QC-Analyst II (Temporary 2 years contract)-1

Posted Yesterday
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Stein, Aargau
Junior
Biotech • Pharmaceutical
The Role
The QC Analyst II will perform bioassays, maintain compliance with SOPs, review data, and support quality control in a laboratory setting.
Summary Generated by Built In

Job Description Summary

QC-Analyst II (Temporary 2 years contract)
Switzerland
About the role
Why join Cell & Gene Therapy?
Because in the Cell & Gene Therapy network we are operating on a daily basis (including weekend days) to deliver our life changing medicines the most rapidly to the patient. We are helped do this by facilities and infrastructure that are top class, but also by an environment that is open-minded, and one which supports people to develop with mentoring, training and the opportunity to experience different disciplines.
This role is limited for 24 months.


 

Job Description

Key Responsibilities: 

• Plan and perform Bioassays (e.g. Flow Cytometry, ELISA) and qPCR assays of release testing
• Perform all testing and activities compliantly following appropriate SOPs and procedures and maintain controls, reagents and reference standards to support testing
• Review data generated by other team members.
• Evaluate/qualify and maintain lab equipment and execute validation/transfers/optimization of test methods as per appropriate protocols
• Contribute to OOS/OOE and deviation investigations; interface with regulatory agencies during audits; support 6S and Lean projects; continually identify areas for improvements in project work.
• Knowledge of LabWare LIMS, SAP and/or other QC data systems
• Maintain GMP quality systems; review of laboratory logbooks and laboratory cleaning; performing daily equipment startup and PQ; assure stock of reagents and materials
Commitment to Diversity & Inclusion: :
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
• Education - BA in biology, chemistry, biochemistry, microbiology or other related science
• 0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry
• Biological techniques (Flow Cytometry, ELISA, qPCR, Cell Count...)
• Thorough knowledge of cGMP requirements
• Results oriented, team player and able to work with all levels of the organization
• Strong written and verbal communication skills are essential
• Fluent in English language, German desirable

You’ll receive: 

Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well. You’ll have to work on a shift model.

Why Novartis?  

766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.

We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working.

We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying!

Imagine what you could do here at Novartis!

Commitment to Diversity & Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve.

Accessibility and accommodation

Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. 

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/network
Division
Operations
Business Unit
QUALITY
Work Location
Stein (Säckingen)
Company/Legal Entity
Novartis Pharma AG
Functional Area
Quality
Job Type
Full Time
Employment Type
Temporary
Shift Work
Yes
Early Talent
Yes
 


 

Skills Desired

Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management

Top Skills

Elisa
Flow Cytometry
Labware Lims
Qpcr
SAP
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The Company
HQ: Basel
110,000 Employees
Hybrid Workplace
Year Founded: 1996

What We Do

Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.

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