Cleaning/equipment Validation Engineer-pharma

**Responsibilities**: - Working in a biotech/pharmaceutical environment as a consultant / contractor for various clients of PSC - Working closely with client's employees on various projects and various GMP facilities to help client with validation issues - Commuting to PSC clients' manufacturing for validation projects - Protocol development (IQ, OQ, PQ) /...

**Responsibilities**: - Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion. - Manage commission and qualification execution - Support validation deviation investigation encountered in qualification. - Collaborate with...

Support equipment, facilities, utilities qualifications - Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and complete execution in a timely fashion - Manage qualification execution and lead qualification deviation investigations encountered during qualification -...

Support equipment, facilities, utilities qualifications Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and complete execution in a timely fashion Manage qualification execution and lead qualification deviation investigations encountered during...

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements. **Responsibilities**: - Support equipment, facilities, utilities qualifications -...

**Responsibilities**: - Support equipment/system qualification and cleaning validation - Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion - Manage qualification/validation execution and lead the validation deviation investigations...

**Responsibilities**: - Support equipment qualification, system qualification, and cleaning validation. - Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion. - Review Turnover / Vendor Packages as part of the project...

Role Title: Validation Engineer (BioPharma) Duration: 1 year contract **Responsibilities **. - Support project execution from Feasibility through to project completion/handover, including all project stages such as: - Feasibility - Concept Design, Basic Design, Detailed Design - Commissioning & Qualification - Prepare/perform/review process engineering...

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational...

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements **Responsibilities**: - Support equipment, facilities, utilities qualifications, -...