In 1976, 9 independent trucking companies and a business developer joined forces and founded DSV in Denmark. Since then, DSV has evolved to become the world’s 5th largest supplier of global solutions within transport and logistics. Today, we add value to our customers’ entire supply chain by transporting, storing, packaging, re-packaging, processing and ...
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2-3 years’ experience and demonstrable working knowledge of DSV CargoWRITE / RECAP / CAPA (or relevant industry related software)
Proficient in Excel for data management and reporting
Job-related Requirements
Min 2 – 3 years relevant supervisory experience:
2 - 3 years’ experience in Health product identification and compliant storage segregation by resultant UN Code and/or MSDS category
2 - 3 years’ experience in Consumer and/or Retail product;
2 - 3 years’ experience in Specialized packaging for Consumer and/or Retail;
High value product requiring specialized processes and storage arrangements;
Value added services such as promotional bundling, kitting and re-labeling;
Operations: Demonstrable knowledge and hands on skill related to Inbound, Stock Management, Outbound / Order Fulfilment, Return processes, effective packaging, excellent facility housekeeping (5S) and batch / serial number and expiry control;
Problem Solving: Effective Root Cause Analysis, Problem Solving and implementation of Corrective and Preventative Measures;
Communication: Must communicate effectively (written and verbal) to manage and meet both internal and external customer expectations;
Compliance: Must ensure site compliance, including the following: DSV Policies, Regulations, Work Instructions, Maintenance Schedule and Local Authority requirements to give purpose and effect to adopted management system – QSHE / PharmaQMS and similar;
SHERQ and PharmaQMS: Internal measurement and auditing of all site processes to ensure stability and improvement in areas of Health and safety, environment and facility compliance/risk mitigation. Knowledge and experience of QMS such as ISO 9001, 14001, and 45001.
Revise & draft new work instructions / SOP or flow chart and ensure compliance thereto.
Ability to work extended hours and over weekends when required
Assertive & sound negotiator
Be prepared to travel and possibly move to Gauteng
Presentation Skills
Knowledge of various continuous improvement methodologies (Lean, Six Sigma, Theory of Constraints)
Added Advantages
Prepare and implement necessary policies, procedures and codes of practice;
Ability to demonstrate a proactive approach and continuously develop & improve quality, and other related obligations; and
An understanding of pharmaceutical production, whether large- or small-scale; and
An understanding of quality assurance and audit processes in relation to the pharmaceutical industry and associated quality management systems
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