Sr Associate/Associate, Cell Therapy Manufacturing
- $26 to $36 Hourly
- Vision , Medical , Dental , Paid Time Off , Life Insurance , Retirement
- Full-Time
Responsibilities and Duties:
- Perform and/or verify all tasks associated with the manufacture of cell therapy products following batch records and standard operating procedures (SOPs) to ensure safe and compliant operations.
- Work as part of a team to execute GMP production runs in close collaboration with Materials Management, Quality Control and Quality Assurance.
- Perform set-up, operation, cleaning, basic maintenance, and breakdown of simple/routine equipment as per applicable SOPs.
- Draft new and revise existing manufacturing batch records/SOPs/work instructions to support process improvements and maintain cGMP compliance.
- Work in a cleanroom environment that will require a gowning process.
- Raise processing and equipment issues in timely manner to manufacturing management and actively participate in troubleshooting.
- Participate in technology transfers with CBMG internal groups.
- Complete required training assignments to maintain necessary technical skills, and knowledge and to ensure compliance with cGMP requirements.
- Assist in the development of SOPs and batch records.
- Maintain appropriate inventories of materials and supplies within the cleanroom areas to support manufacturing activities.
- Weekend work required.
- Other duties as assigned.
Qualifications and Requirements:
- Bachelor's degree, preferably in biology or other related disciplines. Or Associate Degree with 1+ years of related working experience. Or High School Diploma or GED with 3+ years of related experience
- More than 1+ years of GMP experience is preferred; pharmaceutical, biotechnology or other similar manufacturing environments are preferred.
- Previous training and experience in cell culture, aseptic technique or operations in a biology lab is preferred.
- Experience handling and culturing live cells, including T cells is preferred.
- Rigorous adherence to SOPs and cGMP regulations with the ability to accurately complete documentation associated with the manufacturing process in a timely fashion is required.
- Skilled with Microsoft Office suite of products.
- Ambitious and willing to accept temporary responsibilities outside of initial job description.
- Comfortable in a fast-paced small company environment, able to adjust workload based on changing priorities.
Why You Should Join AbelZeta
- Join a high-growth and fast-paced organization.
- Defined career path and annual performance review and feedback process.
- Comprehensive Benefits Plan, including 100% company paid medical, dental, vision, life Insurance, short-term and long-term disability insurance, and more!
- Competitive company 401k match.
- Paid holidays, sick leave, and annual leave.
AbelZeta is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. AbelZeta validates right to work using E-Verify. Salary at AbelZeta is determined by various factors, including but not limited to location, the individual’s particular combination of education, knowledge, skills, competencies, and experience, as well as contract-specific affordability and organizational requirements. The estimate displayed represents the typical salary range for this position and is just one component of AbelZeta’s total compensation package for employees.
Address
AbelZeta Inc
Rockville, MDIndustry
Manufacturing
Posted date
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