You are viewing a preview of this job. Log in or register to view more details about this job.

Manufacturing Scientist Engineer

Work Environment & Schedule

  • On-site, 5 days per week
  • Standard hours: ~8:30 AM – 4:30/5:00 PM (non-batching periods)

During production cycles:

  • Early starts (~7:00 AM)
  • Second shift shifts (up to midnight)
  • Frequent schedule adjustments (~20 times/year)
  • Occasional weekend work when needed (e.g., batch issues)
  • Requires use of advanced PPE (including full cleanroom/isolator suits)

 

Description

  • We are seeking an entry-level to early-career Manufacturing Scientist/Engineer to support sterile filling and final drug product operations for antibody-drug conjugates in a pharmaceutical setting.
  • This role focuses on aseptic processing, isolator technology, and final product preparation.

 

Key Responsibilities

  • Execute downstream operations including:
  • Sterile filtration
  • Aseptic filling in isolators
  • Lyophilization (freeze-drying)
  • Vial sealing and final processing
  • Perform visual inspection of vials for:
  • Glass defects
  • Product defects
  • Container integrity
  • Support buffer preparation activities as needed
  • Operate and monitor isolator and aseptic equipment
  • Ensure strict adherence to safety and sterility standards

 

Contribute to:

  • Documentation and reporting
  • Process optimization
  • Troubleshooting of manufacturing issues
  • Collaborate with upstream teams to continue production flow

 

Required Qualifications

Bachelor’s degree preferred in:

  • Biology, Chemistry, Engineering, or related field (Equivalent experience may be considered)
  • Ability to follow complex procedures and work in sterile environments

 

Preferred Qualifications

Experience with:

  • Aseptic techniques
  • Cleanroom environments
  • Pharmaceutical manufacturing
  • Strong time management and attention to detail

 

Ideal Candidate Profile

  • Entry-level or early-career professional
  • Detail-oriented with strong procedural discipline
  • Able to work in highly controlled environments
  • Comfortable with schedule variability and hands-on production
  • Strong communication and documentation skills

 

Shared Role Notes (Both Positions)

  • Temporary/contract-to-permanent potential
  • Training duration: extensive (can take 6 months to 2+ years to fully ramp)
  • Roles require long-term commitment due to complexity
  • Candidates should be aligned with expectations and not seeking short-term exposure only