Scientist II (ELISA must have)

Job DescriptionReq Number: 36240 Req Title: Scientist IIClient: A major pharma companyWork Address: 66018, DeSoto, KSDuration: 23 Months with possible extensionHours per Week: 40.0 Position Summary:Responsibilities:Assists in the maintenance of the reference management program for US biologics sites.Maintains compliance according to USDA guidelines and requirements for reference standards and in vitro potency tests.Conducts in vitro testing for stability of reference standards of pre- and post-licensure products.Prepares and tests small-scale vaccines to support formulation of new reference standards.Supports the formulation, dispense and testing of new reference standards as part of the reference qualification process.Participates and collaborates in cross-functional teams with colleagues from R&D, Biotechnology Solutions-Analytics, Production, Quality Control, and Regulatory Affairs to support qualification of new reference standards.May assist in the preparation of protocols or reports for submission to USDA.May participate in critical reagent qualification studies.May provide technical support for approved Quality Control assays.Note:This is an Onsite role at De Soto, KS for 40 hrs/week. Flexible work schedule: 8am-5pm/9am-6pm/8am-4pm/6am-2pm/7am-3pm. The possibility of conversion to permanent employee or extension depending upon the performance. Managers are open to non-local candidates who are comfortable relocating at their expense. Panel interviews will be conducted for this role for approximately 60 minutes. Qualifications:Education:Bachelor’s degree/Master’s degree in a relevant biological area (Bacteriology, Biology, Microbiology, Virology).Either Candidates should have a biological education with 1-3 years ELISA experience in a lab setting (not college but industry).Required Experience and Skills:1-3 years laboratory experience with ELISA, preferably in Animal Health/industry.Detail-oriented with good documentation skills.Ability to conduct scientific experiments, interpret results, and communicate with relevant team members and stakeholders.Effective written and oral communication.Experience with Microsoft Office programs: Excel, PowerPoint, and Word.Preferred Experience and Skills: Ability to independently design scientific experiments.Experience working in an R&D or Quality Control laboratory.Experience developing, working with, and troubleshooting in vitro analytical tests mainly ELISA.Knowledgeable of USDA regulations for biological products.Company DescriptionWe Are Standing With 30+ Years Of Experience.NewAge Clinical is a Division of NewAgeSys Inc., a Favored Provider to the major Drug/Biotech/Medical Devices Organizations in the USA offering broadened types of assistance to our clients, similar to medical care staffing administrations, clinical staffing, and R & D contract jobs. Established in 1994, NewAgeSys has exhibited phenomenal development winning lofty honors for being one of the quickest-developing organizations in New Jersey. We are an inventive association with a forceful business procedure, supplementing amount with quality and using a clever interaction that conveys a full help arrangement. With regards to medical care staffing administrations, clinical staffing, R and D contract jobs, and staffing administrations in New Jersey, NewAge Clinical stands separated concerning quality, when contrasted with others. We understand that the process of selecting a consultant for a clinical trial or pre-clinical project often takes some time. We regard the time that this cycle takes by guaranteeing a completely thorough screening interaction to guarantee shared accomplishment to assure mutual success for our candidate's and client's proficient staffing needs.We Are Standing With 30+ Years Of Experience. NewAge Clinical is a Division of NewAgeSys Inc., a Favored Provider to the major Drug/Biotech/Medical Devices Organizations in the USA offering broadened types of assistance to our clients, similar to medical care staffing administrations, clinical staffing, and R & D contract jobs. Established in 1994, NewAgeSys has exhibited phenomenal development winning lofty honors for being one of the quickest-developing organizations in New Jersey. We are an inventive association with a forceful business procedure, supplementing amount with quality and using a clever interaction that conveys a full help arrangement. With regards to medical care staffing administrations, clinical staffing, R and D contract jobs, and staffing administrations in New Jersey, NewAge Clinical stands separated concerning quality, when contrasted with others. We understand that the process of selecting a consultant for a clinical trial or pre-clinical project often takes some time. We regard the time that this cycle takes by guaranteeing a completely thorough screening interaction to guarantee shared accomplishment to assure mutual success for our candidate's and client's proficient staffing needs.