ZipRecruiter

Log In

1

Lims Manager Jobs in Bend, OR (NOW HIRING)

Microbac

Analyst ll

Prineville, OR · On-site

... LIMS * Comply with and promote Safety, and Quality programs * Perform peer review and work with the ... May be asked to perform duties of a Technical Manager or Study Manager * Other duties as assigned ...

Microbac

Analyst I

Prineville, OR · On-site

... LIMS * May be asked to perform duties of a Technical Manager or Study Manager * Comply with and promote Safety, and Quality programs MINIMUM REQUIREMENTS * High School Diploma; plus, two years of ...

All JobsLims JobsLims Manager JobsLims Manager Jobs in Bend, OR

Lims Manager information

See Bend, OR salary details

$24.3K

$64.7K

$108.1K

How much do lims manager jobs pay per year?

As of Aug 28, 2026, the average yearly pay for lims manager in Bend, OR is $64,725.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,400.00 and $72,800.00 per year, depending on experience, location, and employer.

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 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 job categories do people searching Lims Manager jobs in Bend, OR look for?

The top searched job categories for Lims Manager jobs in Bend, OR are:

Lims Manager jobs near you
Infographic showing various Lims Manager job openings in Bend, OR as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $64,725 per year, or $31.1 per hour.

Senior CSV Engineer / MES Validation Lead

Adryan B.V

Bend, OR • On-site

$120 - $170/hr

Other

Posted 8 days ago

Job description

We are looking for a senior CSV professional with strong, hands-on Manufacturing Execution System (MES) validation experience who can independently lead an MES validation workstream in a GMP manufacturing environment.

The Opportunity

Adryan is looking for an experienced Senior Computer System Validation (CSV) Engineer / MES Validation Lead to support a pharmaceutical manufacturing site in Oregon. The successful candidate will take ownership of CSV activities with a strong focus on MES and related manufacturing systems, working closely with Manufacturing, Automation, Engineering, IT/OT and Quality.

Ideally someone who understands how an MES operates in a pharmaceutical manufacturing environment, can translate manufacturing processes into validated system requirements, and can drive the MES validation lifecycle from requirements through testing, release and change control.

Key Responsibilities
  • Lead and execute CSV activities for MES and associated manufacturing systems.
  • Own or lead the MES validation workstream, including planning, risk assessment, documentation, testing and release.
  • Develop and review Validation Plans, URS, functional/design specifications, risk assessments, traceability matrices, IQ/OQ/PQ protocols, test scripts and Validation Summary Reports.
  • Support implementation, configuration, upgrade, expansion and lifecycle management of MES solutions.
  • Translate manufacturing processes, electronic batch records and GMP requirements into MES system and validation requirements.
  • Apply risk-based validation in accordance with GAMP 5 and modern CSA principles where appropriae.
  • Ensure compliance with 21 CFR Part 11, EU GMP Annex 11 and Data Integrity / ALCOA+ expectations.
  • Assess changes to MES and connected systems through formal change control and validation impact assessment.
  • Support deviations, investigations, CAPAs, troubleshooting and inspection readiness related to computerized systems.
  • Validate interfaces between MES and systems such as ERP, LIMS, DCS, SCADA, PLC.
  • Coordinate effectively across Manufacturing, Automation, IT/OT, Engineering and Quality and drive validation activities to agreed milestones.
Required Experience
  • 7+ years of CSV experience in pharmaceutical, biotechnology or another regulated life-sciences environment.
  • Strong, demonstrable hands-on MES validation experience is essential.
  • Experience leading or independently owning an MES/CSV workstream.
  • Strong knowledge of GAMP 5, 21 CFR Part 11, EU GMP Annex 11, Data Integrity and risk-based validation.
  • Experience across the full computerized system lifecycle: requirements, design review, testing, qualification, release, change control and periodic review.
  • Experience working directly within a GMP manufacturing environment.
  • Ability to communicate effectively with Manufacturing, Automation, IT/OT, Engineering and QA stakeholders.
  • Strong documentation, troubleshooting and stakeholder-management skills.
  • Ability to work independently and deliver in a fast-paced project environment.
Highly Preferred
  • Experience with Werum / Körber PAS-X, Rockwell PharmaSuite, Siemens Opcenter or another enterprise MES platform.
  • MES integration with ERP, LIMS, DCS, SCADA, PLC or historian systems.
  • Electronic Batch Records (EBR/eBR), recipe management and master batch record configuration.
  • MES equipment integration, automation interfaces, data migration and system interfaces.
  • CSA / risk-based assurance approaches and validation of manufacturing automation systems.
  • Experience in Oral Solid Dosage, drug product, small-molecule manufacturing, spray drying or related pharmaceutical operations.
  • Experience in greenfield, expansion or major system implementation projects.
About Adryan

Adryan is an international engineering and quality consultancy dedicated to the pharmaceutical and biotechnology industry. We support leading life-sciences organizations across Europe and the United States with specialized expertise in Commissioning & Qualification, Computer System Validation, Quality & Compliance, Engineering and Project Management.

For this assignment we are looking for a senior professional who can make an immediate impact, strengthen our delivery in Oregon and become an important part of our growing US project organization.

#J-18808-Ljbffr

Apply