Engineering Validation jobs in Camarillo

Crystal Equation Corporation

Validation Engineer We are seeking a Validation Engineer to provide guidance and set standards in producing quality documentation, serving as the liaison between the IS and Quality functions. In this role, you will provide testing and IT compliance guidance with timely and effective response and fol

Actalent

Job Title: Validation Associate Job Description The Validation Associate supports equipment and process validation activities for a cosmetics and OTC manufacturing facility. This role assists with IQ/OQ/PQ execution, batching and compounding validation, and routine quality support activities such as

ACL Digital

*Title: Validation Engineer** *Location: Thousand Oaks, CA** *Duration: 12 months** *Description:** *Hybrid - 3 days onsite weekly** *Ideal Candidate: 2 YOE, hands on engineering, validation and qualifying equipment.** *Job Details:** Position involves support of senior staff in the initiation, desi

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of

ACL Digital

Title: Validation Engineer Senior Location: Thousand Oaks CA Duration:12+ Months Please read the following job description thoroughly to ensure you are the right fit for this role before applying. Description: Primarily responsible for leading and/or executing commissioning and qualification activit

Openmind Technologies Inc.

We are seeking a *highly skilled Verification and Validation Engineer (Embedded C)** to work *onsite** for an aerospace project involving the *Smoke Detection System** . The role involves *embedded software development, rig setup, Fixing any bugs in simulator GUI and Verification and validation of O

Payrate $60.00 - $63.44/hr. Responsibilities Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines. Work with project teams to develop the commissioning and qualification strategy and document in qualification plans. Generate/evaluate qualif

Job Overview Local, onsite at least 3 days weekly 8-5 Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating/reviewing/executing C&Q protocol

ALTEN

\*\*Local, onsite at least 3 days weekly 8-5\*\* Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating/reviewing/executing C&Q protocols