Quality Validation Specialist

Description:

Requirement 1
We are looking for a Quality Validation Specialist ( w2 Contractor) to join our client’s Los Angeles facility! This role is 100% onsite

In this role, you’ll be responsible for quality oversight of validation activities, ensuring compliance with regulatory and internal standards. You'll review and approve validation documentation related to facilities, equipment, critical utilities, automation systems, cleaning, and processes.
Qualifications:
4+ years of experience in pharmaceutical/biotech validation
Strong knowledge of FDA regulations & GxPs
Experience in plasma fractionation and purification processes
Excellent problem-solving and communication skills
Ability to manage multiple projects in a fast-paced environment

Requirement 2
hashtag#Hiring: hashtag#GMP Process Engineer! (W2 contractor)
Duration: 12+months
We are looking for an experienced Process Engineers to support GMP design and plant operations for process equipment. This role involves working with upstream and downstream equipment, stainless steel vessels, SCADA systems, and cold room freezers. If you have a passion for ensuring compliance with GMP and industry standards, we want to hear from you!
Key Responsibilities:
Provide technical support for GMP process equipment
Oversee installation, commissioning, and qualification of equipment
Ensure GMP, regulatory, and safety compliance throughout the project lifecycle
Collaborate with engineering, quality, and operations teams
Support troubleshooting, optimization, and validation of process equipment
Qualifications:-
2-4 years of experience in GMP-regulated environments
Hands-on expertise with stainless steel vessels, SCADA systems, and process equipment
Strong understanding of IQ/OQ/PQ qualification & commissioning
Excellent problem-solving and communication skills
Ability to thrive in a fast-paced, collaborative environment