Method Development Scientist for a Leading Global Pharmaceutical Synthesis Company
* Greater Boston Area
* Competitive Salary + Benefits + Long Term Incentives
A fast-growing Pharmaceutical Company has just secured more funding and is looking to build out their Analytical Development team to aid in their COVID relief efforts. This role will be reporting directly into the Director Analytical Services and will be working cross functionally with Regulatory; Quality, Chemistry, and the Project Management teams.
The Director Analytical Development will have the following Responsibilities:
* Develop Analytical Methods for all products in process control, final product release or in stability testing, all while in compliance with cGMP
* Write and execute validation protocols and reports for clinical phase of API,
* Write and revise SOPs to improve laboratory functions and practices in alliance with company and federal regulation standards
* Act as SME (Subject Matter Expert) to aid in delivery of analytical results related to manufacturing and development variations, LIR//OOS, and QI
* Provide Technical Support, problem solving, and training to relevant parties as needed including; R&D, Quality, and Production.
The Ideal Candidate will have the following skill set:
* PH. D in Chemistry, Organic Chemistry, or Analytical Development Required
* 3+ years in Pharmaceutical Industry within cGMP, and a primary focus on method development and validation
* Technical Expertise in Chromatography and Spectroscopy with Analytical expertise with the following techniques: HPLC, GC, FTIR, KF, TOC
* Strong Communication Skills
Back to jobs