Zurück
Project Engineer – GMP Manufacturing 100%
<p><strong>In this role</strong>, you will lead and coordinate technical investment projects within a GMP-regulated biopharmaceutical manufacturing environment. You will act as a key interface between engineering, operations, and quality teams to ensure the successful implementation of mechanical modifications and process improvements. The position combines technical expertise, operational support, and project execution in a highly regulated production setting.</p>
<p><strong>Start Date</strong>: ASAP</p>
<p><strong>Duration</strong>: approx. 6 Months</p>
<p><strong>Place of Work</strong>: Visp</p>
Jetzt bewerben
<p class="isSelectedEnd"><span><strong>Key Responsibilities</strong></span></p>
<ul style="list-style-type:disc">
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Define project requirements, timelines, and technical objectives in alignment with operational and compliance standards</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Support the development and execution of capital investment projects from design phase through qualification activities</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Serve as the main technical contact for mechanical modifications and process optimization initiatives</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Coordinate closely with production, engineering, maintenance, and quality departments to ensure smooth project execution</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Ensure all activities are performed according to GMP requirements and internal quality procedures</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Support change control activities including preparation and review of technical documentation and change records</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Monitor project progress, budget, timelines, and key deliverables</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Identify project risks and implement mitigation strategies to minimize operational impact</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Provide technical guidance and hands-on support during implementation and operational improvement activities</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Lead commissioning and qualification activities including IQ, OQ, and PQ phases</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Collaborate with validation teams to ensure systems and processes meet operational and compliance expectations</span></li>
<li style="line-height:normalmargin-bottom:0cmtab-stops:list 36.0pt"><span lang="EN-US" xml:lang="EN-US">Prepare technical reports, project updates, and stakeholder presentations</span></li>
</ul>
<p style="line-height:normalmargin-bottom:0cm"> </p>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US"><strong>Candidate Profile</strong></span></p>
<p style="line-height:normalmargin-bottom:0cm"> </p>
<ul>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Bachelor’s or Master’s degree in Engineering, Life Sciences, Biotechnology, or a related technical discipline</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Several years of experience within biopharmaceutical or GMP-regulated manufacturing environments</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Strong background in technical project management, operational excellence, or engineering projects</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Hands-on experience with commissioning, qualification, and validation activities within GMP operations</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Solid understanding of GMP regulations, change management, and quality standards</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Experience coordinating cross-functional teams and external partners</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Strong organizational and problem-solving skills with the ability to manage multiple priorities simultaneously</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Excellent communication skills and stakeholder management capabilities</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Structured, detail-oriented, and proactive working style</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm"><span lang="EN-US" xml:lang="EN-US">Fluent German language skills are highly preferred</span></p>
</li>
<li>
<p style="line-height:normalmargin-bottom:0cm">Professional English skills are required</p>
<p style="line-height:normalmargin-bottom:0cm"> </p>
</li>
</ul>
<p style="line-height:normalmargin-bottom:0cmmargin-left:40px">Job ID 19041</p>
Prämiert und zertifiziert – unser Anspruch an Exzellenz.
Top Company seit 2017
Du hast Fragen zum Bewerbungsprozess?