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Validation engineer Jobs in Simi Valley, CA

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Validation engineer • simi valley ca

Last updated: 14 days ago

Senior Validation Engineer

SSi PeopleThousand Oaks/ California
Full-time

Thousand Oaks, California (Hybrid).We are seeking experienced professionals to join our team in supporting critical commissioning and qualification activities for GMP analytical and process equipme...Show more

Controls Design Engineer

ATC AutomationSimi Valley, CA, USA
Full-time
Quick Apply

Join ATC Automation as a Full-Time Controls Design Engineer in Simi Valley, CA, where innovation and high performance thrive.This onsite position offers an exciting opportunity to work on cutting-e...Show more

Quality Control Validation Scientist

Katalyst HealthCares & Life SciencesThousand Oaks, CA
Full-time

As a QC Analytical Scientist, you will support various Quality Control activities within the AQC department.Key responsibilities are to transfer and execute analytical methods, including raw materi...Show more

Computer System Validation (CSV) Lead

Tata Consultancy ServicesThousand Oaks, CA
Full-time

Perform System Assessment, Data Integrity Assessment, Third-party Risk Assessments.Change Record Management in CCMS and ServiceNow.Author all Validation Documents - Validation Plan, Validation Summ...Show more

Engineer

SSi PeopleThousand Oaks/ California
Full-time

Thousand Oaks, California (On-Site).We are seeking an experienced individual to lead the development of packaging solutions for biologics and combination products.Our team values innovation and com...Show more

Device Engineer

SSi PeopleThousand Oaks/ California
Full-time

Thousand Oaks, California (Hybrid).We are seeking a highly skilled professional to support the development and lifecycle management of drug delivery devices.Our team values technical excellence and...Show more

Engineer

US Tech SolutionsThousand Oaks, CA
Temporary

Lead development and optimization of secondary & tertiary packaging packaging for biologics, sterile injectables, and combination products (, prefilled syringes, autoinjectors).Create and maintain ...Show more

Principal Engineer

SSi PeopleThousand Oaks/ California
Full-time

Thousand Oaks, California (On-site).We are seeking a motivated professional to support capital automation projects and day-to-day plant operations within the dynamic life sciences sector.Our team p...Show more

Sr Chatbot Engineer

Teklead CorpWestlake Village, CA, US
Full-time

US CITIZENS & PERMANENT RESIDENTS ONLY.Excellent contract-to-hire job opportunity.Chatbot Engineer to join an Artificial Intelligence team.Join our Tech hub and work in a collaborative environment ...Show more

Senior Validation Engineer

Katalyst HealthCares & Life SciencesThousand Oaks, CA
Full-time

This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specif...Show more

Process Engineer

Sensata TechnologiesThousand Oaks, CA
Full-time

The Process Engineer is responsible for developing or modifying manufacturing processes to increase product performance, improve manufacturing efficiency and boost profits.This position works close...Show more

Process Engineer

Teledyne Scientific & Imaging, LLCCA,Thousand Oaks,US
Full-time

Join Teledyne Scientific & Imaging as a Process Engineer!.Are you ready to launch your career to the next level? Join our mission-focused team, where we value technical excellence, collaboration, a...Show more

Firmware QA Engineer

Motive CompaniesWestlake Village, CA, US
Full-time

Firmware QA Engineer (Embedded Test Engineer) 📍 In-Office - Westlake Village, CA 💰 $80,000 - $110,000Job SummaryWe are seeking a Firmware QA Engineer to improve reliability across an IoT-enabled ...Show more

Quality Engineer

Ensign-Bickford Aerospace & Defense CompanyMoorpark, CA
Full-time

This position provides organizational support for customer programs and supplier quality requirements.The candidate will be responsible for quality engineering, system and process improvements, and...Show more

QC Validation Scientist

ProclinicalThousand Oaks, USA
Full-time

Advance quality excellence by driving analytical method transfer and validation in a cGMP environment.Proclinical is seeking a QC Analytical Scientist to join our client's team in the US.In this ro...Show more

Packaging Engineer

Aditi ConsultingThousand Oaks, CA
Full-time

This role is part of the Packaging Engineering group under Combination Products Operations (CPO).The position involves applying engineering principles to design, qualify, and implement Primary and ...Show more

Software Development Engineer

Teledyne Controls, LLCCA,Thousand Oaks,US
Full-time +1

Teledyne Controls is seeking an experienced Embedded Software Engineer to join our team developing advanced avionics solutions.This role focuses on designing and implementing embedded software for ...Show more

Associate Engineer

SSi PeopleThousand Oaks/ California
Full-time

We are seeking a talented professional to support our team by streamlining data management and monitoring processes.Our team values innovative thinking and is committed to enhancing digital systems...Show more

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Senior Validation Engineer

Senior Validation Engineer

SSi PeopleThousand Oaks/ California
27 days ago
Job type
  • Full-time
Job description

Job Title: Senior Validation Engineer
Location: Thousand Oaks, California (Hybrid)

Job Summary: We are seeking experienced professionals to join our team in supporting critical commissioning and qualification activities for GMP analytical and process equipment, utilities, and facilities. Our team values effective collaboration with cross-functional stakeholders, analytical thinking, and a strong commitment to quality assurance within regulated environments.

Responsibilities:

  • Develop and execute commissioning and qualification strategies in line with project requirements, including protocol generation, review, and completion.
  • Lead implementation and tracking of commissioning and qualification documentation against evolving project timelines.
  • Coordinate and collaborate with project teams to prepare technical and GMP-related documentation, such as risk assessments, master plans, and final reports.
  • Perform execution, investigation, and corrective actions for protocol discrepancies during installation, operational, functional, or performance qualification activities.

Required:

  • Demonstrated experience in a pharmaceutical, biotech, or life science organization performing commissioning, qualification, or validation activities.
  • In-depth knowledge of cGMP commissioning, qualification, and validation practices, with familiarity using digital C&Q systems such as Kneat Gx.
  • Experience working with cross-functional project teams and managing multiple projects simultaneously.
  • One of the following minimum educational/experience requirements: Doctorate degree or Master’s degree and 2+ years of experience or Bachelor’s degree and 4+ years of experience or Associate’s degree and 8+ years of experience or high school diploma/GED and 10+ years of experience.

About SSI People: With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.

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