Biomanufacturing Associate

This Jobot Consulting Job is hosted by: Juan Correa

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Salary: $28 - $38 per hour

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.

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

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 "Apply Now" button.