Analista de Qualificação Pleno
PharmEng TechnologyParaná, Brazil
Posted December 12, 2025
Full Time
About the Company
PharmEng Technology, now part of the Efor Group, delivers specialized compliance engineering services—Commissioning, Qualification, and Validation (CQV)—to the pharmaceutical, biotechnology, and healthcare sectors, drawing on 25 years of industry expertise. The firm designs, constructs, and validates facilities, utilities, equipment, and computer systems in strict adherence to cGMP, GEP, and GLP, covering areas such as API production, laboratory, and medical device manufacturing. Leveraging Efor’s global network of 3,000 experts across 12 countries, PharmEng combines worldwide best practices with local proximity to offer flexible, innovative, and cost‑effective solutions that meet regulatory and business demands. Its culture prioritizes quality, safety, and client partnership, ensuring customized, measurable outcomes for leading industry players.
Job Description
PharmEng is a leading pharmaceutical and biopharmaceutical consulting firm looking for a highly qualified Senior Quality Analyst to join their team.
Requirements
- Bachelor's degree in Engineering and/or Pharmacy.
- Minimum 4 years of experience in qualification and validation in the pharmaceutical industry.
- Knowledge of RDC 658, IN 138, ANVISA Guide 33, Data Integrity, GAMP 5, CFR 21 part 11, qualification, and validation.
Benefits
- Competitive remuneration
- Opportunities for professional growth