Remote Senior Associate Project Manager - Biosimilars Ops

Biopharma Careers; United States; Hybrid; USD 89,000 - 121,000; Full time

Benefits offered by this job

Flexible work models

Total Rewards Plan

Stock-based incentives

Job summary

Amgen in the United States is seeking a Sr Associate Project Manager to drive biosimilar programs from development through regulatory submission. You will manage/optimize workflows, coordinate cross-functional teams, and ensure data integrity across ELN/LIMS and related systems.

Qualified candidates bring strong analytical skills, experience with document management and collaboration tools, and a track record in project management within biotech or pharma environments.

Qualifications

• Master’s degree or 2 years PM experience withBachelor’s degree or 6 years PM experience or High school diploma with 8 years PM experience.
• Experience with pharmaceutical development or biotech environments preferred.
• Experience coordinating regulatory documents and data review processes.

Responsibilities

• Provide project management to technical teams developing biosimilar candidates through regulatory approval.
• Oversee biosimilar business unit analytical sample management and workflow optimization.
• Collaborate with cross-functional teams to plan and maintain inventory.
• Manage sample distribution logistics and communicate data for biosimilar projects.
• Create ELN entries for submission and manage data in LIMS/ELN systems.
• Verify data and support regulatory filings in controlled document systems.

Skills

Analytical skills

MS Word

MS Excel

Data verification

Collaboration tools

Communication skills

Education

Master’s degree

Bachelor’s degree

Associate’s degree

High school diploma

Tools

Document management systems

Collaboration platforms

Project management tools

Job description

Amgen in the United States is seeking a Sr Associate Project Manager to drive biosimilar programs from development through regulatory submission. You will manage/optimize workflows, coordinate cross-functional teams, and ensure data integrity across ELN/LIMS and related systems.

Qualified candidates bring strong analytical skills, experience with document management and collaboration tools, and a track record in project management within biotech or pharma environments.