Quality Assurance Pharmacist

SUMMARY:
a Big Giant within the Pharmaceutical Industry is looking to employ skillful Quality Assurance Pharmacist to join their dynamic team of experts!!!!

POSITION INFO:

Overview

Position: Quality Assurance Pharmacist

Salary: Market Related

Location: Port Elizabeth

Send detailed CV in Word Document, certified copy of Id, head and shoulders photo of yourself, pay slip, plus certified Qualifications. This is to speed up your application and get the correct documentation to the Employer!!!!!!

Applicants are invited to apply for this excellent opportunity that exists for the above mentioned position. The successful incumbent will report to the QA Manager.

 We encourage all suitable employees to apply.

Overview

• Conduct in-process compliance to quality procedures, standards and specifications for value stream operations
• Review and approve quality related activities for value streams
• Identify and provide solutions to systematic issues
• Review Annual Performance Quality Review (APQR)
• Related administrative tasks

Responsibilities

Planning and Process

• Provide technical and operational input during drafting of plans and procedures specific to unit.

 Process Compliance

• Execute day-to-day QA activities for value streams
• Identify systematic technical and process issues by reviewing CAPA requests and trends
• Systematic investigation of the root causes of identified problems and risks for corrective action or prevention
• Develop CAPA plans and change incidents to address process compliance
• Implement operational changes to SOPs and processes, in compliance with control processes
• Ensure deviations (planned/ unplanned) and concessions are documented, reviewed, and analysed; and recommend validation activities to be performed
• Execute change control process by ensuring changes are documented, reviewed and approved

 Annual Performance Quality Review

• Review APQRs to assess production risks and quality of in-process control programs
• Review and analyse CAPA plans to assess impact on quality procedures and standards

 Retention Sample Management

• Store and manage retention samples as per guidelines

 In Process Quality Management

• Review and approve outcome of in-process internal inspections

 Reporting

• Monitor the storage of documents on the soft and hard copy filing systems
• Maintain and update records and systems as required
• Provide information for reports on weekly/monthly basis, as required by superior
• Compile standardised reports and consolidate documents

 Skills Required

 Background/experience

• Bachelor’s degree (B Pharm) with 4-6 years’ related work experience experience
• 2 – 4 years Pharmaceutical manufacturing experience

Specific job skills

• Advanced understanding of the 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
• Offering Insights
• Taking Action

NB! This job is now closed. You can apply for other jobs by uploading your CV.