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Temporary Lims Jobs in Rodeo, CA (NOW HIRING)

Logistics Specialist

Vacaville, CA · On-site

$20 - $25/hr

Temporary Assignment Work Type: Onsite Shifts: Monday to Friday from 06:00 AM to 03:00 PM Summary ... Accurately enter data into business and quality systems (DCS, POMS, SAP, LIMS, PQS, etc.

Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook ... Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the ...

Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook ... Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the ...

Temporary Lims information

See Rodeo, CA salary details

$11

$20

$28

How much do temporary lims jobs pay per hour?

As of Jul 17, 2026, the average hourly pay for temporary lims in Rodeo, CA is $20.30, according to ZipRecruiter salary data. Most workers in this role earn between $16.97 and $22.02 per hour, depending on experience, location, and employer.

What are some common challenges faced when working as a Temporary LIMS (Laboratory Information Management System) professional, and how can they be addressed?

As a Temporary LIMS professional, you may face challenges such as quickly adapting to different laboratory workflows, learning proprietary or customized LIMS platforms, and integrating smoothly into existing teams. Since the role is temporary, you'll need to rapidly familiarize yourself with the lab's data management protocols and ensure data integrity under tight timelines. Proactively communicating with permanent staff, utilizing available documentation, and seeking clarification on lab-specific processes can help you overcome these obstacles and contribute effectively during your assignment.

What are the key skills and qualifications needed to thrive as a Temporary LIMS (Laboratory Information Management System) Specialist, and why are they important?

To excel as a Temporary LIMS Specialist, you typically need a background in laboratory science, strong data management skills, and familiarity with laboratory workflows. Hands-on experience with LIMS software platforms such as LabWare, STARLIMS, or Thermo Fischer, as well as knowledge of database systems and relevant certifications, is highly valued. Strong analytical thinking, problem-solving abilities, and effective communication help you adapt quickly and support laboratory teams efficiently. These skills ensure accurate data handling, regulatory compliance, and seamless lab operations during temporary assignments.

What are Temporary LIMS positions?

Temporary LIMS positions refer to short-term jobs involving Laboratory Information Management Systems (LIMS). These roles typically require managing, maintaining, or supporting LIMS software, which is used to track samples, tests, and laboratory data. Temporary LIMS jobs are often found in laboratories, biotech companies, and research organizations, and may involve data entry, quality control, system administration, or user support. These positions are ideal for candidates seeking contract or project-based work, often to support specific projects or during busy periods.
What job categories do people searching Temporary Lims jobs in Rodeo, CA look for? The top searched job categories for Temporary Lims jobs in Rodeo, CA are:
What cities near Rodeo, CA are hiring for Temporary Lims jobs? Cities near Rodeo, CA with the most Temporary Lims job openings:
(CW) Manufacturing Associate (Temporary/Contract)

(CW) Manufacturing Associate (Temporary/Contract)

BIOMARIN PHARMACEUTICAL

Novato, CA

Full-time

Re-posted 18 days ago


BioMarin Pharmaceutical rating

8.3

Company rating: 8.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

23rd of 74 rated pharmaceutical


Job description

Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Our manufacturing and process development teams manage the production of our therapies for clinical trials and commercial markets. These engineers, technicians, scientists, and support professionals continually provide quality assurance and ensure we meet all regulatory standards. We have manufacturing facilities in Northern California and in Cork, Ireland. Additionally, our supply chain teams procure the goods and services needed to support manufacturing and worldwide distribution.
About Technical Operations
BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

This a contract /Temporary role - Contract length 1 year Multiple roles (3)

Shift is Sunday - Tuesday 6:00 p.m. - 7:00 a.m., with alternating Saturdays
Job Description:
PROCESS KNOWLEDGE: Understanding of process theory and equipment operation. Ability to learn biopharmaceutical manufacturing processes including mammalian cell culture, depth filtration, tangential flow filtration, column chromatography, centrifugation, protein purification, and formulation of bulk drug substance. Support initiatives for process optimization. Identify and elevate processing issues and support solutions. Gain experience with automation systems (LIMS, MES, PI, etc.).
TECHNICAL DOCUMENTATION: Provide feedback and/or suggested changes to operational procedures. Assist in the incorporation of new technologies, practices, and standards into procedures. Capable of writing and reviewing process documents.
QUALITY AND COMPLIANCE: Understanding of cGMPs as related to Commercial Operations. Ability to utilize Quality systems (Deviations, CAPAs, Change Requests, Action/Alert Reports, etc.).
BUSINESS: Ability to participate on projects and contribute to outcomes. Capability to learn and support new business systems (Track wise, ERP, etc.). Support trending of defined department metrics.
WORK ENVIRONMENT/PHYSICAL DEMANDS
Consists of strenuous, repetitive work. The following list of physical movements may be used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands.
Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds.
May require work around loud equipment. The use of personal protective equipment will be required.
Requires various shift based work and off hours.
Skills
Strong communication skills-verbal and written
Ability to work in a team environment which includes good conflict resolution and collaboration
Displays good initiative to identify areas for improvement and implement solutions
Education
-Bachelor's degree in science related area or engineering
-Associate's degree in science related area or Biotech certificate with 2+ years of experience in a biotech
Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Employment Type: Fulltime-Temporary

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