P

CQV Engineer

salary Salary :

$85,000 - 100,000 yearly

icon briefcase Job Type : Full Time

Number of Applicants

 : 

000+

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Job Description - CQV Engineer

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
experienced validation engineers 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.

  • Develop and execute
    commissioning, qualification, and validation protocols for
    required equipment and systems.

  • 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.


Requirements


  • Bachelor’s degree
    in Engineering, Life Sciences, or a related field.

  • 2 -7 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, and work environments are essential, as
    it allows our team members to collaborate
    effectively with clients and colleagues nationally.

  • Must be authorized to
    work in the US.

  • No C2C at this time.

Benefits

Offering a full suite
of benefits, PSC Biotech™ is firmly focused on diligently
investing in our employees who enable our company to fulfill
our mission and achieve success. We want to promote balance,
so you not only enjoy your work, but also have the time and
resources to live your life happy and healthy.


  • Medical, Dental,
    and Vision - PSC pays 100% of all qualifying employee
    medical premiums and 50% for qualifying
    dependents

  • Insurance options
    for Employee Assistance Programs, Basic Life
    Insurance, Short/Long Term Disability and
    more.

  • 401(k) and 401(k)
    matching

  • PTO, Sick Time, and
    Paid Holidays

  • Education
    Assistance

  • Pet
    Insurance

  • Discounted rate at
    Anytime Fitness

  • Financial Perks and
    Discounts

Adhering to the requirements of California's law on salary transparency, the salary bracket for this role is set between $85,000 - $100,000 annually. The salary offered may be adjusted based on various factors such as the applicant's qualifications, skills, and professional experience.

Equal Opportunity
Employment Statement


PSC Biotech is committed to a policy of Equal Employment Opportunity with respect
to all employees, interns, and applicants for employment.
Consistent with this commitment, our policy is to comply with all
applicable federal, state and local laws concerning employment
discrimination. Accordingly, the Company prohibits discrimination
against qualified employees, interns and applicants in all aspects
of employment including, but not limited to: recruitment,
interviewing, hiring (or failure or refusal to hire), evaluation,
compensation, promotion, job assignment, transfer, demotion,
training, leaves of absence, layoff, benefits, use of facilities,
working conditions, termination and employer -sponsored activities
and programs,  including wellness, social and recreational
programs. Employment decisions will be made without regard to an
applicant’s, employee’s, or intern’s actual or perceived: race,
color, religion, sex (including pregnancy, gender identity, and
sexual orientation), national origin, age (40 or older),
disability, genetic information, or any other status protected by
law.


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