Project Management Senior AssociateAdvanced Bio-Logic Solutions Corp • Thousand Oaks, California, United States
Project Management Senior Associate
Advanced Bio-Logic Solutions Corp
- Thousand Oaks, California, United States
- Thousand Oaks, California, United States
Über
Remote
- Thousand Oaks, CA (EST or PST preferred)
Employment Type:
Contingent Worker (Contract, W2)
Contract Length:
12 months (possible extension)
Compensation:
$52/$58 per hour (based on experience)
Summary of the Role Join a big biopharma leader as a Supply Chain Project Manager, responsible for executing product lifecycle management activities across manufacturing, regulatory, and supply chain functions. You will translate product launch and variation strategies into actionable implementation plans and oversee change control execution for compliance. This fully remote role requires 3-5 years of experience managing change controls and lifecycle processes in a regulated industry.
Key Responsibilities
Manage change control timelines with input from Variation and Regional Operations Leads
Maintain compliance in Change Control Management systems for Global Distribution Change Records (GDCR) and Customer Facing SKU Change Records (CFSCR)
Provide timely stakeholder updates on GDCR and CFSCR status and readiness activities
Represent the SCPM Hub in project planning, execution, and operational meetings
Build and maintain effective relationships across key functional areas
Identify opportunities to streamline departmental activities and lead improvement projects
Develop and implement new procedures and processes to optimize results
Share and implement best practices with cross-functional stakeholders
Adapt quickly to changing priorities in a dynamic, global environment
Independently execute projects and business cases as assigned
Required Experience & Skills
3-5 years’ experience with lifecycle management across full product manufacturing stages
Experience with change control in regulated (biotech/pharmaceutical) environments
Knowledge of GMPs and supply chain or quality processes
Trackwise or similar Quality System experience
Strong stakeholder management and cross-functional collaboration skills
Excellent communication and analytical abilities
Self-starter who thrives in dynamic, fast-paced settings
Preferred Qualifications
ASCM/APICS and/or PMP certification
Top 3 Must Have Skills 1. Change Control experience in Lifecycle Management, with Trackwise or other Quality System background
2. Knowledge of GMPs and biotech/pharmaceutical industry practices
3. Supply Chain and/or Quality background, especially in lifecycle management
Day-to-Day Responsibilities
Quickly train and gain system access; independently follow SOPs and participate in project forums/meetings; gather requirements and translate them into compliant Change Control records (CFSCR or GDCR); ensure all activities are completed on schedule to support product launches and variations; actively partner with assessors and task owners to drive timely completion and regulatory compliance.
Basic Qualifications
Master degree
Bachelor degree and 2 years of experience
Associate degree and 6 years of experience
High school diploma / GED and 8 years of experience
This posting is for Contingent Worker, not an FTE
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Sprachkenntnisse
- English
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