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Engineer ll, Upstream Manufacturing

Job in Elizabeth, Union County, New Jersey, 07215, USA
Listing for: WuXi Biologics Group
Full Time position
Listed on 2026-02-12
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

A true single-source provider from concept to commercialization for biologics produced from mammalian cell culture.

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Recombinant Proteins / Enzymes / Cytokines

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

High quality, expert services for biologics produced from microbial fermentation.

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

Discover information about the various drug development services we provide for this product type

We offer customized antibody discovery platforms for monoclonal antibodies (mAbs), bispecific antibodies (bsAbs), multispecific antibodies (msAbs), immunocytokines, and other therapeutic modalities, to accelerate biology-driven lead identification.

At WuXi Biologics, we specialize in the production and engineering of monoclonal, bispecific, and multi-specific antibodies, fusion-proteins, cytokines, enzymes, and novel biologics. With industry-leading expertise, state-of-the-art facilities and proprietary technologies, we offer our customers high-quality protein engineering and production services for research use.

At WuXi Biologics, we provide comprehensive protein characterization testing to help you triage and optimize your lead candidates. Our integrated protein characterization and analytics platform includes purity/impurity testing, structure characterization assessment, including MS-based protein  post-translational modification analysis, and function testing (e.g., SPR/ELISA/cell-based activity assays).

Leveraging advanced in vitro assay technologies such as cellular, biochemical, molecular, immune, and Fc effector function assays, we deliver reproducible, high-quality results with data interpretation to support biologics discovery and development.

Our multi-species in vivo pharmacology services provide science-driven solutions for preclinical studies, including pharmacokinetic (PK) and pharmacodynamic (PD) evaluations, efficacy models, toxicology studies, and immunohistology.

Industry-leading expertise, state-of-the-art facilities, and multiple antibody generation technology platforms for the discovery of novel monoclonal, bispecific and multispecific antibodies, immunocytokines and other biologics.

Provided as either a standalone service offering or as part of our integrated CMC development platforms, WuXi Biologics provides extensive expertise and industry-leading timelines for cell line engineering and strain development across a wide range of biotherapeutics.

Our extensive analytical testing services offer top-tier expertise in method development for in-process, release, and stability assays, and support of cell line, process, and formulation development activities, product characterization, develop ability assessments and other key IND- and BLA-enabling studies.

Multiple upstream and downstream PD labs facilitate the establishment and scale-up of fed-batch, intensified fed-batch, and continuous manufacturing approaches for diverse biotherapeutic modalities in both early and late-stage development.

Late-stage development scales processes for commercialization, culminating in biologic characterization, characterization, and validation.

Process characterization supports drug substance production within a data-driven framework that streamlines PPQ and meets global compliance requirements.

We provide advanced drug product development services spanning biologics, vaccines, and small molecules, with expertise in formulating clinical and commercial products in liquid, frozen, and lyophilized forms, compatible with various container closure systems such as vials, prefilled syringes, and other combination product types.

Offering in-house, one-stop cell banking and cell line characterization services, compliant with global GMP regulations and ICH guidelines, we operate over 20 cGMP cell banking suites ensuring capacity availability and timely execution of this critical CMC development activity.

Our extensive experience and expertise, along with EMA, ISO (CNAS), and CMA-certified laboratories, and exceptional track record for IND- and…

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