Process Development Associate Jobs in Cranston, RI

Position: Associate Principal Scientist, Process Development

Salary Range: $120,000 - $160,000

Location: Coventry, RI (On-site)

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

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.

• 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)

Pharmaron is a premier 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 CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

• 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

As an Equal Employment Opportunity and Aff…