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Compliance Specialist at Haleon
Haleon
September 21, 2026
Full-time
On-site
About the role
The responsibility of the Compliance Specialist is to support compliance activities in Auditing, Inspection Readiness, Change Control, CAPA management, Risk Management, Training & PLM oversight.
Key responsibilities
Review and assess change controls for quality impact and ensure changes are implemented in compliance with regulatory and Haleon standards.
Coordinate CAPA management through oversight of timely CAPA closures ensuring adequate supporting evidence is provided, and effectiveness checks are undertaken.
Coordinate the site internal audit program and ensure timely monitoring and closure of audits as per the annual audit schedule.
Support risk assessments across quality systems and operations aligned with HQS, regulatory requirements, ICH and ISO standards.
Support site training program and ensure timely monitoring and completion of monthly training requirements for the site.
Support in audit readiness assessments and preparations.
Coordinate site problem solving program.
Oversight product lifecycle management activities including specification updates and change tracking.
Monitor and update monthly KPI status for site compliance activities.
Stand in as a backup for Quality Systems & Compliance Lead and Data Integrity Lead.
Responsibilities of the role can be delegated to the Data Integrity Lead supported by appropriate training and competence.
Qualifications and skills
Essential
Bachelor's degree in chemistry, Pharmacy, Microbiology, Chemical Engineering, Biochemistry, Social or Physical Sciences
3-5 years in a pharmaceutical or consumer healthcare manufacturing environment with direct exposure to GMP compliance activities
Preferred
Strong knowledge of GMP, quality systems and regulatory compliance requirements.
Previous experience working in an analytical lab or production.
Excellent analytical and interpersonal and facilitation skills
Ability to influence without authority and communicate to all levels of team structure to enable and drive change.
Analytical mindset with attention to detail and accuracy in documentation.
Organizational, planning and prioritization skills.
Good verbal and written communication skills.
Result-oriented.
High level of integrity, accountability and commitment to fostering a quality-driven culture.
Ability to balance regulatory compliance with business objectives while mitigating risks.
The responsibility of the Compliance Specialist is to support compliance activities in Auditing, Inspection Readiness, Change Control, CAPA management, Risk Management, Training & PLM oversight.
Key responsibilities
Review and assess change controls for quality impact and ensure changes are implemented in compliance with regulatory and Haleon standards.
Coordinate CAPA management through oversight of timely CAPA closures ensuring adequate supporting evidence is provided, and effectiveness checks are undertaken.
Coordinate the site internal audit program and ensure timely monitoring and closure of audits as per the annual audit schedule.
Support risk assessments across quality systems and operations aligned with HQS, regulatory requirements, ICH and ISO standards.
Support site training program and ensure timely monitoring and completion of monthly training requirements for the site.
Support in audit readiness assessments and preparations.
Coordinate site problem solving program.
Oversight product lifecycle management activities including specification updates and change tracking.
Monitor and update monthly KPI status for site compliance activities.
Stand in as a backup for Quality Systems & Compliance Lead and Data Integrity Lead.
Responsibilities of the role can be delegated to the Data Integrity Lead supported by appropriate training and competence.
Qualifications and skills
Essential
Bachelor's degree in chemistry, Pharmacy, Microbiology, Chemical Engineering, Biochemistry, Social or Physical Sciences
3-5 years in a pharmaceutical or consumer healthcare manufacturing environment with direct exposure to GMP compliance activities
Preferred
Strong knowledge of GMP, quality systems and regulatory compliance requirements.
Previous experience working in an analytical lab or production.
Excellent analytical and interpersonal and facilitation skills
Ability to influence without authority and communicate to all levels of team structure to enable and drive change.
Analytical mindset with attention to detail and accuracy in documentation.
Organizational, planning and prioritization skills.
Good verbal and written communication skills.
Result-oriented.
High level of integrity, accountability and commitment to fostering a quality-driven culture.
Ability to balance regulatory compliance with business objectives while mitigating risks.