Analyst I, QC - Swing Shift

LGC Group • Petaluma, CA

1d • $52,000 - $72,800 • Onsite

About The Position

The Quality Control Analyst I performs routine analytical and functional testing of custom and research-use-only (ISO9001) oligonucleotides, raw materials, intermediates, and final chemical products. The role operates analytical laboratory equipment, evaluates results against specifications and customer requirements, and supports product disposition through accurate documentation and record updates. It works closely with Quality Control leadership, Quality Assurance, internal suppliers, and maintenance personnel in a fast-paced, regulated laboratory environment. The position also supports laboratory safety, equipment readiness, and continuous improvement activities.

The role focuses on analytical and functional testing of ISO9001 oligonucleotides, Prime CPG, and BTI Legacy CPG. Testing uses equipment such as HPLC, LC/MS, spectrophotometers, pH meters, and DNA synthesizers. The Analyst maintains and verifies laboratory equipment, performs standard lab operations and general maintenance, and communicates testing status, equipment needs, and process issues to relevant colleagues.

The position is on-site and is identified as a swing-shift role in the job title. The stated California-based hourly pay range is $25 to $34.855; the posting also lists compensation of $52,000 to $72,800 yearly. LGC describes its work as supporting mission-critical genomics and research into treatments for disease and illness.

Requirements

• Bachelor's degree in chemistry, biology, biochemistry, chemical engineering, pharmaceutical sciences, or a related field.
• Hands-on experience working in an analytical laboratory.
• Working knowledge of basic laboratory etiquette, chemical handling, and laboratory safety practices.
• Ability to execute approved analytical procedures and follow standard operating procedures.
• Ability to perform volumetric and gravimetric measurements, dilutions, and solution preparation.
• Ability to analyze data and compare test results with specifications and customer requirements.
• Knowledge of good documentation practices and accurate laboratory recordkeeping.
• Ability to use Microsoft Office applications, including Word, Excel, and Outlook.
• Ability to communicate testing information clearly to laboratory leadership and cross-functional stakeholders.
• Ability to work independently, manage time effectively, and take initiative in a fast-paced laboratory environment.
• Current U.S. work authorization; the company is unable to sponsor or assume sponsorship for temporary visas.

Nice To Haves

• Bachelor's degree in Analytical Chemistry.
• Industry experience with HPLC, LC/MS, and Quality Control testing.
• Experience working in a regulated environment with strong good documentation practices.
• Familiarity with FileMaker Pro, MassLynx, or Empower laboratory software.
• Demonstrated experience meeting the technical and operational requirements of a Quality Control Analyst I role.
• Attention to detail, effective verbal and written communication, problem-solving and critical-thinking skills, task prioritization, proactive independent work, flexibility, and effective stakeholder collaboration.

Responsibilities

• Execute approved Quality Control procedures using HPLC, LC/MS, spectrophotometers, pH meters, DNA synthesizers, and other applicable analytical tools.
• Perform analytical and functional testing of raw materials, intermediates, and final products, including ISO9001 oligonucleotides, Prime CPG, and BTI Legacy CPG.
• Analyze and interpret test data against approved specifications and customer requirements.
• Recommend product disposition and update applicable records for Quality Control and Quality Assurance review.
• Label products and incoming goods with the appropriate quality status.
• Maintain, calibrate, and verify laboratory equipment in accordance with approved procedures.
• Perform standard laboratory operations, including chemical dispensing, volumetric and gravimetric measurements, dilutions, and solution preparation.
• Follow standard operating procedures and good documentation practices to create complete and accurate records.
• Perform general laboratory maintenance, including cleaning, buffer loading, reagent stocking, and hazardous-waste handling.
• Communicate testing status, equipment needs, and process issues to Quality Control leadership, internal suppliers, and maintenance personnel.
• Support laboratory safety, team objectives, and continuous improvement initiatives.
• Collaborate with laboratory colleagues and cross-functional partners.

Benefits

• Competitive compensation with a strong bonus program.
• Medical, dental, and vision benefits for employees and dependents.
• FSA/HSA pre-tax savings plans for health care, childcare, and elder care.
• Voluntary accident, critical illness, and hospital indemnity programs.
• 401(k) retirement plan with matching employer contribution.
• Company-paid short- and long-term disability and life insurance.
• Employee assistance program.
• Pet insurance.
• Eight weeks of parental leave for qualifying life events.
• Monthly Town Hall meetings, employee recognition through the Cheer program, companywide social events, and frequent catered lunches.

What This Job Offers

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