Process Specialist (Pharmacuetical)

  South of Malta

  • Our client who specializes in the Pharmaceutical industry is looking for a Process Specialist. Your roles and responsibilities will include: 
  • Coordinating scientific and technical Pharmaceutical Technology projects (study, design, evaluate, conclude, implement, control and follow-up) and ensuring that projects are completed in time according to the pre-established time schedule.
  • Liaising with the relevant departments, as necessary, to ensure information is disseminated and coordination of activities across the site is achieved to ensure projects are completed on time.
  • ·Aiding in issuing, checking and approving all Submission, Process Optimisation, Validation and Cleaning Validation documents, in accordance with company and GMP standards
  • Coordinating with the QC, Production, and Supply Chain departments the manufacturing of the submission/ optimization and validation batches.
  • Actively assisting and following up on any investigations that might arise during manufacturing and testing of submission, optimization and validation batches.
  • Assisting in the issuing of manufacturing methods by the requirements defined within the Product Registration Dossiers and filings
  • Coordinating all aspects of manufacturing process transfers for individual products
  • Ensuring that all transfer activities are successfully concluded in time for product submission, product launch or any regulatory requirements
  • Supporting technical and scientific investigations into manufacturing and product-related issues and assisting Production and Quality with troubleshooting related to the formulation, process-related difficulties and validation issues.
  • Ensuring that appropriate process optimization is carried out when deemed necessary.

Requirements

  • At least five (5) years of experience in manufacturing or QA of solid oral doses
  • A good understanding of formulations

Education and Experience

  • A first degree in a science background or a number of years experience in a manufacturing environment in the Pharma industry or related business

Job Reference: GC330


  • Category
    Quality Assurance
  • Job type
    Full Time
  • Employment level
    Experienced (3 years +)
  • Employer industry
    Healthcare, Pharmaceuticals
  • Languages
    English, Maltese
  • Job Reference
    GC330
  • Closing Date
    30/06/2024
  • Date Published
    30/05/2024
  • Status
    Evaluating CVs

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