Process Engineer II
Full time, Permanent Contract
Are you looking to become a valued member of an award-winning clinical research organisation, with a collective goal of positively improving the health and wellbeing of others? Clintec is looking for an experienced Process Engineer to join our specialist Biotech team in Lucerne, Switzerland, and we are currently accepting applications.
You will have the opportunity to work dedicated to a world-renowned pharmaceutical leader, on some of the most prestigious and ground-breaking drug development projects impacting lives all over the world. Every employee strives to find innovative ways to overcome obstacles together, and this team centric ethos is crucial to the continued success of Clintec.
Our management team recognise that every employee is different, so we offer individual training and development plans to suit your goals and expectations. You’ll enjoy a fast-paced and dynamic environment, where we value inclusion and promote team work.
What we can offer you:
A competitive salary and benefits package; performance related bonus, private healthcare allowance, pension contribution and flexible working options
25 day’s annual leave per year plus 15 days bank holiday entitlement
Career development/training opportunities and a life-long career with an innovative, forward-thinking clinical research company
Team focused social events throughout the year, subsidised food canteen and a high-quality working environment
What your responsibilities are:
Participating in the planning, coordination, and implementation of the Biotech next generation continuous manufacturing platform
Support the initial qualification and operations of continuous manufacturing unit operations.
Provide oversight and leadership of day to day operations of the continuous processing during water-based field testing and engineering runs and lead the day to day operations of the MSD next generation continuous manufacturing process.
Support in helping shape the development of the shop floor operations including in the development and authoring of batch records, sampling plans, and standard operating procedures.
Support the area’s implementation of process changes, and root cause investigation of deviations.
Participate in shop floor activities for GMP Batch or Continuous Manufacturing.
Embody Safe by Choice – know and follow the Safety, Health and Environment guidelines and work towards company safety and environment goals.
What we require of you:
2+ years of work experience in the pharmaceutical or biotech industry
Familiarity with Unit Operations for mAb manufacturing.
Experience with MVDA and PAT Technologies such as (MAM, Raman and UPLC)
Familiarity with Emerson DeltaV, SIPAT, and the use of Automation in a manufacturing Process.
Minimum C1 level of English and German (written, spoken, understanding)
Swiss Citizen, or legal status to work full time in Switzerland
*Previous experience of working within a Biotech, Pharma or Medical Device environment with a focus on GMP/GLP is an essential requirement
If you would like additional information on any of our job opportunities, please contact the Clintec recruitment team at email@example.com or visit our website for more information www.clintec.com
Clinical Research / Clinical Trials / Analytics / Biologics / Chemistry / Engineering / Validation / Process