Manufacturing Manager (Purification)

Location:  Novato, California Category: Manufacturing

Description

BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.

BioMarin’s Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin’s cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients. Come join our team and make a meaningful impact on patients’ lives. 
 

RESPONSIBILITIES

The position is responsible for the Downstream Purification area within one of the BioMarin commercial manufacturing facilities. Collaborates with support groups to ensure accurate and well managed transfer of process changes and improvements to floor operations. Integrates best practices, where appropriate, into manufacturing. Oversees the planning, implementation and execution of manufacturing operations for new and/or existing products and technologies in a cGMP environment.

 

Leadership

  • Accountable for the daily operations of an area that requires making appropriate decisions including the trouble shooting of equipment, response to process deviations and schedule adjustments.
  • Accomplishes tasks through direct & effective management of staff
  • Interact with department leaders to ensure production objectives are met
  • Accomplishes results through professional staff and/or employees
  • Sets project timeframes and priorities based on objectives with effective tracking and management of progress
  • Provides guidance and technical advice and becomes actively involved as required
  • Manages a team of supervisors and/or professionals
  • Contributes to the standards around which others operate

Process Knowledge

  • Experience with column purification processes
  • Experience with automated process equipment and control
  • Working knowledge with disposable systems, filtration, centrifuge
  • Experience with troubleshooting and problem solving with process and equipment
  • Experience with Buffer and Media operations
  • Support the closure of manufacturing discrepancies and change requests
  • Knowledge and experience in all aspects of GMP manufacturing
  • Ability to troubleshoot, identify issues and support resolutions with technical groups
  • Effectively communicates relevant information with team & department
  • Ensure consistent product quality through implementation of effective systems and collaboration with key support groups (QA, MSG, ENG, FAC, etc.) knowledge in area of responsibility for and provide technical instruction

People

  • Involved in hiring process to maintain staffing levels
  • Provides effective leadership through:
    • Managing performance and expectations of direct reports, team and self 
    • Manage performance issues, development and policies
    • Ensure the use of safe and compliant work practices and behaviors

Quality

  • Provide technical expertise to resolve manufacturing issues. Interact with support groups to ensure targets are met and product and process comply with cGMPs
  • Owner of Standard Operating Procedures and Batch Records
  • Ensure staffing levels and skill sets are maintained and training is in compliance
  • Complete understanding and adherence to cGMP’s as related to commercial operations
  • Lead or oversee individuals responsible for drafting standard operating procedures

Strategic Influence

  • General Look-Ahead: 1 year
  • Develop manufacturing flows and process steps in production area
  • Influences approach for operations at campaign and daily execution
  • Adheres to and executes policies and guidelines that directly affect work activities
  • Champion self-initiated projects and drive area of control within context of defined priorities

Business

  • Experience with various business systems (Process historian, CMMS, LIMS, TrackWise, ERP, MES, etc.)
  • Lead trending and communication of key department metrics
  • Identify and drive opportunities for process & business optimization

Contribution

  • Accountable for operations and results of assigned area in production plant
  • Ability to independently manage work and assigned projects
  • Responsible for projects that span multiple functional areas
  • Receive assignments in the form of objectives with goals and steps to meet as defined
  • Work is reviewed by management to measure meeting of defined objectives
  • Establishes and influences operations policies with focus on alignment across manufacturing plants when appropriate
  • Communicate, interact and influence with peers and plant leadership

 

EXPERIENCE

Required Skills:

  • 8+ years of directly related industry experience, including at least 4+ years with proven leadership role
  • Ability to independently manage work, actions and expectations is essential
  • Strong organizational, collaborating and communication skills

Other Valued Skills:

  • Curiosity and propensity to learn
  • Experience with Human and Organization Performance
  • Six Sigma or Lean training and certification
  •  

EDUCATION

  • B.S. degree in Life Sciences, Engineering, Applied Physics, etc., or acceptable equivalent combination of education and experience.

 
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.