Senior Manager, Process Engineering Drug Substance and Drug Product
- Compensation
- $138.8K–$183.8K / yr
- Location
- Hopewell
- Work setup
- Not specified
- Seniority
- Senior
- Employment
- Not specified
- Experience
- 5+ years
- Category
- Not specified
- Posted
Skills
Must have
- Minimum 7 years of experience GMP pharmaceutical operations support. in biopharmaceutical manufacturing, engineering, and/or project management and at least 5 years of project management experience in
- Effective leadership of technical teams.
- Passion and expertise developing a team of Engineers
- Effectively gives and receives feedback.
- Proactively identifies, shares, and implements improvement opportunities that supports the site.
- Proven ability to manage multiple complex priorities simultaneously under tight timelines.
- Analytical problem-solving skills and proactive decision-making.
Nice to have
- OE and/or LEAN Methodologies
Full description
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
BeOne Medicines is seeking a highly motivated and organized Senior Manager of Process Engineering for Dug Substance and Drug Product to join our team at the Hopewell, NJ site. The successful candidate will be responsible for leading a hands-on team of subject matter experts focused on supporting technology transfers and new equipment selections, troubleshooting and supporting day-to-day manufacturing, supporting deviation/investigation root cause analysis, regulatory inspections, and continuous improvement. This role works independently, with minimal supervision and direction and will provide technical direction, Project Management support.
Responsibilities
- Effective leadership of technical teams with focus on right-first time Quality.
- Prior hands-on experience in the design, selection, and troubleshooting of systems and equipment used in commercial Drug Substance and Drug Product manufacturing.
- Support of technology transfer and qualification studies associated with the development and implementation of processes, systems, and facilities related to drug product manufacturing.
- Partner with Operations, Quality, and Automation functional areas.
- Develop and review technical documentation
- Participate and lead in controls fault analysis and remediation
- Directly support operations with troubleshooting and issue resolution
- Requires working in an industrial manufacturing environment including gowning
- Support operations and ensure compliance with regulatory, corporate and site requirements
Required Skills/Experience
- Minimum 7 years of experience GMP pharmaceutical operations support. in biopharmaceutical manufacturing, engineering, and/or project management and at least 5 years of project management experience in biologics or GMP.
- Effective leadership of technical teams.
- Passion and expertise developing a team of Engineers
- Effectively gives and receives feedback.
- Proactively identifies, shares, and implements improvement opportunities that supports the site.
- Proven ability to manage multiple complex priorities simultaneously under tight timelines.
- Analytical problem-solving skills and proactive decision-making.