Contract - Quality Operations Consultant

Be Bio is seeking a highly motivated Contract Quality Operations professional to join our Quality Assurance team. This new role will be a key leader, responsible for ensuring the success of our GMP manufacturing and quality control operations through oversight of our Contract Development and Manufacturing Organization (CDMO) partner. The successful candidate will play a critical role in technology transfer activities while also supporting daily external GMP quality operations. The role is hybrid, the ideal person would be on-site 2 to 3 days a week.

Key Responsibilities:

• Partner closely with internal Manufacturing, MSAT, and AD/PD teams, and with external CDMO partners to provide GMP quality oversight, supporting Manufacturing and Quality Control activities.
• Act as a quality lead for technology transfer, collaborating closely with internal technical teams and the CDMO to ensure robust and compliant transfer of processes.
• Review and approve GMP documentation, including batch records, deviations, change controls, and CAPAs.
• Lead timely product disposition by ensuring all quality requirements are met.
• Partner internally to enhance the Be Bio Quality Management System and implement industry best practices.
• Travel to CDMO sites as needed (up to ~20%).
• Be Awesome: Exhibit a positive attitude and a proactive approach to problem-solving, embracing challenges with enthusiasm and a solutions-oriented mindset.

Minimum Experience, Education, and Specialized Knowledge and Skills:

Must thrive in a fast-paced, growing, and innovative environment where flexibility, resourcefulness, resiliency, and communication skills are key. Excellent interpersonal and communication skills, ability to develop important relationships with colleagues, and being an all-around good company citizen are essential.

• Bachelor’s or Master’s degree in Life Sciences, or a related field.
• 5+ Experience in a GMP Quality Assurance manufacturing environment, with a focus on product disposition, deviation support, change control, and technology transfer.
• Strong knowledge of manufacturing processes, root cause analysis, and corrective action planning.
• Excellent communication and leadership skills, with the ability to coordinate cross-functional teams and manage relationships with CDMO partners.
• Ability to work independently and collaboratively in a dynamic environment.
• Demonstrated positive attitude and enthusiasm for problem-solving and overcoming challenges.
• This position will require up to 20% domestic travel during tech transfer activities to ensure proper oversight at the CDMO. After tech transfer is complete, travel requirements will reduce to < 10%.

Preferred Skills:

• 5+ years of experience supporting early phase cell therapy processes in a Quality Assurance role.
• Preferred experience in the development and transfer of early phase cell therapy processes.
• Preferred experience working with external CDMOs in a Quality Oversight capacity.
• Preferred experience drafting quality agreements.
• Familiarity with regulatory requirements for early-phase submissions and inspections.

At Be Bio, we recognize that our people are our most valuable resources, and we are committed to offering a competitive rate. The anticipated hourly pay range for this role is $48.00/hr - $55.00/hr, effective for the current calendar year and is subject to market changes. Final rate will be determined based on a range of considerations, including—but not limited to—location, experience, skills, and alignment with role responsibilities.