Qa Manager
Posted on Sep 29, 2024 by CV-Library
Croydon, Greater London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
QA Manager
Working exclusively with a long-standing client, I am now working to grow out their Quality team with a crucial, hands on management hire.
Given that the business is expanding headcount, introducing new systems, new products and also looking to bring in new equipment across all European facilities, this is both an exciting and positively challenging time to become a part of the business.
Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities.
A core aspect of the role will be leadership – leading a small team through hands on coaching, mentoring and training. Given the size of the site, I’ll emphasise again that this is hands on – as well as delegating out to the team, you must be willing and able to get stuck in yourself with investigations, documentation generation and other areas of quality department requirements.
If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information.
Key experience:
* Experienced within a QA capacity, working in a GMP environment
* Aseptic experience is beneficial but non-sterile environments will also be considered
* Leadership and management experience is preferred
* Strong hands on experience of a range of quality activities, especially in relation to QMS oversight
* Auditing experience essential – if you have been a lead auditor, this would be advantageous
* Knowledge and experience of validation activities
Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints, sterile, non-sterile, powders, APIs, raw, materials, biologics, cell, gene, atmp, vaccine, plasma, tablet, liquid, capsules
Working exclusively with a long-standing client, I am now working to grow out their Quality team with a crucial, hands on management hire.
Given that the business is expanding headcount, introducing new systems, new products and also looking to bring in new equipment across all European facilities, this is both an exciting and positively challenging time to become a part of the business.
Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities.
A core aspect of the role will be leadership – leading a small team through hands on coaching, mentoring and training. Given the size of the site, I’ll emphasise again that this is hands on – as well as delegating out to the team, you must be willing and able to get stuck in yourself with investigations, documentation generation and other areas of quality department requirements.
If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information.
Key experience:
* Experienced within a QA capacity, working in a GMP environment
* Aseptic experience is beneficial but non-sterile environments will also be considered
* Leadership and management experience is preferred
* Strong hands on experience of a range of quality activities, especially in relation to QMS oversight
* Auditing experience essential – if you have been a lead auditor, this would be advantageous
* Knowledge and experience of validation activities
Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints, sterile, non-sterile, powders, APIs, raw, materials, biologics, cell, gene, atmp, vaccine, plasma, tablet, liquid, capsules
Reference: 222102124
https://jobs.careeraddict.com/post/95647535
Qa Manager
Posted on Sep 29, 2024 by CV-Library
Croydon, Greater London, United Kingdom
Pharmaceutical
Immediate Start
Annual Salary
Full-Time
QA Manager
Working exclusively with a long-standing client, I am now working to grow out their Quality team with a crucial, hands on management hire.
Given that the business is expanding headcount, introducing new systems, new products and also looking to bring in new equipment across all European facilities, this is both an exciting and positively challenging time to become a part of the business.
Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities.
A core aspect of the role will be leadership – leading a small team through hands on coaching, mentoring and training. Given the size of the site, I’ll emphasise again that this is hands on – as well as delegating out to the team, you must be willing and able to get stuck in yourself with investigations, documentation generation and other areas of quality department requirements.
If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information.
Key experience:
* Experienced within a QA capacity, working in a GMP environment
* Aseptic experience is beneficial but non-sterile environments will also be considered
* Leadership and management experience is preferred
* Strong hands on experience of a range of quality activities, especially in relation to QMS oversight
* Auditing experience essential – if you have been a lead auditor, this would be advantageous
* Knowledge and experience of validation activities
Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints, sterile, non-sterile, powders, APIs, raw, materials, biologics, cell, gene, atmp, vaccine, plasma, tablet, liquid, capsules
Working exclusively with a long-standing client, I am now working to grow out their Quality team with a crucial, hands on management hire.
Given that the business is expanding headcount, introducing new systems, new products and also looking to bring in new equipment across all European facilities, this is both an exciting and positively challenging time to become a part of the business.
Working as a form of QA head for their own respective site, this position will manage a small team and remain fully hands on in all areas of quality. This includes systems oversight, operational delivery and validation activities.
A core aspect of the role will be leadership – leading a small team through hands on coaching, mentoring and training. Given the size of the site, I’ll emphasise again that this is hands on – as well as delegating out to the team, you must be willing and able to get stuck in yourself with investigations, documentation generation and other areas of quality department requirements.
If you are looking for a varied position that offers you a chance to make a real impact on your own site and play a significant part in the way that quality assurance is adopted and implemented business wide, please apply below or contact Mark Bux-Ryan for further information.
Key experience:
* Experienced within a QA capacity, working in a GMP environment
* Aseptic experience is beneficial but non-sterile environments will also be considered
* Leadership and management experience is preferred
* Strong hands on experience of a range of quality activities, especially in relation to QMS oversight
* Auditing experience essential – if you have been a lead auditor, this would be advantageous
* Knowledge and experience of validation activities
Quality, assurance, qa, GMP, manufacturing, pharmaceutical, QMS, system, operational, manager, supervisor, team, leader, specialist, compliance, regulatory, audit, lead, complaints, sterile, non-sterile, powders, APIs, raw, materials, biologics, cell, gene, atmp, vaccine, plasma, tablet, liquid, capsules
Reference: 222102124
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