulatory compliance, and optimizing workflows within the lab’s digital infrastructure. You'll play a key role in keeping laboratory operations streamlined, secure, and in alignment with industry standards.

What are the most commonly searched types of Lims jobs in Minnesota?

The most popular types of Lims jobs in Minnesota are:

What are popular job titles related to Lims Manager jobs in Minnesota?

For Lims Manager jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Lims Manager jobs?

Cities in Minnesota with the most Lims Manager job openings:

Infographic showing various Lims Manager job openings in Minnesota as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $60,088 per year, or $28.9 per hour.

PLS QA Document Control Specialist

Pace

Oakdale, MN • On-site

$21 - $24/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

Shift:
Monday through Friday, 8:00 AM - 5:00 PM
Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.
This is an onsite, full-time, PLS Document Control Specialist position located in Oakdale, MN, Monday - Friday, from 8:00 a.m. - 5:00 p.m.
Compensation: $21.00 - $24.00 per hour
The salary for this position reflects a variety of factors. Compensation will be determined based on the candidate's geographic location, relevant experience, education, skills, and alignment with internal equity. Market conditions, budgetary considerations, and organizational compensation guidelines may also influence the final offer.
Make an Impact. Build a Career.
Pace® Life Sciences delivers a comprehensive suite of contract CMC development, CTM manufacturing, regulatory compliance, consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene therapy industries. Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing support centers, we partner with clients to efficiently advance programs from early development through commercialization.
Our experienced industry experts and continued investment in state-of-the-art facilities reflect our commitment to quality, speed, and reliability. United by a shared purpose, we bring meaningful value to patients, healthcare professionals, and health businesses worldwide by delivering services that support a safer, healthier future.
SUMMARY
Responsible for performing and managing QA administrative and document control tasks while following current Good Manufacturing Practice (cGMP), under the supervision of experienced Quality Professionals.
ESSENTIAL FUNCTIONS
This job description lists the major duties and requirements of the position and is not all-inclusive. Applicable essential functions may vary by site. Incumbent(s) may be expected to perform job-related duties other than those contained in this document and may be required to have specific job-related knowledge and skills.
  • Performs quality assurance and record management tasks with strong attention to detail
  • Provides excellent customer service and QA support to all internal and external PLS customers
  • Maintains various filing systems, including labeling of folders, scanning/filing records, maintaining folder inventory and filing system
  • Scans and files technical and quality records and maintains records in a readily retrievable state
  • Prepares and coordinates records for off-site archival and retrieval
  • Maintains the QA report databases by entering and updating all relevant data within the related system
  • Prepares and assembles logbooks for data entry and assigns tracking numbers for notebooks
  • Provides administrative support to remote and on-site QA team members
  • Contributes to the efficiency and effectiveness of the department's services to its customers by participating as an active member of a work team
  • Promotes and supports the overall mission of Pace® by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment.

QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.
Education and Experience
High School Diploma/GED; AND one year of administrative experience, specifically with administrative document control; OR an equivalent combination of education, training, and experience.
Required Knowledge and Skills
Required Knowledge:
  • Excellent organizational and time management skills
  • Strong attention to detail and accuracy
  • Flexibility to handle multiple tasks concurrently and in a timely manner
  • Good interpersonal skills and ability to work both independently and in a team environment
  • Ability to communicate effectively with both internal and external customers
  • Adaptability to manage changing task assignments and priorities

Required Skills:
Proficiency in Microsoft Word and Microsoft Excel.
Desirable Knowledge and Skills:
  • Proficiency in Microsoft Office 365, including Outlook and Teams
  • Proficiency with Adobe Acrobat
  • Experience with electronic document management systems (e.g., MasterControl eDMS)
  • Experience using laboratory information management system (LIMS)
  • Experience working in an FDA regulated environment or familiarity with FDA cGMP regulations

PHYSICAL/MENTAL REQUIREMENTS
The physical demands described herein are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Mobility to work in a lab and office setting, use standard office and lab equipment and stamina to sit for extended periods of time; exerting up to 20 pounds of force occasionally and/or up to 10 pounds of force frequently to lift, carry, push, pull or move objects; vision to read printed materials and computer screens; and hearing and speech to communicate in person or over the telephone.
WORKING ENVIRONMENT
Work is performed in a lab and office setting. Work is subject chemicals, fumes, gasses, noxious odors and related items in a lab setting.
Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.
Benefits
When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.
Equal Opportunity Employer
Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.