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...

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 -...

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 -...

The Senior Validation Engineer is responsible for the qualification or requalification of laboratory equipment within the targeted schedule. **Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and...

**Who are we?**: **Amaris Consulting** is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 7500 people spread across 5 continents and more than 60...

**Job description**: **About the job**: - Develop, review and/or approve validation lifecycle documents and protocols/reports in accordance with relevant policies, standards, procedures, and guidelines, and completed in a timely fashion. - Lead project validation activities and provide basic guidance and direction to junior project engineers as required. -...

Company Description **Amaris Consulting** is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1000 clients across the globe, we have been rolling out solutions in major projects for over a decade - this is made possible by an international team of 6000 people spread across 5 continents and more than 60...

**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/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/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...

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, -...

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, -...

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, -...

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...

**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...

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...

**Responsibilities**: - Monitor day-to-day Validation activities in accordance with approved SOPs / Plan / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility - Participate in review and approval of Validation Protocols / Reports including site discrepancies and deviations investigation / closure - Support / participate in...

**Responsibilities**: - Monitor day-to-day Validation activities in accordance with approved SOPs / Plan / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility - Participate in review and approval of Validation Protocols / Reports including site discrepancies and deviations investigation / closure - Support / participate in...