Group Leader, Analytical Development
Germer International Pharmaceutical Recruiting · Waterloo, Iowa, United States
FULL TIMEpermanent
Job Description
Our client is seeking an experienced Analytical Development Group Leader to lead a team of scientists in a dynamic and fast-paced environment. This individual will be responsible for the safe and efficient management of the group, while driving the development, establishment, and validation of analytical testing methodologies.
Ensure all your application information is up to date and in order before applying for this opportunity.
Responsibilities:Safely and efficiently managing a group of 5-8 direct reports with varying levels of experience and degrees to develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products.Effectively and professionally communicating project status to internal and external clients during weekly teleconferences and email correspondence.Investigating and solving analytical technical issues.Assisting with or leading efforts to transfer documented analytical methods to Quality Control and Process Support departmentsProviding guidance and/or project leadership for cross functional project teamsProviding guidance to laboratory personnel on safe laboratory practicesPerform analytical chemistry assays based on new and existing methodologies and qualify reference materials. xzbcwsv Training staff on analytical techniques and instrumentationParticipating in the evaluation of new business opportunitiesMaintaining laboratory notebooks documenting work and writing technical reports to document analytical methodsMaintain compliance with GMP SOPs and DEA regulationsCoordinate off-site testing as necessaryParticipation in design/execution in R&D initiatives
Qualifications:4 year degree in Chemistry, with analytical emphasis. Advanced degree beneficial8 or more years of industrial experience in a method development and validation role with a focus on small scale pharmaceutical method validation
Ensure all your application information is up to date and in order before applying for this opportunity.
Responsibilities:Safely and efficiently managing a group of 5-8 direct reports with varying levels of experience and degrees to develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products.Effectively and professionally communicating project status to internal and external clients during weekly teleconferences and email correspondence.Investigating and solving analytical technical issues.Assisting with or leading efforts to transfer documented analytical methods to Quality Control and Process Support departmentsProviding guidance and/or project leadership for cross functional project teamsProviding guidance to laboratory personnel on safe laboratory practicesPerform analytical chemistry assays based on new and existing methodologies and qualify reference materials. xzbcwsv Training staff on analytical techniques and instrumentationParticipating in the evaluation of new business opportunitiesMaintaining laboratory notebooks documenting work and writing technical reports to document analytical methodsMaintain compliance with GMP SOPs and DEA regulationsCoordinate off-site testing as necessaryParticipation in design/execution in R&D initiatives
Qualifications:4 year degree in Chemistry, with analytical emphasis. Advanced degree beneficial8 or more years of industrial experience in a method development and validation role with a focus on small scale pharmaceutical method validation