Description:
ENVIRONMENT:
Our client, established in 1987 within the realm of biotechnology, has consistently focused on crafting implant devices that adhere to rigorous standards of quality and biocompatibility. They are presently in search of a QA and Regulatory Officer tasked with drafting validation protocols and reports encompassing process, packaging, sterilization, and equipment validations (as relevant). Applicants should possess a tertiary degree in natural sciences or engineering, along with a minimum of two years of experience.
DUTIES:
- Writing validation protocols and reports. This will Include but is not limited to: Process, Packaging, sterilization and equipment validations (Equipment qualification as applicable).
- Document control of all documents used in implementing and maintaining the quality management system.
- Perform Quality review of documentation (Procedures and related forms and records).
- Facilitating the effective and appropriate close out of Nonconformances, by
- Liaising with the appropriate departments to ensure actions and corrective actions are taken to address the root cause.
- Ensuring the process has been documented and supporting evidence has been included.
- Where applicable, facilitate the process risk management procedure and ensure appropriate preventative actions are taken and all activities are documented.
- Facilitate Departmental internal audits
- Assisting with the facilitation of all third-party audits as directed by the department manager
- Assisting with the facilitation of supplier audits as directed by the department manager
- Identify areas to improve the QMS and facilitate required action.
- Offering Regulatory support to departments related to product development including, where needed, assisting in the writing or reviewing of technical documentation and clinical evaluations.
- Provide and facilitate training to staff for quality related processes and procedures.
- To support day-to-day activities associated with maintaining QMS compliance
REQUIREMENTS:
- Required minimum education: Tertiary degree required in the natural sciences or engineering
- Required minimum experience: 2 years
- Good understanding of statistics
- Computer literate: Microsoft Office
- ATTRIBUTES:
- Good communication skills – writing, presentation and interpersonal communication (Good writing skills a fundamental requirement).
- High ethical standards
While we would really like to respond to every application, should you not be contacted for this position within 10 working days please consider your application unsuccessful.
COMMENTS:
When applying for jobs, ensure that you have the minimum job requirements. Only SA Citizens will be considered for this role. If you are not in the mentioned location of any of the jobs, please note your relocation plans in all applications for jobs and correspondence. Apply here https://www.datafin.com/job/qa-and-regulatory-officer/
OR e-mail a Word copy of your CV to wendy@datafin.com and mention the reference number of the job.
Requirements:
- Writing validation protocols and reports. This will Include but is not limited to: Process, Packaging, sterilization and equipment validations (Equipment qualification as applicable).
- Document control of all documents used in implementing and maintaining the quality management system.
- Perform Quality review of documentation (Procedures and related forms and records).
- Facilitating the effective and appropriate close out of Nonconformances, by
- Liaising with the appropriate departments to ensure actions and corrective actions are taken to address the root cause.
- Ensuring the process has been documented and supporting evidence has been included.
- Where applicable, facilitate the process risk management procedure and ensure appropriate preventative actions are taken and all activities are documented.
- Facilitate Departmental internal audits
- Assisting with the facilitation of all third-party audits as directed by the department manager
- Assisting with the facilitation of supplier audits as directed by the department manager
- Identify areas to improve the QMS and facilitate required action.
- Offering Regulatory support to departments related to product development including, where needed, assisting in the writing or reviewing of technical documentation and clinical evaluations.
- Provide and facilitate training to staff for quality related processes and procedures.
- To support day-to-day activities associated with maintaining QMS compliance
- Required minimum education: Tertiary degree required in the natural sciences or engineering
- Required minimum experience: 2 years
- Good understanding of statistics
- Computer literate: Microsoft Office
- ATTRIBUTES:
- Good communication skills – writing, presentation and interpersonal communication (Good writing skills a fundamental requirement).
- High ethical standards