Senior Analytical Chemistry Director

2 weeks ago


Coventry, Rhode Island, United States Pharmaron Full time

**Job Summary:**

We are seeking an experienced Analytical Chemistry Director to join our dynamic team in Coventry, RI.

The successful candidate will oversee analytical services including development, optimization, validation, and transfer of drug substance-related analytical test methods in alignment with the overall business strategy.

Key Responsibilities:

  • Provide input to the scientific strategic direction of the department, influencing the mission, vision, and culture of the organization in alignment with department/company goals
  • Identify best practices directly impacting functional deliverables, leveraging resources to capitalize on them
  • Create and encourage a transparent and trustworthy work environment
  • Promote a culture where quality is everyone's responsibility
  • Review RFPs, assist with providing information for the analytical portion of proposal, participate in customer visits, audits, or project meetings
  • Ensure initial and continued personal training, adapting according to need, and ensure all employees are suitably trained before undertaking tasks
  • Assist scientific staff in reaching critical decisions aligning with current functional or cross-functional strategies
  • Oversee high-quality analytical work and GMP compliance: accurate documentation, instrument qualification, software validation, training, sample handling, testing, record keeping
  • Establish and validate robust analytical methods that are GMP-friendly based on quality-by-design, documenting formal protocols and reports
  • Manage multiple projects requiring analytical or process-related activities
  • Establish or revise procedures covering all GMP activities, harmonizing or integrating with other Pharmaron sites
  • Communicate with Pharmaron colleagues and customers on projects
  • Review experimental data, notebooks, and instrument qualification protocols/reports as needed
  • Actively participate in investigations, problem-solving, and troubleshooting, assisting with investigation reports
  • Prepare and present data summaries (written and oral) as necessary, presenting to cross-functional teams and effectively communicating critical analytical issues and solutions
  • Direct the development of SOPs appropriate for CDMO activities
  • Communicate openly within the group to provide and gather information, optimize resource use, and optimize efficiency


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