Downstream Process Development Scientist
at Clinical Professionals
Liverpool, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 27 May, 2024 | GBP 20 Hourly | 01 Mar, 2024 | N/A | Good communication skills | No | No |
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Description:
REFERENCE NUMBER: JO-2402-530351
Downstream Process Development Scientist
Rate: Negotiable
Job Type: Contract
Location: Speke, Liverpool
Downstream Process Development Scientist (R&D)
Speke, Liverpool
£15.38 to £20.51 per hour
6 month contract
CPL Life Sciences are currently partnering with a large global healthcare company to support a 6-month contract hire in the Speke area. The responsibilities of the role will include working within downstream purification to support the development of novel vaccine and biopharmaceutical products.
Responsibilities:
- Providing technical knowledge for delivering downstream purification projects across development laboratories.
- Assisting process scale-up and supply deliveries in laboratories and plant-pilot areas, such as GMP production of clinical trial products as per business requirements.
- Responsible for adhering and encouraging compliance in different quality and safety aspects for process development processes, and driving continuous improvement through innovation and collective technical expertise.
- Providing regular updates for project progress to technical teams and global stakeholders, delivering peer reviewed technical reports, and operating collaboratively with different teams.
- Able to work collaboratively, communicating effectively and building strong professional relationships at various levels in the organization.
- At least 2 years of experience in downstream purification of cell culture based or fermenter-based products or similar experience, such as PhD, is preferable.
- Analytical skills to help with process optimization and making critical decisions on development data, and ability to solve problems independently and proactively for early to late phase development.
- Competency in cGMP environments and ability to write high quality technical documentation.
- Experience with AKTAs, TFF, or reaction chemistry is desirable.
For further information please apply within or send your CV to arshaan.sindhwani@cpl.com
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
IT Software - Other
Software Engineering
Graduate
Proficient
1
Liverpool, United Kingdom