Regulatory Affairs Scientist (Epping) needed at Aspen Pharma Group

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Job title : Regulatory Affairs Scientist (Epping)

Job Location : Western Cape,

Deadline : November 18, 2024

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Description

  • Fine Chemicals requires the services of a highly competent Regulatory Affairs Scientist for the Regulatory Affairs Department.  To qualify for this position the most suitable candidate must fulfil the following requirements.

Requirements

JOB REQUIREMENTS:

  • Degree in Chemistry/Pharmaceutical Sciences or equivalent qualification.
  • Good knowledge of chemistry (Analytical and Organic).  Knowledge of local and international pharmaceutical regulations and guidelines would be highly advantageous.
  • Excellent written and verbal communication skills and the ability to interact well with internal and external customers.
  • Minimum of 3 years’ experience in pharmaceutical, cGMP, or chemical manufacturing environment.
  • Proven technical documentation compilation skills, with the ability to critically evaluate and interpret data.
  • MS Office computer literacy, particularly the following applications: Word, Excel, Outlook, Teams, Access and PowerPoint.  Minitab and/or EXTEDO proficiency would be advantageous.

JOB FUNCTIONS (Brief Summary)

  • Compilation and update of documents to be submitted to Regulatory Authorities.  This includes the compilation of Common Technical Documents (CTDs) in accordance with relevant guidelines and regional requirements.
  • Compilation, update and/or amendment of internal documentation relating to the testing and manufacture of Active Pharmaceutical Ingredients (APIs).
  • Responding to customer (both internal and external) and regulatory authority queries.
  • Ensuring that annual product quality reviews are compiled according to cGMP standards and adverse trends and potential process improvements identified.
  • Implementing changes according to established company procedures relating to the testing and manufacturing process.
  • Compilation and/or update of manufacturing and cleaning instructions according to internal procedures and in line with regulatory expectations.
  • Compilation of process qualification protocols and reports.
  • Ensuring that related databases are updated to allow for the capturing of API data.

PERSONAL ATTRIBUTES (Brief Summary)

  • Good interpersonal skills.
  • Good organisational and systems implementation skills.
  • Exceptional attention to detail and accuracy.
  • Good communication (written and verbal) with excellent report writing and document reviewing skills, including the ability to evaluate data critically.
  • Ability to perform tasks concurrently.

How to Apply for this Offer

Interested and Qualified candidates should Click here to Apply Now

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