Supervisor, QC (Swing Shift)

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 DescriptionSwing Shift Working Hours: Monday to Friday, 3:00 PM to 11:30 PM PT.Position SummaryThe 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 DutiesProvide leadership and operational oversight for multiple Quality Control laboratory teams and functional areasAssign work, establish priorities, train and mentor staff, support recruiting and succession planning, and evaluate team performanceDevelop and implement mid-term capacity, cross-training, and resource-allocation strategies that align testing activities with production needsOversee analytical testing of chemical products and oligonucleotides using high-performance liquid chromatography, liquid chromatography-mass spectrometry, spectrophotometry, DNA synthesizers, and related laboratory equipmentReview analytical results against specifications and customer requirements and support product-disposition recommendationsOversee investigations, deviation support, risk assessments, technical decisions, and summary reporting with broader impact across Quality Control operationsEnsure compliant documentation and testing practices under applicable Good Documentation Practice, Good Manufacturing Practice, ISO 9001, and ISO 13485 requirementsPartner with Manufacturing, Research and Development, Quality, and internal customers to align testing schedules, deadlines, results, and quality expectationsAuthor, review, and maintain standard operating procedures, work instructions, safety documentation, and Quality Control recordsIdentify and implement process improvements that strengthen safety, efficiency, documentation accuracy, laboratory organization, and operational performanceEnsure safe handling, labeling, storage, and disposal of samples, reagents, hazardous materials, and waste in accordance with training and policyPerform other duties as required or assigned by management to meet business needsWork Conditions and EnvironmentTravel & 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 levelsDistinctive Safety Conditions: Potential exposure to hazardous chemicals, materials, and waste requiring adherence to safety precautions, chemical-handling practices, and required trainingRequired Personal Protective Equipment (PPE): Laboratory coat, gloves, goggles, closed-toe non-slip shoes, and other personal protective equipment as required by policy and taskQualificationsKnowledge, Experience, Skills, and CertificationsEssential Knowledge and QualificationsBachelor’s degree in Analytical Chemistry, Biochemistry, Biology, Chemical Engineering, Chemistry, Pharmaceutical Sciences, or a related fieldHands-on laboratory experience in a regulated Quality Control environment with demonstrated ability to lead laboratory priorities and staffWorking knowledge of analytical testing for chemical products and oligonucleotidesProficiency operating, maintaining, and troubleshooting relevant laboratory equipment, including high-performance liquid chromatography, liquid chromatography-mass spectrometry, spectrophotometers, DNA synthesizers, and pH metersKnowledge of ISO 9001, ISO 13485, Good Manufacturing Practice, Good Documentation Practice, and quality documentation expectations applicable to laboratory testingAbility to review analytical results against specifications and customer requirements and support scientifically sound technical decisionsExperience supporting investigations, deviations, risk assessments, process improvements, and technical summary reportsKnowledge of hazardous chemical handling, laboratory safety, personal protective equipment, waste management, and applicable compliance practicesDemonstrated ability to schedule and prioritize analytical work, manage multiple tasks, and communicate deadlines and results to stakeholdersDemonstrated ability to train, mentor, and develop Quality Control staff while promoting consistency, accountability, and safe work practicesDesired Knowledge and QualificationsAdvanced experience with high-performance liquid chromatography and Quality Control testing in an industry laboratoryProficiency with laboratory and business software such as FileMaker Pro, MassLynx, Empower, IFS, and Microsoft OfficeExperience in Good Manufacturing Practice, ISO 9001, or ISO 13485 environmentsProven success in mentoring, project management, succession planning, and continuous improvementStrong understanding of hazardous chemical safety and laboratory complianceBehavioural and Interpersonal CompetenciesResonate and operate in line with LGC’s core value behaviours: Passion, Curiosity, Integrity, Brilliance, and RespectApply a strategic and developmental leadership style that promotes growth, accountability, and cross-team consistencyDemonstrate strong attention to detail and documentation accuracyCommunicate clearly and effectively in verbal and written formats with individuals, teams, departments, and organizational unitsUse critical thinking and problem-solving skills to evaluate data, investigations, risks, and operational prioritiesPrioritize and manage multiple tasks in a fast-paced environmentWork proactively, independently, and flexibly while engaging stakeholders at the appropriate timeCollaborate across functions to align Quality Control activities with business, production, and quality expectationsAdditional InformationWhat we offer (US based-employees):Competitive compensation with strong bonus programComprehensive medical, dental, and vision benefits for employees and dependentsFSA/HSA Pre-tax savings plans for health care, childcare, and elder careVoluntary Accident, Critical Illness and Hospital Indemnity programs401(k) retirement plan with matching employer contributionCompany-paid short- and long- term disability, life insurance, and employee assistance programPet Insurance for our furry friends8 weeks of parental leave for qualifying life eventTown 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 VALUESPASSIONCURIOSITY INTEGRITYBRILLIANCERESPECTEQUAL 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