Key Skills

Job Description

We are looking for a Junior CQV Engineer to join our team and support commissioning, qualification, and validation activities within the pharmaceutical and biotechnology industries. This is an excellent opportunity for someone looking to develop their career in CQV and gain hands-on experience in a GMP-regulated environment. Responsibilities Support commissioning, qualification, and validation (CQV) activities for pharmaceutical equipment, utilities, and facilities. Assist with the preparation and execution of IQ, OQ, and PQ protocols. Prepare and review technical documentation in accordance with GMP requirements. Support the execution of qualification tests and document the results. Collaborate with engineering, quality, and validation teams. Help investigate deviations and support the implementation of corrective actions. Ensure activities comply with applicable GMP standards and procedures. Requirements A degree or background in engineering, biotechnology, life sciences, chemistry, or a related field. An interest in CQV, validation, and the pharmaceutical or biotechnology industry. Basic knowledge of GMP is an advantage. Strong attention to detail and good documentation skills. A proactive attitude and willingness to learn. Good communication skills. What We Offer The opportunity to build a career in CQV within the pharmaceutical and biotechnology industries. Training, guidance, and support from experienced professionals. Exposure to a variety of projects and GMP-regulated environments. Opportunities for professional development and career progression. The chance to work with leading companies in the life sciences sector. Interested? Apply now and take the next step in your career as a Junior CQV Engineer.

Core Responsibilities

Support commissioning, qualification, and validation activities for pharmaceutical equipment, utilities, and facilities, including preparing and executing IQ, OQ, and PQ protocols and documenting test results. Prepare and review GMP-compliant technical documentation, collaborate with engineering, quality, and validation teams, and assist with deviation investigations and corrective actions.

Requirements

A degree or background in engineering, biotechnology, life sciences, chemistry, or a related field is sought, along with an interest in CQV, validation, and the pharmaceutical or biotechnology industry. Basic GMP knowledge is advantageous; candidates should have strong attention to detail, good documentation and communication skills, and a proactive willingness to learn.

Benefits

• Training
• Professional Development
• Career Progression