Pharmaron Beijing Co. Ltd.
Associate Principal Scientist, Analytical Chemistry and Quality Control
Pharmaron Beijing Co. Ltd., Coventry, Rhode Island, us, 02816
Position: Associate Principal Scientist, Analytical Chemistry & Quality Control
Location: Coventry, RI (ON-SITE)
FLSA Status: Exempt
We are on the search for an Associate Principal Scientist to join our team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Associate Principal Scientist, Analytical will support process chemistry and manufacturing activities through analytical method development, optimization, validation, and transfer in compliance with all applicable guidelines.
Primary Responsibilities:
Provides independent analytical leadership of projects, accountable for project deliverables.
Develop / improve and/or validate robust analytical methods that are GMP friendly based on quality-by-design and document formal protocols and reports.
Participate in method transfer activities, including writing protocols and reports.
Manage stability studies, perform the testing and data trending, as required.
Ownership of equipment, participate in computer system validation.
Draft, review and Approval of Scientific Protocols, Reports and SOPs.
Overseeing leadership on several analytical project teams working to tight deadlines.
Supervises multiple members of staff and support management team with workload management
Implementing new analytical techniques and strategies to expand departmental capabilities.
Solving multiple complex scientific problems.
Ensuring adherence to GMP.
Presenting and communicating clearly and effectively with clients.
Experience and Education:
PhD in Chemistry with 7 years of experience or MSc/BS in Chemistry or related field with 12 years of experience with the following instrumentation: HPLC, GC, FTIR, UV, LC/MS, GC/MS. Experience with NMR is a plus.
Excellent communication skills, both verbal and written.
Effective in managing multiple competing activities and delivering to timelines.
Previous supervisor experience is a plus
Ability to work in a cross-functional environment.
Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred.
High level of awareness of innovative technologies and ability to adapt to in-house needs.
Why Pharmaron?
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.
Collaborative Culture:
You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Our core cultural values are 'Employees Number One' and 'Clients Centered,' setting Pharmaron apart from other organizations.
Benefits:
Medical, Dental & Vision Insurance with significant employer contributions.
Employer-funded Health Reimbursement Account.
Healthcare & Dependent Care Flexible Spending Accounts.
100% Employer-paid Employee Life and AD&D Insurance.
Short- and Long-Term Disability Insurance.
401(k) plan with generous employer match.
Access to an Employee Assistance Program.
Pharmaron is an Equal Employment Opportunity and Affirmative Action employer, valuing diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed.
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