EMPQ Validation Specialist

Veg Group; Puerto Rico; Presencial; USD 90.000 - 120.000; Jornada completa

Descripción de la vacante

Validation & Engineering Group, Inc. seeks an EMPQ Validation Specialist to support environmental monitoring performance qualification activities in a biotechnology manufacturing facility.

You will prepare, review, and execute EMPQ protocols while collaborating with Microbiology, Validation, Manufacturing, and Quality teams to ensure GMP-compliant qualification work. We value a strong scientific foundation, hands-on initiative, and clear communication as you help advance healthcare and

Formación

• Bachelor’s degree in Microbiology or Biology.
• At least 5 years of relevant GMP biotech/pharma experience.
• Experience with environmental monitoring and cleanroom practices.
• Strong technical writing and communication skills.
• Willingness to learn and support hands-on work.

Responsabilidades

• Prepare, review, and execute EMPQ protocols and documentation.
• Perform environmental sampling and document results.
• Review data, identify discrepancies, and support investigations.
• Collaborate with Microbiology, Validation, Manufacturing, and Quality teams.
• Maintain records and follow GMP/site procedures.

Conocimientos

Technical writing

Attention to detail

Communication skills

Team collaboration

Educación

Bachelor’s degree in Microbiology or Biology

Descripción del empleo

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking an EMPQ Validation Specialist to support environmental monitoring performance qualification activities in a biotechnology manufacturing facility. We are looking for someone with a strong scientific foundation who enjoys working in the field, collaborates well with others, and approaches challenges with a positive, proactive attitude.

EMPQ Validation Specialist

Description

• Prepare, review, and execute EMPQ protocols and supporting documentation.
• Perform environmental sampling and document results in accordance with approved procedures.
• Review data, identify discrepancies, and support investigations and corrective actions.
• Work closely with Microbiology, Validation, Manufacturing, and Quality teams to complete qualification activities.
• Maintain accurate records and follow GMP and site procedures.

Qualifications

• Bachelor’s degree in Microbiology or Biology
• At least 5 years of relevant experience in a biotechnology or pharmaceutical GMP environment.
• Experience with environmental monitoring, cleanroom practices, and qualification documentation.
• Strong technical writing, attention to detail, and communication skills.
• Willingness to learn, take initiative, and support hands‑on work as project needs evolve.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.