Biomanufacturing Associate- GMP at Jobot
Pasadena, CA 91108
About the Job
Join the Future of Cancer Treatment: Help Us Revolutionize Gene Therapies and Immunotherapy!
This Jobot Consulting Job is hosted by: Juan Correa
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $28 - $38 per hour
A bit about us:
We create innovative gene therapies to treat cancer and extend patients' lives. Our approach not only destroys tumors but also activates the immune system to fight cancer. By combining this with advanced companion diagnostics, we are at the forefront of cancer immunotherapy and leading clinical-stage cancer companies.
Why join us?
401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Retirement plan
Vision insurance
8 hour shift
Monday to Friday
Weekends as needed
Job Details
Responsibilities
As part of a talented and highly motivated multi-disciplinary team advancing an exciting new approach to drug discovery, development, and manufacturing, the successful candidate will be part of a skilled Manufacturing team working to execute GMP production campaigns in close collaboration with the Process Development Team to supply the company’s clinical pipeline targets
Responsibilities for this position include on-the-floor operations in Cell Culture, Purification, and Aseptic Fill/Finish
Additionally, this role will perform manufacturing support activities including, inventory control, and other assigned activities
Perform Cell Culture (Seed Train Expansion and Maintenance, Wave/Rocker Bioreactor Systems, and Single-Use Bioreactor Systems), Purification (Chromatography, Filtration), Buffer and Media preparation, Formulation, and Aseptic Fill/Finish, while adhering to all cGMP and GDP standards
Effectively engage cross-functionally with other departments to troubleshoot and continuously improve all operations supporting cGMP manufacturing instruments, equipment, and processes
Generate, review, and/or revise batch production records, logbooks, and technically sound Standard Operating Procedures (SOPs) to support manufacturing operations
Maintain and sustain all organizational training profile requirements with strict adherence to safety and compliance
Engage with external vendors and internal stakeholders to procure and manage equipment and inventory levels
Identify, recommend, and implement process improvement initiatives
Ensure high-quality and timely completion of assignments and projects
Perform other duties as assigned
Qualifications
Experience in cGMP operations working with manufacturing equipment
Years of experience will determine the hiring level
High degree of self-motivation and the ability to take initiative and work under pressure and against tight timelines
Ability to take direction well; follow documents and policies at all times
Ability to lift 30 lbs
Proficient in computer skills including Microsoft Office (Word, Excel, PowerPoint) and others
Excellent organizational skills with attention to detail and accurate record-keeping
General knowledge of Federal and State regulatory requirements in a GxP environment
High degree of discretion in dealing with confidential information
Ability and willingness to work flexible hours when needed
Demonstrated ability to work independently and in a team environment
Excellent written, verbal, and, interpersonal communication skills
Eligible to work in the U.S
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
This Jobot Consulting Job is hosted by: Juan Correa
Are you a fit? Easy Apply now by clicking the "Quick Apply" button
and sending us your resume.
Salary: $28 - $38 per hour
A bit about us:
We create innovative gene therapies to treat cancer and extend patients' lives. Our approach not only destroys tumors but also activates the immune system to fight cancer. By combining this with advanced companion diagnostics, we are at the forefront of cancer immunotherapy and leading clinical-stage cancer companies.
Why join us?
401(k)
401(k) matching
Dental insurance
Health insurance
Life insurance
Paid time off
Retirement plan
Vision insurance
8 hour shift
Monday to Friday
Weekends as needed
Job Details
Responsibilities
As part of a talented and highly motivated multi-disciplinary team advancing an exciting new approach to drug discovery, development, and manufacturing, the successful candidate will be part of a skilled Manufacturing team working to execute GMP production campaigns in close collaboration with the Process Development Team to supply the company’s clinical pipeline targets
Responsibilities for this position include on-the-floor operations in Cell Culture, Purification, and Aseptic Fill/Finish
Additionally, this role will perform manufacturing support activities including, inventory control, and other assigned activities
Perform Cell Culture (Seed Train Expansion and Maintenance, Wave/Rocker Bioreactor Systems, and Single-Use Bioreactor Systems), Purification (Chromatography, Filtration), Buffer and Media preparation, Formulation, and Aseptic Fill/Finish, while adhering to all cGMP and GDP standards
Effectively engage cross-functionally with other departments to troubleshoot and continuously improve all operations supporting cGMP manufacturing instruments, equipment, and processes
Generate, review, and/or revise batch production records, logbooks, and technically sound Standard Operating Procedures (SOPs) to support manufacturing operations
Maintain and sustain all organizational training profile requirements with strict adherence to safety and compliance
Engage with external vendors and internal stakeholders to procure and manage equipment and inventory levels
Identify, recommend, and implement process improvement initiatives
Ensure high-quality and timely completion of assignments and projects
Perform other duties as assigned
Qualifications
Experience in cGMP operations working with manufacturing equipment
Years of experience will determine the hiring level
High degree of self-motivation and the ability to take initiative and work under pressure and against tight timelines
Ability to take direction well; follow documents and policies at all times
Ability to lift 30 lbs
Proficient in computer skills including Microsoft Office (Word, Excel, PowerPoint) and others
Excellent organizational skills with attention to detail and accurate record-keeping
General knowledge of Federal and State regulatory requirements in a GxP environment
High degree of discretion in dealing with confidential information
Ability and willingness to work flexible hours when needed
Demonstrated ability to work independently and in a team environment
Excellent written, verbal, and, interpersonal communication skills
Eligible to work in the U.S
Interested in hearing more? Easy Apply now by clicking the "Quick Apply" button.
Salary
28 - 38 /year
