Production Operator
View: 115
Update day: 21-03-2024
Location:
Category: Pharmaceutical / Chemical / Biotech
Industry:
Job content
Lucerne/Schachen,
Switzerland
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 Production Specialist to join our 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 teamwork.
What we can offer you:
- A competitive salary and benefits package; performance related bonus, private healthcare allowance, pension contribution and flexible working option
- 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:
- Working in a manufacturing environment, conducting the weighing of materials in preparation of buffer, provision of sterile material ordering, maintenance and calibration of required equipment.
- Creating SOP’s and development of GMP documents, cGMP plant experiences for medium and solution preparation. Experience in scheduling of group activities and technical writing capabilities
What we require of you:
- 2+ years of work experience in the pharmaceutical or biotech industry
- Experience creating and developing SOP’s and GMP documentation
- Minimum C1 level of English and German (written, spoken, understanding)
- Swiss Citizen, or legal status to work full time in Switzerland
If you would like additional information on any of our job opportunities, please contact the Clintec recruitment team at careers@clintec.com or visit our website for more information www.clintec.com
KEYWORDS
Clinical Research / Clinical Trials / Analytics / Biologics / Chemistry / Engineering / Validation / Process
Deadline: 05-05-2024
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