Job Description
We are seeking an experienced contract scientist specializing in chemometric method development and validation using Raman spectroscopy. The successful candidate will support pharmaceutical analysis through the creation, optimization and validation of multivariate models and spectroscopic methods to be used in pharmaceutical manufacturing or QC lab environments.
This role requires strong expertise in Raman spectroscopy and HPLC/UPLC-UV analysis, chemometric modeling and regulatory expectations for method validation and lifecycle management.
Pay rate between $63-68/hr based on experience.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Required Skills & Experience
• MS or PhD in Chemometrics, Analytical Chemistry, Pharmaceutical Sciences or related discipline.
• Minimum 3-5 years of industry experience in chemometric method development and validation within the pharmaceutical or biotech industry
• Hands-on expertise with Raman spectroscopy
• Strong understanding of multivariate statistical analysis and chemometric modeling techniques
• Experience with pharmaceutical method validation and GMP documentation practices
Knowledge of ICH Q2, PAT guidance and data integrity
Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.