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Associate Scientist II, Downstream

Catalent

Baltimore, MDOnsitePosted 1 day ago$70,000 - $90,000/year
Full TimeEntry LevelManufacturing & CMCCDMO
Original posting ↗

Summary

The role supports downstream process development, pilot scale execution, and technology transfer to GMP manufacturing. The position involves hands-on laboratory work, collaboration with cross-functional teams, and contribution to process development activities.

Job description

Position Summary

The role supports downstream process development, pilot scale execution, and technology transfer to GMP manufacturing. The position involves hands-on laboratory work, collaboration with cross-functional teams, and contribution to process development activities.

The Role

  • Perform downstream processing of macromolecules expressed in mammalian cell lines, insect cells, or microbes.
  • Develop and execute purification protocols from bench scale to large scale.
  • Collaborate with analytical and upstream teams for purification and analysis of target molecules.
  • Execute laboratory procedures and methods with high quality and moderate guidance.
  • Build credibility within the group by delivering high-quality work.
  • Assist other members of the Downstream Process Development group as needed.
  • Follow standard operating procedures, protocols, and maintain required training.
  • Manage data, complete batch and experimental records according to Good Documentation Practices (GDP).
  • Document and communicate results through presentations, discussions, and meetings.
  • Manage samples and inventory related to experiments.
  • Assist with lab maintenance, stocking, cleaning, and troubleshooting equipment.
  • Participate in project team decision-making and scientific discussions.
  • Accommodate occasional weekend and evening work.
  • Perform other duties as assigned.

The Candidate

Minimum Requirements

  • Degree in Engineering or Life Science discipline with relevant experience (Bachelor of Arts or Bachelor of Science – at least 1+ years; or Master of Science – 0+ years).
  • At least 1 year of relevant experience in biologics purification including chromatography and aseptic processing.
  • Ability to sit at a desk or computer for documentation and data analysis.
  • Ability to work in a laboratory environment for extended periods, including standing, walking, or sitting.
  • Manual dexterity to handle laboratory instruments, pipettes, chromatography equipment, and tubing.
  • Occasional lifting of containers or lab equipment up to 30 pounds.
  • Good vision and hand-eye coordination for detailed work.
  • Use of personal protective equipment (PPE) such as lab coats, gloves, safety goggles, and respiratory protection when required.

Preferred Skills & Background

  • Experience with centrifugation, normal and tangential flow filtration, depth filtration, virus removal, and inactivation steps.
  • Experience operating AKTA chromatography systems, UNICORN software, and chromatography column packing.
  • Downstream process development experience specific to AAV, virus, VLP, or protein production.
  • Awareness of GMP operations and process technical transfer.

Requirements

  • Degree in Engineering or Life Science discipline
  • Bachelor of Arts or Bachelor of Science with at least 1+ years relevant experience, or Master of Science with 0+ years
  • At least 1 year of relevant experience in biologics purification including chromatography and aseptic processing
  • Ability to sit at a desk or computer for documentation and data analysis
  • Ability to work in a laboratory environment for extended periods, including standing, walking, or sitting
  • Manual dexterity to handle laboratory instruments, pipettes, chromatography equipment, and tubing
  • Occasional lifting of containers or lab equipment up to 30 pounds
  • Good vision and hand-eye coordination for detailed work
  • Use of personal protective equipment (PPE) such as lab coats, gloves, safety goggles, and respiratory protection when required

Benefits

  • Medical, Dental & Vision
  • Paid Time Off
  • 8 Paid Holidays
  • Tuition Reimbursement
  • Annual Performance Review
  • Career Growth Potential

Company overview

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) that serves as a trusted partner to pharmaceutical, biotech, and consumer health companies worldwide. Founded on a legacy dating back to 1933, Catalent has evolved into a comprehensive drug development and delivery leader with over 40 global sites. The company specializes in providing end-to-end solutions spanning oral dose formulations, biologics, specialty products, and clinical supply services. Catalent's expertise includes formulation development, analytical services, commercial manufacturing, and advanced delivery technologies such as Zydis® fast-dissolve tablets and softgel technologies. With over 1,000 active development programs at any given time, the company launches more than 100 new products and line extensions annually and has supported half of all FDA approvals over the past decade. Catalent produces over 60 billion treatment doses per year, helping approximately 200 million patients annually. Headquartered in Tampa, Florida, the company employs more than 10,000 professionals globally who are dedicated to putting patients first and championing the missions that matter in healthcare innovation.

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