70 Pharmaceutical jobs in Johannesburg
Technical Commercialization Director, Future Injectables Market Steward
Posted 17 days ago
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PATH current employees - please log in and apply
PATH is a global nonprofit dedicated to achieving health equity. With more than 40 years of experience forging multisector partnerships and with expertise in science, economics, technology, advocacy, and dozens of other specialties, PATH develops and scales up innovative solutions to the world’s most pressing heath challenges.
PATH is deeply committed to implementing our strategic vision focused on strengthening people-centered primary health care (PHC) to help countries and health systems adapt and respond to a changing world, move toward Universal Health Coverage (UHC), and achieve the health-related Sustainable Development Goals. The PHC program focuses on advancing integrated people-centered care and systems through a life course approach, and includes capabilities in health systems, integrated maternal and child health and development, nutrition, sexual and reproductive health (SRH), HIV, viral hepatitis, and other STIs, tuberculosis, noncommunicable diseases, and more.
The Future Injectable Market Steward (FIMS) project is a multi-country effort to facilitate the sustainable availability of injectable contraceptive options, including self-injection of DMPA-SC, as part of an expanded range of family planning methods delivered through informed choice programming. DMPA-SC offers a safe and effective injectable contraceptive that clients can, once trained, inject themselves if they choose. At the core of the FIMS mission is the belief that when women and adolescents have access to a variety of contraceptives, including those they can manage themselves, they are more likely to find and consistently use a method that meets their needs and ultimately realize their reproductive intentions.
The Technical Director / Senior Commercialization Officer will be responsible for gathering, analyzing and interpreting market data to inform global strategic decisions for DMPA-SC and the broader injectables market. This individual will also be a key point of contact for private sector stakeholders, including suppliers, distributors, social marketing non-governmental organizations (NGO), and other private sector partners.
Specific roles and responsibilities :
- Lead the development of an annual DMPA-SC Market Strategy that serves as a global roadmap towards a healthy DMPA-SC market and provides data-informed recommendations for donors, governments and manufacturers to align demand with available supply, including generic DMPA-SC products.
- Apply a total market approach to DMPA-SC introduction and scale, including engaging proactively with private sector partners, including suppliers and delivery partners around financing / pricing, application of available data to guide new product introduction, and general recommendations based on market research.
- Responsible for managing external relationships with key stakeholders, including UNFPA, product manufacturers, WHO, and Consensus Planning group, ensuring effective collaboration and alignment.
- Collaborate with internal and external partners, including donors, advisory bodies, manufacturers, commercial distributors, and NGOs, develop and provide analytics to inform discussions and to identify and resolve key market barriers.
- Facilitate and guide the regional resource teams, who provide technical assistance to country teams related to supply chain strengthening, monitoring and evaluation, sustainable financing, and evidence-informed advocacy.
- Engage with ministries of health, regional bodies, donors, and other partners, serving as a technical / scientific expert and external representative for global advocacy and policy efforts, including through webinars and presentations at international conferences and other fora.
Required expertise :
- Master’s degree in business administration, marketing, life sciences, or a related field.
- Advanced commercialization expertise, including 10+ years of comprehensive experience in commercial market access work for a pharmaceutical, life sciences, or commercial wholesaler, or distribution company, preferably related to women’s health products.
- Experience commercializing health products from market entry to saturation in low-resource settings, including experience with regulatory processes and compliance.
- Experience ideating and implementing strategies to ensure supply availability of health commodities within low and middle-income country (LMIC) supply chains.
- Experience utilizing complicated or nuanced data for strategic decision-making. Familiarity with data systems and data availability in low-resource settings preferred.
- Proven experience in ideating and developing data-driven solutions that address the needs and challenges of private sector distributors and partners in delivering new products and services.
- Deep expertise with rigorous quantitative analysis and modeling is required. Analyses led by the Technical Commercialization Director may include : rapid demand forecasting, product uptake and quantification analyses, and supply management scenario planning analyses.
- Proven ability to lead cross-cultural teams, demonstrate cultural sensitivity, and manage people with a commitment to building a shared vision and positive team culture across multiple country sites. At least three years of management or supervisory experience is required, along with above-average emotional intelligence and the ability to give and receive constructive feedback
- Experience building and managing relationships at global, regional, and national levels, including with donors, multilateral organizations, implementing partners, governments, local organizations, academic institutions, and the private sector.
Technical Director • South Africa, Johannesburg Project Office
#J-18808-LjbffrSenior Biostatistician (Home Based - South Africa)
Posted 17 days ago
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Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn .
Senior Biostatistician:
Roles & Responsibilities
- Providesinput into statistical sections and overall consistency of clinical study protocols.
- Develops and reviews statistical analysis plans (SAP). Determines appropriate analyses for clinical endpoints based on input from the protocol and the client.
- Performs senior-level reviews and is responsible for the datasets and outputs of a project. Ensures consistency with the SAP and reviews for correctness and quality.
- Works with programming team to provide inputfor analysis/ADaM datasets to be used for final analyses. Develops specifications and reviews datasets based on what is needed for the planned tables, listings and graphs (TLGs).
- Prepares TLG shells/specifications and programming notes based on SAP and analysis/ADaM datasets.
- Works with data management team to review data collection (e.g., CRFs) and helps ensure data quality throughout the clinical trial.
- Performs and/or coordinates the preparation, execution, reporting and documentation of high-quality statistical analysis according to the SAP.
- Provides high level of support to the programmers and medical writers on all statistical matters according to client requirements.
- Prepares and reviews statistical methods and results sections for the clinical study report (CSR) with in-house medical writers.
- Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
- Generates sample size calculations appropriate for the primary endpoint and based on input from the protocol.
- Generates and reviews randomization schedules per the protocol and randomization specifications.
- Works with the project management group to ensure timelines are appropriate given the scope of the project.
- Is familiar with and stays current with the latest industry practices and updated regulatory guidelines.
- Communicates competently and independently with client to coordinate the statistical and programming considerations of the project.
- Demonstrates strong understanding of ICH guidelines, as applicable to statistics.
- Practices good internal and external customer service.
Requirements
- Master of Science (in statistics of equivalent) with four (4) plus years relevant work experience or PhD (in statistics of equivalent) with two (2) plus years of relevant years of work experience.
- Strong knowledge of and experience with SAS (SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph).
- Able to be in a hands-on role by digging into data and using SAS to validate datasets and outputs.
- Excellent mathematical and problem-solving skills.
- Advanced knowledge of the statistical considerations involved in drug development including hands-on experience with clinical trial data.
- Strong knowledge of study designs and statistical analysis methods (e.g., GLMs, non-parametric methods, survival analysis techniques, general imputation methods, common descriptive stats).
- Strong familiarity with a variety of clinical data and databases (including EDC systems)
- Working knowledge of SDTM/ADaM standards (in the absence of ADaM experience, considerable experience working with analysis or derived datasets).
- At least three (3) years of experience in pharmaceutical industry.
- Ability to coordinate the analytical aspects of multiple projects or clinical trials at the same time.
- Proficiency with MS Office applications (e.g., Word, PowerPoint and Excel).
- Good interpersonal, oral, and written communication skills.
- Self-motivated, hardworking, dependable, and positive team-oriented personality.
- Ability to communicate effectively and provide clear directions to Statistical Programmers
Please consider your application unsuccessful if we do not reach out to you within 14days of your submission.
#J-18808-LjbffrBrand Manager (Pharmaceutical)
Posted 1 day ago
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Job Description
We are looking for an experienced Brand Manager in the Pharmaceutical industry (or a qualified pharmacist looking to pivot into the exciting world of brand management).
POSITION INFO :
Our client is looking for a dynamic Pharmaceutical Brand Manager ready to shape brand narratives, drive impactful campaigns, and grow within an innovative marketing team.
No prior marketing experience? No problem — we offer full training and mentorship to get you there.
Minimum Requirements :
- B Pharm degree + 3 years’ experience as a Retail Pharmacist
- Strong communication skills and a flair for storytelling
- Curiosity, drive, and a genuine love for marketing
- A team spirit and eagerness to grow in a cross-functional environment
Key Responsibilities :
- Craft and support brand strategies powered by your pharmacy insights
- Collaborate with marketing, sales, and affairs to bring campaigns to life
- Conduct market research and gain real-world marketing experience
- Receive world-class training in brand management and campaign development
Please apply directly by clicking the apply button or visiting for more exciting opportunities.
If you have not received a response within one week,
Create a job alert for this searchBrand Manager • Johannesburg, South Africa
#J-18808-LjbffrMaster Data Analyst (FMCG/ Medical/ Pharmaceutical) - Hybrid Remote
Posted 2 days ago
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Our client has a track record of nearly 3 decades in the medical industry! They are a leading South African based distributor of high-quality medical consumables and equipment, working with professionals in both private practice and state health facilities.
They are looking for their next superstar Master Data Analyst!
Duties & ResponsibilitiesAs their new Master Data Analyst, you will:
- Support the efficient purchasing and management of inventory.
- Be responsible for the data integrity of item master data.
- Be responsible for costing of foreign shipments received.
Here’s what you will need:
- Higher Education qualification with a Certificate in Informatics or equivalent.
- Minimum 5 years experience as a Master Data Analyst from the FMCG/Medical/Pharmaceutical industry essential.
- Knowledge of logistics and documents required to freight cargo.
- Microsoft Navision and Bi Wise.
Are you the MASTER of your craft? Apply Now!
#J-18808-LjbffrQuality Assurance Analyst (FMCG Sector)
Posted 3 days ago
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Job Description
This role is responsible for supporting the ongoing maintenance and continuous improvement of product, service, and process quality standards. The ideal candidate will have a foundational understanding of quality control methodologies and a proactive approach to identifying and resolving quality issues in a fast-paced production environment.
Requirements :
- Diploma or degree in Food Tech / Biotech / Food and Nutrition or Anaylitcal Chemistry
- 1-2 years relevant experience
- Proven abililty to manage, maintain and deliver against Customer requirements.
- Analytical skills, communication skills, conflict management and report writing skills.
Duties :
- Support the establishment, implementation, maintenance and continuous improvement of the food safety and quality systems such as FSSC 22000, product safety and regulatory standards.
- Enhance the sites food safety and product quality culture.
- Conduct data-based statistical analysis to identify trends, quality, and food safety improvement in product and process performance.
- Ensure adherence to established quality standards and regulatory standards and procedures.
- Develop and maintain quality standards and procedures in collaboration with functional departments.
- Assist with trend analysis and documentation, actionable reports.
- Develop inspection methods to analyze product.
- Identify areas for improvement, identifying root causes and supporting continuous improvement.
- Enforce customer requirements, company policies, and procedures.
- Participate in house quality complaints investigations, investigation on non-conformance and ensure close out procedures.
- CCP / OPRP Monitoring / Verification, Quality and other inspections, product specifications and failure investigations.
- Departmental audits and traceability.
- Monitor, maintain and practice food safety.
Leadership Standards
- Provide exemplary character for food safety and culture.
- Maintain inter-departmental relationships for overall good work ethic.
- Communication skills on all levels.
Key Performance Indicators
- Quality output
- Reduction of non-conformances
- Teamwork
- Customer service levels and reduction of customer complaints
Skills and Attributes
- Analytical skills
- Problem-solving skills
- Computer proficiency
- Technical and non-verbal communication
- Good planning and organizational intelligence
- Ability to work as team
Quality Assurance Analyst • Johannesburg, South Africa
#J-18808-LjbffrFinancial Controller (Medical/ Pharmaceutical) - Midrand Hybrid WFH
Posted 3 days ago
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Job Description
Our client has a track record of nearly 3 decades in the Medical industry! They are a leading South African based distributor of high-quality medical consumables and equipment, working with professionals in both private practice and state health facilities.
They are looking for their next superstar Financial Controller!
Duties & ResponsibilitiesAs their new Financial Controller, you will lead financial operations, drive cost efficiency, and offer strategic guidance.
Desired Experience & QualificationHere’s what you will need:
- BCom Financial Accounting with articles (SAICA or SAIPA) completed
- Minimum 2 years post articles experience as a Financial Controller from the Medical/Pharmaceutical industry essential
- Advanced Excel skills with Microsoft Navision and Bi Wise
We’re going to fill this one by the end of April so move fast!
#J-18808-LjbffrPharmaceutical Production Manager (Pharmaceutical Company) - Johannesburg, Gauteng
Posted 3 days ago
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Job Description
As a Pharmacy/Production Manager, you will oversee the day-to-day operations of our client’s pharmacy and ensure the delivery of high-quality pharmaceutical services.
You will be responsible for managing a team of pharmacists and pharmacy assistants, optimising workflow efficiency, and maintaining compliance with regulatory standards.
Minimum Requirements:
- Minimum of bachelor’s degree in Pharmacy (B.Pharm)
- 1-6 years’ related work experience
- Pharmaceutical Production Experience and Retail Pharmacy Experience
- Registration with Pharmacy Council
Specific Job Skills:
- Comprehensive knowledge of pharmaceutical manufacturing, standards, and compliance requirements
- Ability to interpret and implement policies, processes, and objectives
- Entrepreneurial spirit and a proactive approach to problem-solving
- Highly organised with strong time management skills
- Excellent leadership and team-building skills
- Understanding of the complementary medicine’s environment
- Strong financial acumen and business acumen
- Information gathering
- Interrogating information
- Taking action
Duties & Responsibilities:
Planning and Procedures:- Plan and prioritise daily, weekly, and monthly activities
- Determine, request, and use resources/assets optimally
- Verify certified clean status of equipment
- Verify, review, and approve verification of measuring equipment performance, calibrations, and sampling, and dispensing of materials
- Perform, review, and approve line sign-no’s, closures, and clearance authorisations
- Perform, review, and approve batch reconciliations to product specifications and quality
- Ensure production process adherence to standards and specifications
- Manage review, and approve change control programs and deviations/concessions comply to standards and specifications
- Manage and resolve customer complaints
- Optimise processes and identify gaps in policies/procedures
- Drive Corrective Action and Preventative Action investigations in area of focus
- Ensure compliance with regulatory requirements, including those set forth by the South African Pharmacy Council and other relevant authorities
- Perform and review shift Good Manufacturing Practice checks, and agent expiry dates, and ensure continued compliance
- Verify good document practice as per Standard Operating Procedures and regulation
- Verify the identity of bulk product and printed packaging materials, and conduct intermix checks to assess uniformity
- Verify In Process Controls are in line with product quality and specifications
- Review and approve preliminary batch records
- Audit logbooks and systems
- Investigate deviations and concessions, and assess risk
- Raise deviations and implement corrective action
- Raise maintenance notifications as and when required
- Provide clinical guidance and support to pharmacy staff, including counselling patients on medication use and adherence
- Train new Pharmacists and Post Basic Assistance on SOP’s in transition period
- Identify refresher or awareness training needs
- Monitor inventory levels and ordering processes to maintain adequate stock
- Complete batch records and labels
- Query documents and sign off declarations
- Perform and verify calculations in relation to production targets
- Maintain and update records and systems as required
- Retrieve supporting documentation and records to facilitate and support query resolution
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Jnr Quality/Assurance ANALYST
Posted 3 days ago
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Jnr Quality/Assurance ANALYST
(MUST currently work as an Analyst with Minimum 1-2 Year's experience in the FMCG Industry)
Location: Nasrec, Jhb area (MUST stay within reasonable distance )
Note: Clearly stipulate if you are willing to relocate at own cost on your Resume/CV.
- MUST currently work as an ANALYST
- MUST live within a reasonable distance of Nasrec, Jhb (Gauteng)
- Willing to work shifts
- Diploma/Degree in:
Food Tech, Biotech, Food & Nutrition OR Analytical Chemistry - MINIMUM 1-2 Year's working experience in the FMCG / Manufacturing Industry - ESSENTIAL
- Clean Criminal & Credit record - will be verified
Monthly
#J-18808-LjbffrQuality Assurance Analyst JHB - Central
Posted 3 days ago
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Job Description
Jnr Quality Assurance Analyst
(MUST currently work as an Analyst with a minimum of 1-2 years' experience in the FMCG Industry)
Location: Nasrec, Jhb area (MUST stay within reasonable distance)
*** Clearly stipulate if you are willing to relocate at own cost on your Resume/CV
- MUST currently work as an Analyst
- MUST live within a reasonable distance of Nasrec, Jhb (Gauteng)
- Willing to work shifts
- Diploma/Degree in:
- Food Tech
- Biotech
- Food & Nutrition
- Analytical Chemistry
- Minimum 1-2 years working experience in the FMCG/Manufacturing Industry - ESSENTIAL
- Clean Criminal & Credit record - will be verified
Monthly
#J-18808-LjbffrSupply Manager (Pharmaceutical)
Posted 3 days ago
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Job Description
- Engage with vendors to deliver quality, cost-effective products and services.
- Ensure effective price management and identify/participate in cost-saving initiatives across products and services.
- Manage the acquisition, utilization, and value chain across products and services to ensure cost efficiencies.
- Build and maintain internal and external stakeholder relationships.
- Negotiate contract terms and conditions.
- Manage vendor performance proactively in accordance with their contracts.
- Drive vendor compliance and performance.
- Provide direction and inspire positive work behavior.
- Provide procurement-related support based on:
- Serious reportable events and adverse events.
- Product complaints and service delivery issues.
- Monitor business compliance to preferred agreements and keep management informed of compliance.
- Participate in new growth projects as required.
- Build effective working relationships with hospital and functional teams.
- Drive initiatives to foster the development of new or existing suppliers in line with the company's BBEEE requirements.
- Relevant Bachelor’s degree in pharmacy, nursing, or other relevant clinical field / Bachelor of Commerce in Supply Chain Management or equivalent.
- CIPS certification (level 2) would be advantageous.
- Knowledge of products and supply chain management (i.e., medicines and surgical devices) in the healthcare industry would be advantageous.
- Working experience in a hospital environment would be advantageous.
- Understanding of management and relationship structures within an operating environment.
- Good computer proficiency especially in Excel, Word, and PowerPoint.
- Knowledge of SAP would be advantageous.
- Must have a valid driver’s license and own transportation.