Group Leader, Analytical Development at Cambrex

Posted in Other 24 days ago.

Location: Charles City, Iowa





Job Description:

Cambrex


Group Leader, Analytical Development

US-IA-Charles City

Job ID: 2024-3688
Type: Regular Full-Time
# of Openings: 1
Category: Analytical Development
Cambrex - Charles City

Overview

Reporting to the Director, Analytical Development, the Group Leader of Analytical Development will provide management oversight and leadership to a group of approximately 5 to 8 direct reports with varying levels of degrees and experience. Strict compliance with cGMP guidelines is required to perform most job tasks.



Responsibilities

  • Safety and efficiently manage a group of 5-8 direct reports with varying levels of experience and degrees, in order to develop, establish, and validate analytical testing methodologies used to control raw materials, production intermediates, and final products
  • Effectively and professionally communicate project status to internal and external clients during weekly teleconferences and email correspondence
  • Investigate and solve analytical technical issues
  • Assist with or lead efforts to transfer documented analytical methods to QC and PSG departments
  • Provide guidance and/or project leadership for cross-functional project teams
  • Provide guidance to lab personnel on safe lab practices
  • Perform analytical chemistry assays based on new and existing methodologies and qualify reference materials
  • Training staff on analytical techniques and instrumentation
  • Participate in the evaluation of new business opportunities
  • Maintain lab notebooks documenting work and writing technical reports to document analytical methods
  • Maintain compliance with cGMP SOPs and DEA regulations
  • Coordinate off-site testing as necessary


Qualifications

  • 4 year degree in Chemistry, with analytical emphasis. Advanced degree preferred.
  • At least 5 years of industrial experience in a method development role and validation role with a focus on small scale pharmaceutical method validation






PI239476883


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