Associate Principal Scientist, Process Development

Pharmaron • Coventry, RI

2d • Onsite

About The Position

As a subject matter expert, the Associate Principal Scientist will solve high complexity chemical development issues for assigned projects and /or initiatives. In a multidisciplinary environment, solve problems of higher complexity for assigned projects and / or initiatives with limited guidance from a scientific supervisor / Line Manager. Fully competent in the core chemistry laboratory skills required to support development and / or scale up of chemical processes. Such skills include, but are not limited to, expert application of core laboratory techniques and instrumentation to positively impact API drug development. From time to time use of selected higher end instrumentation or methodologies with supervisor guidance may be required. Design and execute core experiments, interpret results, and plan additional experiments in a timely manner to solve assigned problems of high complexity. Actively participate in the development of new technologies or methodologies, as appropriate within the functional area. Effectively communicate, coordinate and collaborate with cross-functional project groups to ensure that scientific work is appropriately documented such that the broader collaborative inputs and efforts are combined to maximum effect in the production of reports, manuscripts, and presentations. Document and report results of all experiments in a manner consistent with department practices and governing policies, as applicable, which may include significant contributions to manufacture of API for GLP toxicology studies or for GMP manufacture of clinical supplies. Contribute to effective team planning and mentor less experienced staff on core functional technical and procedural matters as opportunities arise. Follow all key internal business practices and external regulations governing the role (e.g. GLP or GMP), and adhere to all corporate policies governing the business activities. Contributes to ongoing client updates and final reports in a timely manner and present data at client meetings. Support client projects either as an individual contributor or as a PC project leader: performing experiments, reporting results, hosting and presenting data at project meetings, delegating work, being accountable for project deliverables and demonstrating leadership behaviours. In addition, supervise multiple individual contributors and be accountable for the whole teams' deliverables on a project. Responsible for any mixed model projects and tech transfer within the Pharmaron network.

Requirements

• PhD or equivalent in chemistry or related field MSc or BSc in chemistry or related field
• For those with PhD: Evidence of strong academic or industrial achievement with at least 7-11 years' experience in such role
• For those with MSc or BSc: Evidence of strong academic or industrial achievement with at least 11-15 (MSc) or 12-16 (BSc) years' experience in such role
• Evidence of strong academic or industrial laboratory experience with at least 5 years' experience in such roles
• Evidence of experience in successful application of analytical / physical skill sets to resolve high complexity chemical problems such as those required within the role
• Evidence of ability to effectively contribute to multi-disciplinary scientific teams
• Evidence of ability to effectively supervise staff
• Management of small teams (2-3 people)

Responsibilities

• Solve high complexity chemical development issues for assigned projects and /or initiatives.
• Solve problems of higher complexity for assigned projects and / or initiatives with limited guidance from a scientific supervisor / Line Manager.
• Expert application of core laboratory techniques and instrumentation to positively impact API drug development.
• Design and execute core experiments, interpret results, and plan additional experiments in a timely manner to solve assigned problems of high complexity.
• Actively participate in the development of new technologies or methodologies, as appropriate within the functional area.
• Effectively communicate, coordinate and collaborate with cross-functional project groups to ensure that scientific work is appropriately documented.
• Document and report results of all experiments in a manner consistent with department practices and governing policies.
• Contribute to effective team planning and mentor less experienced staff on core functional technical and procedural matters as opportunities arise.
• Follow all key internal business practices and external regulations governing the role (e.g. GLP or GMP), and adhere to all corporate policies governing the business activities.
• Contributes to ongoing client updates and final reports in a timely manner and present data at client meetings.
• Support client projects either as an individual contributor or as a PC project leader.
• Supervise multiple individual contributors and be accountable for the whole teams' deliverables on a project.
• Responsible for any mixed model projects and tech transfer within the Pharmaron network.

Benefits

• Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
• 401(k) Retirement Plan with generous employer matching
• Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
• Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
• Employee Assistance Program (EAP), mental health resources, and wellness programs
• Family-friendly benefits, including fertility support and maternity resources
• Professional development and career growth opportunities within a leading global CRO/CDMO

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree