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Quality Control Associate Scientist

Company Description

LGC’s Diagnostics & Genomics Division develops and manufactures a comprehensive portfolio of catalogue and custom-developed diagnostic quality solutions and component materials in addition our Genomic side of the business has integrated portfolio of products, services and expert support for your entire genomic work flow including Nucleic acid sample preparation, Oligos, probes, primers, Sequencing cloning, protein expression, PCR instruments, reagents and consumables for the extended life sciences industry. We partner with IVD assay developers, and pharmaceutical, CRO and academic institutions in commercialization activities across the entire diagnostic pipeline - from concept and early-stage research, through expedited product development and onwards into routine clinical use. Laboratorians and diagnostic professionals across disciplines of clinical chemistry, immunochemistry, serology, molecular diagnostics, and clinical genomics rely on LGC’s products to support accurate and reliable diagnostic results.

Each day, our world-class staff, scientific expertise, operational efficiency, and superior quality systems are ready to support the range of advanced technologies that collectively improve patient outcomes - from the widely adopted and established through to cutting-edge NGS and precision diagnostics.

 

Job Description

Job Description

Join an outstanding team at LGC as a Quality Control Associate Scientist, ensuring excellence in product quality. This role offers a remarkable opportunity to work in a dynamic, daring, and world-class environment where you can truly make a difference.

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

  • Independently carry out operational workflows adhering to approved documentation while applying standard microbiology, analytical chemistry, and aseptic techniques.
  • Process, record, and analyze data in compliance with test methods, good documentation practices, and ISO-13485 requirements.
  • Support quality control operations to maintain standards in safety, quality, and efficiency.
  • Contribute to commercial and development activities, ensuring adherence to quality and regulatory standards. Identify improvement opportunities through observation and data analysis. Fulfill training requirements and support continuous improvement projects.
  • Strictly adhere to the company’s PPE policy and undertake additional duties as assigned to meet organizational needs.

Qualifications

Minimum Qualifications:

  • An associate degree in a relevant life sciences field, such as molecular biology or biochemistry, or equivalent work experience is essential.
  • Proven success in operationally oriented or technical teams, particularly within pharma, biotech, or medical device sectors, is highly valued.
  • Candidates should demonstrate proficiency in biological techniques, including cell-based assays, ELISA, and PCR, as well as analytical techniques like chromatography and mass spectrometry.
  • Adherence to SOPs is crucial, alongside strong data coordination and recommendation skills.
  • Proficiency in Microsoft Office, specifically Outlook, Word, and Excel, is required to support effective communication and reporting.

Preferred Qualifications:

  • Resonate and operate in line with LGC’s core value behaviors: Passion, Curiosity, Integrity, Brilliance, and Respect.
  • Effective written and verbal communication skills.
  • Showed independence: capable of initiating and leading while recognizing the right moment for collaboration.
  • Effective problem-solving, time management, and organizational skills.
  • Passion for continuous improvement, with demonstrated initiative.
  • Aptitude to work in a complex and rapidly growing company.
  • Dedicated to meeting targets promptly and within budget restrictions.
  • Ability to work well in a team environment and possess an ability to adapt to change in the environment.
  • Demonstrated good professional judgment and reliability.
  • Promotes partnership and dedication within a team to achieve goals and results.

Additional Information

Additional information

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
  • Deductible Buffer Insurance and Critical Illness Insurance
  • 401(k) retirement plan with matching employer contribution
  • Company-paid short- and long-term disability, life insurance, and employee assistance program
  • Flexible work options
  • Pet Insurance for our furry friends
  • Improved Parental leave of 8 additional weeks
  • PTO that begins immediately
  • Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events, frequent catered lunches and much more!

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 birthing parent, religion, or belief. Shortlisting, 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.

Average salary estimate

$70000 / YEARLY (est.)
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$60000K
$80000K

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What You Should Know About Quality Control Associate Scientist, LGC Group

Join the fantastic team at LGC as a Quality Control Associate Scientist, where ensuring product excellence is your primary mission! Located in Middleton, WI, our Diagnostics & Genomics Division is on the cutting edge of developing an extensive array of diagnostic quality solutions for both the genomic and life sciences sectors. As a Quality Control Associate Scientist, you'll thrive in a vibrant and collaborative environment that encourages you to make a real impact. You'll independently manage operational workflows, utilizing your expertise in microbiology and analytical chemistry. Your role will also involve processing and analyzing data while adhering to ISO-13485 regulations and good documentation practices. Continuous improvement is at the heart of what we do, and you'll contribute by identifying areas for enhancement through data analysis. We believe in working safely and effectively, and that means strictly adhering to our PPE policies, too. If you have a background in life sciences—particularly molecular biology or biochemistry—and possess hands-on experience with techniques like ELISA and PCR, you’ll be right at home with us. We're excited to welcome a proactive individual who not only meets our technical standards but also aligns with LGC’s core values of passion, curiosity, and integrity. Let's work together to support accurate diagnostic results and improve patient outcomes!

Frequently Asked Questions (FAQs) for Quality Control Associate Scientist Role at LGC Group
What are the primary responsibilities of a Quality Control Associate Scientist at LGC?

As a Quality Control Associate Scientist at LGC, your main responsibilities will include independently managing operational workflows according to approved documentations, applying standard microbiology, and analytical techniques. You will process and analyze data while ensuring compliance with the ISO-13485 regulations and good documentation practices. Supporting quality control operations to uphold safety and quality standards is also a key part of your role, alongside contributing to commercial and development activities.

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What qualifications do you need to be a Quality Control Associate Scientist at LGC?

To be a successful Quality Control Associate Scientist at LGC, you should have at least an associate degree in a relevant life sciences field such as molecular biology or biochemistry, or possess equivalent work experience. Proven success in technical teams within the pharma, biotech, or medical device sectors is highly valued, and proficiency in biological techniques, including cell-based assays, ELISA, and PCR, is essential.

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What skills will help you succeed as a Quality Control Associate Scientist at LGC?

Success as a Quality Control Associate Scientist at LGC hinges on proficiency in biological and analytical techniques, strong data coordination skills, and adherence to standard operating procedures (SOPs). Demonstrating effective problem-solving abilities, organizational skills, and the capacity to work both independently and collaboratively will also be beneficial in this role.

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What kind of work environment can a Quality Control Associate Scientist expect at LGC?

At LGC, a Quality Control Associate Scientist will find a dynamic and world-class work environment that fosters collaboration and innovation. The team values passion, integrity, and curiosity—creating a supportive atmosphere where you can make a meaningful difference in patient outcomes while growing your professional skills through continuous improvement projects.

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What additional benefits does LGC offer to Quality Control Associate Scientists?

LGC provides its Quality Control Associate Scientists with a comprehensive benefits package that includes competitive compensation, medical, dental, and vision benefits, along with flexible work options. Additional perks include a strong bonus program,401(k) retirement plans with employer contributions, family-friendly leave policies, and even pet insurance for your furry friends!

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Common Interview Questions for Quality Control Associate Scientist
Can you describe your experience with microbiology techniques relevant to the Quality Control Associate Scientist position?

When answering this question, highlight specific microbiology techniques you have used in previous roles, such as conducting microbiological assays or using aseptic techniques. Be sure to underscore your attention to detail and adherence to standard procedures, as these are crucial in ensuring product quality.

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How do you handle compliance with ISO-13485 standards in your work?

Discuss your understanding of ISO-13485 and how you have implemented compliance in your previous roles. Emphasize your experience in maintaining documentation, performing audits, and your commitment to quality standards as necessary for a Quality Control Associate Scientist at LGC.

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Can you give an example of a time you identified a quality improvement opportunity?

Use the STAR (Situation, Task, Action, Result) method to describe a specific situation. Explain what the challenge was, the actions you took to analyze the data, and the positive outcomes resulting from your efforts. This showcases your analytical abilities and commitment to continuous improvement.

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What techniques do you find most effective for data analysis within quality control?

Discuss your proficiency with data analysis tools and techniques, mentioning specific software or methods you've used. Give examples of how you've utilized these techniques to impact quality control decisions positively, ensuring you convey your analytical mindset.

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How do you prioritize your tasks in a fast-paced laboratory environment?

Talk about your time management and organizational skills. Share strategies you employ to prioritize urgent tasks while ensuring that quality control standards are met, highlighting your adaptability to changing priorities.

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What motivates you to work in quality control within the life sciences sector?

Express your passion for improving patient outcomes and how this role at LGC aligns with your career goals. Discuss your commitment to collaboration, integrity, and excellence in quality management, which resonates with LGC's values.

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How do you ensure effective communication within your team?

Illustrate your approach to maintaining open and influential communication channels within a team. Share examples of successful collaborations and how you ensure that everyone is well-informed about tasks and quality standards.

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What experience do you have with regulatory standards in your previous roles?

Provide examples of your hands-on experience meeting regulatory standards within quality control, especially those relevant to pharmaceuticals or medical devices. Discuss your familiarity with guidelines and how you ensured compliance in your previous positions.

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Can you discuss a challenging situation you faced in quality control and how you overcame it?

Use another STAR response to detail a relevant challenging situation. Focus on your problem-solving approach, the steps you took to resolve the issue, and the lessons learned, emphasizing resilience and adaptability.

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Why do you believe continuous improvement is essential in quality control?

Explain that continuous improvement is vital for ensuring product quality, enhancing operational efficiency, and complying with evolving regulatory requirements. Share your personal experiences with continuous improvement initiatives and how they can lead to better patient outcomes.

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LGC is a life sciences measurement and testing company providing laboratory services, reference materials, analytical testing products and services along with genomics solutions for the pharmaceutical, food, agricultural biotechnology, government,...

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Full-time, on-site
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March 15, 2025

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