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QC Manager
- Posted 07 September 2023
- Salary Competitive Package
- LocationCambridge
- Job type Permanent
- Reference92580
- Contact NameDixie Rowley
Job description
QC Manager – UK – Competitive Package
I am currently working with an exciting pharmaceutical company on their search for a Quality Control Manager. You will play an integral role within the QC department, working closely with senior leadership to help support and oversee testing which is testing place on the manufacturing site.
This role will offer you:
The opportunity for future growth into senior leadership positions.
The chance to join an organisation that offers a creative and flexible working environment.
The opportunity to be part of a company that is contributing to the development of products that have the ability to save lives.
You will be responsible for:
Helping to drive Process Changes on site and continuous improvements across the lab and manufacturing site.
Acting as the SME for QC, hosting internal audits.
Ensuring stability assurance reviews are taken place in a timely manner.
Line managing a large team of motivated QC professionals.
You will bring the following:
Well versed in sterility assurance and endotoxin testing.
Previous experience working within GMP pharmaceutical environment.
Proven leader, having line managed teams in the past.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: dixie.rowley@biotalent.com
Mobile: 02039115888
I look forward to hearing from you!
I am currently working with an exciting pharmaceutical company on their search for a Quality Control Manager. You will play an integral role within the QC department, working closely with senior leadership to help support and oversee testing which is testing place on the manufacturing site.
This role will offer you:
The opportunity for future growth into senior leadership positions.
The chance to join an organisation that offers a creative and flexible working environment.
The opportunity to be part of a company that is contributing to the development of products that have the ability to save lives.
You will be responsible for:
Helping to drive Process Changes on site and continuous improvements across the lab and manufacturing site.
Acting as the SME for QC, hosting internal audits.
Ensuring stability assurance reviews are taken place in a timely manner.
Line managing a large team of motivated QC professionals.
You will bring the following:
Well versed in sterility assurance and endotoxin testing.
Previous experience working within GMP pharmaceutical environment.
Proven leader, having line managed teams in the past.
If this role is for you or someone that you know, then please get in touch by reaching out to me on:
Email: dixie.rowley@biotalent.com
Mobile: 02039115888
I look forward to hearing from you!
