Compliance Pharmacist (Port Elizabeth) at Aspen Pharma Group June, 2024

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Aspen has a proud heritage dating back more than 160 years and is committed to sustaining life and promoting healthcare through increasing access to its high quality affordable medicines and products. Aspen has a market capitalisation of approximately US$10 billion, is the largest pharmaceutical company listed on the JSE Limited (share code: APN) and rank…

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Compliance Pharmacist (Port Elizabeth)

Overview 

  • Monitor manufacturing compliance to GMP and statutory requirements
  • Monitor adherence to guidelines, procedures and document controls
  • Deliver expected value stream targets as per business requirements
  • Facility GMP compliance
  • Team and process development

Responsibilities

Staff development

  • Train new Pharmacists and PMAs on SOPs in transition period
  • Ensure pharmaceutical and supervisory team training is compliant
  • Oversee staff professional development to ensure team value add is realized
  • Facilitate training sessions as required
  • Mentorship and guidance to pharmaceutical teams

Product release management

  • Facilitate end to end product release process withing production department
  • Deviation management and adherence to daily, weekly targets
  • Raise deviations, complete forms and investigations as required and implement corrective action
  • Facilitate incident review process
  • Maintain and update records and systems as required
  • Retrieve supporting documentation and records to facilitate and support query resolution
  • Ensure deviation owner allocation and re-allocation in accordance to priorities
  • Ensure CAPA actions are implemented (deviations, CAPAs, Change controls)

Process and system improvements

  • Continuously review process impacting manufacturing and release to identify and implement optimization measures to improve efficiency and effectiveness
  • Manage, review and approve change control programs and deviations/ concessions comply to standards and specifications
  • Optimise processes and identify gaps in policies/ procedures
  • Drive CAPA investigations in area of focus
  • Implement and maintain KPIs and trackers supporting business objectives

Planning

  • Plan and prioritise own and team daily, weekly and monthly activities
  • Determine, request and use resources/ assets optimally
  • Align activities with business and customer product release priorities

Stakeholder management

  • Key interface between production and support departments with main interface being with the QA department
  • Customer interface as needed to share information, feedback on open items,  
    retrieve guidance and facilitate priorities

GMP Compliance

  • Facilitate and support audit management
  • Enforce and control area compliance (personnel, documentation, process, product)
  • Ensure production process adherence to standards and specifications
  • Enable teams and process to achieve documentation and deviation right first time targets

Requirements

Background/experience

  • BPharm Degree
  • 1-3 years’ related work experience
  • Pharmaceutical manufacturing experience

Specific job skills

  • Comprehensive knowledge of pharmaceutical manufacturing, standards and compliance requirements
  • Ability to interpret and implement policies, processes and objectives

Competencies

  • Leadership
  • Managing complex task and integration of multiple variables
  • Interrogating information
  • Meeting deadlines
  • Finalising output
  • Taking action

Method of Application

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