| Need submission details for Research Associate Quality Control, Somerville, NJ at Somerville, Alabama, USA |
| Email: [email protected] |
| From: Bhavani, nukasanigroup [email protected] Reply to: [email protected] Dear Partner, Good Morning , GreetingsfromNukasanigroupInc!,Wehavebelowurgentlongtermcontractprojectimmediatelyavailable for** Research Associate Quality Control, Somerville, NJ ** need submissions you please review the below role, if you are available, could you please send me updated word resume, and below candidate submission format details, immediately. If you are not available, any referrals would be greatly appreciated.Interviews are in progress, urgent response is appreciated. Looking forward for your immediate response and working with you. **Candidate Submission Format - needed from you** Full Legal Name Personal Cell No ( Not google phone number) Email Id Skype Id Interview Availability Availability to start, if selected Current Location Open to Relocate Work Authorization Total Relevant Experience Education./ Year of graduation University Name, Location Last 4 digits of SSN Country of Birth Contractor Type DOB: mm/dd Home Zip Code Assigned Job Details Job Title : Research Associate Quality Control Location: Somerville, NJ Rate : Best competitive rate on w2/hr Visa: USC/GC/EAD(Don't submit any other visa) the manager is looking for candidates with 1-3 yrs exp. Onsite Role Position Title: Research Associate Biochemistry - QC Location: Branchburg, NJ Job Function: Quality Control (QC) Tech Ladder (Y/N): Yes Lilly employees embrace Operational Excellence in everything we do, ot achieve our mission of Making Medicine with Safety First & Quality Always; following our common purpose under TEAM Lilly and our Manufacturing Standards under the strict code of conduct guided by our Red Book assuring data integrity ni al we do ni order ot deliver a reliable supply of medicine for people around the world. Position Brand Description: Conduct routine and non-routine analyses of in-process materials, raw materials, envroin sa alivate ys supe,r r : deP go od duo ability sponseis yb as necaiet phemical acceptable GMP practices during execution of al work tasks. Work independently with moderate supervisory guidance. Key Objectives/Deliverables: Manage for Results /Strategic Planning: 1. Perform routine QC responsibilities as assigned by supervisor such as (as applicable): .a Conduct routine and non-routine analyses of test articles as assigned by supervisor by appropriate biochemical methods such as: SDS-PAGE, HPLC,CE- SDS, ELISA, Cell Based Bioassay, etc. b. 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. c. Monitor laboratory equipment for temperature and conformance to specifications. d. Apply acceptable cGMP practices during execution of al work tasks. e. Work independently with minimal supervisory guidance. Exhibit strong teamwork skills. f. g. Update supervisor of progress at scheduled intervals. Seek additional guidance as needed. Use scientific expertise to provide assistance for troubleshooting, laboratory investigations and problem resolution. Suggest process improvements to QC management. h. Perform assay data review. .2 Perform independent assignments such as: a. Compile data and prepare graphs for documentation of test procedures and preparation of reports. b. Conduct document reviews, author standard operating procedures (SOPs), and assay review. c. Lead special projects such as method validation, troubleshooting, optimization, and investigations. Resource Management: N/A Basic Requirements: 1. BS requires 3-5 years and MS requires 1-3 years of previous related experience. 2. Good working knowledge of cGMP regulations is required. 3. Ability to work independently with moderate supervisory guidance. 4. Excellent teamwork and communication skills. Attentive to detail. Good computer skills. Additional Preferences: .1 N/A Education Requirements: 1. BS or MS in a related science such as a Biology or Biochemistry is required. Other Information: 1. Travel not required 2. Lifting not required 3. Not required to be on call. 4. Shift work may apply. Thanks re gards Bhavani |Technical recruitment| Nukasani Group | 1001 E Chicago Ave, Unit B 111, Naperville IL 60540. Email: bhavaniAT nukasanigroupusa.com People, Process, Technology Integrator. An E-Verified Company Keywords: materials management rlang golang container edition green card wtwo microsoft Alabama Idaho Illinois New Jersey Need submission details for Research Associate Quality Control, Somerville, NJ [email protected] |
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| Wed Sep 18 19:49:00 UTC 2024 |