Associate Scientist II, Quality Control

The Associate Scientist II, Quality Control supports and independently executes quality control activities for microbiological, next generation sequencing, biologics, and related products.

The role applies established technical knowledge to perform and troubleshoot routine and moderately complex laboratory workflows, analyze and communicate results, support investigations and process improvements, and maintain compliance with the quality management system.

This position works closely with Manufacturing, Process Development, Quality Assurance, and operational partners.

To perform this job successfully, an individual must be able to capably perform each of the following essential duties:

Independently execute routine and moderately complex QC testing and operational workflows to support production schedules, product release, development activities, and customer requirements

Identify assay, documentation, and process improvement opportunities through first-hand observation and data review; implement approved improvements and contribute technical input to change activities

Perform primarily tactical laboratory work with responsibility for planning assigned daily activities, prioritizing work, and completing defined technical assignments with limited day-to-day direction

Collaborate with local QC, Manufacturing, Process Development, Quality Assurance, and Operations partners; provide reliable technical information to support cross-functional work

Document laboratory activities and quality records clearly; summarize results, observations, risks, and recommended next steps to technical staff, peers, and leadership

Provide task-level guidance, peer support, and on-the-job training to less experienced team members when assigned

Own assigned workflows, test methods, equipment, or product-family activities within established procedures; support scheduling, readiness, documentation, and issue resolution

Apply working knowledge of microbiology, molecular biology, analytical methods, aseptic technique, and standard laboratory equipment; serve as a developing technical resource in assigned areas

Participate in and independently complete defined improvement projects, lean initiatives, investigations, and corrective or preventive action activities

Process, review, trend, and interpret test data using approved methods and good documentation practices; contribute to reporting of quality, productivity, right-first-time, and other relevant performance indicators

Perform laboratory and light manufacturing activities requiring repetitive hand movement, close visual work, standing, walking, and handling materials in accordance with the physical requirements below

Perform work in accordance with approved SOPs, work instructions, applicable regulatory requirements, ISO 13485 quality system requirements, safety expectations, and PPE policies

Perform other duties as required or assigned by management to meet business needs

• Bachelor's degree in a relevant life sciences field such as molecular biology, microbiology, biochemistry, or a related discipline with relevant laboratory or industry experience—or an equivalent combination of education and applicable work experience.
• Experience independently executing laboratory workflows in a regulated, production, biotechnology, pharmaceutical, or medical-device environment.
• Demonstrated capability with applicable biological techniques, which may include cell-based assays, enzyme activity assays, ELISA, PCR, next generation sequencing, microbiology, and aseptic technique.
• Demonstrated capability with applicable analytical techniques, which may include electrophoresis, chromatography, mass spectrometry, or spectroscopy.
• Ability to operate standard laboratory equipment and to process, record, review, and interpret data using approved methods and good documentation practices.
• Ability to follow SOPs and work instructions, recognize deviations or atypical results, perform initial troubleshooting, and escalate appropriately.
• Experience contributing to investigations, process improvements, method updates, or controlled documentation.
• Effective written and verbal communication skills and the ability to work successfully on cross-functional teams.
• Working knowledge and proficiency with Microsoft Office, particularly Outlook, Word, and Excel.

• Two or more years of relevant laboratory or industry experience in biotechnology, pharmaceutical, medical-device, or regulated manufacturing operations.
• Experience with ISO 13485 or a comparable regulated quality management system.
• Experience writing or revising SOPs, work instructions, test methods, or manufacturing protocols.
• Experience supporting investigations, corrective and preventive actions, statistical analysis, method transfer, validation, or implementation of new technical processes.
• Experience providing task-level training or technical guidance to peers.

• Resonate and operate in line with LGC's core value behaviors: Passion, Curiosity, Integrity, Brilliance, and Respect.
• Work with a high degree of accuracy, attention to detail, reliability, and professional judgment.
• Demonstrate autonomy by organizing assigned work, taking initiative, and recognizing when stakeholder engagement or escalation is appropriate.
• Apply analytical problem-solving skills to organize information, interpret results, and recommend effective action within the scope of the role.
• Communicate clearly and respectfully with technical staff, peers, cross-functional stakeholders, and leadership.
• Adapt to changing priorities while managing multiple tasks in a dynamic laboratory environment.
• Promote cooperation, accountability, and commitment within the team to achieve goals and deliverables.
• Demonstrate a continuous-improvement mindset and willingness to learn new methods, technologies, products, and responsibilities.
• Meet quality, safety, schedule, and productivity expectations while maintaining compliance with approved procedures.

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.

• PASSION
• CURIOSITY
• INTEGRITY
• BRILLIANCE
• RESPECT

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.

All your information will be kept confidential according to EEO guidelines.

For more information about LGC, please visit our website www.lgcgroup.com

#scienceforasaferworld

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.