QA Compliance Manager

Hobson Prior; Worthing; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player seeks a dedicated QA Compliance Manager to uphold high standards in quality management and data integrity. This role is pivotal in ensuring IT systems critical to GxP operations comply with regulations. You will lead compliance efforts, support adherence to manufacturing regulations, and collaborate closely with IT teams. If you are passionate about quality and precision, this opportunity offers a chance to make a significant impact within a supportive team environment. Join us in delivering exceptional quality in the life sciences sector.

Qualifications

• Experience in pharmaceuticals or biotechnology required.
• Strong knowledge of IT compliance and GxP systems.

Responsibilities

• Ensure IT systems meet GxP compliance standards.
• Oversee system validation and compliance processes.
• Collaborate with IT teams to maintain compliance.

Skills

GxP compliance

Data integrity

System validation

Communication skills

Stakeholder management

Word and Excel proficiency

Detail-oriented

Job description

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Consultant - Engineering at Hobson Prior

Are you passionate about quality and precision? Join the team as QA Compliance Manager and help ensure top-tier standards every day.

Hobson Prior is seeking a QA Compliance Manager for a 12 month Fixed Term Contract. This role will lead and ensure that IT systems critical to GxP operations comply with regulations. You will be part of a supportive team focused on maintaining high standards in quality management and data integrity.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Ensure IT systems meet GxP compliance standards.
• Support adherence to manufacturing and data integrity regulations.
• Oversee system validation and compliance processes.
• Review and manage changes to IT systems.
• Provide guidance on data integrity and quality systems.
• Collaborate with IT teams to maintain compliance.
• Stay updated on industry regulations and best practices.

Key Skills and Requirements:

• Previous experience within pharmaceuticals or biotechnology companies
• Must have previous experience in data integrity and system validation.
• Knowledge of IT compliance and GxP systems.
• Strong communication and stakeholder management skills.
• Proficient in using Word and Excel for data analysis.
• Detail-oriented with excellent report writing skills.
• Ability to be onsite in Worthing for 3 days a week

For more information, please contact Will Hay.

Apply now

If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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