What Data Warehousing Jobs are in Gauteng?
Showing 50 Data Warehousing jobs in Gauteng
Job Description
Our client is looking for Logistics Supervisor for each of these regions: KZN, Cape Town, East London, Polokwane and Johannesburg
THE ROLE:
A Logistics Supervisor is responsible for assisting and supporting the Logistics Manager. This includes the management and administration of the company’s fleet and the departments associated functions. The role involves supervising the implemented strategies for the movement of goods, inventory control, and coordination of transportation and distribution.
KEY RESPONSIBILITIES:
1. Drive the company's values and leadership principles, ensuring alignment across the business.
2. Manage drivers, assistants, and forklift drivers, coordinating shift rosters and addressing personnel shortages.
3. Conducting monthly inspections on driver certifications
4. Supervise daytime loading tasks and handle the submission of insurance-related documents.
5. Manage vehicle and forklift inspection sheets, maintenance registers, and fuel authorization for forklifts.
6. Coordinate all fleet maintenance and repair work with service providers after manager approval.
7. Build and maintain a high-performance team, ensuring the enforcement of the company's disciplinary code. Conduct performance appraisals and CDPs for department members above GW level.
8. Manage clock-in reports, investigate transgressions, and handle first approvals of leave within the department.
9. Enforce uniform policies for all drivers and conductors, ensuring full compliance.
10. Ensure timeous deliveries and rectify shortfalls and damages.
11. Maintain excellent communication standards and customer service with stores, responding to queries swiftly.
12. Ensure adherence to all Logistics SOPs, providing necessary training where required and maintaining training registers.
13. Provide after-hours assistance for truck breakdowns, coordinating with mechanics and tow trucks to protect the fleet and stock.
14. Manage Lug Recon processes and associated tasks efficiently.
15. Directly manage the Logistics Administrator and Fleet Controller, overseeing associated tasks and KPIs.
16. Compile the Daily Delivery Schedule, gaining final approval from the Logistics Manager.
QUALIFICATIONS & EXPERIENCE REQUIRED:
- Bachelor’s degree in Logistics, Supply Chain Management, or related field
- At least 5 years of prior experience in a supervisory role in logistics or related field
- Knowledge of, receiving, distribution processes and procedures
- Fleet supervision and maintenance experience
- Effective communication: Communicate clearly and openly with team members, superiors, suppliers, and other departments to ensure smooth information flow and effective problem-solving.
- Problem-Solving: Identify and address challenges, obstacles, and inefficiencies in distribution centre operations to maintain smooth functioning.
- Team Management: Supervise, mentor, and guide logistics staff, including task delegation, performance evaluations, and skills development.
- Conflict Resolution: Address and resolve conflicts or issues within the distribution centre team, promoting a harmonious work environment.
- Key Performance Areas: Consumption, Invoicing, Variable Cost, On Time Dispatches, OTIF (On Time in Full)
TECHINICAL EXPERIENCE:
- Supply Chain Experience
- Inventory Maintenance
- Transportation Management
- Distribution Management
- Organisational and time management skills
- Strong verbal and written skills
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0
Job Description
Key Responsibilities:
Apply now!
Data Leadership & Delivery:
- Lead the design, development, and optimisation of data platforms, pipelines, and models.
- Translate business requirements into scalable, high-quality data solutions.
- Provide technical leadership and best practice guidance across the data function.
- Design and implement data architectures, integration layers, APIs, and data marts.
- Ensure efficient data ingestion, transformation, and integration across systems.
- Drive platform scalability, performance, and continuous improvement.
- Establish and maintain data quality, monitoring, and validation processes.
- Ensure the accuracy, reliability, and availability of critical data assets.
- Implement data governance standards and ensure compliance with POPIA, PAIA, and internal policies.
- Relevant Degree in Data Engineering, Computer Science, Business
- 10 - 15 + years experience in data-related
- 5 years in Data Management
- Experience in platforms, engineering and architecture
- Understanding end-to-end data lifecycle management, including retention, archiving and deletion aligned to legal and business requirements
- Strong understanding of modern data architecture, data platforms and integration patterns (ETL, APIs) across on-prem and cloud environments
Apply now!
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1
Job Description
**IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.**
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Is this job a match or a miss?
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2
Job Description
**Base level role**
+ Perform comprehensive data management tasks including data review, query generation and query resolution.This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc.Data Management tasks should be inclusive of Study Start-up, Execution, Database Lock and Close-out.
+ Perform ongoing Data Reconciliation of all data streams
+ Attend study related meetings/teleconferences
+ Perform Study Closeout/Archiving Activities including QC of subject/site Archival CRFs
+ Create and provide status/metric reports
+ Generate reports on EDC and track cleaning progress
+ Manage Freeze / lock of eCRF
+ File documentation in the virtual Trial Master File (TMF)
+ Receives and enters lab normal ranges
Education and Experience Guidelines:
+ Bachelor's degree in a Health or Science discipline with experience in clinical research.
+ Data Management experience and experience working on a clinical trial mandatory.
+ Rave experience mandatory
+ Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
+ Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
+ Knowledge of technology platforms and systems to capture and process data
+ Project management skills.
+ Vendor management skills.
+ Proficiency with Microsoft Office tools
+ Experience CDA BASE level: 1-3 years of experience in Data Management at a CRO/Pharma
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
+ Perform comprehensive data management tasks including data review, query generation and query resolution.This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc.Data Management tasks should be inclusive of Study Start-up, Execution, Database Lock and Close-out.
+ Perform ongoing Data Reconciliation of all data streams
+ Attend study related meetings/teleconferences
+ Perform Study Closeout/Archiving Activities including QC of subject/site Archival CRFs
+ Create and provide status/metric reports
+ Generate reports on EDC and track cleaning progress
+ Manage Freeze / lock of eCRF
+ File documentation in the virtual Trial Master File (TMF)
+ Receives and enters lab normal ranges
Education and Experience Guidelines:
+ Bachelor's degree in a Health or Science discipline with experience in clinical research.
+ Data Management experience and experience working on a clinical trial mandatory.
+ Rave experience mandatory
+ Experience working in highly diverse teams within clinical research; cross-functional, global, multi- regional.
+ Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA.
+ Knowledge of technology platforms and systems to capture and process data
+ Project management skills.
+ Vendor management skills.
+ Proficiency with Microsoft Office tools
+ Experience CDA BASE level: 1-3 years of experience in Data Management at a CRO/Pharma
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Is this job a match or a miss?
Apply Now
3
Job Description
**IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models.**
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
**Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams - allowing us to match you with the best-fit project and client environment for your experience and interests!**
IQVIA is seeking experienced Clinical Data Management Leads to oversee end-to-end data management delivery for global clinical trials. You'll ensure quality, accuracy, and compliance while leading cross-functional teams that help bring new therapies to life. _This is a remote/WFH position with all necessary equipment provided._
**What You'll Do**
+ Lead data management for complex, global clinical trials from study setup to database lock.
+ Serve as the main client contact for all data management deliverables.
+ Oversee SAE, PK, and external data reconciliation and database deployment.
+ Manage timelines, budgets, and resource allocation to meet customer expectations.
+ Mentor junior data management staff and promote best practices.
+ Drive process improvements and ensure regulatory and SOP compliance.
**Who We're Looking For**
Ideal candidates will have.
+ Bachelor's degree in life sciences, health, clinical, biological, or mathematical field.
+ No less than 10 years of direct clinical data management experience, with 5+ years in a Lead Clinical Data Management role.
+ Your previous roles/job titles may include _Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager_ .
+ Proven success managing large global studies (1000+ patients).
+ Expertise with Medidata Rave, Oracle InForm, or similar EDC systems.
+ Strong understanding of GCP, ICH, and clinical research processes.
+ Excellent communication and leadership skills.
**What IQVIA Offers**
+ Fully remote role - company equipment provided
+ Competitive salary and performance-based incentives
+ Career growth and learning opportunities through mentoring and internal mobility
+ Inclusive, global culture focused on innovation and collaboration
**What to Expect After Applying**
+ Recruiter video chat (20 min)
+ Hiring manager interview (1 hour, MS Teams - Offer decisions are typically made within one or two weeks of the final interview.)
**Apply now to join IQVIA, where your expertise shapes the future of data-driven healthcare!**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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4
Job Description
- Grade 12 essential
- 5 Years working experience in a warehouse of which 1 year in a supervisory capacity
- MS Office
- Experience on SAP Erp system
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5
Job Description
At Omega HR Solutions, we believe that a motivated and cohesive team creates the foundation for excellent service. We are proud to support a well-established logistics company in Gauteng that values leadership, process efficiency, and continuous improvement. If you’re an experienced transportation professional with a passion for leading teams and optimizing operations, this is your chance to thrive in a dynamic environment.
Join a company where your expertise in transportation and logistics will directly impact daily operations and customer satisfaction. You will be part of a team that values innovation, teamwork, and professional growth.
Duties:
Build and streamline transportation processes to ensure smooth daily operations
Lead and manage the branch transportation team, ensuring effective delivery of customer orders
Train and empower staff to maintain high service standards
Analyze logistics efficiency and costs, identifying areas for ongoing improvement
Control budgets, optimize resources, and work to reduce transportation expenses
Requirements:
Bachelor’s degree or higher
Minimum of 5 years experience in transportation or logistics management
Proven leadership and team management skills
Fluency in Mandarin and understanding of Chinese business culture will be an advantage.
Strong ability to meet deadlines and manage budgets
Proficiency in process optimization
Ability to work effectively in a fast-paced environment
Familiarity with the following:
Logistics and supply chain industry best practices
Cost management and process improvement strategies
What We'll Give You:
A full-time, on-site role with a reputable employer
Opportunities to make a meaningful impact through process improvement and team leadership
A collaborative environment that values your skills and experience
Competitive salary aligned with your expertise
If you are ready to lead and innovate within a respected logistics organization, we would love to hear from you. Take the next step in your career and apply today to be part of a team that values dedication and excellence.
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6
Job Description
Key Responsibilities
- Supervise all inbound and outbound logistics activities.
- Manage material flow to production lines, ensuring uninterrupted supply.
- Lead warehouse, dispatch, receiving and line-feeding teams.
- Monitor inventory accuracy through cycle counts and stock control.
- Coordinate deliveries with customers, suppliers and transport providers.
- Ensure compliance with FIFO, JIT and Kanban principles.
- Drive continuous improvement in logistics processes, safety and cost reduction.
- Maintain 5S and housekeeping standards within the logistics area.
- Monitor logistics KPIs including inventory accuracy, delivery performance and stock variances.
- Ensure compliance with customer, quality, safety and company requirements.
- Grade 12 (Matric).
- Diploma or Degree in Logistics, Supply Chain, Warehousing or related field advantageous.
- 3 to 5 years supervisory experience in an automotive manufacturing environment.
- Sound knowledge of JIT, FIFO, Kanban, SAP/ERP systems and warehouse management.
- Strong leadership, planning and problem-solving skills.
- Computer literate (MS Office and ERP systems).
- Valid driver'''s licence.
- Experience with OEM customer requirements in the Automotive Industry Essential.
- Knowledge of IATF 16949 and ISO 14001.
- Lean Manufacturing and Continuous Improvement experience.
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7
Job Description
**Company Description**
**AECOM** is seeking a **Senior Technologist - Architecture (DATA Centres)** to be based in South Africa's Enterprise Capabilities office in **Centurion** . This position will support a team locally based in South Africa and Global Teams. As a part of AECOM's culture, it offers a flexible hybrid work arrangement which accommodates both office and out-of-office work schedules.
**About Enterprise Capabilities**
Fundamental to our _Think and Act Globally_ strategy and digital adoption, Enterprise Capabilities (EC) is AECOM's primary vehicle for workshare. Operating across geographic boundaries and time-zones, EC partners with regional and Global Business Line project teams to provide technical expertise, accelerate delivery and keep AECOM competitive in the industry.
With a team of over 3000 technical professionals located across nine countries and remote technical anchors, EC teams are trusted to deliver high-quality, specialist services that help to fill capability gaps, resourcing needs and technical constraints on projects of all scopes and sizes.
**Start here. Grow here.**
**Job Description**
The Senior Technologist serves as a capable professional in an architectural design team, leading work on specific elements of a project with minimal direction and supervision of a Senior Architect or designated senior team members.
**Here is what you will be doing:**
+ Architectural Design
+ BIM Model and Drawing production (Design Brief compliance, completeness & accuracy)
+ Design co-ordination (within Architecture & Cross Discipline)
+ Performing basic architectural/engineering calculations.
+ Preparing specifications, reports and related data tables.
+ Maintaining liaison with design and drafting groups.
+ Preparing, reviewing, and approving drawings as required.
+ Under some supervision, may complete design assignments of moderate to high complexity.
+ Limited familiarity with codes, permits, and software applications related to the discipline.
+ Introduced to the process of preparing designs and drawings using project specifications and discipline-associated written and verbal instructions in accordance with established design practices, standards and procedures.
+ Intermediate to advanced understanding of the purpose and use of vendor documents.
+ Introduced to the process of performing material take-offs for the discipline.
**Qualifications**
+ Degree in Architectural Technology (BTech) from an accredited University
+ 8 years experience within the built environment
+ Registered as a Professional Architectural Technologist (SACAP)
**Additional Information**
**At AECOM, you will have freedom to grow in a world of opportunity**
_At AECOM, our Freedom to Grow philosophy supports flexibility and balance to help our people thrive. As part of this approach, we ask all hybrid employees to work from an AECOM office at least three days per week._
**ReqID:** J
**Business Line:** Architecture
**Business Group:** DCS
**Strategic Business Unit:** Enterprise Capabilities
**Career Area:** Design
**Work Location Model:** Hybrid
**AECOM** is seeking a **Senior Technologist - Architecture (DATA Centres)** to be based in South Africa's Enterprise Capabilities office in **Centurion** . This position will support a team locally based in South Africa and Global Teams. As a part of AECOM's culture, it offers a flexible hybrid work arrangement which accommodates both office and out-of-office work schedules.
**About Enterprise Capabilities**
Fundamental to our _Think and Act Globally_ strategy and digital adoption, Enterprise Capabilities (EC) is AECOM's primary vehicle for workshare. Operating across geographic boundaries and time-zones, EC partners with regional and Global Business Line project teams to provide technical expertise, accelerate delivery and keep AECOM competitive in the industry.
With a team of over 3000 technical professionals located across nine countries and remote technical anchors, EC teams are trusted to deliver high-quality, specialist services that help to fill capability gaps, resourcing needs and technical constraints on projects of all scopes and sizes.
**Start here. Grow here.**
**Job Description**
The Senior Technologist serves as a capable professional in an architectural design team, leading work on specific elements of a project with minimal direction and supervision of a Senior Architect or designated senior team members.
**Here is what you will be doing:**
+ Architectural Design
+ BIM Model and Drawing production (Design Brief compliance, completeness & accuracy)
+ Design co-ordination (within Architecture & Cross Discipline)
+ Performing basic architectural/engineering calculations.
+ Preparing specifications, reports and related data tables.
+ Maintaining liaison with design and drafting groups.
+ Preparing, reviewing, and approving drawings as required.
+ Under some supervision, may complete design assignments of moderate to high complexity.
+ Limited familiarity with codes, permits, and software applications related to the discipline.
+ Introduced to the process of preparing designs and drawings using project specifications and discipline-associated written and verbal instructions in accordance with established design practices, standards and procedures.
+ Intermediate to advanced understanding of the purpose and use of vendor documents.
+ Introduced to the process of performing material take-offs for the discipline.
**Qualifications**
+ Degree in Architectural Technology (BTech) from an accredited University
+ 8 years experience within the built environment
+ Registered as a Professional Architectural Technologist (SACAP)
**Additional Information**
**At AECOM, you will have freedom to grow in a world of opportunity**
_At AECOM, our Freedom to Grow philosophy supports flexibility and balance to help our people thrive. As part of this approach, we ask all hybrid employees to work from an AECOM office at least three days per week._
**ReqID:** J
**Business Line:** Architecture
**Business Group:** DCS
**Strategic Business Unit:** Enterprise Capabilities
**Career Area:** Design
**Work Location Model:** Hybrid
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8