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Lims Project Manager Jobs in California (NOW HIRING)

... LIMS and project management tools. • Coordinate and support new product stability programs, ensuring timely shelflife assignment critical for global product registration and market readiness. • ...

The Sample Accessioner will work in a team environment which includes project managers and clinical ... This will entail following SOPs and working with Laboratory Information Management System (LIMS ...

The Sample Accessioner will work in a team environment which includes project managers and clinical ... This will entail following SOPs and working with Laboratory Information Management System (LIMS ...

We specialize in helping companies strategize, architect, implement and support scientific data management and laboratory automation projects. Senior LIMS/ELN Business Analysts Duties: Work with ...

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Lims Project Manager information

See California salary details

$43.9K

$95.3K

$152.5K

How much do lims project manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for lims project manager in California is $95,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,000.00 and $111,500.00 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 California?

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

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

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

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

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

Infographic showing various Lims Project Manager job openings in California as of August 2026, with employment types broken down into 82% Full Time, 15% Part Time, and 3% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $95,295 per year, or $45.8 per hour.

Manager, Stability

Torrance, CA • Hybrid

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago


Job description

ROLE AT A GLANCE: 
The Stability Manager leads the execution, coordination, and continuous improvement of the stability program for Dietary Supplement, Food, and Personal Care products. This role serves as a key technical and communication hub, ensuring stability data is scientifically sound, compliant, delivered on time, and clearly communicated to project teams to support product development, registration, and lifecycle management across regions.

HOW YOU’LL MAKE AN IMPACT: 
•    Lead and oversee stability studies, including protocol execution, sample management, data review, statistical analysis, trending, and reporting. 
•    Serve as a primary communication lead for stability, proactively updating project teams, QC managers, R&D, Regulatory, and regional stakeholders on study status, milestones, risks, and outcomes. 
•    Ensure stability timelines are met by actively tracking deadlines, stability pull schedules, testing completion, and reporting deliverables using LIMS and project management tools.
•    Coordinate and support new product stability programs, ensuring timely shelflife assignment critical for global product registration and market readiness. 
•    Apply statistical analysis and trending techniques to stability data to support shelf life determination, identify emerging risks, and drive data based decisions, and provide technical review and approval of stability protocols, acceptance criteria, and reports prior to cross functional or regional use
•    Lead and coordinate the resolution of stabilityrelated OOS, deviations, and adverse trends, collaborating with QC, QA, and scientific teams to determine root cause and corrective actions. 
•    Maintain strong alignment with QC managers, analytical teams, and R&D partners by leveraging knowledge of analytical methods to support data interpretation, investigations, formulation development, specification setting, and interpretation of stability results for new and reformulated products.
•    Ensure compliance with FDA 21 CFR Part 111, ISO/IEC 17025, cGMP, GDP, and applicable ICH stability guidelines. 
•    Identify industry best practices and implement continuous improvement initiatives to enhance stability processes, tools, templates, and efficiency. 
•    Additional duties as assigned.

TEAM DYNAMICS:  
•    This role leads Technicians, Stability Coordinators and/or Senior Stability Coordinators and works closely with QC managers, scientists, R&D, Regulatory, Licensing, and regional partners. The position operates in a matrixed environment requiring strong influencing skills, technical credibility, and clear, timely communication.

LEADERSHIP AND SUPERVISORY RESPONSIBILITIES: 
•    Directly manages Technicians, Stability Coordinators and/or Senior Stability Coordinators.
•    Responsible for onboarding, training, performance management, coaching, and development of stability team members.
•    Supports workload planning and readiness as stability oversight expands across regions or sites.


QUALIFICATIONS FOR SUCCESS: 

Education
•    Bachelor of Science degree in Chemistry, Biochemistry, Biology, Microbiology, or a related scientific discipline.


Experience
•    7+ years
•    Demonstrated experience with stability protocol oversight, data interpretation, statistical trending, and shelf life assignment for regulated products.
•    Strong working knowledge of FDA 21 CFR Part 111, ISO/IEC 17025, cGMP, GDP, and ICH stability guidelines applicable to food and dietary supplements.
•    Experience resolving OOS, deviations, and stability related investigations in collaboration with QC and QA.


Skills/Certifications:
•    Advanced understanding of stability science, regulatory expectations, and industry best practices.
•    Strong communication and stakeholder alignment skills, with the ability to clearly convey technical stability data to diverse audiences.
•    Proficiency in statistical analysis and data trending for stability and shelf life determination.
•    Preferred familiarity with analytical methods used in QC testing (e.g., HPLC, ICP, GC) to support data interpretation.
•    Experience using Laboratory Information Management Systems (LIMS), preferably LabWare.

#LI-GB1

#LI-Hybrid 


Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D; Short-Term and Long-Term Disability, and an Employee Assistance Program (EAP). Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company-observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.