Analyst I, QC - Swing Shift
- Full-time
- Work Arrangement: On-site
- Department: Quality Assurance and Regulatory Affairs
- Compensation: USD 52000 - USD 72800 - yearly
Company Description
ABOUT LGC BIOSEARCH TECHNOLOGIES:
With manufacturing sites across the US, UK, Germany and Denmark, LGC Biosearch Technologies has plans to continue growing. We deliver mission critical genomics to our diverse customer base in molecular diagnostics, pharma/biotech and agrigenomics. Our integrated portfolio of products, services and expertise supports our purpose of Science for a Safer World and we have embodied our mission by working with customers to enable research into life-altering treatment for disease and illness worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organisation.
Job Description
Position Summary
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. The position works closely with Quality Control leadership, Quality Assurance, internal suppliers, and maintenance personnel in a fast-paced, regulated laboratory environment. The role also supports laboratory safety, equipment readiness, and continuous improvement activities.
To perform this job successfully, an individual must be able to capably perform each of the following essential duties:
Execute approved Quality Control procedures using high-performance liquid chromatography (HPLC), liquid chromatography-mass spectrometry (LC/MS), spectrophotometers, pH meters, DNA synthesizers, and other applicable analytical tools
Perform analytical and functional testing of raw materials, intermediates, and final products with a focus on:
ISO9001 Oligonucleotides
Prime CPG
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
Qualifications
Knowledge, Experience, Skills, and Certifications
Essential Knowledge and Qualifications:
Bachelor's degree in chemistry, biology, biochemistry, chemical engineering, pharmaceutical sciences, or a related field
Hands-on experience working in a 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
Desired Knowledge and Qualifications
Bachelor's degree in Analytical Chemistry
Industry experience with high-performance liquid chromatography and liquid chromatography mass spectrometry 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
Behavioural and Interpersonal Competencies
Operate in line with LGC's core value behaviours: Passion, Curiosity, Integrity, Brilliance, and Respect
Apply strong attention to detail and maintain accurate documentation
Communicate effectively in verbal and written formats
Use problem-solving and critical-thinking skills to evaluate laboratory issues
Prioritize and manage multiple tasks in a dynamic work environment
Work proactively, independently, and flexibly while engaging stakeholders at the appropriate time
Collaborate effectively with laboratory colleagues and cross-functional partners
Additional Information
Additional information
The typical pay range for this role is:
Minimum: $ 25/ Hourly
Maximum: $ 34.855/ Hourly
This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location.
What we offer (US based-employees):
- Competitive compensation with strong bonus program
- Comprehensive 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, life insurance, and employee assistance program
- Pet Insurance for our furry friends
- 8 weeks of parental leave for qualifying life event
- Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Companywide social events, frequent catered lunches and much more!
This position requires current U.S. work authorization. We are unable to sponsor or assume sponsorship for temporary visas (including H‑1B, H‑2B, OPT, O‑1, TN).
ABOUT LGC:
LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers’ products and workflows and are valued for their performance, quality, and range.
OUR VALUES
- PASSION
- CURIOSITY
- INTEGRITY
- BRILLIANCE
- RESPECT
EQUAL OPPORTUNITIES
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.
For more information about LGC, please visit our website www.lgcgroup.com
#scienceforasaferworld
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