CQV Engineer Projects
Drive validation for pharmaceutical projects, lead commissioning, manage quality, and work with top tech. Must have 5 years’ experience and strong problem-solving.
What You’ll Do Every Day
This CQV Engineer role involves spearheading commissioning, qualification, and validation projects, focusing on advanced process and packaging equipment as well as systems documentation.
You’ll be responsible for maintaining cGMP documentation, reviewing technical documents, and ensuring every step, from design to implementation, aligns with regulatory standards.
Managing vendor relationships and compliance will also fall under your remit, giving you the autonomy to influence project outcomes from start to finish.
Innovative thinking and technical skills are crucial in identifying validation risks, drafting robust qualification protocols, and working through challenging project milestones.
If you enjoy collaborating with highly skilled teams and driving operational success in pharma manufacturing, this role is a great match.
Pros of This Opportunity
This job provides exposure to state-of-the-art pharmaceutical projects, where you’ll lead validation processes that directly impact manufacturing excellence.
You will be recognised for your expertise and innovation, bringing your technical knowledge to a company that encourages continuous improvement and professional growth.
Cons to Keep in Mind
The role requires at least five years’ experience, so it’s not suitable for new graduates or those without direct pharma validation expertise.
The need for a valid work visa may also limit accessibility for some applicants who are seeking sponsorship.
Final Verdict
The CQV Engineer Projects role is an outstanding fit for skilled engineers driven by excellence in pharma validation and passionate about leading complex projects. If you meet the requirements, it’s a solid next career step.
