Forum Topic Biotechnology
  • Conversation: ***Bio-pharmaceutical Process Specialists*** Required

    • October 24, 2017 3:12 PM BST
    • ***Bio-pharmaceutical Process Specialists*** Required

      I'm looking to speak with Bio-pharma process specialists with SIP / CIP experience urgently. If you're interested in a new role in Switzerland I welcome your contact.
    • July 2, 2020 8:02 AM BST
      • Post(s)

      Good morning sir.

      i am interestes. My name is Jithesh cp. I have completed Diploma chemical Engineering. I have 8 years Experience  in the Chemical field of small molecule volume downstream (analytical and Batch Process, SCADA, PLC, DCS Operations) Presently I am working in Gulf Pharmaceutical industry Julphar ( UAE Ras Al Khaimah) as an Assistant Officer insulin department (Buffer and media Preparation) and i have 5 years of experience in Biotechnology plant with the knowledge of downstream biopharmaceutical unit operations. Previously I worked at Biocon LTD (India - Bangalore) as a junior Executive.


      Main duties performed

      • Experience executing operations in accordance to SOPs, Batch Records and Manufacturing Controls Systems (Delta V or Unicorn) is essential

      • Experience to include activities such as Clean in Place/Steam in Place Systems, Washers, Autoclaves, Large and Small Buffer/Media Preparation, Conjugation, Column Packing, Ultrafiltration/Diafiltration, Chromatography, Sterile Filtration, Manual and Automated Filling Systems

      • Experience in training Technicians and troubleshooting equipment and/or processing issues during startup and cGMP production within Grade C/D manufacturing areas.

      • Experience with use of Lean Tools such as Standard Work/5S and Six Sigma Tools such as Method 1 and 5 Whys

      • Excellent interpersonal skills, positive influence, team orientation, attention to detail, documentation skills, problem identification and problem-solving skills

      • An ability to work independently, and as a member of a self – managed shift team in a dynamic, fast-paced environment that requires flexibility and initiative.

      • Cleans, sanitize, and sterilize manufacturing area rooms and equipment’s

      • Performs CIP and SIP (Cleaning in Place and Sterilization in Place) of the tanks

      • Performs integrity test of all filters used in the process before and after each use

      • Monitors critical process parameters and proactively takes necessary action to prevent process deviation and/or product losses

      • Performs GMP Safety and Environmental regulatory tasks required in the manufacturing area.

      • v  Handling of chemical and biological spillages, and handles Hazardous and Non-hazardous waste according to EHS procedures.


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