Interim QP / QD
- Recruiter
- Hyper Recruitment Solutions Ltd
- Location
-
Oxford
South East EnglandUnited Kingdom
- Salary
- 700.00 - 800.00 GBP Daily
- Posted
- 15 Oct 2021
- Closes
- 23 Oct 2021
- Job Title
- Non-Executive Director
- Category
- Scientific and Pharmaceutical
- Contract Type
- Contract
- Hours
- Full Time
Oxfordshire area. As the Interim Quality Director you will be responsible for providing quality leadership and technical guidance to contribute to the build of a new site.
KEY DUTIES AND RESPONSIBILITIES:
1. You will need to ensure that the site will be eligible to operate within MHRA regulations and that all quality systems are in compliance with these regulations. You will need to keep updated with changes in regulations and own the development plans of the quality systems, cultures and teams.
2. You will work extremely closely with the Senior Leadership Team and will need to have the gravitas and commercial awareness to advise and encourage stakeholders. As the Quality Director, you will advise the senior leadership during their exciting growth, on quality standards.
3. As the Quality Director, you will take charge of all relevant Quality areas and will need to show managerial experience. The team will consist of various departments, including QA, QC and Operations. You will need to oversee the Audit plans, manufacturing and procedure Quality whilst ensuring there is adequate QA coverage throughout.
4. Although you are not expected to be a QP for this position, it would be advantageous.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Quality Director we are looking to identify the following on your profile and past history:
1. Prior experience managing a Quality Assurance unit within a Pharmaceutical or Life Science industry. Any experience at executive or board level would be beneficial, along with experience working within a sterile business.
2. Prior experience working and liaising with regulatory bodies, such as the MHRA, FDA or EMA is essential. You will be the lead contact with the regulatory bodies and will be the point of contact.
3. Experience in a commercial manufacturing site.
Key Words: Quality Director | Quality Assurance Director | Director | QA | Quality Assurance | MHRA | Life Science | Pharma | Biologics | Regulatory | Audit | ISO13485 | Med Device | QMS | Development | Commercial | Manufacturing | Aseptic
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.
KEY DUTIES AND RESPONSIBILITIES:
1. You will need to ensure that the site will be eligible to operate within MHRA regulations and that all quality systems are in compliance with these regulations. You will need to keep updated with changes in regulations and own the development plans of the quality systems, cultures and teams.
2. You will work extremely closely with the Senior Leadership Team and will need to have the gravitas and commercial awareness to advise and encourage stakeholders. As the Quality Director, you will advise the senior leadership during their exciting growth, on quality standards.
3. As the Quality Director, you will take charge of all relevant Quality areas and will need to show managerial experience. The team will consist of various departments, including QA, QC and Operations. You will need to oversee the Audit plans, manufacturing and procedure Quality whilst ensuring there is adequate QA coverage throughout.
4. Although you are not expected to be a QP for this position, it would be advantageous.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Quality Director we are looking to identify the following on your profile and past history:
1. Prior experience managing a Quality Assurance unit within a Pharmaceutical or Life Science industry. Any experience at executive or board level would be beneficial, along with experience working within a sterile business.
2. Prior experience working and liaising with regulatory bodies, such as the MHRA, FDA or EMA is essential. You will be the lead contact with the regulatory bodies and will be the point of contact.
3. Experience in a commercial manufacturing site.
Key Words: Quality Director | Quality Assurance Director | Director | QA | Quality Assurance | MHRA | Life Science | Pharma | Biologics | Regulatory | Audit | ISO13485 | Med Device | QMS | Development | Commercial | Manufacturing | Aseptic
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.