Avid Bioservices is a leading CDMO specializing in biologics manufacturing with over three decades of experience. Offering a range of services including Mabs, biosimilars, and recombinant proteins, the company boasts world-class facilities and a flawless quality record. Avid Bioservices personalizes every stage of development from early to late stages, ensuring their clients' success through expertise and partnership.
Open Positions
Engineer, MSAT (Upstream)
2+ years of biologic upstream manufacturing experience, Bachelor’s degree in a scientific or engineering discipline, strong understanding of cGMPs
Sr. Microbiologist, Quality Control
B.S. in Microbiology or related field with 4–5 years of experience in a GMP facility, or master’s degree with 1-3 years of experience
Manufacturing Associate Downstream
2+ years of experience with large-scale liquid chromatography columns or similar equipment. 1+ years of related experience in the life sciences industry
Scientist, Cell Line Development
2-5 years of industry experience in cell development for biologics, M.S. in Cell Biology, Molecular Biology, Biochemistry, or related field, and hands-on experience with CHO cell systems
Engineer, GxP Systems
Bachelor's degree, 1+ years' experience in technical writing, complex systems design, and support
Technician, Environmental Monitoring
Associate's degree or equivalent experience, knowledge of GMP environment, and ability to work overtime
Associate Engineer, MSAT (Downstream)
Bachelor's degree in scientific or engineering discipline, 1+ year of downstream biologic manufacturing experience, quality assurance knowledge, and hands-on experience with downstream process equipment
Associate Scientist, Analytical Development
5+ years of biotech industry experience, HPLC, CE, or Potency/ELISA experience, and a BS degree in Biochemistry, Chemistry, Biology or a related field
Manufacturing Associate Downstream
2+ years of experience with large-scale liquid chromatography columns or similar equipment. 1+ years of related experience in the life sciences industry. Proficiency in working within a GMP production environment with aseptic techniques
Engineer, IT Systems Compliance
3+ years of experience in biopharmaceutical/pharmaceutical manufacturing with 1 year of validation experience
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