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Job Description
“Parkville is committed to diversity, equity, and inclusion, and all employees are expected to support these values in all aspects of their work.”
Responsibilities:
- Assist in implementing and maintaining the QMS in accordance with GMP and ISO standards.
- Contribute to the development, review, and revision of Standard Operating Procedures (SOPs) and other quality documentation.
- Support complaint investigations with related CAPA & Recall systems.
- Participate in documentation control activities.
- Perform Vendor qualification for all suppliers & service providers.
- Conduct internal training sessions on quality procedures and compliance requirements.
- Support the execution of quality audits, inspections, and assessments of facilities and processes.
- Assist in performing risk assessments and developing mitigation plans for operational activities.
- Maintain accurate records of quality activities, audits, and training sessions.
- Collaborate with cross-functional teams to ensure compliance with GMP and quality standards.
- Understand and comply with the organization's information security policies, procedures, and controls relevant to the role.
- Implement security measures and controls to protect organizational information assets.
- Ensure the confidentiality, integrity, and availability of information within the scope of work.
Job Requirements
Education :
- Bachelor’s degree in pharmaceutical sciences or Equivalent.
Experience :
- From 1 -3 years in Quality Assurance, or Operational Compliance within a regulated industry (pharmaceutical, biotech, or similar).
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