Lab Technician (Biotech: Plasmids)
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Currently hiring a Entry Level Lab Technician in a cell and gene therapy lab.
Looking for someone finishing their B.S. or has a completed scientific degree. Full time or part time to start. This opportunity has a ton of room for growth!
Job Description
The Plasmids Technician is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working in collaboration with the Manager of GMP and Plasmids Operations and staff, you will provide hands-on assistance for all day-to-day Plasmids Core production operations. This includes the execution of production processes, documentation, and facility and equipment maintenance. You will mainly help and support solution preparation, prep sampling, mini prep, gel making, and lab maintenance. You will also anticipate and troubleshoot issues with operations to avoid interruptions in production. Your responsibilities will include assuring the availability of materials and proper documentation surrounding GMP activities and product quality, operating within the Quality Management System applicable to the manufacture of phase-appropriate material in the CMF, and maintaining compliance with applicable regulatory requirements for cellular and gene therapy products. Attention to detail is crucial in all job functions. You will perform tasks in accordance with established policies, procedures, and techniques and require training, common experience, or working knowledge related to the tasks performed. You will work towards specific measurable objectives requiring operational planning skills with little direct supervision. Documentation of all activities performed according to SOPs is essential. Additionally, you will support GMP resources and supply chain by ordering and maintaining materials inventory to meet production goals and support daily operational activities related to the manufacturing of biological products.
You will spend 50-75% of your time working in the lab and about 25% at a desk doing documentation and report writing. The shift is Monday to Friday, 8 AM to 5 PM, but we are open to part-time candidates able to work 24+ hours a week
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Looking for someone finishing their B.S. or has a completed scientific degree. Full time or part time to start. This opportunity has a ton of room for growth!
Job Description
The Plasmids Technician is responsible for supporting all aspects of Good Manufacturing Practices (GMP) and production in the Clinical Manufacturing (CMF). Working in collaboration with the Manager of GMP and Plasmids Operations and staff, you will provide hands-on assistance for all day-to-day Plasmids Core production operations. This includes the execution of production processes, documentation, and facility and equipment maintenance. You will mainly help and support solution preparation, prep sampling, mini prep, gel making, and lab maintenance. You will also anticipate and troubleshoot issues with operations to avoid interruptions in production. Your responsibilities will include assuring the availability of materials and proper documentation surrounding GMP activities and product quality, operating within the Quality Management System applicable to the manufacture of phase-appropriate material in the CMF, and maintaining compliance with applicable regulatory requirements for cellular and gene therapy products. Attention to detail is crucial in all job functions. You will perform tasks in accordance with established policies, procedures, and techniques and require training, common experience, or working knowledge related to the tasks performed. You will work towards specific measurable objectives requiring operational planning skills with little direct supervision. Documentation of all activities performed according to SOPs is essential. Additionally, you will support GMP resources and supply chain by ordering and maintaining materials inventory to meet production goals and support daily operational activities related to the manufacturing of biological products.
You will spend 50-75% of your time working in the lab and about 25% at a desk doing documentation and report writing. The shift is Monday to Friday, 8 AM to 5 PM, but we are open to part-time candidates able to work 24+ hours a week
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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