Is there a job opening for a Hands-On Upstream Manufacturing Associate in Piscataway, NJ, USA?

Pharma Universe is currently hiring a Hands-On Upstream Manufacturing Associate in Piscataway, NJ, USA.

Does Pharma Universe hire Hands-On Upstream Manufacturing Associate?

Pharma Universe looking to hire a qualified Hands-On Upstream Manufacturing Associate in Piscataway, NJ, USA.

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Hands-On Upstream Manufacturing Associate

Piscataway, NJ, USA

328 Days ago

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Job Description

Upstream Manufacturing Associate Biologics cGMP Environment (Full-Time, Onsite New Jersey, USA)

Relocation support offered for US Citizens

Upstream Manufacturing Associate to support cell culture operations in a fast-paced, cGMP biopharmaceutical environment focused on mammalian-based biosimilar production. This role involves hands-on execution of upstream processes for engineering and clinical-scale batches ranging from 50 L to 1000 L.

Key Responsibilities:

Execute upstream manufacturing activities including cell culture and bioreactor operations at various scales
Support the production of engineering and clinical batches in compliance with cGMP standards
Operate and troubleshoot bioreactors, single-use systems, and associated upstream equipment
Collaborate with cross-functional teams including engineering and quality to ensure batch readiness and execution
Accurately document batch execution, deviations, and investigations as required
Assist in reviewing executed batch records and supporting documentation
Follow all safety procedures and maintain compliance with environmental, health, and safety policies
Contribute to continuous improvement initiatives in manufacturing processes and equipment operation

Requirements:

Bachelor's or Master's degree in Biochemistry, Chemical Engineering, Biology, or related field
Minimum 3 years' experience in upstream biologics manufacturing in a cGMP environment
Proficiency in aseptic technique and working with single-use technologies (bags, tubing, manifolds, etc.)
Strong understanding of cell culture processes and bioreactor operations
Experience initiating and executing GMP documentation including batch records and protocols
Comfortable working independently with minimal supervision while contributing to a team-based environment
Strong attention to detail, written documentation skills, and basic computer proficiency (Word, Excel, etc.)

This role is ideal for candidates with hands-on bioprocessing experience who are confident operating in a clinical and GMP-regulated setting.

Key Skills Required

ManufacturingBasic computerAseptic TechniqueAttention to DetailBatch RecordsBiochemistryBiologyCell CultureChemical EngineeringComplianceComputer ProficiencyDocumentationEnvironmentalFocusedMinimal SupervisionSupervisionSupporting DocumentationUpstream

Job Overview

Job Function: Other

Job Type: Full Time

Workplace Type: Not Specified

Experience Level: Associate

Salary: Competitive & Based on Experience

Experience: 0 - 0 yrs

Contact Information

Company Name: Pharma Universe

Recruiting People: HR Department

Website: http://www.pharmauniverse.co.uk

Location

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