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Full Time Biotech Project Management Jobs (NOW HIRING)

MENTOR TECHNICAL GROUP CORP

PR · On-site

... biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, ... Proactively identify of opportunities to improve project management processes across the board.

BioIVT

Project Management Coordinator

Detroit, MI · On-site

$23 - $26.92/hr

This position is in Detroit and the employee will be expected to be on site, full time. ... With 2 years' work experience in Biotechnology or Health Care industries is preferred. Other Skills ...

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Full Time Biotech Project Management information

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How much do full time biotech project management jobs pay per year?

As of Jun 9, 2026, the average yearly pay for full time biotech project management in the United States is $102,682.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,500.00 and $123,000.00 per year, depending on experience, location, and employer.
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Full Time Biotech Project Management jobs near you
Project Management Senior Associate

Project Management Senior Associate

Advanced Bio-Logic Solutions Corp.

Thousand Oaks, CA • On-site

$52 - $58/hr

Full-time

Posted 4 days ago

Job description

Location: 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
Advanced Bio-Logic Solutions logo

About Advanced Bio-Logic Solutions

Sourced by ZipRecruiter

At ABL, we combine our 15 years of staffing experience with our excellent relationships with top-rated companies to find you the perfect career fit. Our long-term client relationships allow us to find and facilitate rewarding engagements for our employees. You can count on ABL to deliver the right career match, whether you are looking for a consulting assignment or a permanent position. In the field of technology, there are many options that might interest a potential consultant. Whether you specialize in software development, design, analysis or support, we have technology career opportunities in the following areas:

Industry

Biotechnology research and development

Company size

1 - 10 Employees

Headquarters location

Westlake Village, CA, US

Year founded

2002

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