21 hours ago
Job title : MBR Automation Specialist (Port Elizabeth)
Job Location : Eastern Cape, Port Elizabeth
Deadline : November 16, 2024
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Description
Responsibilities
Service Operations
- Request Fulfillment related to e.g., new recipe creation, updates to existing recipes withing agreed SLAs
- Incident and problem management related to MBR design
- Co-ordination of technical resources to ensure adherence to agreed Service request SLAs
- Application Management throughout entire system lifecycle
Service Design
- Design and coordination with key business stakeholders
- Compliance of IT services, processes and systems with company policies and regulatory requirements
- Alignment to architecture strategy, policies, and standards
- Ensure confidentiality, integrity, and availability of data in line with regulatory requirements and company policies.
Service Transition
- Change management, risk and impact evaluation
- Manage and execute project activities, stakeholders and report on Deliverables, Risks, Assumptions, Issues and Decisions.
- Batch Record Validation and Testing – Compiling requirements, risk assessments, specifications, and test protocols; testing and validation reporting
- Service Release as per Service Introduction procedures
- Asset and Configuration Management.
- Update Knowledge Base to improve efficiency.
Service Strategy
- Understand and anticipate customer demand through demand management processes
Continuous Service Improvement
- Regularly review services to improve quality and identify areas where processes can be improved
- Implement and monitor CSI Initiatives
Requirements
Skills Required
Background/Experience
- Pharmaceutical (B Pharm) / Engineering / IT Business Degree or diploma
- 1-3 years pharmaceutical manufacturing experience or Control & Automation, relevant IT development experience
- Extensive experience working within a Pharma Quality Management System (QMS) with automated workflows
Specific Job Skills
- Good knowledge of local registrations and regulations and of international regulations/guidelines concerning GDP/GMP
- Advanced understanding of the pharmaceutical manufacturing processes
- Pharmaceutical standards and compliance requirements
- Excellent computer/IT system skills and competencies
- Information Gathering and Interrogating information
- Offering Insights
- Endorsing Quality Standards
How to Apply for this Offer
Interested and Qualified candidates should Click here to Apply Now
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