Scientist II

Core Responsibilities

• Performs sample analysis, interprets results, and reports data.
• Documents all analyses per SOPs.
• Aids in method development, method qualification/validation/transfer activities, drafts weekly reports, method qualification/validation protocols/reports for analytical procedures.
• Prepares high quality written documentation (notebook entry, summary reports, SOPs, analytical procedures, etc.).
• Troubleshoots analytical instrumentation.
• Communicates effectively in verbal and written form on research results and plans.
• Demonstrates initiative in handling responsibilities and collaborates with the team members.
• Participates in self-development activities.
• Applies cGMP, quality, regulatory, and EH&S standards in compliance with company procedures and state and federal regulations.
• Promotes a safe and compliant work environment by following EH&S policies, reporting incidents, and supporting corrective actions and sustainability initiatives.

Qualifications

• BS in Analytical chemistry or equivalent with 2+ years relevant experience or MS in Analytical chemistry or equivalent with 1+ years of related experience in analytical development (R&D and method qualification/validation) environment within pharmaceutical industry in a cGMP environment.
• Proficiency in standard analytical techniques such as: HPLC, GC, UV, KF, and FTIR.
• Good written and verbal communication skills.
• Ability to work independently and in a team environment.
• Knowledge of MS Project.
• Experience in establishing integrated plans with resource and task constraints.

Additional Information

• The position is full-time, Monday-Friday, 8:00am-5:00pm, with overtime as needed.
• Candidates living within a commutable range of Devens, MA are encouraged to apply.
• Compensation: $65,000-72,000/year
• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays