Manufacturing Associate III, Downstream Processing (3rd shift)

System One; Pennington (NJ); On-site; USD 45,000 - 52,000; Full time

Benefits offered by this job

Health and welfare benefits

401(k) plan

Job summary

System One, Inc. is seeking a Manufacturing Associate III, Downstream Processing for the 3rd shift on-site in Pennnington, NJ. You will lead downstream operations, manage campaigns, ensure readiness of equipment and materials, and serve as the primary technical resource on the floor.

You will guide SOPs, MBRs, batch records, and documentation while supporting CAPAs, deviations, and process improvements in a GMP environment.

Qualifications

• Bachelor’s degree in Biotechnology, Biochemistry, Chemical Engineering, or Life Sciences with 5+ years of biopharma experience.
• Extensive hands-on experience with Protein A, polishing chromatography, and AKTA systems.
• Strong GMP knowledge and documentation practices; leadership abilities.

Responsibilities

• Lead daily downstream manufacturing operations and provide shop-floor technical support.
• Coordinate execution of manufacturing campaigns and purification schedules.
• Oversee chromatography skids, AKTA systems, BioSC and TFF platforms.

Skills

Downstream purification operations

AKTA chromatography

TFF platforms

Viral filtration

GMP compliance

Leadership

Troubleshooting

Education

Bachelor's degree in Biotechnology or Life Sciences

Tools

AKTA systems

TFF systems

BioSC

Protein A capture

Sterile filtration

Job description

Job Title: Manufacturing Associate III, Downstream Processing (3rd shift)
Location: Pennnington, New Jersey
Type: Contract To Hire
Work Model: Onsite- Monday-Friday 10pm-6am
Pay Rate: $33-00-$37.50hr (Based on experience)
plus $3 differential for 3rd shift

Responsibilities

• Lead daily downstream manufacturing operations and provide shop-floor technical support.
• Coordinate execution of manufacturing campaigns and purification schedules.
• Ensure manufacturing readiness, equipment availability, and material preparedness for batch execution.
• Serve as the primary technical resource during downstream manufacturing operations.
• Provide real-time decision support during process execution and batch recovery activities.
• Lead all purification operations including Protein A capture, viral inactivation, ion exchange chromatography, UF/DF, viral filtration, and final bulk drug substance processing.
• Oversee operation and performance of chromatography skids, AKTA systems, BioSC, TFF systems, and filtration equipment.
• Monitor critical process parameters and ensure adherence to process specifications.
• Troubleshoot process and equipment issues to maintain operational continuity.
• Support implementation of process improvements and manufacturing optimization efforts.
• Lead preparation and revision of:
  • Standard Operating Procedures (SOPs)
  • Master Batch Records (MBRs)
  • Manufacturing Forms and Logbooks
  • Equipment and Process Documentation
• Support deviation investigations, CAPAs, change controls, and risk assessments.
• Ensure continuous inspection readiness and GMP compliance.
• Participate directly in regulatory inspections and client audits.
• Support review and approval of manufacturing documentation for batch release readiness.
• Coordinate activities between Manufacturing, QA, QC, MSAT, Validation, Engineering, Facilities, Warehouse, and Supply Chain teams.
• Support technology transfer projects from process development through GMP manufacturing.
• Participate in process validation, PPQ campaigns, and commercial manufacturing programs.
• Lead manufacturing readiness reviews and campaign planning meetings.
• Drive continuous improvement and operational excellence initiatives.
• Train, mentor, and develop Associate I and Associate II personnel.
• Provide technical coaching and floor-based leadership.
• Support qualification programs and onboarding activities.
• Assist supervisors with scheduling, work assignments, and personnel development plans.

Requirements

• Advanced expertise in downstream purification operations and biologics manufacturing.
• Extensive experience with Protein A and polishing chromatography processes.
• Strong hands- on experience operating AKTA chromatography systems and TFF platforms.
• Advanced knowledge of viral filtration, UF/DF, and sterile filtration processes.
• Strong understanding of GMP regulations, manufacturing systems, and documentation requirements.
• Proven leadership, decision-making, and organizational skills.
• Excellent troubleshooting and problem-solving capabilities.
• Ability to effectively coordinate cross-functional manufacturing activities.
• Ability to stand for extended periods.
• Ability to bend, reach, and lift up to 50 pounds.
• Ability to work in cleanroom environments while wearing required PPE.
• Bachelor's degree in Biotechnology, Biochemistry, Chemical Engineering, Life Sciences, or a related discipline with 5+ years of relevant biopharmaceutical manufacturing experience.
• Previous lead operator, project coordination, or team leadership experience preferred.
• Experience supporting late-stage clinical or commercial biologics manufacturing preferred.
• Preferred Skills Technology Transfers
• Process Validation and PPQ Campaigns
• Commercial Manufacturing Operations
• Regulatory Inspections and Client Audits
• CAPA and Deviation Management
• Continuous Improvement and Lean Manufacturing Initiatives

System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Ref: #558-Scientific