This position is no longer open for applications

A Global Pharmaceutical and R&D Company are looking for Snr Analytical Scientists in New Jersey and Boston.

Position Responsibilities:

Responsible for the design, development, qualification, validation, and implementation of analytical procedures in support of research, GMP production, and stability testing.  The Senior Analytical Chemist is expected to provide quality ideas and contribution to the assigned challenges and to offer recommendations and knowledge to other staff.

Job Responsibilities:

• Develops efficient and selective analytical procedures (with emphasis on HPLC and GC) for assigned projects
• Prepares qualification and validation protocols and reports for analytical procedures and instrumentation
• Performs sample analysis and reviews data packages
• Documents all analyses per SOPs
• Prepares high quality written documentations (notebooks, SOPs, and analytical procedures) and assists with regulatory documentation
• Troubleshoots analytical instrumentation
• Communicates effectively in verbal and written form on research results and plans
• Volunteers to assist with task not directly related to a specific project
• Demonstrates initiative in handling responsibilities
• Contributes to the technical growth of the department and company
• Attends project meetings and prepares project updates
• Participates in self-development activities
• Other duties as assigned

Quality/Regulatory Responsibilities:

• Demonstrates technical proficiency and self-assuredness in applying cGMP standards
• Applies cGMP concepts in association with department specific responsibilities
• Ensures all documentation produced is in compliance with cGMP standards
• Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed
• Ensures work is in compliance with all state and federal regulations, including but not limited to GMP, DEA, FDA, etc

Essential Skills and Experience:

• BS in Analytical Chemistry or equivalent with 5-7 years related experience in a pharmaceutical  industry
• MS in Analytical Chemistry or equivalent with 3-5 years related experience in a pharmaceutical  industry
• Ability to write clear and concise technical reports
• Good understanding of Microsoft Office and statistical software
• Demonstrates ability to exercise good judgment and make decisions quickly
• Good written and verbal communication skills
• Experience with common analytical techniques such as HPLC, GC, LC-MS, GC-MS
• Experience communicating effectively to management
• Ability to work independently and in a team environment