View all jobs
Project Manager Senior – REMOTE - (JP10121)
Thousand Oaks, CA · Biotech/PharmaceuticalJob Title: Project Manager Senior – REMOTE - (JP10121)
Location: Thousand Oaks, CA. 91320 (100% REMOTE)
Employment Type: Contract
Duration: 1+ years (with likely extensions)
Notes: Remote. PMP/Prince2/PM Certification Highly Preferred
Posting Date: 04/26/2022
3 Key Consulting is hiring a Project Manager Senior for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Project Manager will be responsible for managing one or multiple workstreams within a critical project within the Quality organization. Duties Include:
Basic Qualifications:
Preferred Qualifications:
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
Day to Day Responsibilities:
Manage project meetings, keep project documentation and tracking up to date, and trouble-shoot project obstacles.
Employee Value Proposition:
The person in this role will join a group that reports to senior VP in quality. You will be exposed to many different groups at client and have an opportunity to network.
Red Flags:
Lack of pharmaceutical industry experience, lack of project management skills or experience,, poor time management
Interview process:
Phone screening followed by in-person interview.
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Location: Thousand Oaks, CA. 91320 (100% REMOTE)
Employment Type: Contract
Duration: 1+ years (with likely extensions)
Notes: Remote. PMP/Prince2/PM Certification Highly Preferred
Posting Date: 04/26/2022
3 Key Consulting is hiring a Project Manager Senior for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
The Project Manager will be responsible for managing one or multiple workstreams within a critical project within the Quality organization. Duties Include:
- The PM will create and maintain detailed project timelines based on input from workstream leads and workstream team members.
- Follow up with action owners and document progress and risks.
- Maintain detailed dashboards and action trackers
- Act as meeting manager including but not limited to scheduling, agenda creation, write and distribute meeting minutes.
Basic Qualifications:
- Master’s degree and 3 years of Project Management experience OR Bachelor’s degree and 5 years of Project Management experience OR Associate’s degree and 10 years of Project Management experience OR High school diploma / GED and 12 years of Project Management experience
- Certified Project Manager
- Expert in Microsoft Project
Preferred Qualifications:
- Experience in the Pharmaceutical, Biotechnology or other Healthcare related field
- Master’s degree with 4 or more years of projects management experience, OR Bachelor’s degree with 6 or more years of project management experience.
- Ability to cultivate collaboration and work effectively on cross-functional teams
- Strong interpersonal and communication skills with the ability to effectively interface across all levels of the organization
- Workshop planning and facilitation skills
- Critical thinking and problem-solving skills
- Apply standard Project Management tools, and practices, experience with Excel, SharePoint, and Smartsheet highly desirable
- Self-driven
- Able to work independently
Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
- Self-starter, detail oriented project manager, excellent facilitation skills (Meeting, workshop, helping with decision making, objective delivery).
- Pharmaceutical industry preferred but not required
- 3 YOE with masters degree
- 5 YOE with Bachelors degree
- Must be able to work with minimal supervision
- PMP preferred
Day to Day Responsibilities:
Manage project meetings, keep project documentation and tracking up to date, and trouble-shoot project obstacles.
Employee Value Proposition:
The person in this role will join a group that reports to senior VP in quality. You will be exposed to many different groups at client and have an opportunity to network.
Red Flags:
Lack of pharmaceutical industry experience, lack of project management skills or experience,, poor time management
Interview process:
Phone screening followed by in-person interview.
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
Regards,
3KC Talent Acquisition Team