Compliance Specialist
AI summary
Haleon is hiring a Compliance Specialist in Nairobi to support quality and regulatory compliance activities including auditing, CAPA management, change control, risk management, and training oversight. The role requires a relevant science or engineering degree and 3-5 years of GMP compliance experience in pharmaceutical or consumer healthcare manufacturing.
- Support auditing, inspection readiness, change control, CAPA, risk management, and training oversight
- Coordinate internal audit program and ensure timely closure per annual schedule
- Require Bachelor's degree in science/engineering and 3-5 years GMP manufacturing experience
- Stand in as backup for Quality Systems & Compliance Lead and Data Integrity Lead
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- Required3+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in internship, compliance specialist, quality assuranceThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in NairobiThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Compliance Specialist evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Haleon and the role in Nairobi.
- Add concrete examples related to internship, compliance specialist, quality assurance, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from JobWeb Kenya; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- JobWeb Kenya
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Compliance Specialist role in internship, compliance specialist?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Nairobi under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Haleon before the interview.
Ask what the first priorities will be in the role and how success will be measured.
Similar jobs to consider
Use AI to apply better
After confirming the original source, use Career Assistant to check role fit, tailor your CV and prepare a cover letter or employer message.
Original source description
- 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
- of the role can be delegated to the Data Integrity Lead supported by appropriate training and competence.
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.
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 Qualifications
- 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.
