Quality Control Specialist I
Location Switzerland - Luzern
Job Code WAG - 10411
Category QA / QC
Quality Control Specialist I
Full time, FTC
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 well-being of others? Clintec is looking for a Quality Control 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 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:
The Quality Control Specialist (QC) is supporting the Quality Unit and acts as registered contact to the Swiss Health Authorities for quality issues and his Deputy (QRP).
The QC works together with the QRP and the to maintain an open and transparent relationship with the Health Agency Swissmedic, the Regional Health Inspectorate, and the Cantonal Health Authority.
The QC supports the QRP in overseeing the quality systems and processes, in accordance with local and international regulations and internal standards.
Control of batch certificates and comparison with regulatory requirements (approved release specifications, shelf-life, authorized sites involved in the manufacturing process, further regulatory filings etc.)
What we require of you:
1+ years of experience in Quality Assurance (GMP/GDP) within pharmaceutical industry and local Swiss, European and international GxP regulations would be an asset
Excellent analytical and problem solving skills, based on science, data and understanding of regulatory requirements
Degree in Life Sciences
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 email@example.com or visit our website for more information www.clintec.com
Clinical Research / Clinical Trials / Analytics / Biologics / Chemistry / Small Mo lecule / HPLC / GMP