Senior Scientist II – Analytical Chemistry

Pharmaron; Coventry (RI); In loco; USD 90.000 - 130.000; Tempo pieno

Vantaggi offerti da questo lavoro

Insurance including Medical, Dental &

Vision with significant employer con-

Employer-funded Health Reimbursement A

Healthcare & Dependent Care Flexible S

100% Employer-paid Employee Life and A

401k plan with generous employer match

Access to an Employee Assistance Progr

Descrizione del lavoro

Pharmaron Beijing Co. Ltd. in Coventry, RI is seeking a Senior Scientist II– Analytical Chemistry to serve as a key technical resource in the QC laboratory supporting API manufacturing and development programs.

The role focuses on analytical method validation, transfer, troubleshooting, and QC testing of raw materials, intermediates, and active pharmaceutical ingredients in a cGMP environment. You will contribute technical expertise to complex analytical challenges, mentor QC scientists, and

Competenze

• Ph.D. in Chemistry or a related field with 1–4 years of postdoctoral or industry experience.
• MS with 5–8 years of pharmaceutical industry experience; BS with 7–10 years of experience.
• 3 years of experience with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.
• Experience applying analytical techniques to support method validation, troubleshooting, and implementation.
• Strong hands-on expertise with HPLC/UPLC, GC, FTIR, UV, and Mass Spectrometry.

Mansioni

• Support analytical method validation, verification, and transfer activities within the QC laboratory.
• Troubleshoot complex analytical challenges related to API characterization and GMP testing.
• Review analytical data, notebooks, and instrument qualification documentation for accuracy and regulatory compliance.
• Lead or support laboratory investigations, deviations, and root cause analyses.
• Maintain laboratory equipment and act as system owner for analytical instrumentation.
• Provide technical mentorship to QC scientists and staff.
• Prepare and revise SOPs and analytical methods.
• Support regulatory inspections and client audits as an analytical SME.
• Collaborate with Manufacturing, Process Chemistry, QA, and Regulatory Affairs.
• Contribute to continuous improvement initiatives for QC efficiency.
• Perform other related assignments as required.

Conoscenze

HPLC/UPLC

GC

FTIR

UV

Mass Spectrometry

Formazione

PhD in Chemistry or related field

MS in Chemistry or related field

BS in Chemistry or related field

Descrizione del lavoro

Position: Senior Scientist II– Analytical Chemistry

Salary Range: $90k - $130k

Location: Coventry, RI

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, 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 over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ 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 3,000 global customers. To learn more, visit www.pharmaron.com.

Job Overview

The Senior Scientist - Analytical Chemistry will serve as a key technical resource within the Quality Control laboratory supporting API manufacturing and development programs at Pharmaron's Coventry, RI facility.

This role is responsible for supporting analytical method validation, transfer, troubleshooting, and QC testing of raw materials, intermediates, and active pharmaceutical ingredients in a cGMP-regulated laboratory environment. The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations.

Key Responsibilities

• Support analytical method validation, verification, and transfer activities within the QC laboratory.
• Troubleshoot complex analytical challenges related to API characterization and GMP testing.
• Review analytical data, laboratory notebooks, and instrument qualification documentation to ensure scientific accuracy and regulatory compliance.
• Lead or support laboratory investigations, deviations, and root cause analyses.
• Maintain laboratory equipment and serve as system owner for analytical instrumentation, including qualification and maintenance activities.
• Provide technical mentorship and scientific guidance to QC scientists and laboratory personnel.
• Prepare and revise standard operating procedures (SOPs), analytical methods, and technical documentation.
• Support internal and external regulatory inspections and client audits as an analytical subject matter expert.
• Collaborate with cross-functional teams including Manufacturing, Process Chemistry, Quality Assurance, and Regulatory Affairs.
• Contribute to continuous improvement initiatives that enhance QC laboratory efficiency and analytical capabilities.
• Perform other related assignments and duties, as required and assigned.

What We're Looking For

• Ph.D. in Chemistry or a related field with 1–4 years of postdoctoral or industry experience.
• MS with 5–8 years of pharmaceutical industry experience, BS with 7–10 years of relevant pharmaceutical industry experience
• 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.
• Demonstrated experience applying analytical techniques to solve complex scientific problems related to method validation, troubleshooting, and implementation
• Strong hands‑on expertise with analytical instrumentation including:
• HPLC / UPLC
• GC
• FTIR
• UV
• Mass Spectrometry
• Experience supporting API manufacturing or pharmaceutical QC laboratories
• Proven ability to troubleshoot analytical instrumentation and laboratory methods
• Working knowledge of cGLP / cGMP and applicable FDA, EMA, and ICH regulatory guidelines
• Experience contributing to multidisciplinary scientific teams and cross-functional projects
• Experience mentoring or supervising laboratory personnel preferred
• Strong analytical thinking, scientific judgment, and problem-solving skills
• Excellent written and verbal communication skills

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 across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture:

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.

Benefits:

• Insurance including Medical, Dental & Vision 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
• 401k plan with generous employer match
• Access to an Employee Assistance Program

As an Equal Employment Opportunity and Aff…?