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Jr. Tech Transfer Project Manager

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Bytecubit Technologies

Ridgefield, NJ (In Person)

$112,320 Salary, Full-Time

Posted 6 weeks ago (Updated 5 weeks ago) • Actively hiring

Expires 5/27/2026

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Job Description

Jr. Tech Transfer Project Manager Ridgefield, NJ Job Details Contract $45 - $63 an hour 1 day ago Qualifications Project team coordination Project timeline management GMP Mid-level Pharmaceutical plant experience Organizational skills Technical project management Manufacturing Cross-functional collaboration Cross-functional team management 2 years Communication skills Project scheduling Cross-functional communication Pharmaceutical manufacturing facility experience
Full Job Description Job Title:
Jr.
Tech Transfer Project Manager Location:
Ridgefield, New Jersey Project Duration:
12+
Months Pay Rate :
$45/hr - $63/hr all-in rate (depending on experience)
Job Description:
Looking for a junior-level Technical Transfer Project Manager to support a PMO group at a pharmaceutical manufacturing site transitioning into a CDMO. This person will help oversee line installations and support tech transfer activities for sterile injectable products, including syringes and vials across formulation, filling, inspection, and packaging. Will be responsible for managing project plans, timelines, change controls, and coordinating across cross-functional teams.
Must Have Skills:
2+ years of technical transfer project management experience within sterile injectables Pharma industry experience Strong communication and organizational skills W2 position - only US Citizens, Green Card holders, or candidates with EADs, OPT need apply (no C2C).
Pay:
$45.00 - $63.00 per hour Application Question(s): Do you have at least 2 years of experience in Tech Transfer Project Management in the pharmaceutical industry? Do you have experience with sterile injectable products (vials, syringes, aseptic filling)? Do you have pharmaceutical manufacturing experience (not just research or clinical)? Do you have experience working with change control systems in a GMP environment? Have you coordinated with cross-functional teams (Manufacturing, Quality, Validation, Engineering, Regulatory)? Do you have experience managing project timelines, schedules, and project plans?
Work Location:
In person

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