Commissioning, Qualification and Validation CQV activities play a crucial role in delivering operationally effective and compliant facilities, utilities, equipment and process. We support our clients throughout the full CQV life cycle, from early stage of user requirements gathering to start-up and operations handover. During the course of our engagement, we continually educate your team, to facilitate knowledge transfer and ensure long-term sustainability. Process Control Systems PCS comprise of the majority of the manufacturing systems used on the pharma shop floor. We apply an effective science-based Quality Risk Management QRM approach in PCS qualification based on the product and process understanding to reduce risk to product quality, patient safety, data integrity, while potentially saving time and effort.
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CQV Engineer - Utilities
This position is also open to high potential graduated and Junior Engineers. Besides an exciting flexible environment, a unique chance to participate in challenging and innovative projects and interaction with inspiring colleagues who have a professional attitude and attach considerable importance to teamwork; we stand for. CQV Engineer for pharmaceutical projects Belgium-based with international missions. Your key tasks and responsibilities. You could be our ideal colleague if. You have a field experience with: System start-up and CQV Project scheduling Change management Project document management You are a structured, conscientious and precise fast-learner You are a real team player who can also work independently You are ready to travel and you are flexible on schedules and duties You are resourceful with a CAN DO mentality who can think proactively.
We offer you. We are looking forward to meeting you soon. Your application. If this is you, please address your application, CV and a short motivation text, to us: hr phenx. Guldensporenpark , Merelbeke 09 57 00 info phenx.
The Complete CQV: Where to Start
We offer an opportunity to help support our teams of industry subject matter experts and thought leaders while consulting with some of the biggest companies in the Life Sciences industries. This includes preparing and executing protocols independently, analyzing test results, and preparing technical reports. Contributes directly to the completion of commissioning and validation projects through the development of protocols and reports for systems that may be complex in nature, to support clinical and commercial manufacturing. VTI offers professional development, training, competitive compensation, excellent benefits, K plus a stimulating and collaborative work environment. We are committed to providing exciting career opportunities in a work environment that values trust, respect, openness, teamwork, creative talent, enthusiasm and diligence. As one of the leading global Commissioning, Qualification and Validation Services organizations, VTI is always looking for innovative, talented and experienced validation professionals for our multinational and global offices. VTI Life Sciences provides contract services to a wide variety of clients around the world. For a typical service contract, it is necessary for VTI employees to travel to project sites and perform a variety of validation and laboratory work without the assistance of another worker or special accommodations. To perform these services safely and effectively, the following minimum physical requirements are indicated for the position offered:. Must be able to don standard clean room attire: bunny suit, lab coat, gloves, head cover, and booties, without contaminating garments, gloves, or the facility.
CQV (Validation Engineer)
This national-level award also recognized its members for outstanding engineering leadership and service support to ISPE Cleaning Validation and Contamination Control Practices - May This is a modal window. We will update our schedule here as new trainings are booked. You may unsubscribe from these communications at any time.
Freelance CQV Engineer for pharmaceutical projects in Belgium
Sort by: Date Relevance. Asset Recruitment Ltd - Dundalk, Louth. We have both short and long term contracts and all are with biotech client project site based. We Cqv Engineer opportunity PM Group - Carlow.
CQV Engineer – Wicklow
Apply for this job. About CAI. We provide commissioning, qualification, validation, start-up, project management and other consulting services associated with operational readiness to FDA regulated and other mission-critical industries. As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally:. That is how we have grown exponentially. You will have an opportunity to work with recognized subject matter experts allowing YOU to be a key player in bringing life saving therapies to patients. As part of our company culture, we invest in YOUR future, and commit to hands on certifications as well as professional training. The CQV Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
Cqv Engineer jobs
We are looking for Intermediate to Senior Engineers who will bring their expertise with them and drive our projects to completion. All roles are with Biotech clients. Attractive rates, while working in a multi-disciplinary environment, in a vibrant expanding international company.
My client is a renowned Biotech in Belgium who are currently searching for several Engineers CQV; Process; Utilities to support on-going projects and expansion to existing plants. They are a fast-paced, innovative company, and look for dynamic people who can enjoy the ride with them! Right now, they urgently need a CQ Engineer to support the teams in achieving their project goals. Job purpose:.
Minimum Qualifications and Experience:. If you would like to discuss this vacancy or to discuss your career and other job opportunities in confidence, contact us: recruitment prochem. Your Name:. Your Email Address:. The project involves upgrades and installation of new equipment associated with an existing API facility. It will involve ties in to existing or installation of new glass lined reactors, receivers, holding tanks, centrifuges and dryers for the manufacture of a new pharmaceutical.
Commissioning, Qualification and Validation, more commonly known as CQV, is a process that is primarily associated with the pharmaceutical industry. The role focuses on equipment, ensuring systems and facilities are meeting the correct design requirements for creating various products. Engineers in this position usually have experience of working in each aspect of CQV and our expert Life sciences team know how to pair the best people in the right position. By dividing our consultants into vertical market areas within your industry, you can rely on the premise that you are only going to deal with a technical expert who understands the terminology and nuances of the sector - something most agencies do not offer.