Lonza

Research Associate III

Lonza  •  Houston, TX (Onsite)  •  1 month ago
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Job Description

Research Associate III

Location: This is an on-site position located in Pearland, TX

The purpose of this role is to provide technical support to Lead Scientists in conducting analytical tests for the evaluation of cellular products and in support of process development activities. Has the ability to conduct and execute complex scientific experiments and interprets the experimental results with minimal supervision.

What you will get:

A competitive compensation. 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:

  • Perform Development Studies concerning complex unit operations involving cellular, biochemical and molecular techniques, including but not limited to, cell culture, qPCR/RT-PCR, dd/dPCR, flow cytometry, microscopy, ELISA and spectrophotometric, fluorometric cell-based potency assays, for the characterization Cell & Gene Therapy products.

  • Provides study design, trouble-shooting and technical support for analytical method optimization, qualification and transfer to QC.

  • Maintains accurate, detailed records, experimental data and protocols following Lonza’s best documentation practices.

  • Prepares data summary and data reports. Works with Lead Scientists to communicate and summarize results for internal and client meetings, written reports and presentations.

  • Participates in laboratory Lean Six Sigma processes, such as, but not limited to, maintaining stock of lab supplies and reagents in support of ongoing programs and regular scheduled instrument maintenance programs.

  • Becomes knowledgeable and complies with all pertinent safety policies, rules and regulations.

  • Engage and maintain collaboration with various C & GT departments including Operations, Research and Development (R&D), Quality Control (QC), Quality Assurance (QA) and Project Management (PM).

What we are looking for:

  • Master's with at least 2 years of experience, or bachelor's with 4 or more years of experience.

  • PCR, SDS-PAGE, cell-based assays, flow cytometry, ELISA, data analysis.

  • Analytical Methods and/or Primary cell culture techniques.

  • Knowledge of cellular biology/chemistry, various types of laboratory equipment, strong aseptic technique.

  • Technical writing skills. GMP documentation practices is a plus.

  • Experience with statistical analysis of data preferred (Excel, JMP, Prism, etc.).

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. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Lonza

About Lonza

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.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Basel, CH
Year Founded
1897
Website
lonza.com
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