What are the responsibilities and job description for the Project Manager position at BioPhase?
The Project Manager will develop, plan, direct and control projects associated with drug product manufacturing, aseptic processing and filling. They will oversee all aspects of projects by working directly with customers and internal support teams. The Project Manager will manage project timelines by setting milestones and assigning tasks as well as monitor and summarize project progress. They should possess a broad range of skills in process analysis, project planning, coordination, and project execution.
Pay Rate: $90,000k - 115,000k (depending on experience)
Location: Orange County
Responsibilities
- Assemble project teams, develop project plans and timelines, manage project budgets and costs, and conduct routine project meetings. Closely follow-up with projects to ensure project deliverables are met.
- Conduct routine project meetings with external customers and generate meeting minutes and action item logs.
- Assist in developing scope of work for drug product manufacturing projects and technical transfer.
- Manage project teams with strong communication and interpersonal relationship skills to ensure project objectives and milestones are reached.
- Direct and coordinate the activities of internal cross-functional project team members such as Engineering, Supply Chain, Quality Assurance, Manufacturing and Maintenance, demonstrating a strong ability to function well in a team environment.
- Responsible for the entire project lifecycle including project initiation, planning, execution, monitoring and closing.
- Report on Project budget and schedule adherence, issues and mitigations, scope changes to senior leadership.
Qualifications
- BS Degree in science, engineering or related field
- PMP Certification preferred
- 2-4 Years of Industry PM-related experience
- Experience in the Pharmaceutical or Medical Device industry with knowledge and experience with pharmaceutical manufacturing processes and equipment strongly desired.
- Project Management experience in a pharmaceutical or biotechnology environment is preferred.
- Demonstrate Project Management knowledge tools, techniques and culture. Strong computer skills. A solid knowledge of Microsoft Office programs.
- Aseptic manufacturing experience preferred. Sterile solution and suspension as well as sterile semi solids experience desired.
- Product development and sustaining engineering knowledge is a plus.
- Solid organizational skills including attention to detail and multi-tasking skills.
- Capable of motivating others in a dynamic and fast-pace environment. Ability to shift and change priorities as needed.
- Strong knowledge of GMP’s, CFR’s, ICH and ISO Regulations.
- Familiarity with OSHA, EPA and other federal and local regulatory requirements.
- Must be a self-starter with the aptitude to work independently and use good judgment while performing multiple tasks.
Salary : $90,000
