Principal QC Scientist
- Permanent
- Technical Operations, Quality Control, Chemist
This vacancy has now expired. Please see similar roles below...
Hobson Prior are looking for a Principal QC Scientist to join a brilliant biotech corporation on a permanent basis. Our client is focused on inventing innovative remedies for people suffering from cancer.
Please note that to be considered for this role you must have the right to work in this location.
Key Responsibilities:
- For this role, you will direct the GMP investigations and produce CAPAs for out-of-specifications and aberrations.
- Produce protocols, as well as conduct the implementation and creation of documents for validation and qualification of analytical strategies as per suitable phase of development rendering to ICH and GSP regulations.
- You will manage processing, documenting, evaluating and consenting of analytical data.
- Uphold laboratories in an audit prompt state as well as be included in the alignment of crucial QC techniques across the company's new manufacturing sites.
- Handle the data storage, as well as the outputs and trending.
- To assist in continuous professional development, you will train junior personnel across the QC function and design and execute systems and processes.
- The ideal candidate will form and uphold efficient operating relations with all crucial shareholders.
- Any other assigned duties.
Key Skills:
- Capable of leading a team.
- A solution-oriented individual with the capacity to be agile, flexible, and comfortable with change.
- Able to adjust to changing priorities.
- An organised individual with the ability to plan and manage time efficiently.
- A focused individual with a passion for delivery and able to be proactive.
- Capable of working within a fast-paced setting, as well as cross-functionally.
- Communication skills both verbally and in writing.
- Works well in a team environment as well as independently.
Requirements:
- Educated to a degree level in a life science discipline.
- Experienced with flow cytometry.
- Know-how of GXP, Quality Control and Quality Systems.
- At least 3 years of experience within a biotech or ATMP organisation.
- Familiarity with cell culture strategies and aseptic processing.
- Computer systems and data veracity procedure knowledge.
- Know-how of the guidelines and regulations on ATMP manufacture.
- Past involvement with data lifecycle, data management and analysis tools.
Apply now:
If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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