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Validation Engineer

  • ... Posted on: Apr 17, 2026
  • ... Veg Group
  • ... Barceloneta, null
  • ... Salary: Not Available
  • ... Full-time

Validation Engineer   

Job Title :

Validation Engineer

Job Type :

Full-time

Job Location :

Barceloneta null United States

Remote :

No

Jobcon Logo Job Description :

Validation Engineer We are seeking a Validation Engineer with hands‑on experience in biotech/pharmaceutical manufacturing, specifically supporting aseptic filling operations (vials). This role will be responsible for executing and supporting validation activities for equipment, processes, and computerized systems in compliance with regulatory requirements and industry standards. Responsibilities Develop, review, and execute validation protocols including IQ, OQ, PQ for: Aseptic filling lines (vial filling, stoppering, capping) Lyophilization (if applicable) Support equipment (autoclaves, washers, depyrogenation tunnels) Perform process validation activities related to sterile manufacturing, including media fills (APS). Ensure compliance with cGMP, FDA, EMA, and ICH guidelines. Support commissioning and qualification (C&Q) activities for new equipment and facility upgrades. Generate and review: Validation master plans (VMPs) SOPs, protocols, and final reports Collaborate with cross‑functional teams (Manufacturing, QA, Engineering, MSAT). Investigate deviations, CAPAs, and implement corrective actions related to validation activities. Support risk assessments (FMEA, impact assessments) for validation scope. Ensure data integrity and adherence to 21 CFR Part 11 requirements (if applicable to systems). Qualifications Bachelor’s degree in Engineering, Chemistry, Biology, or related field. 3–7+ years of validation experience in biotech or pharmaceutical industry. Strong experience with: Aseptic processing Vial filling operations Sterile manufacturing environments Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation. Available to work extended hours, possibility of weekends and holidays. 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. #J-18808-Ljbffr

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Jobcon Logo Position Details

Posted:

Apr 17, 2026

Reference Number:

14660_CAAC49D98DE9C86D2DA5BAE38FA91B62

Employment:

Full-time

Salary:

Not Available

City:

Barceloneta

Job Origin:

APPCAST_CPC

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Validation Engineer We are seeking a Validation Engineer with hands‑on experience in biotech/pharmaceutical manufacturing, specifically supporting aseptic filling operations (vials). This role will be responsible for executing and supporting validation activities for equipment, processes, and computerized systems in compliance with regulatory requirements and industry standards. Responsibilities Develop, review, and execute validation protocols including IQ, OQ, PQ for: Aseptic filling lines (vial filling, stoppering, capping) Lyophilization (if applicable) Support equipment (autoclaves, washers, depyrogenation tunnels) Perform process validation activities related to sterile manufacturing, including media fills (APS). Ensure compliance with cGMP, FDA, EMA, and ICH guidelines. Support commissioning and qualification (C&Q) activities for new equipment and facility upgrades. Generate and review: Validation master plans (VMPs) SOPs, protocols, and final reports Collaborate with cross‑functional teams (Manufacturing, QA, Engineering, MSAT). Investigate deviations, CAPAs, and implement corrective actions related to validation activities. Support risk assessments (FMEA, impact assessments) for validation scope. Ensure data integrity and adherence to 21 CFR Part 11 requirements (if applicable to systems). Qualifications Bachelor’s degree in Engineering, Chemistry, Biology, or related field. 3–7+ years of validation experience in biotech or pharmaceutical industry. Strong experience with: Aseptic processing Vial filling operations Sterile manufacturing environments Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation. Available to work extended hours, possibility of weekends and holidays. 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. #J-18808-Ljbffr

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