CQV Engineer
Vor 6 Tagen
CQV Engineer – 6219
Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for aCQV Engineer based in Visp,Switzerland for a 6-month contract with possible extension.
The Commissioning Qualification Validation engineer carries out a variety of tasks related to the validation of equipment and facilities. The scope of activities includes the coordination on the installation of equipment, drafting the IQ/OQ/PQ protocols, execution of the IQ/OQ/PQ and documenting the results according cGMP requirements.
Main Responsibilities:
- Validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
- The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
- Prepare validation documents.
- Execution of IQ/OQ and PQ for equipment, systems and utilities.
- Write reports of completed validation activities.
- Work to identify efficiencies in the validation program approach
- Work to apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation.
- Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s.
- Writing and/or revising procedures applicable to the Engineering activities.
- Support the Engineering group to prepare the validation, requalification, and maintenance program.
- Perform other duties as assigned.
Qualifications and Experience:
- Relevant working/residency permit or Swiss/EU-Citizenship required.
- Education Required: Bachelor’s Degree in Science or Technical field.
- Language: English.
- Work Experience: Advanced Level Pharma Industry 5-10 years.
- Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
- Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.
- Excellent organizational and time management skills.
-
CQV Engineer
Vor 3 Tagen
Visp, Schweiz Coopers Group AG VollzeitFor our client, a leading company in the Biotech sector, we are currently looking for a CQV Engineer.Background:The CQV Engineer is primarily responsible for the preparation of documentation in compliance with cGMP and all internal standards pertaining to their specific project and the execution of the CQV activities corresponding to their project’s area...
-
CQV engineer
Vor 5 Tagen
Visp, Schweiz Panda International VollzeitWe are looking for a CQV Engineer that will be responsible for the validation of equipment and facilities within a regulated pharmaceutical environment. This role involves overseeing the installation of equipment, drafting and executing IQ/OQ/PQ protocols, and documenting results in compliance with cGMP requirements. The CQV Engineer ensures that all...
-
CQV Engineer
Vor 2 Tagen
Visp, Schweiz CTC Resourcing Solutions VollzeitCQV Engineer – 6219 Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for aCQV Engineer based in Visp,Switzerland for a 6-month contract with possible extension. The Commissioning Qualification Validation engineer carries out a variety of...
-
CQV Engineer
Vor 3 Tagen
Visp, Schweiz Lonza VollzeitThe CQV Engineer is primarily responsible for the preparation and execution of CQV activities.Accountabilities:Includes, but is not limited to, execution of the following activities for the relevant systems in accordance with Project procedures/guidelines:System Boundary development + approval.Design Qualification preparation, execution, and approval....
-
CQV Engineer
vor 23 Stunden
Visp, Schweiz Proclinical Staffing Vollzeit3 days ago Be among the first 25 applicantsDirect message the job poster from Proclinical StaffingSenior Research Associate @ Proclinical Staffing - DACH | EngineeringProclinical is seeking a CQV Engineer to join our client's team on a contract basis. In this role, you will focus on the validation of equipment and facilities, ensuring compliance with cGMP...
-
CQV Engineer
vor 2 Stunden
Visp, Schweiz Lonza Group Ltd. VollzeitCQV Engineer / Qualification & Validation Engineer 80-100%(f/m/d)Apply locations CH - Visp time type Full time posted on Posted 5 Days Ago job requisition id R46721Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is...
-
CQV Specialist
Vor 6 Tagen
Visp, Schweiz Coopers Group AG Vollzeit1 week ago Be among the first 25 applicantsTalent Acquisition Consultant at Coopers Group AG - Life ScienceDuration: 31.07.2025The Commissioning Qualification Validation engineer carries out a variety of tasks related to the validation of equipment and facilities. The scope of activities includes the coordination on the installation of equipment, drafting...
-
CQV Specialist LZAJP00004921
Vor 3 Tagen
Visp, Schweiz Coopers Group GmbH VollzeitKey Accountabilities:The CQV Engineer will be involved in all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others. The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ,...
-
CQV Specialist
Vor 3 Tagen
Visp, Schweiz CTC Resourcing Solutions AG Vollzeit2 days ago Be among the first 25 applicantsDirect message the job poster from CTC Resourcing Solutions AGSenior Recruitment Consultant | Life Sciences | Pharmaceuticals | Biotech | Medical Devices | Business DevelopmentCQV Specialist - 6073Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in...
-
CSV Engineer
vor 1 Tag
Visp, Schweiz NRL VollzeitBackground:Supporting assigned project(s) in Visp as CSV-Engineer:Create the requested CSV documents according to the client’s SOPs.Execute the CSV tests.Support the CSV timelines with PM & CQV-Lead.Close interaction with Process Engineers, Automation Team (EMR), PM, and QA.Responsibilities:80%Acting as subject matter expert (SME) on following client’s...
-
CQ engineer
Vor 6 Tagen
Visp, Schweiz Proclinical Group VollzeitProclinical is seeking a CQ Engineer to join our client's team on a contract basis in Switzerland. This role focuses on commissioning, qualification, and validation (CQV) activities within the dermatology sector. We are looking for individuals who are eager to contribute to impactful projects in a dynamic and inclusive environment.Please note that to be...
-
QA Engineer
Vor 6 Tagen
Visp, Schweiz Capgemini Engineering VollzeitDirect message the job poster from Capgemini EngineeringTalent Acquisition Professional at Capgemini EngineeringFollow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as,Responsibilities:QA Oversight of CQV Activities: Provide comprehensive quality...
-
CSV Engineer
vor 1 Tag
Visp, Schweiz CTC Resourcing Solutions AG VollzeitOur client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a CSV Engineer for a 12 months contract in Visp, Valais area of Switzerland.In this role you will support the assigned project, create the requested CSV documents according to Companies...
-
Validation Engineer
Vor 2 Tagen
Visp, Schweiz Talentify VollzeitDescriptionSummary: The Commissioning Qualification Validation engineer carries out a variety of tasks related to the validation of equipment and facilities. The scope of activities includes the coordination on the installation of equipment, drafting the IQ/OQ/PQ protocols, execution of the IQ/OQ/PQ and documenting the results according to cGMP...
-
Instrument & Controls Engineer
vor 1 Tag
Visp, Schweiz NRL VollzeitInstrument & Controls Engineer – Stein, SwitzerlandThe Instrumentation and Control (I&C) Engineer will report directly to the Automation Technical Lead and is responsible for providing hands-on support to the commissioning and qualification of the Utility and HVAC Systems installed at the site in Stein. The I&C Engineer will provide hands-on support and...
-
Project/ Process Engineer
Vor 3 Tagen
Visp, Schweiz Capgemini Engineering VollzeitDirect message the job poster from Capgemini EngineeringTalent Acquisition Professional at Capgemini EngineeringFollow your passion in a role where you will be exposed to the technologies and processes that leading global companies utilize, and join our innovative team as,Project/ Process EngineerResponsibilities:Act as the primary representative for the...
-
Engineer, Project Engineering
Vor 2 Tagen
Visp, Schweiz public.client.lonza.display.name Vollzeitp>Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. And that’s the kind of work we want to be part of.As a Senior CSV Engineer,...
-
Senior Bioprocess Engineer BioConjugates
vor 1 Tag
Visp, Schweiz Lonza Group Ltd. VollzeitSenior Bioprocess Engineer BioConjugates (m/w/d) Apply locations CH - Visp time type Full time posted on Posted Yesterday job requisition id R62678 The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Today, Lonza is a global leader in life sciences operating across...
-
Automation Engineer
vor 1 Tag
Visp, Schweiz Hays VollzeitResponsibilities:Participate in automation projects within a team consisting of Automation Engineers, CQV engineers, and CSV engineers, contributing as an essential member of the DeltaV team.Write code in a DeltaV System.Code testing.Commissioning.Apply Good Manufacturing Procedures (cGMP) principles.Support the definition, execution, and documentation of...
-
Senior CSV Engineer 80-100%
Vor 3 Tagen
Visp, Schweiz public.client.lonza.display.name VollzeitToday, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small,...