Pilot Plant Associate Chromatography ultrafiltration
Job in
San Diego, San Diego County, California, 92189, USA
Listed on 2025-12-15
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.
- 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.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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