We are seeking a skilled Analytical Scientist II or Senior to join our laboratory team. This role focuses on supporting formulation development through comprehensive analytical testing, method development, and validation activities for both generic (ANDA) and new drug application (NDA) projects.
Responsibilities:
Method Development & Validation
Design, develop, and optimize analytical test methods for raw materials, in-process samples, and finished pharmaceutical products
Execute method verification and validation studies following established protocols, company procedures, FDA guidance documents, and ICH guidelines
Document all analytical work comprehensively to ensure regulatory compliance
Testing & Analysis
Perform chemical and physical characterization of APIs, raw materials, in-process samples, and finished products
Conduct routine product release testing and stability studies using validated analytical methods
Support formulation development teams through timely and accurate analytical data generation
Documentation & Communication
Author technical protocols, validation reports, and analytical documentation
Collaborate effectively with cross-functional teams including Formulation Development, Quality Control, Quality Assurance, Compliance, and Regulatory Affairs
Maintain clear communication channels to support project timelines and objectives
Compliance & Professional Development
Adhere to current Good Manufacturing Practice (cGMP) regulations and company standard operating procedures
Participate in ongoing training programs covering SOPs, laboratory safety, and current scientific methodologies
Stay current with FDA guidance documents and ICH guidelines relevant to analytical testing
Required Qualifications:
Education & Experience
Bachelor's degree in Chemistry, Chemical Engineering, Materials Science, or related scientific discipline
Minimum 5 years of relevant analytical laboratory experience
Level (II vs Senior) determined by depth of experience and demonstrated expertise
Technical Skills
Strong foundation in analytical chemistry principles and physical characterization techniques
Proven experience in analytical method development and optimization
Working knowledge of GMP requirements, ICH guidelines, and FDA regulatory expectations
Professional Skills
Excellent written and verbal communication abilities
Strong interpersonal skills for effective cross-functional collaboration
Detail-oriented approach with strong documentation practices
Ability to work independently while supporting team objectives
If you meet the required qualifications and are interested in this role, please apply today.
Clinical Resource Network Distinction
CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit and connect with us on Facebook and LinkedIn .
Opportunity Awaits.