Cell Therapy Specialist - All levels of experience

Have you a minimum term 6-motnhs experience in Cell Therapy? Looking to join a company that support motivated employees who strive for success? Would you want to be part of a unique project changing cancer patients' lives? Read on as this is the opportunity for you!

One of our most trusted clients here at i-Pharm is looking to give motivated and talented Cell Therapy Specialist/Process Operators the opportunity to get involved with a project based in the outskirts of Amsterdam! Our client is looking for not just experienced CTTs but those who have limited experience (minimum 6-months) to join their State-of-the-Art facility to conduct cell manipulation for cancer patients. Currently they are the only company worldwide conducting this type of live product thus are looking for driven CTTs with the desire to really make an impact.

My client is an Global biotech company who in the last 5 years have really made an impact in the pharmaceutical world, conducting revolutionary research around cancer therapies. Of recently they have established themselves in the market and since made partnership with one of the global market leaders as well as ranking 7^th in MITs 50 smartest companies.

Your Responsibilities

Responsibilities (include but are not limited to):

• To perform tasks associated with the manufacturing of clinical and commercial products following batch records and standard operating procedures (SOPs) in B, D and CNC grade areas
• To work as part of a dedicated and committed team to execute GMP runs in close collaboration with Product Sciences, Material Management, and Quality Assurance & Quality Control
• To assist in optimization of SOPs and Batch records, revise existing Manufacturing Batch Records, SOPs, WIs to support process improvements and maintain GMP compliance
• Assist in investigations required to manage deviations
• Assist in managing change controls
• To strictly comply with SOPs and cGMP regulations; accurately complete documentation associated with clinical and commercial manufacturing
• To ensure a consistent process execution to guarantee high quality output
• To maintain cleanroom in an optimal state
• To continuously look for improvements to the processes to increase quality and efficiency.

Education/experience

• Requires MBO and/or Bachelor's degree OR 2 or more years of cGMP experience in a manufacturing pharmaceutical/biotechnology environment
• Demonstrated knowledge of pharmaceutical manufacturing of biotechnology products, aseptic processing, cell culture products
• Experience with handling and propagation of human primary cells, including T cells
• Excellent skill in Microsoft word, Excel and data analysis
• Ability to think critically, and demonstrated troubleshooting and problem-solving skills
• Self-motivated and willing to accept temporary responsibilities outside of initial job description
• Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
• Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities

If you feel your experience in cGMP and GDP as well as knowledge of SOP is paramount and you are looking to ignite this amazing opportunity for yourself, please do not hesitate to apply for this role, I would love to discuss this opportunity further and get your CV submitted today! Looking forward to seeing your application and speaking with you too!