Biotech Manufacturing Support

Rockville, MD
Temporary
Entry Level
Job Title: Biotech Manufacturing Support
Duration: 12 months with possible extension
Office: Rockville, MD 20850
Shift: 09:00 am to 05:00 pm
Pay rate: $28/hr.


Job Description:
  • Perform and/or verify all tasks associated with the manufacture of cell therapy product 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 break down 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, knowledge and to ensure compliance with cGMP requirements.
  • Assist in the development of SOPs and batch records.
  • Maintain appropriate inventories of material and supplies within the cleanroom areas to support manufacturing activities.
  • Other duties as assigned.

Qualifications and Requirements:
  • Bachelor’s degree, preferably in biology other related disciplines. Or, Associate degree with 1+ years of related working 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 priority

About Us:
Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.
IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.

Compensation: The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.
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