C&Q Engineer

Are you ready for a change? Tired of the same routine? Join our team and make your mark in the industry!
Have a look below and apply or send me your CV directly.
Title: C&Q Engineer
Location: Bern, Switzerland
Rate: Open
Openings: 2 Engineers
Contract/Perm: Contract (4-Months)
Join the team and be part of an innovative company that values inclusion, growth, and impact. Our dynamic work environment offers brilliant opportunities for advancement. We're seeking talented and driven individuals who share our passion for making a difference within the Life Science industry.
Key responsibilities

• We are seeking 2 highly skilled Commissioning and Qualification Engineers for a 4-month contract position to support a capital expenditure (CAPEX) project in Bern. As a Commissioning and Qualification Engineer, you will play a crucial role in ensuring the successful commissioning and qualification of facilities, systems, and equipment in compliance with applicable regulations and industry standards.
• Support the overall commissioning and qualification activities for the 4-month CAPEX project in Bern.
• Collaborate with project stakeholders to develop commissioning and qualification plans, protocols, and reports.
• Execute commissioning activities, including system turnover verification, alignment checks, functional testing, and documentation of results.
• Perform qualification activities, including installation and operational qualifications (IQ/OQ).
• Work closely with cross-functional teams to coordinate and integrate commissioning and qualification activities within project timelines.
• Identify and mitigate risks during the commissioning and qualification phase, ensuring compliance with regulatory requirements and safety standards.
• Utilize industry best practices and standard operating procedures to conduct commissioning and qualification activities.
• Collaborate with project team members to ensure documentation is completed accurately and on schedule.

Requirements

• Bachelor's or Master's degree in Engineering or a related field.
• Minimum of 5 years of experience in commissioning and qualification activities in in pharmaceuticals or biotechnology industry.
• Strong knowledge and understanding of GMP (Good Manufacturing Practice) guidelines and regulatory requirements.
• Experience in developing and executing commissioning and qualification plans, protocols, and methodologies.
• Proficient in conducting system turnover verification, functional testing, and documentation of results.
• Familiarity with qualification activities such as IQ/OQ.
• Excellent problem-solving and analytical skills, with the ability to identify and resolve issues proactively.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
• Detail-oriented, with exceptional organizational skills and the ability to manage multiple tasks and priorities simultaneously.
• Availability to commit to a 4-month contract duration.
• Business fluency in English, German language is a plus

S.Hubert@Proclinical.com
DL: +44 203 949 8594
CH: +41 61 508 7073
Mob: +44 7592 053 700