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Lims Project Manager Jobs in Virginia (NOW HIRING)

Director, Biorepository Core

Richmond, VA · On-site

$120 - $180/hr

Support future development and enhancement of LIMS infrastructure and laboratory technologies. Personnel & Project Management * Supervise all biorepository and laboratory personnel. * Recruit, mentor ...

Managing and driving wastewater surveillance projects. Assisting with validation efforts ... Experience using laboratory information management systems (LIMS) Education: Bachelor of Science ...

ADay in theLife As a QA Associate ,you'llbe responsible forassistingmultiple projects where you ... Experience with LIMS. * Proficiency using and data visualization tools for reports and graphs.

... LIMS system * Travel 3-4 times a week including at least one day of overnight travel, during ... Ability to control and manage several projects simultaneously Required 2 Years * Working knowledge ...

Showing results 21-30

Lims Project Manager information

See Virginia salary details

$44.1K

$95.7K

$153.2K

How much do lims project manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for lims project manager in Virginia is $95,732.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,400.00 and $112,000.00 per year, depending on experience, location, and employer.

What is a LIMS Project Manager?

LIMS Project Managers are professionals who oversee the implementation and maintenance of Laboratory Information Management Systems (LIMS) within organizations. Their responsibilities include coordinating between laboratory staff, IT teams, and vendors to ensure the system meets the needs of the laboratory. They manage project timelines, budgets, and ensure compliance with industry regulations. LIMS Project Managers also handle troubleshooting, training, and post-implementation support to ensure the system operates efficiently and effectively.

What are the key skills and qualifications needed to thrive as a LIMS Project Manager?

To thrive as a LIMS Project Manager, you need a strong background in laboratory processes, project management experience, and a relevant degree in science or IT. Familiarity with Laboratory Information Management Systems (LIMS), project management software, and often certifications like PMP or Six Sigma are typically required. Excellent communication, leadership, and problem-solving skills help manage cross-functional teams and client expectations effectively. These skills and qualifications are crucial to ensure timely, successful LIMS implementations that meet organizational and regulatory requirements.

What are some common challenges faced by LIMS Project Managers during system implementation, and how can they be addressed?

LIMS Project Managers often encounter challenges such as aligning system functionality with diverse laboratory workflows, managing stakeholder expectations, and ensuring data integrity during migration. Effective communication with lab staff and IT teams, thorough documentation of requirements, and phased implementation strategies can help mitigate these issues. It's also important to provide robust training and prioritize user feedback during the rollout to ensure successful adoption.

What is the difference between Lims Project Manager vs Laboratory Technician?

AspectLims Project ManagerLaboratory Technician
CredentialsBachelor's in Life Sciences, Project Management CertificationAssociate's or Bachelor's in Science, relevant lab certifications
Work EnvironmentOffice-based, overseeing projects in labs or biotech companiesLaboratory setting, performing tests and sample analysis
Industry UsageUsed in biotech, pharmaceutical, and clinical labs for project oversight

The Lims Project Manager focuses on planning, coordinating, and managing laboratory information system projects, ensuring timely delivery and compliance. In contrast, a Laboratory Technician performs hands-on testing and sample analysis. While both roles work within laboratory environments, their responsibilities and required skills differ significantly.

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

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

What job categories do people searching Lims Project Manager jobs in Virginia look for?

The top searched job categories for Lims Project Manager jobs in Virginia are:

What cities in Virginia are hiring for Lims Project Manager jobs?

Cities in Virginia with the most Lims Project Manager job openings:

Infographic showing various Lims Project Manager job openings in Virginia as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $95,732 per year, or $46 per hour.

Associate Director, QC Microbiology

BeiGene USA

Hopewell, VA

$22.75 - $30/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago


Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

Leads and manages all QC Microbiology laboratory activities to support GMP manufacturing, including Environmental Monitoring (EM) and microbiological testing of materials, intermediates, and finished products in accordance with FDA/EU regulations, applicable International Regulations, and BeOne processes and procedures. Establishes a new QC Microbiology laboratory and implements QC Microbiology procedures. Supports commissioning and qualification of a new manufacturing facility. Participates in regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the Microbiology laboratory.

Essential Functions of the job:

  • Lead the new QC Microbiology laboratory (Micro-Lab) set up, including commissioning/qualification of cleanrooms and equipment.
  • Establish an environmental monitoring (EM) program in accordance with FDA/EU regulations and applicable International Regulations.
  • Support critical utility qualification, including water for injection (WFI), clean steam, and process gases.
  • Lead the Environmental Monitoring Performance Qualification (EMPQ) of cleanrooms.
  • Establish QC microbiology laboratory procedures and test methods in accordance with health authority regulations and BeOne Global quality standards.
  • Manage QC Micro-Lab routine operations, including but not limited to microbiological testing, data review, personnel training, and equipment maintenance.
  • Lead the establishment of a cross contamination strategy for the manufacturing site.
  • Ensure Micro-Lab EHS compliance.
  • Ensure timely completion of testing (DS, DP release and stability testing, raw materials testing) to ensure timely generation and reporting of test results in support of manufacturing operations.
  • Ensure appropriate investigation of OOS events and Microbial Data Deviations (MDD).
  • Ensure appropriate corrective actions and preventive actions (CAPAs) are implemented to prevent recurrence of OOS and MDDs.
  • Significant participation in internal and external GMP audits.
  • Manage microbial method verification activities, including the verification strategy and approval of protocols and reports.
  • Ensure that the QC Micro-Lab meets or improves on budget, cost, volume and efficiency targets (KPIs) in line with business objectives.
  • Introduce advanced concept of microbiology laboratory to keep the laboratory forward-looking and competitive in the industry.
  • Build a highly efficient QC microbiology team. Identify and develop key talents by mentoring, motivating, coaching direct reports to higher levels of capability.
  • Undertake any other duties as required.
Other Qualifications:
  • Minimum of 8 years relevant working experience in an FDA-regulated biotechnology or pharmaceutical company.
  • Minimum of 5 years team management experience in an FDA-regulated biotechnology, pharmaceutical company with progressive levels of responsibility are required.
  • Expert with pharmaceutical microbial testing and related equipment/instruments.
  • Knowledgeable with USP/EP and cGMP/EU GMP regulations.
  • Experience with microbial contamination control of aseptic process.
  • Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
  • Wide knowledge of analytical methods and electronic systems (LIMS, MODA) used in the QC Micro-Lab.
  • Strong leadership/team management skills and experience.
  • Credible and confident communicator (written and verbal) at all levels.
  • Strong analytical and problem-solving ability.
  • Excellent project management skills.
  • Hands-on approach, with a 'can do' attitude.
  • Ability to prioritize, demonstrating good time management skills.
  • Excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
  • Self-motivated, with the ability to work proactively using own initiative.
  • Committed to learning and development.

Education:

  • Bachelor's Degree in Science (ideally microbiology, pharmaceutical sciences, biotechnology or related).

Computer Skills:

  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint)

Travel:

  • Must be willing to travel approximately 10%
  • Ability to work on a computer for extended periods of time

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity
Salary Range: $133,800.00 - $183,800.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.