Address
SalaryContract Type: Permanent
Closing date:
Reference: VN1417
Who we are
Vectura Fertin Pharma’s ambition is to become a market-leading wellness and healthcare business. Formed in March 2022, the business brings together two unique organizations: Vectura, experts in inhalation technology and Fertin Pharma, experts in oral and intra-oral delivery systems.
We are driven by the exciting and unique goal of addressing unmet patient and consumer needs by revitalizing, repurposing, and reimagining existing therapies to better serve people in taking care of their health and wellbeing.
What we will deliver
We focus on the development of a proprietary pipeline of wellness and healthcare products, with a specific focus on highly differentiated products that address unmet medical and consumer needs.
By leveraging our unique and enabling R&D capabilities, we are building a pipeline that includes inhalable medicines, nicotine replacement therapies (NRT), and consumer wellness products.
This will a highly varied role, with exposure to the full range of quality duties associated with pharmaceutical manufacture.
You will be working with a small, friendly team, providing support to teams across our site.
Your role
Working within the Quality department, you’ll be an advocate for embedding a ‘culture of quality’ across Vectura. You’ll provide quality systems expertise to facilitate maintenance and continual improvement of Vectura’s QMS.
Other key responsibilities will include (but not limited to):
Maintain the existing quality system by completing a range of tasks across the QMS; e.g. supplier approval.
Generate, review and maintain all relevant Quality documentation required by GMP/ISO
Identify and implement improvements to the QMS
Provide Quality support to project teams and business functions
Actively support a continuous improvement culture
Perform internal and external audits, and act as subject matter expert for client and regulatory audits
Maintain a broad awareness of GMP/ISO requirements, and a detailed knowledge of those pertinent to areas of specialism
Lead continuous improvement activities and internal Quality projects as required
Provide formal induction and refresher training to individuals across our business
About you
You’ll be educated to bachelor degree standard in a scientific discipline, with experience in a pharmaceutical environment and an understanding of applicable GMP/ISO requirements. You’ll be IT literate with good working knowledge of MS Office applications.
If you’re looking for a quality role with breadth and variety then we’d love to hear from you.
Vectura Fertin Pharma’s ambition is to become a market-leading wellness and healthcare business. Formed in March 2022, the business brings together two unique organizations: Vectura, experts in inhalation technology and Fertin Pharma, experts in oral and intra-oral delivery systems.
We are driven by the exciting and unique goal of addressing unmet patient and consumer needs by revitalizing, repurposing, and reimagining existing therapies to better serve people in taking care of their health and wellbeing.
What we will deliver
We focus on the development of a proprietary pipeline of wellness and healthcare products, with a specific focus on highly differentiated products that address unmet medical and consumer needs.
By leveraging our unique and enabling R&D capabilities, we are building a pipeline that includes inhalable medicines, nicotine replacement therapies (NRT), and consumer wellness products.
This will a highly varied role, with exposure to the full range of quality duties associated with pharmaceutical manufacture.
You will be working with a small, friendly team, providing support to teams across our site.
Your role
Working within the Quality department, you’ll be an advocate for embedding a ‘culture of quality’ across Vectura. You’ll provide quality systems expertise to facilitate maintenance and continual improvement of Vectura’s QMS.
Other key responsibilities will include (but not limited to):
Maintain the existing quality system by completing a range of tasks across the QMS; e.g. supplier approval.
Generate, review and maintain all relevant Quality documentation required by GMP/ISO
Identify and implement improvements to the QMS
Provide Quality support to project teams and business functions
Actively support a continuous improvement culture
Perform internal and external audits, and act as subject matter expert for client and regulatory audits
Maintain a broad awareness of GMP/ISO requirements, and a detailed knowledge of those pertinent to areas of specialism
Lead continuous improvement activities and internal Quality projects as required
Provide formal induction and refresher training to individuals across our business
About you
You’ll be educated to bachelor degree standard in a scientific discipline, with experience in a pharmaceutical environment and an understanding of applicable GMP/ISO requirements. You’ll be IT literate with good working knowledge of MS Office applications.
If you’re looking for a quality role with breadth and variety then we’d love to hear from you.
Chippenham, United Kingdom
1-6 Prospect West
Bumpers Way
Chippenham
SN14 6FH
