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Fill Finish Jobs (NOW HIRING)

Scorpion Therapeutics

NY · On-site

$90 - $150/hr

Preferred background in aseptic processing/fill finish, technology transfer, drug product process development, or biopharmaceutical process validation Location/Work model * East Greenbush, New York ...

Scorpion Therapeutics

NY · On-site

$120 - $180/hr

Technology transfer and equipment/process validation experience in aseptic parenteral fill/finish preferred; lyophilization experience a plus; operating/qualifying highly automated equipment a plus.

New

Scorpion Therapeutics

NY · On-site

$92 - $206/hr

Manage all aspects of Manufacturing Support operations across Fill and Finish, including oversight of full-time and contract staff; conduct evaluations, coaching, and disciplinary actions, with ...

Initial Therapeutics, Inc.

NY · On-site

$92 - $206/hr

Manage all aspects of Manufacturing Support operations across Fill and Finish areas, including oversight of full-time employees and contract staff; perform personnel management functions including ...

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Fill Finish information

What is a fill finish?

A Fill Finish job involves the final stages of pharmaceutical manufacturing, where drug products are aseptically filled into vials, syringes, or other containers and then sealed for distribution. This process requires precision, sterile conditions, and adherence to strict regulatory guidelines to ensure product safety and efficacy. Fill Finish roles often include equipment operation, quality control, and compliance with Good Manufacturing Practices (GMP).

What does a fill finish do?

A typical day in Fill Finish involves preparing and operating specialized filling and packaging equipment in a cleanroom setting, following strict aseptic and safety protocols to handle pharmaceutical or biotech products. You may participate in setup, calibration, and troubleshooting of machinery, as well as perform quality checks and detailed documentation to comply with regulatory standards. Team members often work closely with quality assurance, maintenance, and production planning staff to ensure seamless workflow. This collaborative environment offers valuable experience in regulated manufacturing and can open doors to supervisory or technical specialist positions with continued training and experience.

What are the key skills and qualifications needed to thrive in the fill finish position?

To thrive in a Fill Finish role, you should have a background in life sciences or manufacturing, strong attention to detail, and experience working in Good Manufacturing Practice (GMP) environments. Familiarity with automated filling equipment, aseptic techniques, and relevant quality control systems or certifications (such as GMP or ISO) is often required. Strong teamwork, communication skills, and the ability to follow strict protocols set outstanding candidates apart. These skills ensure that pharmaceutical or biotechnology products are safely and efficiently filled, sealed, and packaged with the highest standards of quality and safety.

What cities are hiring for Fill Finish jobs?

Cities with the most Fill Finish job openings:

What are the most commonly searched types of Fill Finish jobs?

The most popular types of Fill Finish jobs are:

What states have the most Fill Finish jobs?

States with the most job openings for Fill Finish jobs include:

What job categories do people searching Fill Finish jobs look for?

The top searched job categories for Fill Finish jobs are:

Fill Finish jobs near you
Infographic showing various Fill Finish job openings in the United States as of August 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 77% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Process Validation Engineer (Fill Finish)

Scorpion Therapeutics

NY • On-site

$90 - $150/hr

Other

Posted 4 days ago

Job description

Discover Your Role
  • Supports technology transfer, process control strategy, validation, and post-commercialization activities
  • Evaluates product and process risks throughout the process lifecycle
  • Analyzes data from development, characterization, and at-scale manufacturing
  • Collaborates with Manufacturing, QC, QA, and CMC Regulatory to support process lifecycle management
  • Authors protocols, reports, and technical documents based on process and product knowledge
  • Ensures SOPs, policies, and validation plans align with industry and regulatory standards (e.g., ICH guidelines)
  • Supports audits, inspections, and CMC regulatory submissions
  • Applies engineering principles to develop and execute process controls and validation strategies
  • Uses statistical and engineering methods to assess manufacturing process performance
  • Supports laboratory and manufacturing-scale studies
This Role Requires
  • BS/BA in Engineering, Chemical Engineering, Biomedical Engineering preferred
  • Process Controls & Validation Engineer: 2+ years of relevant experience
  • Sr. Process Controls & Validation Engineer: 5+ years of relevant experience
  • Level determined based on qualifications relevant to the role
  • Preferred background in aseptic processing/fill finish, technology transfer, drug product process development, or biopharmaceutical process validation
Location/Work model
  • East Greenbush, New York, United States
  • Monday–Friday, 8am–4:30pm
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