Senior Director of Quality Control

3 days ago


Torrance, California, United States Bachem Full time
Job Summary

We are seeking a highly experienced and skilled Senior Director of Quality Control to join our team at Bachem. As a key member of our Executive Committee, you will play a critical role in ensuring the quality of our intermediate and active pharmaceutical ingredient manufacturing operations.

Key Responsibilities
  • Lead and Manage Quality Control Teams: Oversee the Quality Control teams at our Torrance and Vista facilities, ensuring they are equipped to support manufacturing operations and business objectives.
  • Ensure Compliance and Regulatory Adherence: Ensure all laboratory operations comply with pharmaceutical drug manufacturing laws, regulations, and guidance.
  • Drive Financial Performance: Take an active role in achieving expected financial performance, including management of costs and resource utilization.
  • Establish Priorities and Goals: Set priorities and goals for the Quality Control teams, guiding directors and managers to meet business needs and technical requirements.
  • Develop High-Performance Teams: Identify and develop high-performance individuals, supporting their career growth and development.
  • Provide Leadership and Guidance: Offer leadership and guidance throughout the organization, championing analytical science and technology to maintain a competitive advantage.
  • Represent Bachem: Represent the company during customer visits, GMP audits, and regulatory agency inspections.
  • Stay Abreast of Industry Developments: Stay up-to-date with developing analytical science and technology, driving continuous improvement of analytical capabilities.
Requirements
  • Education and Experience: Ph.D. in a science-related field with a minimum of 5 years of industry experience or Master's degree in a science-related field with a minimum of 10 years of industry experience.
  • Knowledge and Skills: Minimum of 10 years of overall experience, with 5 years of managerial experience and 5 years of analytical laboratory experience in the pharmaceutical industry. Knowledge of GMP for drugs and APIs and applicable FDA regulations.
  • Communication and Leadership Skills: Excellent written and oral communication skills, with the ability to lead, motivate, and mentor others.
  • Technical Skills: Proficient in Microsoft Word, Excel, and PowerPoint, with the ability to efficiently and productively use these tools.
Preferred Qualifications
  • Ph.D. in Analytical Chemistry
  • Experience working at a Contract Manufacturing Organization (CMO)
  • Technical experience in drug substance analysis


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