Jobs Career Advice Signup
X

Send this job to a friend

X

Did you notice an error or suspect this job is scam? Tell us.

  • Posted: Aug 17, 2020
    Deadline: Not specified
    • @gmail.com
    • @yahoo.com
    • @outlook.com
  • Never pay for any CBT, test or assessment as part of any recruitment process. When in doubt, contact us

    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...
    Read more about this company

     

    Release Pharmacist

    About

    Ensure in-process materials and finished products comply with GMP guidelines, regulation, and in-house SOPs, Determine product release for use into the marketplace, Control of documentation in compliance with regulation and company policies and procedures as well as related administrative tasks.

    Responsibilities

    Planning and Process

    • Implement and coordinate systems and procedures and make decisions within policies and procedures, or as authorised by superiors

    Product Release

    • Review batch documentation and production conditions to assess compliance to quality procedures, standards and product specifications
    • Review and approve quality of new, in-process and released batches to assess compliance to quality control programs, product specifications, and GMP guidelines
    • Approve and release production batches
    • Execute batch release priorities in line with OTIF and planning schedule
    • Ensure release requirements are met for finished products
    • Determine disposition of in-process and finished products for clinical and commercial use
    • Ensure changes/ deviations in production or quality control have been approved according to QMS
    • Initiate tests/ checks/ inspections/ sampling to mitigate any risk associated with planned changes/ deviations
    • Ensure production and QC documentation are completed in compliance with SOPs
    • Monitor and audit compliance to regulatory and in-house standards with regards to current GMP
    • Report observed deficiencies in process and follow up on corrective action
    • Investigate systematic quality problems and develop preventative plans, in conjunction with Production
    • Provide input into GMP-related training needs

    Reporting

    • Complete and consolidate standard documents
    • File, archive and retrieve documents
    • Maintain and update records and systems as required

    Requirements

    Grade: 9

    Background/experience

    • Bachelor’s degree with 2-4 years’ related work experience, or Post Graduate Degree/ Diploma with 1-3 years’ related work experience
    • Pharmaceutical manufacturing experience

    Specific job skills

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

    Competencies

    • Information Gathering
    • Interrogating Information
    • Meeting Deadlines
    • Finalising Output
    • Taking Action

    Method of Application

    Interested and qualified? Go to Aspen Pharma Group on aspen.mcidirecthire.com to apply

    Build your CV for free. Download in different templates.

  • Send your application

    View All Vacancies at Aspen Pharma Group Back To Home

Subscribe to Job Alert

 

Join our happy subscribers

 
 
Send your application through

GmailGmail YahoomailYahoomail