LabWare LIMS Configuration Specialist

job summary:

Summary

Seeking an experienced LabWare LIMS Configuration Specialist to support a LabWare 8 implementation in a GMP laboratory environment. The role will focus on configuration of raw material, commercial product, stability, and instrument integration workflows, along with support for validation activities.

location: Thousand Oaks, California

job type: Contract

salary: $80 - 90 per hour

work hours: 9am to 5pm

education: Bachelors



responsibilities:

Responsibilities

• Configure LabWare LIMS 8 objects, workflows, master data, specifications, and test templates.
• Support implementation of raw material, commercial product, and stability workflows.
• Configure and support laboratory equipment and system interfaces.
• Translate business, laboratory, and quality requirements into compliant LabWare configurations.
• Support requirements traceability, testing, validation, and change control activities.
• Troubleshoot configuration and integration issues.
• Work with Quality, Validation, IT, and laboratory teams to support successful deployment and operation of LabWare.

Success Measures

• Timely completion of LabWare 8 configurations.
• Successful support of validation and testing activities.
• Stable execution of configured workflows in the laboratory environment.
• Successful integration of laboratory instruments and systems.

qualifications:

Required Qualifications

Hands-on experience configuring LabWare LIMS (LabWare 8 preferred).

Experience in GMP-regulated laboratory environments.

Experience with one or more of the following:

Raw material testing

Commercial product testing

Stability programs

Laboratory equipment integration

Experience supporting LIMS validation and testing activities.

Experience with laboratory systems such as LabX, Empower, or similar platforms.

Strong documentation and communication skills.

Preferred Qualifications

Experience supporting LabWare8 upgrades or LIMS implementations..

Pharmaceutical or biotechnology industry experience.

Familiarity with GMP change control and validation processes.

skills:

master data,LIMS,requirements traceability,communication skills,Troubleshoot,biotechnology,change control,laboratory systems,laboratory equipment,laboratory instruments,product testing,raw material,testing,validation processes,workflows

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad Digital, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad Digital offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.


Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.



Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.



We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.