Director of Quality Assurance
Posted on Jun 23, 2026 by CV-Library
Leicestershire, United Kingdom
Pharmaceutical
Immediate Start
£90k - £90k Annual
Full-Time
ROLE OVERVIEW
Pr
We are currently looking for a Director of QA to join a leading pharmaceutical organisation that specialises in small molecules and operate within the OSD space. This is an exciting opportunity for a candidate with site operational experience to be part of a global company that values stability and growth, particularly in today’s tumultuous market environment.
This role offers the chance to contribute to critical site activities, overseeing operational quality functions, and working closely on quality assurance processes. Based at the site, you will play a pivotal part in ensuring GMP compliance, supporting upcoming digital and system enhancements, and maintaining high standards in manufacturing operations.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Director of QA will be varied however the key duties and responsibilities are as follows:
• Oversee on‑site operational quality activities, ensuring GMP compliance and effective quality management across manufacturing operations.
• Provide hands‑on site leadership, supporting the QA team and ensuring robust quality oversight for small molecule OSD products.
• Collaborate with cross‑functional teams during audits, inspections, and regulatory interactions, particularly with the MHRA.
• Champion the development, maintenance, and continuous improvement of the site’s PQS (Product Quality System).
• As the Senior Quality Operations individual, you will be responsible for maintaining a pragmatic risk-tolerant approach to quality decisions and operational challenges.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Director of QA we are looking to identify the following on your profile and past history:
• A Degree or higher level in a science‑related discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
• Proven site operational experience within a GMP environment, specifically with small molecule OSDs, liquids, or capsules.
• Experience with GMP inspections, MHRA, and managing quality systems such as TrackWise and LIMS.
WHAT’S IN IT FOR YOU?
This role offers a highly competitive package including a base salary example around £100,000, a 25% annual bonus (with deferred bonus potential), private medical cover for you and your family, and a flexible approach to sign-on bonuses. Our client provides notable job security, a collaborative culture, and opportunities for growth within a company where profits are reinvested into the business, helping it grow to over 7,000 employees globally.
Key Words: Quality Assurance / GMP / Site Operations / Small Molecules / OSD / MHRA / LIMS / TrackWise / Regulatory Compliance / Leadership / Digital QA / System Transition / Global PQS / Manufacturing / Sterile/OECD / On-site / Risk Management
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career
Pr
We are currently looking for a Director of QA to join a leading pharmaceutical organisation that specialises in small molecules and operate within the OSD space. This is an exciting opportunity for a candidate with site operational experience to be part of a global company that values stability and growth, particularly in today’s tumultuous market environment.
This role offers the chance to contribute to critical site activities, overseeing operational quality functions, and working closely on quality assurance processes. Based at the site, you will play a pivotal part in ensuring GMP compliance, supporting upcoming digital and system enhancements, and maintaining high standards in manufacturing operations.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Director of QA will be varied however the key duties and responsibilities are as follows:
• Oversee on‑site operational quality activities, ensuring GMP compliance and effective quality management across manufacturing operations.
• Provide hands‑on site leadership, supporting the QA team and ensuring robust quality oversight for small molecule OSD products.
• Collaborate with cross‑functional teams during audits, inspections, and regulatory interactions, particularly with the MHRA.
• Champion the development, maintenance, and continuous improvement of the site’s PQS (Product Quality System).
• As the Senior Quality Operations individual, you will be responsible for maintaining a pragmatic risk-tolerant approach to quality decisions and operational challenges.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Director of QA we are looking to identify the following on your profile and past history:
• A Degree or higher level in a science‑related discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
• Proven site operational experience within a GMP environment, specifically with small molecule OSDs, liquids, or capsules.
• Experience with GMP inspections, MHRA, and managing quality systems such as TrackWise and LIMS.
WHAT’S IN IT FOR YOU?
This role offers a highly competitive package including a base salary example around £100,000, a 25% annual bonus (with deferred bonus potential), private medical cover for you and your family, and a flexible approach to sign-on bonuses. Our client provides notable job security, a collaborative culture, and opportunities for growth within a company where profits are reinvested into the business, helping it grow to over 7,000 employees globally.
Key Words: Quality Assurance / GMP / Site Operations / Small Molecules / OSD / MHRA / LIMS / TrackWise / Regulatory Compliance / Leadership / Digital QA / System Transition / Global PQS / Manufacturing / Sterile/OECD / On-site / Risk Management
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career
Reference: 225280331
https://jobs.careeraddict.com/post/113448945
Director of Quality Assurance
Posted on Jun 23, 2026 by CV-Library
Leicestershire, United Kingdom
Pharmaceutical
Immediate Start
£90k - £90k Annual
Full-Time
ROLE OVERVIEW
Pr
We are currently looking for a Director of QA to join a leading pharmaceutical organisation that specialises in small molecules and operate within the OSD space. This is an exciting opportunity for a candidate with site operational experience to be part of a global company that values stability and growth, particularly in today’s tumultuous market environment.
This role offers the chance to contribute to critical site activities, overseeing operational quality functions, and working closely on quality assurance processes. Based at the site, you will play a pivotal part in ensuring GMP compliance, supporting upcoming digital and system enhancements, and maintaining high standards in manufacturing operations.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Director of QA will be varied however the key duties and responsibilities are as follows:
• Oversee on‑site operational quality activities, ensuring GMP compliance and effective quality management across manufacturing operations.
• Provide hands‑on site leadership, supporting the QA team and ensuring robust quality oversight for small molecule OSD products.
• Collaborate with cross‑functional teams during audits, inspections, and regulatory interactions, particularly with the MHRA.
• Champion the development, maintenance, and continuous improvement of the site’s PQS (Product Quality System).
• As the Senior Quality Operations individual, you will be responsible for maintaining a pragmatic risk-tolerant approach to quality decisions and operational challenges.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Director of QA we are looking to identify the following on your profile and past history:
• A Degree or higher level in a science‑related discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
• Proven site operational experience within a GMP environment, specifically with small molecule OSDs, liquids, or capsules.
• Experience with GMP inspections, MHRA, and managing quality systems such as TrackWise and LIMS.
WHAT’S IN IT FOR YOU?
This role offers a highly competitive package including a base salary example around £100,000, a 25% annual bonus (with deferred bonus potential), private medical cover for you and your family, and a flexible approach to sign-on bonuses. Our client provides notable job security, a collaborative culture, and opportunities for growth within a company where profits are reinvested into the business, helping it grow to over 7,000 employees globally.
Key Words: Quality Assurance / GMP / Site Operations / Small Molecules / OSD / MHRA / LIMS / TrackWise / Regulatory Compliance / Leadership / Digital QA / System Transition / Global PQS / Manufacturing / Sterile/OECD / On-site / Risk Management
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career
Pr
We are currently looking for a Director of QA to join a leading pharmaceutical organisation that specialises in small molecules and operate within the OSD space. This is an exciting opportunity for a candidate with site operational experience to be part of a global company that values stability and growth, particularly in today’s tumultuous market environment.
This role offers the chance to contribute to critical site activities, overseeing operational quality functions, and working closely on quality assurance processes. Based at the site, you will play a pivotal part in ensuring GMP compliance, supporting upcoming digital and system enhancements, and maintaining high standards in manufacturing operations.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Director of QA will be varied however the key duties and responsibilities are as follows:
• Oversee on‑site operational quality activities, ensuring GMP compliance and effective quality management across manufacturing operations.
• Provide hands‑on site leadership, supporting the QA team and ensuring robust quality oversight for small molecule OSD products.
• Collaborate with cross‑functional teams during audits, inspections, and regulatory interactions, particularly with the MHRA.
• Champion the development, maintenance, and continuous improvement of the site’s PQS (Product Quality System).
• As the Senior Quality Operations individual, you will be responsible for maintaining a pragmatic risk-tolerant approach to quality decisions and operational challenges.
ROLE REQUIREMENTS
To be successful in your application to this exciting role as the Director of QA we are looking to identify the following on your profile and past history:
• A Degree or higher level in a science‑related discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
• Proven site operational experience within a GMP environment, specifically with small molecule OSDs, liquids, or capsules.
• Experience with GMP inspections, MHRA, and managing quality systems such as TrackWise and LIMS.
WHAT’S IN IT FOR YOU?
This role offers a highly competitive package including a base salary example around £100,000, a 25% annual bonus (with deferred bonus potential), private medical cover for you and your family, and a flexible approach to sign-on bonuses. Our client provides notable job security, a collaborative culture, and opportunities for growth within a company where profits are reinvested into the business, helping it grow to over 7,000 employees globally.
Key Words: Quality Assurance / GMP / Site Operations / Small Molecules / OSD / MHRA / LIMS / TrackWise / Regulatory Compliance / Leadership / Digital QA / System Transition / Global PQS / Manufacturing / Sterile/OECD / On-site / Risk Management
"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career
Reference: 225280331
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