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
Full description
Swing Shift Working Hours: Monday to Friday, 3:00 PM to 11:30 PM PT.
Position Summary
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.
Primary Duties
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
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
Knowledge, Experience, Skills, and CertificationsEssential 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 Qualifications
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
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!
The typical pay range for this role is: Salary Range: $70,304 (Minimum) - $134,653 (Maximum)
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)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
RESPECTEQUAL 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