Senior Validation Engineer

<p>Job Description</p><p></p><p>We are seeking a <b>Senior Validation Engineer</b> who will play a crucial role in planning and executing qualification activities for our facilities, utilities, equipment, instruments, and processes, ensuring compliance with current Good Manufacturing Practice (cGMP) regulations and company policies. In this role, you will be a technical expert, supporting validation engineers and other departments in areas such as change controls, investigations, and corrective actions.</p><p></p><p><b>Bring energy, knowledge, innovation to carry out the following:</b></p><ul><li>Execute validation activities throughout facility design, build, and qualification phases, ensuring ongoing compliance.</li><li>Perform qualification activities using a life cycle approach (Design Qualification, Installation Qualification, Operational Qualification, Performance Qualification, and Process Validation) in line with cGMP and company procedures.</li><li>Apply regulatory requirements to the qualification of computerized systems, including documentation of protocols and reports.</li><li>Maintain and update validation procedures to meet regulatory standards.</li><li>Author, review, and approve testing protocols and reports.</li><li>Manage complex projects, troubleshooting process systems, and collaborating with vendors.</li><li>Participate in all phases of projects, from conceptual design through to commissioning and qualification.</li><li>Initiate and complete investigations, corrective actions, and change controls for process systems.</li><li>Ensure new process systems are integrated into maintenance and qualification programs.</li><li>Oversee project management of system upgrades and modifications.</li><li>Perform all duties according to cGMP standards and company procedures.</li><li>Be flexible to take on additional tasks and responsibilities as required.</li></ul><p></p><p><b>What skills you will need:</b></p><p>In order to excel in this role, you will more than likely have:</p><ul><li>A postgraduate degree in engineering or a science discipline is a plus.</li><li>Approximately 5 years of experience in a pharmaceutical or similar cGMP environment, focusing on validation or engineering.</li><li>Experience with facility startup projects and the commissioning and qualification of various equipment (e.g., cleanroom, HVAC, utilities, bioreactors, chromatography systems, process, cleaning, shipping).</li><li>Proven skills in troubleshooting and providing technical solutions for GMP operations.</li><li>Experience in managing vendor equipment and coordinating system design.</li><li>Strong problem-solving skills with the ability to analyze and creatively address complex issues.</li><li>Excellent communication and interpersonal skills for effective collaboration.</li><li>Ability to translate strategic plans into actionable operational goals.</li><li>Knowledge of pharmaceutical industry cGMP regulations and <span>qualification/validation</span> processes.</li><li>Collaborative, inclusive, and proactive approach to teamwork.</li><li>Strong project management skills and the ability to lead cross-functional teams.</li></ul><p></p><p>We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.</p><p></p><p>As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.</p><p></p><p>We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.</p><p>Please feel free to speak to us about what flexibility means to you during your application.</p><p></p><p><b>So, if you are ready to:</b></p><p>Invent solutions to meet unmet healthcare needs, <b>please apply today.</b></p><p></p><p>Current Employees apply <a href="https://wd5.myworkday.com/msd/d/task/1422$6687.htmld" rel="noopener noreferrer" target="_blank">HERE</a></p><p></p><p>Current Contingent Workers apply <a href="https://wd5.myworkday.com/msd/d/task/1422$4020.htmld" rel="noopener noreferrer" target="_blank">HERE</a></p><p></p><p><b>Search Firm Representatives Please Read Carefully </b><br/>Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are