Research Scientist II

American Regent•Brea, CA

5d•$91,000 - $100,000•Onsite

About The Position

The Research Scientist II executes activities related to developing and validating methods for product/project, conducts method validation in compliance with ICH, USP/EP etc., and performs sample testing using HPLC, UV, GC, particle sizer, pH meter, etc. to provide support for formulation development and process development. Essential Duties and Responsibilities Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

Requirements

BS or MS degree in pharmaceutical science, chemistry, biology, or life science related field.
4+ years of method development and validation experience in the pharmaceutical industry.
Experience of analytical instrument techniques UV, HPLC, GC etc.
Experience on analytical method development and validation for assay and impurities.
Extensive experience on protocol writing, technical report creation, and lab investigations.
Good working knowledge of HPLC and GC techniques and trouble shooting skills.
Ability to multi-task, focus on priorities, and problem solving.
Ability to work effectively within an interdisciplinary team setting (independently and collaboratively).
Good knowledge of GMP Compliance, ICH, EP / USP Guidelines.
Excellent computer skills (Excel, Word, PowerPoint etc.), documentation and technique writing skills.
Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals.
Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves.
PPE and Respirators are essential for the health and safety of employees.
Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision.
Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly.
Employee must be able to occasionally lift and/or move up to 50 pounds.
Work in a lab and office environment.
The employee is required to safely handle, use, and dispose of chemicals.

Responsibilities

Conduct analytical studies in support of formulation development, process development, process scale-up, and regulatory filing.
Organize and prepare samples for analysis by external laboratories.
Develop and validate analytical methods for raw materials, in-process and finished product under cGLP/cGMP, ICH, USP/EP Guidelines.
Prepare protocols and reports for method validation, analytical test methods, technology transfer, and stability studies.
Provide training new scientists to perform analytical methods and instruments.
Troubleshoot and maintain analytical equipment.
Observe and maintain compliance, safety regulations, cGLP/GMP guidelines, and company policies and procedures.
Perform any other tasks/duties as assigned by management.