QC Laboratory Support Associate

Lonza

Houston (TX)

On-site

Confidential

Full time

14 days+

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Benefits offered by this job

Performance bonus
Medical insurance
Dental insurance
Vision insurance
401(k) matching
Life insurance
Disability insurance
Employee assistance (EAP)
Paid time off

Job summary

Lonza in Houston, TX is seeking a QC Laboratory Support Associate to help manage QC samples, materials, and documentation within a GMP-regulated environment. This onsite role runs Monday through Friday, 8:00 AM to 3:30 PM and supports manufacturing and testing activities.

You will maintain records, assist with LIMS, collaborate with QC/QA, and help manage inventory while pursuing process improvements to ensure timely product releases and site quality objectives.

Qualifications

  • Associate degree required, preferably in a scientific discipline; equivalent relevant experience will also be considered.
  • 0-4 years of relevant experience in laboratory support, materials management, inventory control, logistics, warehouse operations, or similar environments.
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
  • High attention to detail and commitment to accuracy when handling samples, materials, and documentation.
  • Strong communication and interpersonal skills with the ability to work collaboratively across departments.
  • Basic knowledge of GMP principles and regulated environments is preferred.
  • Experience with inventory management, materials movement, supply management, or warehouse interactions is desirable.
  • Proficiency with spreadsheets, databases, and standard business software applications.
  • Demonstrated problem-solving skills and the ability to work effectively in a team environment.
  • Scientific backgrounds are welcome but not required.

Responsibilities

  • Receive, transfer, store, maintain, and inventory QC samples, including raw materials, in-process samples, lot release samples, and stability samples.
  • Support laboratory operations through housekeeping activities, equipment maintenance, inventory management, supply ordering, and training compliance.
  • Attend internal meetings and provide sample status updates to support manufacturing and testing activities.
  • Maintain accurate records and ensure compliance with GMP and documentation requirements.
  • Assist with QC Shared Services functions including sample management, contract laboratory coordination, LIMS administration support, and quality records activities.
  • Ensure quality standards are maintained while meeting established timelines and departmental objectives.
  • Identify and communicate operational issues and escalations to leadership in a timely manner.
  • Collaborate effectively with QC, QA, Manufacturing, Supply Chain, Warehouse Operations, and other cross-functional teams.
  • Contribute to process improvements and support continuous enhancement of laboratory and sample management processes.
  • Perform additional duties as assigned in support of site Quality Control operations.

Skills

Organizational skills
Attention to detail
Communication skills
GMP knowledge
Inventory management
Spreadsheets proficiency

Education

Associate degree

Tools

LIMS

Job description

QC Laboratory Support Associate

Location: Houston, Texas – Onsite

Shift: Monday-Friday | 8:00 AM - 3:30 PM

As a QC Laboratory Support Associate , you will play a vital role in supporting Quality Control operations across the Houston site. This position is responsible for the receipt, storage, tracking, and management of QC samples and materials that support manufacturing, product release, stability programs, and laboratory operations. Working in a regulated GMP environment, you will collaborate with Quality Control, Quality Assurance, Manufacturing, Supply Chain, and other site functions to ensure samples, materials, and documentation are maintained accurately and efficiently.

What you will get:

A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer:

  • Performance-related bonus
  • Medical, dental and vision insurance
  • 401(k) matching plan
  • Life insurance, as well as short-term and long-term disability insurance
  • Employee assistance programs
  • Paid time off (PTO)

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do:
  • Receive, transfer, store, maintain, and inventory QC samples, including raw materials, in-process samples, lot release samples, and stability samples.
  • Support laboratory operations through housekeeping activities, equipment maintenance, inventory management, supply ordering, and training compliance.
  • Attend internal meetings and provide sample status updates to support manufacturing and testing activities.
  • Maintain accurate records and ensure compliance with GMP and documentation requirements.
  • Assist with QC Shared Services functions including sample management, contract laboratory coordination, LIMS administration support, and quality records activities.
  • Ensure quality standards are maintained while meeting established timelines and departmental objectives.
  • Identify and communicate operational issues and escalations to leadership in a timely manner.
  • Collaborate effectively with QC, QA, Manufacturing, Supply Chain, Warehouse Operations, and other cross-functional teams.
  • Contribute to process improvements and support continuous enhancement of laboratory and sample management processes.
  • Perform additional duties as assigned in support of site Quality Control operations.
What we are looking for:
  • Associate degree required, preferably in a scientific discipline; equivalent relevant experience will also be considered.
  • 0-4 years of relevant experience in laboratory support, materials management, inventory control, logistics, warehouse operations, or similar environments.
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.
  • High attention to detail and commitment to accuracy when handling samples, materials, and documentation.
  • Strong communication and interpersonal skills with the ability to work collaboratively across departments.
  • Basic knowledge of GMP principles and regulated environments is preferred.
  • Experience with inventory management, materials movement, supply management, or warehouse interactions is desirable.
  • Proficiency with spreadsheets, databases, and standard business software applications.
  • Demonstrated problem-solving skills and the ability to work effectively in a team environment.
  • Scientific backgrounds are welcome but not required.
About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

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