Chemist

Kelly Services; San Marcos (CA); On-site; USD 41,000 - 44,000; Full time

Job summary

Kelly Services is seeking a Chemistry Associate for a 6-month contract position in the Manufacturing department for our Client in San Marcos, CA. The role focuses on formulation and processing of controls, calibrators, working solutions, and intermediates according to SOPs.

Responsibilities include in-process analysis, final release testing, aseptic procedures, and ongoing documentation. A Bachelor's degree in Chemistry or related field and 1–2 years of relevant experience are preferred.

Qualifications

• Bachelor's degree in chemistry, biochemistry, biological science, or related field preferred.
• 1–2 years of work experience in in vitro diagnostics, medical device, pharmaceutical, or related industry.
• GMP/GLP environment knowledge; familiar with QSR and ISO standards.

Responsibilities

• Prepare products using approved procedures and keep detailed records.
• Perform in-process analysis and adjust to bring analytes into spec.
• Analyze products, stock solutions, and raw materials using instrumentation.
• Evaluate instrumentation and procedures for correct operation; maintain equipment.
• Measure quantities volumetrically and gravimetrically with chemical knowledge.
• Review and update SOPs and related documents.
• Perform processing steps including centrifugation, diafiltration, filtration, and column separation.
• Conduct final release testing and aseptic procedures.
• Assist with efficiency improvements and cost reduction initiatives.
• Maintain laboratory and equipment cleanliness and organization.
• Perform additional duties as required.

Skills

Attention to detail

Multi-tasking

Verbal and written communication

Team collaboration

Education

Bachelor's degree in chemistry or related field

Tools

Laboratory instrumentation

Job description

Chemist

Kelly® Science & Clinical is seeking a Chemistry Associate for a 6-month contract position at our Client in their Manufacturing department.

Pay: $30-32/hour
Schedule: Full-Time | Mon-Fri Day Shift

Overview

Our Client is an industry-leading company in the in vitro diagnostics, medical device, and pharmaceutical manufacturing space, delivering high-quality controls, calibrators, and working solutions to support critical laboratory and clinical applications.

In this role, you will be responsible for the processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures, while manufacturing quality products on schedule.

Responsibilities

• Prepare products using approved procedures and keep detailed and accurate records
• Perform in-process analysis and determine adjustments to bring analytes into specification
• Analyze products, stock solutions, and raw materials using automated and manual instrumentation
• Evaluate instrumentation and procedures for correct operation; verify or perform maintenance prior to use
• Measure accurately quantities of material volumetrically and gravimetrically, employing knowledge of chemical and biochemical properties and handling procedures
• Continually evaluate and/or create work instructions, QCRs, SOPs, and other documents and procedures for effectiveness and modify through formal change process
• Perform processing steps as required including centrifugation, diafiltration, in-process filtration, and column separation
• Perform final release testing
• Perform aseptic procedures such as aliquoting, filtration, and microbial plating
• Perform assay testing for Value Assignment as required
• Assist in developing ways to increase efficiency and/or reduce costs
• Assist with overall maintenance and cleanliness of the laboratory and equipment
• Perform additional functions as required

Qualifications

• Bachelor’s degree in chemistry, Biochemistry, Biological Science, or related field preferred
• 1–2 years of work experience in in vitro diagnostics, medical device, pharmaceutical, or related industry required
• Ability to perform in a GMP and GLP environment; knowledge of QSR and ISO standards
• Familiarity with biohazardous material handling and chemical safety procedures
• Strong attention to detail with excellent verbal and written communication skills
• Ability to show initiative and perform in a multi-task environment
• Ability to work with personnel at all levels