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Analytical chemist Jobs in Indianapolis, IN
- Promoted
Chemist (SK2630)
TechData Service Company LLCIndianapolis, IN, USChemist
Eurofins Lancaster Laboratories Professional Scientific Services, LLCUSA, Indiana, Indianapolis- Promoted
Senior Project Chemist
VirtualVocationsIndianapolis, Indiana, United States- Promoted
Analytical Lab Chemist
Calibi ConsultingIndianapolis, IN, US- Promoted
Chemist
ExperisIndianapolis, IN, United States- Promoted
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Analytical Purification Chemist
Cogent ScientificIndianapolis, IN, US- Promoted
Chemist
Eurofins USA PSS Insourcing SolutionsIndianapolis, IN, US- Promoted
Opioids Chemist
My3TechIndianapolis, Indiana, USA- Promoted
Opioids Chemist
GSK SolutionsIndianapolis, IN, United States- Promoted
QC Chemist
The Fountain GroupIndianapolis, IN, United StatesChemist
ATCIndianapolis, IN, USA- Promoted
Analytical Scientist
ACL DigitalIndianapolis, IN, United States- Promoted
QC Chemist
Novartis Group CompaniesIndianapolis, IN, United States- Promoted
Analytical Biochemist
EurofinsIndianapolis, IN, United StatesManufacturing Chemist
Cardinal HealthIndiana, United StatesChemist-QC
LillyIndianapolis, Indiana, United States of America- Promoted
Chemist - Analytical Chemistry
Eli Lilly and CompanyIndianapolis, Indiana, United StatesChemist (SK2630)
TechData Service Company LLCIndianapolis, IN, US- Full-time
Job Description
Job Description
Contract : 9 Months (Renewable)
Job ID : 2630
Pay Rate : UP to $36 / hr. W2
Perform accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate Good Manufacturing Practices and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executingwell defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of process development / optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conducted and documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems.
Synthetic Molecule Design and Development (SMDD) is comprised of different groups that design and execute the development of all CMC aspects of synthetic molecules from pre-clinical phases through commercialization for drug substances and drug products. 2. Responsibilities SMDD is responsible for developing the portfolio strategy and for the application of the technical capabilities to the portfolio. Through scientific training and relevant experience, a team of scientists and team leaders support the portfolio from early clinical development through the commercialization of new drug candidates. Teams of cross-functional scientists will drive integration of technical elements from internal and external groups enabling the clinical manufacturing and commercialization of new drug candidates. The Scientist or other designated title from above in SMDD :
- Helps ensure that people, and their environment are safe and that company policies concerning safety are followed.
- Understands and complies with corporate, divisional, and departmental procedures, including FRAP, current good manufacturing practices, safety, and other applicable regulations, and participates in the establishment and maintenance of PRD Quality systems.
- Contributes to, leads and / or supervises the formulation, design, or process development and or control strategy of drug substance and / or drug product. Typical responsibilities include : o Development of the manufacturing processes and control strategies for drug substance and / or drug product. o Preparation of the appropriate manufacturing and controls portion of the IND / CTX and preparation of information for annual updates. o Provides technical oversight at external collaboration partners for laboratory and manufacturing activities to support the portfolio and capability development. o Scale-up to manufacturing. o Preparation or oversight and review of the appropriate manufacturing and controls portion of regulatory submissions. o Provides advice and guidance to teams on the development of a commercial development strategy. o Authors, reviews, or approves high quality technical reports and regulatory submissions dealing with the work performed by the department. Ensures that records and technical notebooks are adequately maintained
TechData is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status.
Job Types : Contract, Temporary
Pay : $26.00 - $36.00 per hour
Expected hours : 40 per week
Benefits :
Schedule :
Experience :
Ability to Commute :
Ability to Relocate :
Work Location : In person
Company Description
www.techdataservice.com
Company Description
www.techdataservice.com