Core Technician – Cell Therapy Overnight
Lonza
Summary
As a Core Technician - Cell Therapy Overnight, you will play a critical role in the manufacturing of clinical and commercial cell therapy products within a highly regulated GMP environment. This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life-saving therapies. Working closely with Manufacturing, Quality, and Operational teams, you will help ensure products are produced according to established procedures, quality standards, and production schedules.
Job description
What you will do:
- Participate in the aseptic processing and manufacture of clinical and commercial cell therapy products.
- Perform aseptic cell culture manipulations within Grade A/B cleanroom environments.
- Operate cell processing and manufacturing equipment according to approved SOPs.
- Troubleshoot basic equipment issues and escalate concerns as appropriate.
- Follow contamination control and containment strategies to maintain a compliant GMP manufacturing environment.
- Participate in assigned customer Aseptic Process Simulations (APS).
- Complete GMP documentation accurately, thoroughly, and in a timely manner.
- Review manufacturing batch records (MBRs) and related GMP documentation as required.
- Adhere to all safety policies, procedures, and applicable regulations.
- Identify, document, and communicate deviations from standard procedures and accepted practices.
- Provide accurate information and support during process deviation investigations.
- Follow production schedules and execute assigned manufacturing activities efficiently.
- Collaborate effectively with Manufacturing, Quality Assurance, Quality Control, and other site functions to support operational objectives.
- Perform additional duties as assigned in support of manufacturing operations.
What we are looking for:
- High school diploma or equivalent required; Associate degree in a scientific or technical discipline preferred.
- 1-2 years of experience working with cell therapy technologies or related biopharmaceutical manufacturing processes in a cGMP environment.
- Working knowledge of aseptic processing principles and cleanroom operations.
- Ability to perform aseptic manipulations while maintaining product and environmental integrity.
- Ability to read, understand, and follow SOPs, manufacturing instructions, and production schedules.
- Understanding of cGMP requirements and the importance of regulatory compliance.
- Experience completing GMP documentation and reviewing manufacturing records is preferred.
- Proficiency with Microsoft Office applications, including Excel; experience with SAP and LIMS is desirable.
- Strong organizational, time management, and prioritization skills.
- Effective verbal and written communication skills.
- Ability to work collaboratively within a team environment and resolve issues professionally.
- Self-motivated, solution-oriented, and committed to operational excellence.
- Ability to perform aseptic gowning on a routine basis.
- Ability to stand for extended periods, up to 6 hours.
- Ability to routinely lift up to 50 pounds.
Requirements
- High school diploma or equivalent required
- Associate degree in a scientific or technical discipline preferred
- 1-2 years of experience working with cell therapy technologies or related biopharmaceutical manufacturing processes in a cGMP environment
- Working knowledge of aseptic processing principles and cleanroom operations
- Ability to perform aseptic manipulations while maintaining product and environmental integrity
- Ability to read, understand, and follow SOPs, manufacturing instructions, and production schedules
- Understanding of cGMP requirements and the importance of regulatory compliance
- Experience completing GMP documentation and reviewing manufacturing records is preferred
- Proficiency with Microsoft Office applications, including Excel; experience with SAP and LIMS is desirable
- Strong organizational, time management, and prioritization skills
- Effective verbal and written communication skills
- Ability to work collaboratively within a team environment and resolve issues professionally
- Self-motivated, solution-oriented, and committed to operational excellence
- Ability to perform aseptic gowning on a routine basis
- Ability to stand for extended periods, up to 6 hours
- Ability to routinely lift up to 50 pounds
Benefits
- Performance-related bonus
- Medical, Dental & Vision
- 401(k) Matching
- Life Insurance
- Short-term Disability
- Long-term Disability
- Employee Assistance Programs
- Paid Time Off
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.