Language

QC Associate Scientists

Mycoplasma
QPCR
BIO-Analytical
Microbiology
Biochemistry
CGMP
Analytical Testing
Flow Cytometry
Elisa
Chemistry
GLP
Medical Device
GMP
LIMS
Labware
FDA
Bioassay
Carvikty
assay
Microbiological
Sterile
Environmental Monitoring
Description:

~~~Please note: This is a temporary contractor opportunity at Novartis ~~~
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!

Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com

Ready to work with/through Magnit at Novartis? Please read on... 
QC Associate Scientist
Under general direction, perform testing and other activities in functions supporting the
Quality Control department (Micro/EM, QC Bio-assay and raw materials, as appropriate).

Responsibilities:
• Perform Bio-Analytical testing such as qPCR, Flow Cytometry, ELISA, cell count, cell viability 
• Perform micro/EM testing such as environmental monitoring, gram stain, sterility testing, endotoxin, and mycoplasma.
• Maintain controls and reference standards to support testing.
• Follows quality policies.
• Plan and schedule assigned activities.
• Generate trend reports.
• Review/approve data generated by other team members.
• Perform method qualification/optimization of methods as per appropriate protocols.
• Contribute to OOS/OOE investigations and deviation investigations.
• Support 5S and Lean projects.
• Identify potential improvements in project work.
• Interface with regulatory agencies during audits.
• Contribute to assigned projects.
• Knowledge of LabWare LIMS and/or other QC data systems.
• Maintain GMP/GLP quality systems.
• In addition to these primary duties, provide coverage for all appropriate areas and testing.
• Performs other job duties as assigned.

Education:
BA or MS in chemistry, biochemistry, microbiology or other related science

Language:
Fluent in English

Experience:
▪ -/+1 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry or working knowledge of Carvikty.
▪ Knowledge of cGMP and an understanding of the concepts of GLP, good clinical practices and FDA guidelines, applicable state and foreign regulations, and standards routinely used in the industry (i.e. ANSI, ISO, etc.).
▪ Knowledge of microbiological and environmental monitoring, bioassay, and/or raw material test methods, as appropriate.
▪ Knowledge of LIMS systems.
▪ Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations.
▪ Detail-oriented with expertise in problem solving and solid decision-making abilities.
▪ Strong interpersonal skills which include a professional demeanor when interacting with Novartis personnel.
▪ Sound, practical and appropriate regulations with regards to Novartis
▪ Strong written and verbal communication skills are essential.

Location: Morris Plains, NJ (Onsite)
Pay Rate: AM Rates:$28 - $31/hour or PM Rates:$30.80 - $34.10/hour based on experience and qualifications (W2 Only)  
12 hour Shifts: (shifts subject to change)
    AM:Sun - Wed/Sun - Tues (Week 1/2 Start 7am) OR 
    AM:Thurs-Sat/Wed-Sat (Week1/2 Start 7am) OR 
    PM:Sun- Tues/Sun- Wed (Week1/2 Start 3pm) OR 
    PM:Wed-Sat/Thurs-Sat (Week 1/2 Start 3pm)
Contract: 6+ months
Health, dental, vision, 401k

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 we can reinvent what's possible when we collaborate with courage to ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! 
Imagine the impact you could make here at Novartis! 
 
Commitment to Diversity & Inclusion: 
Novartis is committed to building an outstanding, inclusive work environment with diverse teams representative of the patients and communities we serve. 
To do our best work we need different viewpoints, which is why here at Magnit, we celebrate diversity and embrace inclusion. As an equal opportunity employer, Magnit is dedicated to building a team that represents a variety of backgrounds, perspectives, and skills. We strive to ensure that we maintain a positive and enriching work environment for all. 
 
Accommodation: 
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.

Commitment to Diversity and Inclusion / EEO

 

QUALIFICATION/ LICENSURE :
  • Work Authorization : Green Card, US Citizen, Other valid work visa
  • Preferred years of experience : 1+ Years
  • Travel Required : No travel required
  • Shift timings: Onsite: Morris Plains, NJ (shifts in J/D)
Job Location Morris Plains, New Jersey
Pay USD 28.00 - USD 34.10 Per Hour
Contract Duration 6 month(s)