Analytical Chemistry Development Group Lead
Job DescriptionJob DescriptionParticipates in method optimization and qualification for clinical chemistry methods.
Participates in technical transfer and impurity clearance testing for clinical drug products.
Reviews documentation and data to ensure completeness and compliance with standards; reports any quality anomalies.
Complies with all pertinent regulatory agency requirements including but not limited to good manufacturing, documentation, and laboratory practices.
Participates in required training activities.
Maintains laboratory supplies.
Calibrates or verifies calibration of instruments/devices prior to use.
Performs instrument maintenance and troubleshooting activities.
Interacts with outside customers or functional peer groups.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivated, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesLeadership ResponsibilitiesLead an Chemistry Development team of three other analysts in a GMP regulated development labCoordinates, supports, and monitors performance of team through testing and quality metrics while ensuring client deadlines are metCoordinates with client contacts to communicate status of deliverables, determine priorities, and set timelines.
Set individual and team goals to develop the scope of work and responsibilities of the teamManage time off and payroll entries of the teamMay participate in new hire interviewsSupports the on-boarding process of new employeesParticipates in training of other employees.
SDL2017 Recommended Skills Adaptability Attention To Detail Calibration Clinical Works Communication Coordinating Estimated Salary: $20 to $28 per hour based on qualifications.
Participates in technical transfer and impurity clearance testing for clinical drug products.
Reviews documentation and data to ensure completeness and compliance with standards; reports any quality anomalies.
Complies with all pertinent regulatory agency requirements including but not limited to good manufacturing, documentation, and laboratory practices.
Participates in required training activities.
Maintains laboratory supplies.
Calibrates or verifies calibration of instruments/devices prior to use.
Performs instrument maintenance and troubleshooting activities.
Interacts with outside customers or functional peer groups.
Strong computer, scientific, and organizational skills.
Excellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivated, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesLeadership ResponsibilitiesLead an Chemistry Development team of three other analysts in a GMP regulated development labCoordinates, supports, and monitors performance of team through testing and quality metrics while ensuring client deadlines are metCoordinates with client contacts to communicate status of deliverables, determine priorities, and set timelines.
Set individual and team goals to develop the scope of work and responsibilities of the teamManage time off and payroll entries of the teamMay participate in new hire interviewsSupports the on-boarding process of new employeesParticipates in training of other employees.
SDL2017 Recommended Skills Adaptability Attention To Detail Calibration Clinical Works Communication Coordinating Estimated Salary: $20 to $28 per hour based on qualifications.
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