Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
Core Technician – Cell Therapy Location: This is an on-site position located in Houston, TX. The purpose of this role is to support the GMP production of viral therapeutics through aseptic processing, including cell cult…
Skills: Aseptic techniques, cGMP manufacturing, Cell culture, Viral production, Bioprocessing
Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
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Houston, Texas, United States · On-site
$18/hr–$21/hr
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The Core Technician will support GMP production of viral therapeutics through aseptic processing, including cell culture, purification, and fill/finish activities. They are also responsible for maintaining cleanroom environments, preparing buffers, and ensuring strict adherence to cGMP standards and documentation.
Candidates should have demonstrated knowledge of aseptic techniques and cGMP manufacturing environments, with experience in cell culture or bioprocessing preferred. A Bachelor’s degree in Life Sciences is preferred, though an Associate’s degree or relevant experience is also acceptable.
Location: This is an on-site position located in Houston, TX.
The purpose of this role is to support the GMP production of viral therapeutics through aseptic processing, including cell culture, purification, formulation, and fill/finish activities. This position is also responsible for maintaining cleanroom environments, preparing buffers and components, and ensuring adherence to cGMP standards and documentation practices.
This is a competitive, hourly paid position. 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.
Perform GMP-compliant production of viral therapeutic products, including large-scale mammalian cell culture.
Execute aseptic processing techniques across production activities such as purification, formulation, and fill/finish.
Prepare buffers and components and operate equipment such as autoclaves and other process systems.
Operate manual, semi-automated, and automated production equipment to support clinical manufacturing.
Maintain cleanroom operations including stocking, setup, and adherence to gowning procedures.
Assist in validation activities, equipment troubleshooting, changeovers, and data collection.
Support cell banking activities and ensure accurate documentation of all performed tasks.
Demonstrated knowledge of aseptic techniques and cGMP manufacturing environments required.
Experience with cell culture, viral production, or related bioprocessing techniques preferred.
Ability to follow detailed SOPs and perform tasks under close supervision while maintaining accuracy and compliance.
Familiarity with cleanroom operations, including gowning qualifications and behavior standards.
Capable of operating and supporting troubleshooting of manufacturing equipment.
Strong documentation skills and working knowledge of Microsoft Office applications.
Effective communication skills and ability to work both independently and in a team-based environment.
Ability to stand for extended periods and perform physically demanding gowning and cleanroom tasks.
Bachelor’s degree in Life Sciences preferred; Associate’s degree or relevant experience also acceptable.
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. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Making the Medicines of Tomorrow
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow. Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs. For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Offices: Muenchensteinerstr. 38, Basel, 4002, CH · 8830 Biggs Ford Road, Walkersville, MD 21793, US · 35 Tuas South Ave 6, SG, 637377, SG · 228 Bath Road, Slough, Berkshire SL1 4DX, GB · Rottenstrasse 6, Visp, VS 3930 , CH
There are currently 4,102 open healthcare positions in Houston, TX listed on Clera. New openings are added daily as companies post roles.
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