Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Apply Offsite

Aseptic Technician - II

Job

Spectraforce

Pearl River, NY (In Person)

Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 7/4/2026

Review key factors to help you decide if the role fits your goals.
How is this calculated?
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
47
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Job Title:
Manufacturing Scientist/Engineer Duration:
9
Months Location:
Pearl River, NY 10965 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 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) Job 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