Skip to content
Find your next chapter

Mentor Technical Group

Validation Specialist – Biotech Downstream Process Equipment

Location not given · Full-time

Posted · Listed from JazzHR

About the job

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 validation protocols (IQ, OQ, PQ) for downstream process equipment.

  • Perform risk assessments, gap analyses, and validation reports for new and existing equipment.

  • Collaborate with engineering, QA, and operations teams to ensure equipment meets regulatory requirements.

  • Support commissioning and qualification activities for bioprocess systems, including filtration, chromatography, and centrifugation equipment.

  • Review and approve validation documentation, SOPs, and change controls.

  • Identify and implement continuous improvement initiatives in validation processes.

  • Support regulatory inspections and audits, providing required validation documentation.

Qualifications:

  • Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or related field.

  • Minimum 3–5 years of experience in validation of biotech downstream process equipment.

  • Strong knowledge of cGMP, FDA, and ICH guidelines.

  • Experience with IQ/OQ/PQ protocols and validation documentation.

  • Familiarity with downstream processes such as chromatography, filtration, and centrifugation.

  • Excellent problem-solving, communication, and organizational skills.

Preferred Qualifications:

  • Advanced degree in relevant scientific field.

  • Experience in a multi-site or global biotech environment.

  • Knowledge of computerized systems validation (CSV) and automated process control systems.

Mentor Technical Group wrote this description; Job Elf found it on JazzHR. Check details with the employer before you share anything sensitive. Never pay to apply for a job.

More jobs at Mentor Technical Group

GxP Auditor

Mentor Technical Group

Location not given

Full-time

Posted 1 week ago Apply on company site

Calibration Technician

Mentor Technical Group

Muskegon, MI

Full-time

Posted 2 weeks ago Apply on company site

Packaging Engineer

Mentor Technical Group

SC

Full-time

Posted 2 weeks ago Apply on company site