Head of Process Operations

Optieum; United States; Remote; USD 90,000 - 150,000; Full time

Job summary

Join a pioneering biotechnology firm dedicated to transforming patient care through innovative CAR-T cell therapies. This role offers the chance to lead process development and production operations, ensuring the efficient manufacture of cutting-edge CAR-T products. Collaborate with internal teams and external partners to optimize workflows and maintain high standards of quality. With a focus on GMP processes and technology transfer, this position is ideal for a dynamic leader ready to make a significant impact in the biotech industry. If you thrive in a fast-paced environment and are passionate about advancing healthcare, this opportunity is for you.

Qualifications

• 10+ years in biotech or pharma focused on CAR-T products.
• Expertise in GMP processes for CAR-T Cell manufacturing.

Responsibilities

• Manage process development and production at CDMOs.
• Lead technology transfer and production process execution.

Skills

Leadership

Process Development

GMP Knowledge

Statistical Analysis

Interpersonal Skills

Organizational Skills

Communication Skills

Education

BSc in Biological Sciences

Ph.D. or MS in Biological Sciences or Process Engineering

Tools

Microsoft Office Suite

Statistical Analysis Software

Job description

This an exciting opportunity for a well-qualified candidate to join Optieum Biotechnologies, Inc., a preclinical stage company focused on transforming the lives of patients with their proprietary Eumbody System, a platform technology that enables the development of advanced CAR constructs that optimize immune-cell function for oncology and other disease targets.

Reporting to the Chief Technology Officer this individual will (i) coordinate internal activities between process development and the research group and (ii) organize and manage external activities with contracted partners, initially in the USA then subsequently different geographies, for the development, validation, and execution of GMP processes for the manufacture of the company's therapeutic CAR-T Cell product candidates.

Responsibilities

• Manage process development and production operations at Contract Development and Manufacturing Organizations (CDMOs) and other company contracted partners for lentiviral vector and CAR T Cell products.

• Coordinate process development activities with the internal research groups.

• Lead the transfer, implementation and execution of production processes and process controls at external partners.

• Review and approval of completed batch production documentation.

• Lead the investigation and resolution of process-related deviations and out-of-specification (OOS)/out-of-trend (OOT) events.

• Lead operational metric review processes, assess data for adverse trends, develop solutions and oversee implementation.

• Author, review, edit and/or approve documents such as master production records, standard operating procedures, development/validation protocols and reports, and Module 3 Common Technical Document (CTD) sections.

• Compile and manage timelines, budgets, and objectives.

• Collaborate with internal and external partners to maximize the efficiency of workflows and ensure supply chain security.

• Assist in negotiation of third-party contracts including clinical supply agreements and associated Quality Agreements.

• Other duties as may be assigned.

Job Requirements

• Hands on, high-energy leader who can operate in a fast-paced, entrepreneurial industrial environment.
• Strong computer and Internet skills with proficiency in Microsoft Office (Outlook, Excel, Word, Project & PowerPoint) as well as statistical analysis software.
• Strong interpersonal and collaborative management skills.
• Outstanding organizational skills.
• Excellent written and oral communication skills.
• Domestic and international travel will be required.
• Demonstrated ability to build and maintain positive and collaborative relationships with management, peers, subordinates and externally with third party contract organizations.
• Self-motivated and detail-oriented, with the highest integrity.

Education and Skills

The ideal candidate for this position will have in-depth experience of the development and execution of GMP processes for the manufacture of CAR-T Cell products.

Candidate must possess:

• Minimum BSc or equivalent in a scientific discipline with likely a Ph.D. or MS advanced degree in biological sciences or process engineering.

• Minimum of 10 years of experience in the biotechnology or pharma industry with a primary focus on the development, manufacture, and delivery of CAR-T or other cell-based products.

• Expert knowledge of state-of-the-art gene-modified CAR-T Cell manufacturing processes and equipment.

• Knowledge of lentiviral vector manufacture a plus.

• Demonstrated track record in successfully managing technology transfer, process development and GMP production operations at CDMOs.

• Excellent interpersonal and strong leadership skills with the ability to influence and liaise in a cross-functional team environment.

• Expert knowledge of GMPs and qualification/validation practices for viral vector and biologics products.

Headquartered in Ehime, Japan, Optieum Biotechnologies, Inc. (www.optieumbio.com) is a pre-clinical stage biotechnology company committed to developing innovative CAR-T cell therapies for treating patients with cancer. Optieum's proprietary platform technology, the Eumbody System, enables the development of advanced CAR constructs that optimize immune-cell function for human disease targets