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4d

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LabWare LIMS Validation Specialist

Experis -
Los Angeles, CA

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Job Details

Contract
$85 an hour

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Vision insurance
401(k) matching
Life insurance

Qualifications

Regulatory inspections
GAMP
Pharmaceutical regulatory compliance
Laboratory information management systems
Quality assurance experience within pharmaceutical industry
Audit support

Full Job Description

Our client, a leading organization in the pharmaceutical and biotechnology industry, is seeking a LabWare LIMS Validation Specialist to join their team. As a LabWare LIMS Validation Specialist, you will be part of the Validation and Compliance team supporting laboratory operations and quality assurance initiatives. The ideal candidate will demonstrate strong analytical skills, meticulous attention to detail, and excellent communication abilities, which will align successfully in the organization.

Job Title:LabWare LIMS Validation Specialist

Location:Los Angeles, California

Pay Range:$85

What's the Job?

Lead validation efforts and ensure requirements traceability across the LabWare LIMS 8 implementation.
Support validation strategy and execution, including IQ, OQ, PQ, and validation documentation review.
Collaborate with configuration and integration teams to validate workflows and system functionality.
Ensure compliance with GxP, CSV, and internal validation procedures to maintain audit readiness.
Assist in preparing for regulatory inspections and review validation reports and deviations.

What's Needed?

Proven experience supporting validation of LabWare LIMS, preferably LabWare 8.
Strong knowledge of CSV, GxP, and GAMP 5 frameworks.
Experience working in GMP laboratory environments.
Demonstrated ability to ensure traceability between requirements and system configuration.
Experience supporting regulatory inspections and audit activities.

What's in it for me?

Opportunity to work on a high-impact project supporting a GMP laboratory environment.
Collaborate with a dedicated team of professionals in a dynamic industry.
Gain valuable experience in validation and compliance within the pharmaceutical sector.
Be part of a company committed to quality and regulatory excellence.
Competitive pay rate reflecting your expertise and contributions.

Upon completion of waiting period consultants are eligible for:

Medical and Prescription Drug Plans
Dental Plan
Vision Plan
Health Savings Account
Health Flexible Spending Account
Dependent Care Flexible Spending Account
Supplemental Life Insurance
Short Term and Long Term Disability Insurance
Business Travel Insurance
401(k), Plus Match
Weekly Pay

If this is a role that interests you and you'd like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells.

ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2023 ManpowerGroup was named one of the World's Most Ethical Companies for the 14th year - all confirming our position as the brand of choice for in-demand talent.

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Refine Your Search

Pharmaceutical Validation Solutions jobs

LabWare LIMS Validation Specialist

Validation Engineer / CQV

Validation Specialist

Computerized System Validation (CSV) Specialist

Validation Writer

Medical Editor

Senior Packaging Engineer

Project Manager Indiana

Electrical SME - Field Consultant

Certification Engineer

Sr. Process Engineer

Senior Mold Maker - A or B Shift

Project Manager in San Diego

Principal Project Engineer

Senior Manufacturing Process Engineer

MedBen Rx Analyst

QC Analyst II, 2nd Shift

Senior Manufacturing Maintenance Technician

Process Engineer

Plant Manager

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