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Manufacturing Scientist/Engineer (Downstream)

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Net2Source (N2S)

Pearl River, NY (In Person)

Full-Time

Posted 1 week ago (Updated 1 day ago) • Actively hiring

Expires 7/12/2026

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Job Description

Manufacturing Scientist/Engineer (Downstream) at Net2Source (N2S) Manufacturing Scientist/Engineer (Downstream) at Net2Source (N2S) in Pearl River, New York Posted in 5 days ago.
Type:
full-time
Job Description:
Join a Global Leader in Workforce Solutions - Net2Source Inc. Who We Are Net2Source Inc. isn't just another staffing company, we're a powerhouse of innovation, connecting top talent with the right opportunities. Recognized for 300% growth in the past three years, we operate in 34 countries with a global team of 5,500+. Our mission? To bridge the talent gap with precision-Right Talent. Right Time. Right Place. Right Price. Title-Manufacturing Scientist/Engineer (Downstream) Duration-9 months contract Location- Pearl River,NY,USA,10965 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) 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
Summary:
The main function of an Aseptic Technician is to support the manufacturing of sterile pharmaceutical products by performing tasks in controlled environments using aseptic techniques. A typical Aseptic Technician ensures product integrity and compliance with regulatory standards through meticulous attention to cleanliness, documentation, and process control. 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.
Job Responsibilities:
Perform aseptic gowning and operate in cleanroom environments Prepare, sterilize, and transfer materials and equipment into cleanrooms Execute aseptic filling, compounding, and packaging processes Monitor environmental conditions and report deviations or contamination risks Follow Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMP) Maintain accurate batch records and documentation Participate in cleaning, sanitization, and routine maintenance of cleanroom areas Support quality assurance and validation activities
Skills:
Knowledge of aseptic techniques and cleanroom protocols Strong attention to detail and adherence to procedures Ability to work in a sterile, regulated environment for extended periods Familiarity with GMP, FDA, and other regulatory requirements Good communication and teamwork skills Basic computer and documentation skills Ability to follow complex procedures and work in sterile environments
Education/Experience:
High school diploma or GED required; associate degree or technical training in life sciences preferred 2-4 years of experience in aseptic processing, pharmaceutical manufacturing, or a related field. Bachelor's degree preferred in: Biology, Chemistry, Engineering, or related field (Equivalent experience may be considered) 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 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 Requires use of advanced PPE (including full cleanroom/isolator suits) Preferred Qualifications Experience with: Aseptic techniques, Cleanroom environments, Pharmaceutical manufacturing Strong time management and attention to detail Why Work With Us? We believe in more than just jobs-we build careers. At Net2Source, we champion leadership at all levels, celebrate diverse perspectives, and empower you to make an impact. Think work-life balance, professional growth, and a collaborative culture where your ideas matter. Our Commitment to Inclusion & Equity Net2Source is an equal opportunity employer, dedicated to fostering a workplace where diverse talents and perspectives are valued. We make all employment decisions based on merit, ensuring a culture of respect, fairness, and opportunity for all, regardless of age, gender, ethnicity, disability, or other protected characteristics. Awards & Recognition
  • America's Most Honored Businesses (Top 10%)
  • Fastest-Growing Staffing Firm by Staffing Industry Analysts
INC 5000
List for Eight Consecutive Years
  • Top 100 by Dallas Business Journal
  • Spirit of Alliance Award by Agile1 Ready to Level Up Your Career?