Analytical Scientist

Key Responsibilities

• Drive special projects that require AQC attention/leadership.
• Drive analytical method development and validation of laboratory methodologies and instrumentation.
• This includes leading analytical/microbiology QC efforts to support the introduction of new product testing, modifying existing laboratory space, planning design new laboratory spaces and working with vendors to purchase new instruments, and the installation and qualification of new instruments.
• Support investigations and manufacturing investigations requiring analytical method support.
• Support the installation, operational qualification (IOQ), maintenance and troubleshooting of instrumentation in the AQC group.
• Serve on project teams, in a leadership role as needed, which will require substantial interaction and communication with other group functions.

Qualifications

• Excellent technical writing skills and able to write technical documents and reports that meet company and regulatory requirements.
• In depth knowledge of analytical methods and operations with strong emphasis in problem-solving.
• Knowledge about analytical method validation and critical reagent qualification.
• Intermediate statistical knowledge and experience with data analysis.
• Knowledge concerning cGMP, especially lab related topics such as method validation and unexpected results investigation.
• Basic knowledge about regulatory requirements concerning analytical instrumentation, test methods and licenses.
• Substantial knowledge and understanding in terms of regulatory standards requirements e.g., CGMP, QSR, USP, 21CFR, ICH etc.
• Ability to complete tasks with minimal direction, demonstration of basic project management skills.
• Ability to multi-task in a highly dynamic and diverse environment.
• Attention to detail, good organization, and time management skills to meet deadlines.
• Proficient in Microsoft Office.
• Strategic and business-oriented thinking.

Education and/or Experience

• Bachelor’s degree in biotechnology, Microbiology, Pharmacy, Chemistry or equivalent.
• Minimum of 3 years of analytical development or validation experience in GMP Pharmaceutical, Biopharmaceutical or related manufacturing environment, or an advanced degree.