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  • Posted: Feb 23, 2026
    Deadline: Not specified
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  • Adcock Ingram is a leading South African pharmaceutical company with a proud 130 year heritage. It has a portfolio of trusted, quality brands and generics and an entrenched value system that assures integrity. Growing from humble beginnings as a small Krugersdorp pharmacy in 1890, Adcock’s portfolio includes an extensive range of Prescription, Over-the-co...
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    Business Unit Manager – LVP, C& D and Nutrition

    Key Job Outputs:

    Strategic and Commercial Leadership

    • Develop and execute business strategies for the LVP, Consumables, Devices and Nutrition portfolio to maximise revenue and profitability.
    • Take full accountability for P&L, pricing, forecasts, and resource allocation.
    • Conduct portfolio analysis and identify new product or acquisition opportunities.

    Marketing and Brand Management

    • Design and implement marketing strategies and campaigns to strengthen brand positioning and market leadership.
    • Drive successful product launches, promotions, and lifecycle management.
    • Monitor market trends and adapt strategies to remain competitive and compliant.
    • Identify and implement value-adding services and solutions beyond core product sales to strengthen long-term partnerships and embed the business as a trusted partner. (e.g Mywalk)

    Tender and Contract Management

    • Support tender activities including pricing, submissions, and negotiations with state and private customers where required.
    • Ensure accurate forecasting and stock planning aligned to tender commitments.
    • Maintain strong relationships with procurement bodies to secure business continuity.
    • Monitor competitor tender activity and adjust strategies accordingly.

    Sales and Customer Engagement

    • Partner with the sales team to deliver sales growth through effective planning, training, and customer engagement.
    • Cultivate strong relationships with hospitals, procurement bodies, distributors, and KOLs.
    • Develop customer proposals and presentations to secure tenders and business opportunities.

    Consumables and Devices Management

    • Lead commercial activities for infusion systems, consumables, and related medical devices.
    • Oversee device roll-out projects, ensuring timely execution, training, and support.
    • Collaborate with technical and regulatory teams to ensure compliance and safe product integration.

    Operational and Financial Management

    • Manage budgets, stock, and supply chain planning to avoid shortages or wastage.
    • Analyse competitor and market share data to inform strategic decisions.
    • Ensure compliance with ROI expectations and financial governance.

    Team Leadership and Development

    • Lead, mentor, and develop cross-functional teams (marketing, sales, key accounts).
    • Promote a culture of innovation, collaboration, and accountability.
    • Drive performance management, succession planning, and talent development.

    Governance and Compliance

    • Ensure all promotional, sales, and marketing activities comply with industry regulations and company SOPs.
    • Maintain readiness for audits and address corrective actions where required.

    Requirements

    Job Requirements:

    • Bachelor of Science in Nursing, Pharmacy, or Life Sciences, or equivalent qualification (preferred).
    • Commercial or Business Degree (advantageous).
    • Sales and Marketing Diploma or equivalent certification.
    • Minimum 8–10 years’ experience in the pharmaceutical and/or medical devices industry.
    • At least 5 years in a senior managerial role with direct P&L accountability.
    • Strong track record in sales and marketing, particularly within Large Volume Parenterals (LVPs) and infusion/medical device portfolios.
    • Experience in product lifecycle management, new product launches, and business development.
    • Demonstrated ability to manage cross-functionally (sales, marketing, and key accounts).

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    Contract Worker: Operator (Viaflex Filling)

    Job Outputs

    • Perform pouching of units on the line.
    • Conduct filling of products.
    • Able to understand process of printing of bags.
    • Assist in loading and sealing of units.
    • Follow SOP process for Products.
    • Follow correct GMP and gowning process
    • Inspect units for missing parts/illegible print and fill volumes
    • Remove defective units and over pouches.
    • Assist in material handling activities.
    • Assist in other departmental needs on a daily basis.
    • Perform cleaning activities in the department as required per SOP.

    Requirements

    • Grade 12 or equivalent
    • 1 to 2 years’ working experience.
    • Experience in pharmaceutical industry – advantageous

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    Industrial Engineering Graduate Programme *2

    Closing Date is 27 February 2026

    Requirements

    Required Learning:

    • BEng in Industrial Engineering /BSc in Supply Chain Management Degree
    • Project Management/Controller certificate and experience will serve as added advantage 
    • NSFAS funding will serve as added advantage
    • PLEASE ATTACH PROOF OF NSFAS FUNDING WITH YOUR CV 

    Core Competencies:

    • Intermediate Computer Literate (MS Package) 
    • Good interpersonal skills and self-driven/starter 
    • Excellent communication, interpersonal and presentation skills 
    • Ability to work under pressure 
    • Must be able to work in a team and/or independently 
    • Outstanding organizational and time-management skills 

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    Instrumentation Qualification Analyst

    Job Outputs:

    Equipment Calibration and Maintenance:

    • Perform scheduled preventative maintenance (PM) and calibration on laboratory equipment as per the qualification protocols and guidelines.
    • Update and manage calibration statuses and ensure all analytical instruments meet calibration requirements.
    • Troubleshoot out-of-limit calibration results, referring to instrument manuals and liaising with suppliers to resolve issues. 

    Instrument Qualification (IQ/OQ/PQ):

    • Coordinate and execute the installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) activities for new and existing equipment.
    • Review and approve equipment qualification protocols, calibration procedures, and change control documents.
    • Ensure all qualification activities are documented, traceable, and stored according to regulatory requirements. 

    Documentation and Records Management:

    • Maintain and update equipment history records, including calibration certificates, repair logs, and qualification reports.
    • Ensure all laboratory equipment has associated SOPs (Standard Operating Procedures) and instrument manuals available for use.
    • Initiate and update new SOPs in line with regulatory and operational requirements.

    Supplier and Vendor Management:

    • Communicate with suppliers for repairs, maintenance, and technical support for laboratory equipment.
    • Coordinate with external vendors for specialised calibration and qualification activities.

    Training and Compliance:

    • Train laboratory personnel on calibration concepts, procedures, and the proper use of laboratory instruments.
    • Ensure adherence to GLP, GMP, safety standards, and regulatory guidelines during all instrument-related activities.
    • Address GLP and safety audit findings within the stipulated timelines.

    Requirements

    Educational Requirement:

    • Bachelor of Science (BSc) degree with a major in Microbiology, Chemistry, or a related field.
    • National Diploma in Microbiology, Medical Technology, Bacteriology, or Chemistry.

    Additional Certifications:

    • Certification in Good Laboratory Practices (GLP) or Instrument Qualification would be advantageous.
    • Training in equipment qualification (IQ/OQ/PQ) is preferred.

    Minimum Required Experience:

    • Minimum of 3–5 years of hands-on experience in the pharmaceutical industry, with specific exposure to laboratory equipment calibration, maintenance, and qualification.
    • Proven experience in IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) activities for analytical instruments.

    Preferred Experience:

    • Practical knowledge of cGMP, GLP, and regulatory requirements for pharmaceutical laboratories.
    • Experience in handling audits related to equipment qualification and maintenance records.

    Method of Application

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