EMPQ Validation Specialist

Pinnaql, Inc.; Manatí (PR); Presencial; USD 70.000 - 110.000; Jornada completa

Descripción de la vacante

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

The role requires a strong scientific foundation, collaborative work style, and a proactive attitude. Responsibilities include preparing EMPQ protocols, executing environmental sampling, reviewing data, and coordinating with Microbiology, Validation, Manufacturing, and Quality teams to ensure compliant

Formación

• Bachelor’s degree in Microbiology or Biology.
• At least 5 years of relevant GMP biotech experience.
• Experience with environmental monitoring, cleanrooms, and qualification docs.

Responsabilidades

• 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.

Conocimientos

Environmental monitoring

GMP compliance

Technical writing

Communication skills

Willingness to learn

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. (V&EG) 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.