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37.5-hour Quality Administrator- Head office Based

Cohens Chemist
Posted 4 days ago, valid for 19 days
Location

Bolton, Lancashire BL6 4SA, England

Salary

not provided

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Contract type

Full Time

Employee Assistance
In order to submit this application, a TotalJobs account will be created for you. As such, in addition to applying for this job, you will be signed up to all TotalJobs’ services as part of the process. By submitting this application, you agree to TotalJobs’ Terms and Conditions and acknowledge that your personal data will be transferred to TotalJobs and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The Cohens Group is seeking a Quality Administrator for their head office in Bolton, offering a permanent 37.5-hour workweek from Monday to Friday, 9am to 5:30pm.
  • The role requires two years of experience in a Good Distribution Practice (GDP) environment and focuses on maintaining quality management systems and regulatory compliance.
  • Key responsibilities include managing quality documentation, preparing KPI reports, and assisting with supplier qualifications and inspections.
  • The position offers a salary of £23,000 to £27,000, along with benefits such as a discretionary bonus scheme, paid holidays, and pension contributions.
  • Candidates should possess strong communication skills, attention to detail, and the ability to work independently or as part of a team.

37.5-hour Quality Administrator- Head office Based

The Company

The Cohens Group offer a friendly and trusted pharmacy service through our network of branches to local communities. We pride ourselves on customer service and offering an excellent service to everyone we work with.

Working Pattern & Location

37.5-hour Permanent contract working Monday to Friday 9am to 5.30pm, with a daily 60-minute unpaid lunch. This role is based at Head office, Lynstock Way, Lostock, Bolton, BL6 4SA.

Brief Role Description

We are seeking a highly motivated and detail-oriented Quality Administrator to join our team in the pharmaceutical wholesale industry. This role is critical to ensure ongoing compliance with current regulatory requirements. The successful candidate will support the maintenance, implementation, and continuous improvement of our quality management systems (QMS) alongside a well-established team.

Key Responsibilities

Assist in the development, implementation, and maintenance of the companys Quality Management System (QMS): raising Change Control, Complaints, Risk Assessments, Deviations and CAPA paperwork as required.

Assist in the identification, investigation, and documentation of non-conformances, deviations, and quality incidents.

Ensure all quality documentation is accurate, up-to-date, and in compliance with regulatory standards.

Maintain an organized system for document control, ensuring that documents are easily retrievable and accessible for audits and inspections.

Preparing KPI reports for Quality Department activities.

Coordinate and maintain training records in accordance with job specific functions.

Assist with the annual qualifications of suppliers and vendors to ensure compliance with regulatory standards.

Assisting with the implementation of new developments and their validation (including all documentation and testing requirements)

Monitoring licence suspension and revoke notifications, communicating to the business and promptly actioning as required.

Monitoring MHRA notifications and communicating to Management promptly and actioning as required

Monitoring Fleet & Warehouse temperature control management and ensuring required temperatures are maintained.

Assisting Quality Management with the planning, implementation and reporting of the Self Inspection Programme.

Assist in preparing for MHRA inspections and handle corrective actions and preventative measures (CAPAs).

Essential Skills and Experience

Two years experience working within a GDP environment/operation.

Proficient written and verbal communicator with a good grasp of English language.

High attention to detail with a commitment to maintaining the highest standards of quality.

Familiarity with quality management and document control systems.

Efficient IT Skills, including MS Word, Excel and Outlook.

Problem-solving skills and the ability to collaborate with cross-functional teams.

Strong planning and organisational skills to manage a busy workload.

Self-motivated with the drive to meet company deadlines, KPIs and continuous professional development.

Proactive, with the ability to work independently and as part of a team.

Desirable

Previous experience in the pharmaceutical wholesale distribution industry.

Good knowledge of warehouse management system (WMS).

Experience of setting up and maintaining controls and documentation procedures.

Previous experience working within a quality or RP department.

Able and willing to potentially grow into a wider role within the business in the future.

Pharmacy, Chemistry or Medical degree.

If successful, additional benefits for you could include:

Discretionary bonus scheme

4 weeks paid holiday, plus statutory holidays, which increase with service. (pro-rata for part time employees)

Pension contributions

Staff discount

Regulatory training where required

Onsite free car park (first come first served)

EAP Provided by BUPA

If you think this role is right for you, please apply, we would love to have you as part of the Cohens Family. We are passionate about equal opportunities and welcome a broad diversity of talent to apply.

To apply for this role please send your CV to humanresourcesdepartment @cohenschemist.co.uk or apply via total jobs.

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In order to submit this application, a TotalJobs account will be created for you. As such, in addition to applying for this job, you will be signed up to all TotalJobs’ services as part of the process. By submitting this application, you agree to TotalJobs’ Terms and Conditions and acknowledge that your personal data will be transferred to TotalJobs and processed by them in accordance with their Privacy Policy.