PRIMARY RESPONSIBILITIES
Implement and maintain the quality system at all the SGS Natural Resources Laboratories (Geochem and Affiliates) to ensure total compliance to ISO17025:2005 SGS SA high level procedures and SGS Global requirements.
SPECIFIC RESPONSIBILITIES
- Operate to the highest standard of ethics as directed by the SGS integrity policy.
- Participate in strategic planning relating to the quality function in all sections within the facility.
- Fulfill the role of Quality Manager as per ISO17025.
- Maintain documentation and standard operating procedures required to comply with laboratory ISO accreditation.
- Facilitate and monitor method validation process under the testing scope.
- Review quality control data for trends and biases. Raise IRs for nonconforming data.
- Determine control limits for standard reference materials and update Lims system.
- Facilitate external audits follow up and resolve external audit action items.
- Reviews PT results and raise IRs for nonconforming data.
- Evaluate review and monitoring reassays within the facility.
- Coordinate the database for reassays billing.
- Manage document control for the laboratory.
- Ensure Management of Change is followed for any quality system changes.
- Coordinate and administer the quality improvement systems.
- Assist with the evaluation and root cause analysis for proficiency testing data.
- Investigate customer complaints and improvement requests with assistance from Section Managers.
- Provide planned quality related training and awareness as required.
- Facilitate and plan all management reviews.
- Comply with health safety and environmental acts regulations and requirements.
- Work with a safety conscious attitude and demonstrates good and safe work habits.
- Actively participate in the Laboratory continuous improvement program (WCS).
- Apply Check status process and use the Stop Work Authority whenever the control of risks is not clearly established and understood.
- Adhere to all quality and safety requirements of the SGS management system.
- Perform any other reasonable tasks as assigned by direct line manager.
- Responsible for training on new methods and/or procedures.
- Responsible for all deadline relating to the quality system. (IRs Audit NCs and Customer Complaints)
- Required to travel
COMPLIANCE & AUTHORITY
- Contribute with scientific and technical leadership and planning to ensure the quality assurance program is effective and efficient.
- Ensure that the quality requirements are not subordinated to any prejudicial interest.
- Responsible for all SANAS matters relating to the accreditation/compliance of the organization (as per responsibilities for Nominated Representative SANAS document R03.
- Ensure that the laboratory accreditation under ISO 17025 is not jeopardized.
- Identify nonconformances with respect to the quality system and address these nonconformances in timely and unbiased approach to achieve customer satisfaction.
- Provide guidance and direction to laboratory personnel with respect to quality control and proper documentation in implementing methodologies and data reporting.
- Plan schedule and perform quality assessments (could be in the form of audits) this provide certainty towards the quality control activities. This also demonstrate that the data produced is at a defined level of precision and accuracy and in accordance with the end users requirements.
- Cease the use of any equipment that may be deemed to constitute a safety hazard or enter hazardous environments without the necessary knowledge and protection and report the situation to higher authority to act and assist with the necessary action.
- Cease to carry on with work that may affect the quality (integrity) of services and report the situation to higher authority to take action and assist with the necessary action.
- Ensure appropriate disciplinary procedures against any instances of nonconformance of any individual / section to the relevant quality protocols and management system.
- Any person has the right to refuse to perform work that may damage the environment in an imminent and serious way and to report such a situation.
- Initiate a formal improvement request when a deviation of the system occurs improvements are identified or when nonconformity is identified.
Qualifications :
Education
- BSc BTech or National Diploma in Analytical Chemistry or Science and/or proven years of laboratory knowledge skills and experience sufficient to be recognized as a qualification through Recognition of Prior Learning
- ISO or College Quality Assurance Program Diploma
- Grade 12 / Matric or N3 with Mathematics and Science as subjects
Experience
- 8 Years work experience in a testing environment
- 5 Years management system experience (ISOor other)
- Advance Microsoft software experience
- Document and report writing experience.
- Statistical Quality Control knowledge
REQUIRED SKILLS
- Selfmotivator
- Excellent problemsolving skills
- Outstanding Attention to detail
- Excellent interpersonal skills and the ability to work with a variety of personalities.
- Good verbal and communication skills
- Ability to consistently meet deadlines.
- Ability to work both independently and as part of a team.
- Superb organizational skills and concern for order
- Effective planning skills
- Ability to multitask and handle several issues simultaneously.
- Ability to maintain a positive and professional attitude when dealing with escalated issues.
Remote Work :
No
Employment Type :
Fulltime