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Job Details

Skills

pharmaceutical
CQV
Packaging
Validation

Summary

Position: CQV Engineer – Packaging Validation

location: Thousand Oaks, CA (fully Onsite)

Contract: 6+ Months

*Applicants must be authorized to work in the U.S. without visa sponsorship now or in the future. The Client is unable to consider candidates who require sponsorship.

Domain : pharmaceutical industry

Job description:

Seeking experienced and ambitious engineering professionals looking to advance their careers within the pharmaceutical, biotechnology, and medical device industries. We support some of the leading organizations across the Life Sciences sector, working alongside highly experienced subject matter experts on technically complex and high-impact projects.

We are currently seeking a Senior CQV Engineer to support a client project based in Thousand Oaks, California. This position requires a highly experienced CQV professional with a strong background in developing, executing, and reporting qualification and validation protocols, including IQ, OQ, and PQ activities across utility, HVAC, filling, and packaging systems.

PROJECT OVERVIEW

Experience Required: Minimum 3+ years of CQV experience within the pharmaceutical or biotechnology industries
Project Duration: Approximately 6 months
Schedule: 40 hours per week, Monday-Friday
Location: 100% onsite in Thousand Oaks, CA
Candidates must be locally based or able to commute to the client site

RESPONSIBILITIES

Develop, execute, and document CQV protocols, reports, risk assessments, and supporting validation documentation in accordance with client procedures and applicable cGMP, FDA, EMA, and regulatory requirements.
Lead and coordinate validation activities with Manufacturing, Quality Assurance, Engineering, and other cross-functional stakeholders.
Investigate protocol deviations, discrepancies, and nonconformities and support their resolution through appropriate corrective actions.
Support change control activities associated with modifications to equipment, systems, processes, and facilities.
Develop, review, and maintain SOPs related to equipment and system operation, qualification, validation, and maintenance.
Ensure all validation documentation meets internal quality standards and remains inspection and audit ready.
Independently manage assigned validation activities while ensuring project timelines, quality expectations, and compliance requirements are met.

REQUIREMENTS

Demonstrated ability to operate as an independent, senior-level contributor with minimal supervision and consistently deliver high-quality results.
Bachelor’s degree or higher in Engineering, Chemistry, Pharmaceutical Sciences, or a related scientific or technical discipline.
Minimum 3+ years of experience within the pharmaceutical or biotechnology industries.
Minimum 2+ years of hands-on Packaging Validation experience.
Strong experience with filling and capping processes, isolators, packaging systems, drop testing, and stress testing.
Strong knowledge of CQV lifecycle activities, including IQ, OQ, PQ, protocol development, execution, deviation management, and final reporting.
Excellent technical writing skills with experience producing clear, compliant validation documentation.
Ability to analyze complex technical data, identify validation issues, and drive effective resolutions.
Strong written and verbal English communication skills with the ability to work effectively across Engineering, Manufacturing, Quality, and Operations teams.
Experience with validation lifecycle management systems and quality management systems such as TrackWise, Kneat, Veeva, or similar platforms is highly desirable.

Manoj Prajapati | Non-IT Recruiter
LinkedIn:

An -E Verified Company
E:

P: +1

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91170457
Position Id: 21089-40870-1790867507
Posted 8 hours ago

Company Info

About Verito Solutions

At Verito Solutions, our core mission is to be an essential partner in our clients’ success. With a strong vision to become a global leader in delivering innovative and value-driven technology solutions, we are committed to exceeding expectations at every step. Our team is fueled by passion, expertise, and an unwavering determination to provide cutting-edge solutions tailored to the evolving needs of businesses.

We understand the challenges organizations face in today’s fast-paced digital landscape. That’s why we focus on delivering technology solutions that not only enhance efficiency but also save our clients valuable time, money, and effort. Whether it’s optimizing workflows, strengthening cybersecurity, or driving digital transformation, Verito Solutions is dedicated to empowering businesses with seamless, scalable, and future-ready technology.

Job Details

Skills

pharmaceutical
CQV
Packaging
Validation

Summary

Position: CQV Engineer – Packaging Validation

location: Thousand Oaks, CA (fully Onsite)

Contract: 6+ Months

*Applicants must be authorized to work in the U.S. without visa sponsorship now or in the future. The Client is unable to consider candidates who require sponsorship.

Domain : pharmaceutical industry

Job description:

PROJECT OVERVIEW

Experience Required: Minimum 3+ years of CQV experience within the pharmaceutical or biotechnology industries
Project Duration: Approximately 6 months
Schedule: 40 hours per week, Monday-Friday
Location: 100% onsite in Thousand Oaks, CA
Candidates must be locally based or able to commute to the client site

RESPONSIBILITIES

Develop, execute, and document CQV protocols, reports, risk assessments, and supporting validation documentation in accordance with client procedures and applicable cGMP, FDA, EMA, and regulatory requirements.
Lead and coordinate validation activities with Manufacturing, Quality Assurance, Engineering, and other cross-functional stakeholders.
Investigate protocol deviations, discrepancies, and nonconformities and support their resolution through appropriate corrective actions.
Support change control activities associated with modifications to equipment, systems, processes, and facilities.
Develop, review, and maintain SOPs related to equipment and system operation, qualification, validation, and maintenance.
Ensure all validation documentation meets internal quality standards and remains inspection and audit ready.
Independently manage assigned validation activities while ensuring project timelines, quality expectations, and compliance requirements are met.

REQUIREMENTS

Demonstrated ability to operate as an independent, senior-level contributor with minimal supervision and consistently deliver high-quality results.
Bachelor’s degree or higher in Engineering, Chemistry, Pharmaceutical Sciences, or a related scientific or technical discipline.
Minimum 3+ years of experience within the pharmaceutical or biotechnology industries.
Minimum 2+ years of hands-on Packaging Validation experience.
Strong experience with filling and capping processes, isolators, packaging systems, drop testing, and stress testing.
Strong knowledge of CQV lifecycle activities, including IQ, OQ, PQ, protocol development, execution, deviation management, and final reporting.
Excellent technical writing skills with experience producing clear, compliant validation documentation.
Ability to analyze complex technical data, identify validation issues, and drive effective resolutions.
Strong written and verbal English communication skills with the ability to work effectively across Engineering, Manufacturing, Quality, and Operations teams.
Experience with validation lifecycle management systems and quality management systems such as TrackWise, Kneat, Veeva, or similar platforms is highly desirable.

Manoj Prajapati | Non-IT Recruiter
LinkedIn:

An -E Verified Company
E:

P: +1

Dice Id: 91170457
Position Id: 21089-40870-1790867507
Posted 8 hours ago

Company Info

About Verito Solutions

Supplier Quality Engineer | Troy, Michigan - (Onsite)

Troy, Michigan

•

Yesterday

Position:Supplier Quality Engineer - Launch location:Troy, Michigan-(Onsite) Contract: 12+Months *Applicants must be authorized to work in the U.S. without visa sponsorship now or in the future. The Client is unable to consider candidates who require sponsorship. Need Month and Day of Birth to submit. Must have - Automotive Domain looking for new vehicle/product launch or Body In White (BIW) SQEExperience. Job description: In this position, the candidate will be responsible for managing the

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Contract, Third Party

Depends on Experience

CQV Engineer - Thousand Oaks, CA - Onsite

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CQV Engineer - Thousand Oaks, CA - Onsite

Verito Solutions

Job Details

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About Verito Solutions

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