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Regulatory Affairs Manager

I am working with a pharmaceutical/ Medical Device manufacturing site based in Deeside specialising in challenge meals, this is a good opportunity for a experienced Regulatory Affairs Manager to develop their career with an expanding company.

Key responsibilities for the Regulatory Affairs Manager

Develop and implement regulatory strategies for FDA and MHRA submissions.Lead the preparation, submission, and lifecycle management of regulatory dossiers.Work closely with the director with FDA and MHRA, coordinating meetings, and inspection readiness.Monitor changes in global regulatory landscapes and assess impact on ongoing and future projects.Provide regulatory guidance during product development, labelling, and promotional review processes.

Requirements for the Regulatory Affairs Manager

Bachelor's degree in a scientific discipline or a related subject.Minimum 5 years' experience in regulatory affairs, with demonstrable expertise in both FDA and MHRA regulatory processes.Strong knowledge of global regulatory standardsProven success in authoring and managing regulatory submissions and renewals.Excellent communication, leadership, and project management skills.

Benefits for the Regulatory Affairs Manager

25 holidays per year + Bank HolidaysChristmas shutdown.Cycle to work schemePrivate healthcareHigh street discount scheme

To apply for the Regulatory Affairs Manager or here more information, please contact Liam Shannon at Smart4Sciences on 01925 239723 or email me at

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Smart4 Sciences are currently working with a Pharmaceutical Company in North Wales to recruit a QA Officer to join a small team responsible for all aspects of GDP and GMP compliance.

This QA Officer position is a brilliant opportunity for candidates with 1+ years GDP/GMP experience to further their career within QA with a company who can provide strong progression opportunities

Key Responsibilities

Respond to and action quality enquiries and quality management activities including deviations, change controls, risk assessments, complaints etc.Support internal and external GDP/GMP auditsAuthor, review and archive quality documentation including SOPs, PQRs, supplier agreementsEnsure GMP/GDP compliance at all times

Key Requirements

Prior GDP/GMP experience within the pharmaceutical/medical device industries is essentialPrior experience working with Pharmaceutical Quality Management Systems is essentialA pro-active, can do attitude is essential

Interviews for this QA Officer position are imminent so please apply now or contact Gareth Gooley at Smart4 Sciences for more information.

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Role: Senior QC Analyst

Salary: Circa £35,000 (Negotiable)

Monday - Friday

Location: Chester area

The role:

Carry out Analytical testing using a range of techniques such as UV, HPLC and GCCoaching/Mentoring junior members of the teamSupport management with timetabling analytical dutiesReporting any issues into Management

The candidate:

Degree in scientific disciplineUnderstanding and previous experience of working in a GMP EnvironmentExperienced in analytical techniques such as HPLC, GC, EVThe ability to lead a team

If you would like to apply for this position or require further information, please email a copy of your CV to Jack Challinor on

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Role: Senior QC Analyst

Salary: Circa £35,000 (Negotiable)

Monday - Friday

Location: Chester area

The role:

Carry out Analytical testing using a range of techniques such as UV, HPLC and GCCoaching/Mentoring junior members of the teamSupport management with timetabling analytical dutiesReporting any issues into Management

The candidate:

Degree in scientific disciplineUnderstanding and previous experience of working in a GMP EnvironmentExperienced in analytical techniques such as HPLC, GC, EVThe ability to lead a team

If you would like to apply for this position or require further information, please email a copy of your CV to Jack Challinor on

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