CCP6 Trainee (MM) at Lonza - Spain

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

31 Dec, 25

Salary

0.0

Posted On

02 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Aseptic Technique, Equipment Monitoring, Laboratory Tasks, Sanitization, Process Troubleshooting, Standard Operating Procedures, Materials Preparation, Solutions Preparation, GMP Manufacturing, Biotechnology, Therapeutic Proteins, Clean Room Operations, CIP, SIP, Batch Records, Logbooks

Industry

Pharmaceutical Manufacturing

Description

Job Description: (Workforce Advancement Federation) Biologics Trainee Job Title: PCP Trainee- Biotechnologist, Mammalian Manufacturing Department: Mammalian Manufacturing Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. Did you know that we are the 1st biologics contract manufacturer in Singapore? We offer you exposure to upcoming biotech and established pharmaceutical companies and to the manufacturing technology needed to produce mammalian treatments and cell therapies of tomorrow. Our global manufacturing network is recognized for its reliable, high-quality services, regulatory track record, global footprint, innovative technology platforms and extensive experience – we, in Singapore are proud to be part of this global network. Responsibilities The Biotechnologist is responsible for the manufacture of therapeutic proteins under cGMP conditions. Expectations for each position are built upon those described in the preceding level. There will be some physical work required to handle equipment and materials. During the course of routine work, the Intern is expected to be working in clean rooms most of the time. This position reports to the Senior/ Section Lead/ Manager of the Manufacturing Large Scale, Small Scale or Centralized Operations Team. Learn and perform well-defined procedures within a GMP manufacturing setting Perform equipment monitoring & and basic 6S housekeeping Perform basic laboratory tasks (e.g. sampling, pH/ conductivity/ osmolality measurements etc.) Perform routine sanitization tasks to maintain facility standards Trained & signed off on Performance Measures (PMs) relating to CIP/ SIP/ basic tank & instrument operations Demonstrate aseptic technique in the handling of product/ materials Perform basic process & equipment troubleshooting Multi-task on equipment preparations & operations to ensure adherence to schedule Attain full competency in the performance of all operations relevant to manufacturing areas assigned. Display basic process & equipment troubleshooting ability under routine scenarios. Become a technical process expert by exhibiting basic understanding of critical process/operational parameters and target/acceptable ranges, as well as interactions between different process parameters. Use Standard Operating Procedures (SOPs), logbooks & Batch Records (BRs) effectively & competently Submit samples via Laboratory Information Management System (LIMS) Materials & Equipment Preparations Able to identify the correct materials by part number and FEFO lots. Select appropriate Dispensing Booths/Hoods and Weight balance. Identify sampling requirements based on material RMS. Assemble Autoclave assembly per SOP. Able to perform equipment wash without stains and residues. Solutions Preparations Enhanced knowledge of the different setup and equipment use between customers for different operations, e.g.: CIPs and buffer/media transfer Able to identify and lead the installation of the different set up and equipment for different customers for different operations, e.g.: CIPs and buffer/media transfer Understand the criticality of setting up the right path and equipment for different customers In depth knowledge of the different set up and the equipment use between single use and the conventional stainless steel equipment Able to formulate plans for executing CIPs to meet different customers requirement, e.g., the CIPs of the HTST. Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Responsibilities

The Biotechnologist is responsible for the manufacture of therapeutic proteins under cGMP conditions. This includes performing well-defined procedures, equipment monitoring, and basic laboratory tasks in a clean room environment.