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Pilot Plant Associate Chromatography ultrafiltration

Job in San Diego, San Diego County, California, 92189, USA
Listing for: VTekis Consulting LLP
Full Time position
Listed on 2025-12-15
Job specializations:
  • Manufacturing / Production
    Operations Engineer, Quality Engineering, Manufacturing Engineer, Validation Engineer
Job Description & How to Apply Below

Job Description

Qualifications
  • B.S. degree in biology or related area with 4-6 years of experience working in process development or Manufacturing support in bioprocessing required
  • Hands on experience with Chromatography, ultrafiltration and depth filtration process acquired through lab, pilot or production scale experience.
  • Good manufacturing practices required
  • Good documentation practices required
  • Ability to effectively collaborate with team members
  • Experience with manufacturing investigations for biologics manufacturing.
  • Familiarity with Quality systems and Enterprise Resource Planning etc.
Responsibilities (Essential Role Responsibilities)
  • Perform downstream purification processes, including chromatography, ultrafiltration, tangential flow filtration and depth filtration, at pilot and production scales.
  • Operate and maintain standard bioprocessing equipment such as chromatography systems, ultracentrifuges, and tangential flow filtration (TFF) units.
  • Adhere strictly to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in all activities.
  • Prepare, review, and maintain batch records, SOPs, logbooks, raw material specifications, campaign summary reports, technology transfer documents, and presentations in compliance with regulatory requirements.
  • Collaborate with cross-functional teams to support manufacturing investigations, root cause analysis, and process troubleshooting.
  • Ensure compliance with company SOPs, training requirements, and scale-up best practices.
  • Maintain facility readiness and support regulatory inspections through vigilant oversight.
  • Utilize Quality Systems and ERP platforms to document and track manufacturing activities.
  • Drive process improvements through the change control process or other initiatives.
  • Apply professional expertise to routine assignments; may supervise or serve as lead during on-floor activities.
  • Provide process subject matter expertise and take ownership of assigned deliverables.
  • Preferred:
    Experience conducting manufacturing investigations in biologics production.
  • Demonstrate strong technical writing and communication skills.
  • Maintain a safe working environment and stay current with all assigned training.

Regards,

Mohammed Ilyas,

PH -  or text -  or you can share the updated resume at

All your information will be kept confidential according to EEO guidelines.

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Position Requirements
10+ Years work experience
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