Chemist

Element Materials Technology • Santa Fe Springs, CA

8h • $25 - $35

About The Position

Overview Element has an opportunity for a Chemist to join our growing team. This Chemist 's main responsibility is to assist the Metals department in testing, sample preparation and preparation of test reports. The Chemist is responsible for performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw materials, pharmaceutical products, medical devices and other samples as needed. Execute method validation, method transfers and routine testing to meet client requirements and in accordance to regulatory and company guidelines. Design sample preparation procedures to fulfill client requirements. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOP’s. $25.00-$35.00hr DOE Responsibilities Design and perform sample preparations with increasing complexity Conducts testing as per applicable regulatory and company guidelines Assists in the execution of method development, transfers, verification and validation as per applicable USP, ICH, and company standards Keep accurate, legible, complete, defensible, and complete records of all experiments and observations Assist in audit preparedness 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. Performs analytical testing of incoming raw materials, release testing of pharmaceutical products and medical devices using ICP-OES and ICP-MS for trace metals analysis

Requirements

• Requires a minimum of a bachelor’s degree in Chemistry, or related field with 2-5 years of experience in pharmaceutical industry or other cGMP regulated environments
• Enthusiastic team player, ready to step in wherever they are needed
• Adaptable, receptive to coaching and feedback
• Willing to learn and make adjustments based on feedback
• Able to work in a dynamic environment within a regulated setting; able to perform work under cGMP environment
• Meticulous, detail oriented, and able to maintain high quality with high throughput
• Punctual and willing to switch shift as needed
• Understanding of good laboratory practices and analytical techniques
• Excellent communication skills, written and verbal
• Excellent skills with Microsoft Office Suite of Products (Power Point, Word and Excel)
• Willingness and ability to work overtime

Nice To Haves

• Expertise in ICPMS analysis on pharmaceutical products preferred.
• Knowledge of analytical instrumentation including ICP-MS and ICP-OES preferred

Responsibilities

• Design and perform sample preparations with increasing complexity
• Conducts testing as per applicable regulatory and company guidelines
• Assists in the execution of method development, transfers, verification and validation as per applicable USP, ICH, and company standards
• Keep accurate, legible, complete, defensible, and complete records of all experiments and observations
• Assist in audit preparedness 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.
• Performs analytical testing of incoming raw materials, release testing of pharmaceutical products and medical devices using ICP-OES and ICP-MS for trace metals analysis

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level