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Investigate identify develop and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline.
Responsibilities:
Independently design develop and optimize robust analytical methods using separations-based techniques (HPLC icIEF CE-SDS) to characterize biopharmaceutical products
Implement and innovate new experimental protocols/techniques.
Understand the goal and maintain a high proficiency in his/her projects as well as the overall program.
Interpret results and draw conclusions from own multistage experiments note significant deviations then suggest design and pursue relevant experiments.
Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.
Perform routine and complex tasks competently and independently and generate reliable and consistent results.
Troubleshoot complex analytical issues and implement innovative solutions to improve method performance and efficiency.
Impact projects mostly through lab and/or pilot plant based activities.
Responsible for compliance with all applicable Corporate and Divisional policies and procedures.
Understand and adhere to corporate standards regarding code of conduct safety appropriate handling of materials controlled drug and radioactive compounds GxP compliance and animal care where applicable
Qualifications :
Bachelors Degree or equivalent education with typically 5 years of experience or Masters Degree or equivalent education with typically two years of experience.
Theoretical and practical knowledge to carry out the job functions.
Preferred Qualifications:
Strong understanding of protein chemistry and analytical method development principles.
Proficiency in operating and troubleshooting analytical instrumentation (e.g. Agilent Waters HPLC systems Maurice PA800 systems).
Experience with qualification and validation of analytical methods in accordance with ICH FDA and USP guidelines ensuring methods are suitable for late-phase development and regulatory submissions.
Familiarity with statistical tools for data analysis Empower and regulatory guidelines.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Full-time