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Cqv engineers / immediate start- 6411

Visp
CTC Resourcing Solutions
EUR 80’000 - EUR 100’000 pro Jahr
Inserat online seit: 5 Juni
Beschreibung

Senior Recruitment Consultant - Life Sciences, Pharmaceuticals, Biotech, Medical Devices, Business Development

Our client, a global market leader in the production and process support of active pharmaceutical ingredients in the chemical and biotechnology sectors, is seeking CQV Engineers based in the Valais area, Switzerland.

We are recruiting CQV Engineers for an initial contract starting ASAP until the end of the year, with potential extension.

The Commissioning Qualification Validation (CQV) Engineer performs tasks related to equipment and facility validation, including coordinating equipment installation, drafting IQ/OQ/PQ protocols, executing these protocols, and documenting results in compliance with cGMP standards.


Responsibilities

* Conduct validation activities such as Facilities, Utilities, Validation Lifecycle, Execution, Technical Documentation, Process, GAP Analysis, and Risk Assessment.
* Prepare validation documentation including URS, DQ, FMEA, Risk Assessments, FAT, SAT, and Protocols (IQ, OQ, PQ).
* Execute IQ/OQ and PQ for equipment, systems, and utilities.
* Write reports on completed validation activities.
* Identify efficiencies in the validation process.
* Apply lessons learned and stay updated on industry regulatory changes affecting equipment and facility validation.
* Perform Quality System activities such as Document Management, Change Control, Non-Conformities, and CAPA’s.
* Revise procedures related to engineering activities.
* Support the engineering team in preparing validation, requalification, and maintenance programs.
* Perform other assigned duties.


Qualifications and Experience

* Relevant working/residency permit or Swiss/EU citizenship required.
* Bachelor’s Degree in Science or a Technical field.
* Minimum 5 years of experience in the pharma industry.
* Strong technical writing skills for thorough and accurate documentation.
* Excellent communication skills, both written and oral, with the ability to work effectively across departments.
* Strong organizational and time management skills.


Additional Details

* Seniority level: Mid-Senior level
* Employment type: Contract
* Industries: Biotechnology Research, Manufacturing, Pharmaceutical Manufacturing
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