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Job Details

Research Associate-QC Biochemistry

Somerville, NJ, United States

Posted on
Aug 13,2019

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Research Associate-QC Biochemistry

Job #969458229
Job Category:
Type of Employment:
Full-Time Employment - FTE
As a Research Associate you will conduct routine and non-routine analyses of in-process materials, raw materials, environmental/water samples, finished goods and stability samples by appropriate biochemical methods as assigned by supervisor. In addition, you will perform routine QC responsibilities as needed, and apply acceptable cGMP practices during execution of all work tasks, while working independently with moderate supervisory guidance.
In this role you will perform routine QC responsibilities as assigned by supervisor such as:
Conduct routine and non-routine analyses of test articles as assigned by supervisor by appropriate analytical methods such as ELISA, Cell Based Bioassay, qPCR, etc.
Demonstrate initiative to perform routine QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed.
Monitor laboratory equipment for temperature and conformance to specifications.
Apply acceptable cGMP practices during execution of all work tasks.
Work independently with moderate supervisory guidance. Exhibit strong teamwork skills.
Update supervisor of progress on frequent basis. Seek additional guidance as needed.
Additionally, you will perform independent assignments such as:
Compile data for documentation of test procedures and preparation of reports.
Conduct document reviews and author standard operating procedures (SOPs).
Basic Qualificiations:
BS in a related science such as a Biology, Chemistry, or Biochemistry is required.
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
Additional Skills/Preferences:
Excellent working knowledge of cGMP regulations .
Excellent teamwork and communication skills.
Attention to detail.
Good computer skills.
Ability to work independently and achieve problem resolution with minimal supervision.
Additional Information:
Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
Company Overview:
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering; developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
We strive to make life better and to be leaders in diversity and inclusion, clinical research, corporate responsibility and employee benefits. For more than 140 years, we have received recognition from several distinguished organizations for our efforts. Here are some of our 2019 honors:
Catalyst Award, for our innovative Employee Journeys and People Strategy
Corporate Knights, Global 100 Most Sustainable Corporations in the World
Ethisphere, World's Most Ethical Companies
Forbes, America's Best Employers for Diversity
Forbes, America's Best Large Employers
Posted Date:
Region: North America
City: Branchburg
State: New Jersey
Country: USA
Location Details:
Req Id: 51433BR

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