Manufacturing Associate I

Job Description

Job Description

job summary:

Step into a vital role supporting the production of a key vaccine product at a well-established pharmaceutical manufacturing site in Pearl River, NY. This 100% onsite opportunity is perfect for candidates with 1-2 years of cGMP manufacturing experience and familiarity with systems like SAP, Veeva, and LIMS. You'll be part of the team responsible for producing drug substance through downstream processing techniques such as filtration, centrifugation, and chromatography, with a strong focus on documentation, compliance, and aseptic technique. The Pearl River site is known for its innovation and history in vaccine development, making it a great place to build hands-on experience in a regulated environment.

location: Pearl River, New York
job type: Contract
salary: $25.00 - 25.63 per hour
work hours: 9 to 5
education: High School

responsibilities:

• Operate, clean, and sanitize downstream processing equipment (e.g., stainless-steel vessels, transfer lines, ancillary tools)
• Perform buffer preparation and support drug substance production using techniques such as:
  • Centrifugation
  • Depth filtration
  • Chromatography column purification and packing
  • Tangential flow filtration
  • Clean-in-place (CIP) and steam-in-place (SIP) procedures
• Maintain and use equipment such as:
  • pH/conductivity meters
  • Turbidity meters
  • Tube welders/sealers
  • Peristaltic pumps
• Weigh and dispense raw materials and intermediate solutions
• Collect samples for analytical testing and perform filter integrity tests
• Document all operations in compliance with Good Documentation Practices (GDP)
• Participate in cGMP training and follow all safety and quality guidelines
• Aid in cleaning biosafety cabinets and facility workspaces
• Support troubleshooting, deviations, and CAPAs in manufacturing areas
• Collaborate with quality and compliance teams
• Work flexible hours, including weekends or holidays as needed

qualifications:

Required Skills:

• High school diploma or GED
• 1-2 years of experience in a cGMP manufacturing environment
• Experience using GMP-related systems: SAP, Veeva, and LIMS
• Strong understanding of cGMP, GDP, and SOPs
• Solid documentation and communication skills
• Ability to operate and maintain basic manufacturing and analytical equipment
• Fluent in English (written and spoken)
• Attention to detail and ability to follow safety/compliance standards

Preferred Skills:

• Familiarity with Baculovirus Expression Vector System (BEVS)
• Preventive maintenance experience for equipment
• Experience supporting deviation management and investigations
• Data entry and basic data analysis related to manufacturing operations
• Aseptic technique and biosafety cabinet handling
• Ability to work cross-functionally and adapt to schedule changes or urgent needs

#LI-ST1

skills: SOP, Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA), Good Documentation Practices (GDP)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.