The role
The Supervisor, Quality Control oversees the Quality Control Chemistry Laboratory and Oligonucleotide Quality Control Analytics Laboratory, supporting high-throughput oligonucleotide testing and production activities within regulated quality systems. The role provides strategic team leadership, coordinates priorities across Quality Control, Manufacturing, Research and Development, and Quality, and drives operational consistency across laboratory teams. This people-management role develops staff, plans capacity and cross-training, and supports resource allocation, investigations, and continuous improvement. The position requires strong analytical, organizational, leadership, and communication skills in a fast-paced laboratory environment.
What you need
Essential Knowledge and Qualifications
- Bachelor’s degree in Analytical Chemistry, Biochemistry, Biology, Chemical Engineering, Chemistry, Pharmaceutical Sciences, or a related field
- Hands-on laboratory experience in a regulated Quality Control environment with demonstrated ability to lead laboratory priorities and staff
- Working knowledge of analytical testing for chemical products and oligonucleotides
- Proficiency operating, maintaining, and troubleshooting relevant laboratory equipment, including high-performance liquid chromatography, liquid chromatography-mass spectrometry, spectrophotometers, DNA synthesizers, and pH meters
- Knowledge of ISO 9001, ISO 13485, Good Manufacturing Practice, Good Documentation Practice, and quality documentation expectations applicable to laboratory testing
- Ability to review analytical results against specifications and customer requirements and support scientifically sound technical decisions
- Experience supporting investigations, deviations, risk assessments, process improvements, and technical summary reports
- Knowledge of hazardous chemical handling, laboratory safety, personal protective equipment, waste management, and applicable compliance practices
- Demonstrated ability to schedule and prioritize analytical work, manage multiple tasks, and communicate deadlines and results to stakeholders
- Demonstrated ability to train, mentor, and develop Quality Control staff while promoting consistency, accountability, and safe work practices
Desired Knowledge and Qualificationsnice to have
- Advanced experience with high-performance liquid chromatography and Quality Control testing in an industry laboratory
- Proficiency with laboratory and business software such as FileMaker Pro, MassLynx, Empower, IFS, and Microsoft Office
- Experience in Good Manufacturing Practice, ISO 9001, or ISO 13485 environments
- Proven success in mentoring, project management, succession planning, and continuous improvement
- Strong understanding of hazardous chemical safety and laboratory compliance
Behavioural and Interpersonal Competencies
- Resonate and operate in line with LGC’s core value behaviours: Passion, Curiosity, Integrity, Brilliance, and Respect
- Apply a strategic and developmental leadership style that promotes growth, accountability, and cross-team consistency
- Demonstrate strong attention to detail and documentation accuracy
- Communicate clearly and effectively in verbal and written formats with individuals, teams, departments, and organizational units
- Use critical thinking and problem-solving skills to evaluate data, investigations, risks, and operational priorities
- Prioritize and manage multiple tasks in a fast-paced environment
- Work proactively, independently, and flexibly while engaging stakeholders at the appropriate time
- Collaborate across functions to align Quality Control activities with business, production, and quality expectations
Skills named in this posting
What you'll do
- Provide leadership and operational oversight for multiple Quality Control laboratory teams and functional areas
- Assign work, establish priorities, train and mentor staff, support recruiting and succession planning, and evaluate team performance
- Develop and implement mid-term capacity, cross-training, and resource-allocation strategies that align testing activities with production needs
- Oversee analytical testing of chemical products and oligonucleotides using high-performance liquid chromatography, liquid chromatography-mass spectrometry, spectrophotometry, DNA synthesizers, and related laboratory equipment
- Review analytical results against specifications and customer requirements and support product-disposition recommendations
- Oversee investigations, deviation support, risk assessments, technical decisions, and summary reporting with broader impact across Quality Control operations
- Ensure compliant documentation and testing practices under applicable Good Documentation Practice, Good Manufacturing Practice, ISO 9001, and ISO 13485 requirements
- Partner with Manufacturing, Research and Development, Quality, and internal customers to align testing schedules, deadlines, results, and quality expectations
- Author, review, and maintain standard operating procedures, work instructions, safety documentation, and Quality Control records
- Identify and implement process improvements that strengthen safety, efficiency, documentation accuracy, laboratory organization, and operational performance
- Ensure safe handling, labeling, storage, and disposal of samples, reagents, hazardous materials, and waste in accordance with training and policy
- Perform other duties as required or assigned by management to meet business needs
Pay and benefits
$70,304 a year
Employer providedThe typical pay range for this role is: Salary Range: $70,304 (Minimum) - $134,653 (Maximum)
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
8weeks
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 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.
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)
Where you'll work
Petaluma, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Petaluma, CAWorking conditions
Work Conditions and Environment
- Travel & Time Expectations: Periodic travel to customer, vendor, or company sites as needed to support the business, less than 20%
- Work Setting: Primarily a laboratory and office environment with regular exposure to manufacturing areas and moderate to loud noise levels
- Distinctive Safety Conditions: Potential exposure to hazardous chemicals, materials, and waste requiring adherence to safety precautions, chemical-handling practices, and required training
- Required Personal Protective Equipment (PPE): Laboratory coat, gloves, goggles, closed-toe non-slip shoes, and other personal protective equipment as required by policy and task
From the posting
About LGC Group
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.
Swing Shift Working Hours: Monday to Friday, 3:00 PM to 11:30 PM PT.
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 opportunity, accessibility and legal noticesLGC Group's statements, word for word
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
Job intelligence
The context around this role
Live data · October 28, 2026
Salary intelligence
How the pay compares
This role's midpoint is 37% below the US median for Quality Control roles at this level.
This roleEmployer provided
Manager roles in California6 roles publishing pay
Manager roles in the US28 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $70,304 | — | $70,304 |
| California (middle half) | $106,625 | $123,750 | $137,125 |
| All US (middle half) | $103,250 | $112,000 | $129,125 |
This role: LGC Group's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 28, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 341 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not LGC Group's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 36 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods20
- Collaboration and leadership13
- Quality systems and risk8
- Documentation and SOPs6
- GMP and compliance5
- Investigations and CAPA4
- Regulatory submissions1
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devices
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
LGC Group on Regulatory Jobs
- 3
- Open roles
- 2
- Distinct roles
- 2
- Locations
By discipline
- Quality3 100%
By level
- Manager2 67%
- Associate & Specialist1 33%
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Supervisor, QC at LGC Group
Open until filled. $70K a year, employer provided.