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Project Y Biotech Jobs (NOW HIRING)

Sr. Project Engineer

Juncos, PR · On-site

$96K - $125K/yr

... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, ... Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los ...

... projects supporting industrial process equipment and biotechnology manufacturing facilities ... Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los ...

... About from Y Combinator's 2015 Summer Demo Day, that is creating a brand new, cloud-based ... biotech, embedded devices, and/or Internet of Things (IoT) experience would be a huge plus About ...

LabWare LIMS Project Manager

Boston, MA

$107K - $126K/yr

Job Requirements Serve as a IT Project Management and UAT resource for a LabWare LIMS ... biotech, clinical trials, forensics, medical device, pharmaceutical, public health and research ...

Porfolio Manager

Gurabo, PR · On-site

$90 - $120/hr

... capital projects. * Proven experience in Pharmaceutical, Biotechnology, or Medical Device ... Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los ...

... capital projects. * Proven experience in Pharmaceutical, Biotechnology, or Medical Device ... Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los ...

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Project Y Biotech information

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How much do project y biotech jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for project y biotech in the United States is $30.31, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $35.58 per hour, depending on experience, location, and employer.

What are some careers in biotech?

Careers in biotech include roles such as research scientist, bioprocess engineer, quality control analyst, regulatory affairs specialist, and laboratory technician. These positions often require knowledge of molecular biology, laboratory skills, and familiarity with biotech tools and regulations.

Why is it so hard to get a job in biotech right now?

Getting a job in biotech can be challenging due to high competition, strict qualification requirements such as advanced degrees or certifications, and limited entry-level positions. The industry often values specialized skills like laboratory techniques, data analysis, and familiarity with biotech tools, which can further narrow opportunities for new applicants.
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What cities are hiring for Project Y Biotech jobs?

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What states have the most Project Y Biotech jobs?

States with the most job openings for Project Y Biotech jobs include:

Infographic showing various Project Y Biotech job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $63,044 per year, or $30.3 per hour.

CQV Specialist - Upstream Process Equipment & Downstream Biotech Process Equipment

Juncos, PR • On-site

MENTOR Technical Group Corporation
Manufacturing • 1 - 10 employees

$70 - $90/hr

Other

Posted 10 days ago


Job description

CQV Specialist – Upstream Process Equipment & Downstream Biotech Process Equipment

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Key Responsibilities
  • Develop, review, and execute qualification and validation protocols (IQ, OQ, PQ) for upstream and downstream process equipment.
  • Participate in equipment installation, start-up, and commissioning projects.
  • Review and approve technical documentation related to equipment, including manuals, procedures, and validation reports.
  • Collaborate with cross-functional teams including Engineering, Operations, and QA/QC to ensure regulatory compliance.
  • Identify risks and opportunities for process and equipment improvement.
  • Provide support during internal and external audits related to CQV activities.
  • Maintain accurate and up-to-date CQV records and documentation in accordance with industry standards.
Qualifications / Requirements
  • Bachelor’s degree in Chemical Engineering, Biochemistry, Biotechnology, or related field.
  • Minimum 3–5 years of experience in commissioning, qualification, and validation of biotech process equipment (both upstream and downstream).
  • Strong knowledge of GMP, FDA, cGMP, and international regulatory requirements.
  • Hands‑on experience developing and executing IQ, OQ, and PQ protocols.
  • Excellent teamwork, communication, and problem‑solving skills.
  • Proficiency in technical documentation software and validation tools (e.g., AutoCAD, TrackWise, Veeva).
Preferred Skills
  • CQV, Process Validation, or Project Management certifications.
  • Experience with fermentation, chromatography, filtration, or downstream process systems.

Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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