Project Management Senior Associate, Biopharma (JP10780)
Company: 3 Key Consulting
Location: Thousand Oaks
Posted on: April 1, 2026
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Job Description:
Job Title: Project Management Senior Associate, Biopharma
(JP10780) Location: Thousand Oaks, CA. Employment Type: Contract
Business Unit: Quality Duration: 1 year with likely extensions or
conversion to FTE Posting Date: 09/08/2022 3 Key Consulting is
hiring a Project Management Senior Associate for a consulting
engagement with our direct client, a leading global
biopharmaceutical company. Job Description: Responsible for overall
coordination, status reporting and stability of projects for the
Quality organization to advance the company-wide Quality Management
System. Establishes and implements project management processes and
methodologies to ensure projects are delivered on time, within
budget, adhere to high quality standards and meet customer
expectations. Responsible for assembling project plans, directing
and monitoring work efforts on a daily basis, identifying resource
needs, reviewing deliverables; and escalating functional, quality,
timeline issues appropriately. Responsible for tracking key project
milestones and adjusting project plans and/or resources to meet the
needs of customers. Coordinates communication with all areas of the
enterprise that impact the scope, budget, risk, and resources of
the work effort being managed. Must possess advanced knowledge and
proficiency in the use of project management methodologies and
tools, resource management practices and change management
techniques. Ability to manage multiple projects/workstreams of
medium to high complexity. Understanding of quality management
systems and principles, especially related to highly regulated
industries. Strong quantitative and qualitative skills including
financial analysis and cost accounting Why is the Position Open?
Supplement additional workload on team. Top Must-Have Skill Sets:
Excellent communication and facilitation skills as well as
attention to detail Must possess advanced knowledge and proficiency
in the use of project management methodologies and tools, resource
management practices and change management techniques Understanding
of quality management systems and principles, especially related to
highly regulated industries Day to Day Responsibilities: Develop
project plans, directing and monitoring work efforts on a daily
basis, identifying resource needs, reviewing deliverables; and
escalating functional, quality, timeline issues appropriately.
Responsible for tracking key project milestones and adjusting
project plans and/or resources to meet the needs of customers.
Coordinates communication with all areas of the enterprise that
impact the scope, budget, risk, and resources of the work effort
being managed. Employee Value Proposition: Career growth/
opportunity. Red Flags: Limited project management experience, has
not worked in a highly regulated industry, poor communication
skills, poor attention to detail. Interview process: Phone and
WebEx interviews We invite qualified candidates to send your resume
to recruiting@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 welcome to also share this
opportunity with anyone you think might be interested in applying
for this role Regards, 3KC Talent Acquisition Team
Keywords: 3 Key Consulting, Camarillo , Project Management Senior Associate, Biopharma (JP10780), IT / Software / Systems , Thousand Oaks, California
