downstream process development
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Manufacturing Associate I, Downstream Processing
The Manufacturing Associate I, Downstream Processing works in a hands-on capacity in the cGMP purification and production support areas to manufacture collagenase clostridium histolyticum bulk drug substance (CCH BDS).
Manufacturing Associate, Downstream, Sun-Wed, Days
Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility.
Manufacturing Lead, Downstream - 15162
San Diego, CA
5+ years of downstream experience in biotech/pharma industries preferred (open to 4+ years in academic and 1+ years in industry)
Validation Engineer- Entry Level
STELLAR CONSULTING GROUP LLC
Validation, IQ, OQ, PQ, Engineering, automation, pharma, commissioning, qualification, Quality control, quality assurance, technical documentation, document control, workflow, files, document management, auditing, engineering, pharma, pharmaceutical, contract to hire, contract, permanent, full time, benefits, 401K, direct hire, cell culture, gene therapy, temperature mapping, lab equipment, KAYE, Fill/finish, sterile, upstream, downstream, process
Manager of Validation Services
An understanding of filtration and single use technology and their applications in the manufacturing process (upstream/downstream/formulation & filling, cGMP, bioprocessing) is preferred
Manufacturing Associates (Downstream/Biopharmaceutical)
San Diego, CA
∙ Reviews completed Production, Buffer and Purification batch records daily for cGMP compliance and completeness.
Manufacturing Associate II-III, Downstream Purification
Vista Biologicals Corp.
San Diego, CA
Vista Biologicals provides highly specialized cell culture, process development, and cGMP manufacturing services for the biopharmaceutical industries, utilizing cell culture to support pre-clinical, Phase I - III production.
Senior Process Engineer
Experience with upstream and downstream biopharmaceutical facility design, comprehensive knowledge of Good Engineering Practices (GEP) and familiarity with ASME BPE, ASTM E2500 methodology is preferred.
Sr. Scientist, Science & Technology
Upstream and downstream unit operation expertise with knowledge in; fermentation, ultrafiltration /diafiltrating, purification, and chromatography in cGMP manufacturing environment.
Manufacturing Tech II
interact cross-functionally with Downstream Operations, Upstream Operations, Facilities, R&D, Quality Assurance, Quality Control, Validation, and other internal and external functions to support successful commercial manufacturing campaigns.
Sr. Scientist, Downstream Process Development
The ideal applicant will be an experienced process engineer/scientist with a strong background in Downstream process development with a background in biologics/AAV processes.
Project Farma (PF)
Conduct experiments supporting the development and implementation of a cell expansion, upstream, and downstream processes for gene therapy.
Process Engineer, Technical Engineering, US - Vaccine
The preferred candidate will have expertise in downstream bioprocessing systems including TFF, chromatography and centrifugation.
Commissioning and Qualification Engineer
Working as part of the Commissioning & Qualification (C&Q) team, you will work with our client which are Pharmaceutical or Bio-Pharmaceutical companies in the areas of manufacturing equipment, upstream or downstream biopharmaceutical manufacturing equipment and processes, performing the C&Q activities listed below.
Manufacturing Associate III/IV (Flexible Volume Manufacturing)- Night Shift
In Purification, we perform critical downstream processing activities within cGMP cleanroom suites at our RTP Facility.