Chemist III at Element Materials Technology

Santa Rosa, California, United States -

Full Time

Start Date

Immediate

Expiry Date

17 Feb, 26

Salary

110000.0

Posted On

19 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Chemistry, Laboratory Skills, Synthetic Techniques, Purification Techniques, cGMP Experience, Process Scale Up, Project Management, Team Leadership, Documentation, Safety Compliance, Research and Development, Equipment Maintenance, Raw Material Handling, Technical Review, Data Summarization, Positive Work Environment

Industry

Manufacturing

Description

Overview Element is seeking a Chemist III to join our growing Santa Rosa, CA team. In this role, you will independently manufacture and accurately document Active Pharmaceutical Ingredients (APIs), intermediates, regulatory starting materials, and other chemicals in accordance with approved batch or laboratory records. You will support daily laboratory operations within our Santa Rosa facility—part of Element’s global network dedicated to advancing safety and quality—while ensuring adherence to rigorous quality, safety, and compliance standards. As assigned, the Chemist III will also take on Project Manager responsibilities, contributing to efficient workflow, customer support, and the delivery of high-quality results. You can read more about the work our Santa Rosa Lab does here: EMT Santa Rosa Lab Page $80k-$110k DOE Responsibilities Supervising and or participating in manufacturing APIs, intermediates, and regulatory starting materials according to approved batch production records Writing and technical review of cGMP documentation Setup, use and cleaning of process equipment and maintenance of corresponding equipment logs, as applicable Ensuring a secure supply of raw materials from reliable and qualified vendors Dispensing and use of raw materials, and maintenance of corresponding material logs, as applicable Maintaining schedule of manufacture activities Participating in research and development activities without direct supervision Maintaining accurate cGMP records and R&D lab records Preparing project reports and/or data summaries, as needed Understanding of and compliance with appropriate SOPs Directing and overseeing the activities of other laboratory personnel, as assigned Design and execution of scalable processes Assisting in preparation of project proposals and quotations Acting as Project Manager, when assigned Ensuring safety and cleanliness of laboratory work areas Cleaning glassware Helping create a positive work environment Other reasonable duties may be assigned as necessary Skills / Qualifications Bachelor’s degree in chemistry and significant experience in kilo lab/cGMP operations 3 to 6 years as Production Chemist (BS) 2 to 5 years Master's degree or PhD. Strong laboratory skills Skilled in the scale up of processes Demonstrated strength in synthetic and purification techniques Extensive cGMP experience Demonstrates in depth understanding of the chemistry in production Contributes and shares ideas across projects Comfortably prepares and presents information to group and clients Ability to work as a team member and a team leader Physical Demands: Ability to safely handle hazardous materials Ability to move/lift 50 pounds Ability to safely handle large glassware Ability to wear respirator #LI-TK1 Diversity Statement At Element, we always take pride in putting our people first. We are an equal opportunity employer that recognizes diversity and inclusion as fundamental to our Vision of becoming “the world’s most trusted testing partner”. All suitably qualified candidates will receive consideration for employment on the basis of objective work related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws or other characteristics in accordance with the applicable governing laws. The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c) “If you need an accommodation filling out an application, or applying to a job, please email Recruitment@element.com”

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

The Chemist III will independently manufacture and document Active Pharmaceutical Ingredients (APIs) and other chemicals while supporting daily laboratory operations. They will also take on Project Manager responsibilities to ensure efficient workflow and high-quality results.