Associate Director of Analytical Chemistry
1 month ago
Come Join Our Growing Team
We are seeking an Associate Director, Analytical Chemistry to join our dynamic and growing team in Coventry, RI
Position Summary:
The Associate Director oversees analytical services including development, optimization, validation and transfer of drug substance-related analytical test methods in alignment with the overall business strategy.
Principal Accountabilities:
- Provide input to the scientific strategic direction of the department, including influencing the mission, vision, and culture of the organization in alignment with department/company goals
- Identify best practices directly impacting functional deliverables, and leverage resources to capitalize on them.
- Create and encourage a transparent and trustworthy work environment.
- Promote the culture that "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 both initial and continued personal training is carried out and adapted according to need, and ensure that all employees are suitably trained in all processes before undertaking tasks
- Assist scientific staff in reaching appropriate critical decisions which align with current functional or cross-functional strategies
- Ensure high quality in analytical work and GMP compliance: accurate documentation, instrument qualification, software validation, training, sample handling, testing, record keeping
- Oversee the development/improvement and validation of robust analytical methods that are GMP-friendly based on quality-by-design and document formal protocols and reports.
- Oversee method transfer activities, including writing protocols and reports as needed.
- Establishment and qualification of GMP-compliant analytical laboratories.
- Manage multiple projects requiring analytical or process-related activities.
- Establish or revise procedures to cover all GMP activities, as well as harmonizing or integrating with other Pharmaron sites
- Communication with Pharmaron colleagues as well as 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. Present to cross-functional teams and effectively communicate critical analytical issues and solutions.
- Direct the development of SOPs appropriate for CDMO activities.
- Communicate openly within the group to provide and gather information, to optimize the use of resources, and to optimize efficiency.
Education and Experience:
- PhD with 10+ years of experience in pharmaceutical analysis with 5+ years of management experience.
- Ability to effectively lead and supervise staff
- Proven technical skills in analytical method development and validation of small molecules
- Proven scientific skill and ability to oversee complex scientific work
- Effective in managing multiple competing activities and delivering to timelines
- Highly commercially oriented, able to demonstrate how delivery excellence can create competitive advantage to deliver and sustain business growth
- Highly organized, but flexible to changing priorities
- Ability to work in a cross-functional environment
- High level of awareness to innovative technologies and ability to adapt to in-house needs
- Broad experience in analytical instrumentation and selected higher end laboratory techniques.
- Ability to contribute to multi-disciplinary scientific teams
- Ability to drive continuous improvement
- Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance
- Excellent communication skills, both verbal and written
Benefits:
Pharmaron cares about our work community and offers a variety of benefits allowing employees the opportunity to customize a benefits package that meets their personal needs. Company benefits include the following:
- Medical, Dental & Vision Insurance Plan with Employer Contribution
- Health Reimbursement Account Funded by Employer
- Healthcare & Dependent Care Flexible Spending Accounts
- Employee Life and AD&D Insurance 100% Employer Paid
- Voluntary Life and AD&D Insurance for Employee, Spouse & Child(ren)
- Short and Long Term Disability 100% Employer Paid
- 401k with Employer Match
- Employee Assistance Program
About Pharmaron
Pharmaron is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and Cell & Gene Therapy products. With over 19,000 employees, and operations in the U.S., the U.K., and China. Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China.
Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.
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