Chemist I bei PREMIER MAGNESIA

Description

The primary responsibility of this position is to provide laboratory and technical support for multiple business units. The incumbent will perform laboratory functions such as analytical testing, technical assistance, research and development and product development. Will be responsible for data analysis, writing reports, maintaining equipment and supplies. This position is expected to function as a team member with the ability to perform all tests conducted in the QA laboratory. Will comply with Good Manufacturing Practices and Good Laboratory Practices, follow Good Documentation Practices, and abide by Safety & Housekeeping Policies.

Responsibilities

• Provide routine analytical services using ICP, wet chemistry techniques and other typical analytical techniques used for raw materials, in-process and finish product assays
•  Support Research and Development projects
• Interpret results of analyses to provide information to production, sales and customers
• Document test results in Notebooks, Controlled Documents and Forms; maintain accurate and complete quality records
• Assist with Product Development requests.
• Schedule/perform laboratory equipment calibration (daily and third-party annual)
• Maintain all laboratory equipment and supplies to prevent testing delays
• Conduct OOS investigations, as needed.
• Maintain Chemical Inventory and Master Chemical lists
• Maintain Chemical CoA binders
• Will provide validation and qualification support for instrumentation, methods, including, writing and reviewing protocols while maintaining a laboratory notebook
• Maintain a clean, safe and organized lab area and potentially assume responsibility to ensure that others maintain their lab areas
• Follow, understand and comply with Giles/Premier SOP’s and policies on cGMPs and Safety
• Support improvement projects and drive efficiency through utilization of LEAN management principles
• Perform other Laboratory, Quality and/or Safety support functions as assigned.

Qualifications

• Fundamental understanding of cGMP and Safety regulations.
• Experience in an analytical laboratory setting.
• Ability to develop and implement test methods.
• Experience in a supervisory role a plus.
• Possess oral and written communication skills, strong interpersonal skills, strong organizational abilities, and able to work in a team environment.
• Must have strong personal time management skills with the ability to meet deadlines and to work with minimal supervision.
• Intermediate computer skills (Microsoft Word and Excel).
• Customer oriented mindset.
• Background in medical, food, or pharmaceutical manufacturing a plus
• Minimum BS/BA Degree in Chemistry or allied fields
• Two years’ work experience in Quality Laboratory and/or manufacturing with a demonstrated track-record of accomplishments.