Jobs and Careers
PS
CQV Engineer
PSC BiotechLos Angeles, United Statesfull_timeVerifiedPosted 5 Dec 2025
💰 $120,000/yr($100,000/yr – $120,000/yr)
About the role
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 our
team’s achievements. Employing a global team of skilled
professionals and experts that span across strategically
located offices in North America, Europe, Asia and the Middle
East, we are proud of the roles we have fulfilled to help our
clients achieve success.
The
Experience
With operations
spanning the globe and featuring a multi-cultural team, PSC
Biotech® is passionate about bringing the best and brightest
together in an effort to form something truly special. When
you make the decision to join our team, you will be offered
the ability to feel inspired in your career, explore your
professional passions, and work alongside a group of people
who will value and nurture your talents.
We are firm believers
in coaching and developing the next generation of industry
leaders and influencers. As such, you will not only be
offered compensation and benefits structure that rewards you,
but also be provided with the tools that will help you grow
and learn.
At PSC Biotech®, it’s
about more than just a job—it’s about your career and your
future.
Your Role
We are hiring an experienced CQV engineer responsible for the
commissioning, qualification, and validation for facilities,
utilities, and equipment in the pharmaceutical and biotech
industries. Our engineers play a critical role in driving
project success, while supporting validation planning,
development, documentation, and execution, and ensuring
regulatory standards and quality requirements are met.
Prepare and
maintain comprehensive documentation, including
validation protocols, plans, reports, and standard
operating procedures.
Identify and assess
risks associated with CQV activities and develop effective
mitigation strategies.
Troubleshoot and
resolve issues related to equipment and process
performance.
Collaborative with
cross-functional teams to ensure alignment on CQV activities
and project timelines.
Ensure compliance
with regulatory requirements (FDA, EMA, etc.) and industry
standards (GMP, GAMP, etc.).
Additional
responsibilities as required to drive successful validation
project deliverables.
6-10 years of
equipment commissioning, qualification, and validation
engineering experience in the pharmaceutical and/or biotech industries.
Strong knowledge of
regulatory requirements and industry standards.
Experience with
validation lifecycle management and risk-based approaches.
Excellent
analytical and technical problem solving skills.
Strong technical
writing skills and understanding of full lifecycle
documentation (protocols, reports, procedures, risk
assessments, specifications and requirements, etc.)
Effective
communication and interpersonal skills.
Proactive with
strong organization, time management, and project
management abilities.
Excellent attention
to detail with commitment to quality and compliance.
At PSC Biotech,
many of our projects and clients are located in
various regions around the country. Therefore, we
value candidates who are willing and able to travel
as needed for project assignments and client
engagements. The ability to adapt to different
locations, cultures, a
- Develop and execute commissioning, qualification, and validation protocols for required systems and equipment (i.e process skids, chromatography skids).
Requirements
- Bachelor’s degree in Engineering, Life Sciences, or a related field.
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