QC Team Leader (East London)

Aspen Pharma Group
East London
ZAR 300 000 - 600 000
Job description

Job title: QC Team Leader (East London)

Job Location: Eastern Cape, East London

Deadline: April 13, 2025

Description

Overview

  • Manage and co-ordinate lab preparation and QC activities.
  • Manage and co-ordinate sampling and testing of external environment.
  • Provide analytical, maintenance and QC lab support.
  • Ensure continuous compliance of lab with GMP standards.
  • Ensure that products are produced, tested, and stored according to the required SOPs and documentation.
  • Performance management of direct reports.

Responsibilities

Planning and Section Management

  • Provide input into operational planning of section, and prioritisation of objectives.
  • Provide input into, interpret, and execute policies and procedures.
  • Provide input into and manage budgets and resource requirements for section.
  • Provide section staff with day-to-day direction and tasks.
  • Manage and monitor compliance of QC lab testing activities to GMP, quality standards and product specifications.
  • Manage and co-ordinate lab preparation activities according to SOPs (samples, working area(s), PPE, and lab equipment).
  • Prepare and implement maintenance and calibration schedules and records.
  • Ensure set priorities and targets are achieved, identifying constraints and solutions.
  • Investigate and report Out of Specifications (OOS).
  • Manage and co-ordinate sampling and testing of external environmental, according to SOPs and sampling plan/schedule.

Lab Quality Reviews & Training

  • Review and approve corrections in batch documentation.
  • Identify and coordinate training of staff on SOPs.

Deviations Investigations

  • Manage and coordinate deviation investigations and reporting.
  • Coordinate and initiate risk/impact assessments and plans to address quality deficiencies.
  • Manage implementation of operational changes to SOPs and processes.

Governance, Risk and Compliance

  • Provide input to QC for improvement of risk-based compliance systems.
  • Monitor implementation and ensure own and team compliance with legislation, policies, and procedures.

Requirements

Skills Required

  • Bachelor’s degree in chemistry/microbiology with 5 years of related experience.
  • Laboratory and Good Laboratory Practice experience.
  • Supervisory experience.
  • Advanced understanding of pharmaceutical testing methods.
  • Knowledge of value chain and MCC principles.
  • Understanding of pharmaceutical manufacturing and corrective action programs.
  • Pharmaceutical standards and compliance requirements.
  • Ability to interpret and implement policies, processes, and objectives.
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