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24 Feb 2022

Full-Time QA Team Leader – Re advertisement

Sheila Port Elizabeth

Job Description


Interpret and implement quality procedures, standards and specifications for value streams
Manage and coordinate value stream QA activities
Coordinate and execute the review and approval of in-process quality programs
Manage and coordinate admin functions within quality systems
Performance management of direct reports
Perform activities for process compliance and product release, when required


Planning & Section Management

Provide technical and operational input on operational planning of the unit and on the prioritisation of objectives
Provide input into budget and resource requirements of section
Request and allocate assets and resources for the fulfilment of work objectives and monitor their use
Provide section staff with day-to-day direction and tasks
Run effective performance review meetings
Attend L1-2 meetings
Ensure visual performance boards are updated
Completion and monitoring of time and attendance

Product Release

Verify batch release conditions and documentation
Manage and coordinate process to determine disposition of products
Manage and coordinate batch release priorities in line with On Time In Full (OTIF) and planning schedule requirements
Perform batch release when required

Process Compliance

Issue, track and approve CAPA requests
Manage implementation of operational changes to SOPs and processes
Manage and coordinate process compliance activities to ensure that batch release is consistent with OTIF and planning schedule
Leading deviations related to country requirements

In Process Quality Management

Manage and coordinate in-process internal inspections

Governance, Risk & Compliance
Monitor implementation and correct compliance with legislation, policies and procedures

Skills Required Background/experience
Minimum of Bachelor’s degree (B Pharm)
Minimum 4-6 years’ related work experience
Pharmaceutical manufacturing experience

Specific Job Skills

Strong working knowledge of pharmaceutical manufacturing and corrective action programs
Pharmaceutical standards and compliance requirements
People management
Ability to interpret and implement policies, processes and objectives


Interrogating Information
Managing Performance
Planning and Organising
Finalising Outputs

Accountability & Decision Rights

Set overall direction for team in alignment with unit policies, objectives and OTIF and planning schedules
Manage budget(s) for teams and/ or small projects
Exercise interpersonal, communication, training and problem-solving skills to optimise team performance
Escalate highly complex problems or out-of-policy issues
Provide support to production operations to ensure quality at source, providing the necessary quality references and policies and executes problem solving and risk-based approaches to operational activities

Independent decisions relating to:

Resources, approach and tactical operations
Staff productivity and operational processes, tools and services
Establishing own and team work priorities and timelines
Interpretation of policies, standards, requirements and approaches

How to Apply

Check out this job from Aspen Pharma Group

Job Categories: WordPress. Job Types: Full-Time. Job Tags: QA Team Leader - Re advertisement.

Job expires in 82 years.

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