~~~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

Shifts Available -
(1 week Sun-Wed 7:30 AM-7:30 PM, then 2-week Sun-Tue 7:30 AM-7:30 PM)
(1 week Sun-Wed 3:30 PM-3:30 AM, then 2-week Sun-Tue 3:30 PM-3:30 AM)
(1 week Wed-Sat 7:30 AM-7:30 PM, then 2-week Thu-Sat 7:30 AM-7:30 PM)
(1 week Wed-Sat 3:30 PM-3:30 AM, then 2-week Thu-Sat 3:30PM-3:30 AM)
Please Note - Will have 4 different rotational shifts while submitting candidates please mention the shift at the top of the resume

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).

Major Accountabilities:
· 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.
· Provide coverage for all appropriate areas and test-ng.
· Performs other job duties as assigned.

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

Experience: 
2 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry. 
§ 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.

Competency Profile:
Specific Professional Competencies: Indicate any other soft/technical/professional knowledge and skills requirements
Internal orientation
- Thorough understanding of cGMP requirements
- Good communication and organizational skills
- Ensure customer satisfaction and react to customer requests
- Is seen as a competent team player
Others
- Strong ability to work independently, compliantly and results driven.
- Strong analysis and decision-making skills surrounding documentation
- Pays attention to detail
- Able to proof work and identify non-standard format or wording, and errors within
documents

Location: Morris Plains, NJ (onsite)
(1 week Sun-Wed 7:30 AM-7:30 PM, then 2-week Sun-Tue 7:30 AM-7:30 PM)
(1 week Sun-Wed 3:30 PM-3:30 AM, then 2-week Sun-Tue 3:30 PM-3:30 AM)
(1 week Wed-Sat 7:30 AM-7:30 PM, then 2-week Thu-Sat 7:30 AM-7:30 PM)
(1 week Wed-Sat 3:30 PM-3:30 AM, then 2-week Thu-Sat 3:30PM-3:30 AM)
Pay Rate: $30 - $35/hr based on experience and qualifications (W2 Only)
Contract: 6-month 
Health, dental, vision, 401k

Why Novartis: 
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?

EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

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.