Job Field: Sector in Pharmaceutical

  • Pharmaceutical Technologist

    Pharmaceutical Technologist

    Details:
    As a growing Retail Pharmacy entity with envisioned Branch extension and current branch in Kitengela, on the Outskirts of Nairobi, we are looking to recruit a Pharmaceutical Technologist who is a result oriented, self-driven and dynamic individual to share in the company’s ideals and vision and contribute to its growth.
    Reporting directly to the Pharmacist in charge the incumbent shall be responsible for the day to day running of the pharmacy with the following duties and responsibilities:

    Dispensing of prescriptions, Patient counseling and counter- prescribing to optimize the Pharmacy Sales.
    Making Extemporaneous Preparations, and technical supervision of Pharmacy Assistant/s as required.
    Stock control and Inventory Management including monitoring of expiries, with good working Knowledge of Phamacore-Inventory/Financial management system.
    Short listing items sold for ordering, conducting stock counts as and when required by the management and receiving deliveries from suppliers.
    Maintaining cleanliness of the Pharmacy and all storage areas and conforming to good storage practices.
    Providing inventory, Sales and Cash collection reports to the management as needed.
    Keeping appropriate patient records and doing follow ups to ensure optimal pharmaceutical care and treatment outcomes, and ensuring storage of prescription records for Two years as required by Cap 244 of the Kenyan laws.
    Performing Blood Glucose Monitoring, Blood Pressure check, Weight and BMI Check and providing the required advice on medicines and doing the necessary referrals.
    Sale of Medical Aids, Self testing Kits and Medical Equipment and training of patients on their use.
    Sale of Vaccines, Insulin and other cold chain products and ensuring optimal cold chain maintenance until use by the end consumer. Also provision of technical advice on cold chain management to clients.
    Participating in Health Promotion and Marketing initiatives organized by the Pharmacy.
    Performing any other duties as may be required by the management.

    Minimum Qualifications/Education Requirements:

    A Diploma in Pharmacy/Pharmaceutical Technology from a recognized Institution
    Enrollment Certificate from Kenya’s Pharmacy & Poisons Board (Mandatory)
    Valid Practice license (if currently employed)

    Work Experience:

    A minimum of One Year Post Enrollment Experience in a busy Retail Pharmacy.
    Good Working knowledge of Phamacore-inventory management System and other data bases.

  • Pharmaceutical Technologist

    Pharmaceutical Technologist

    The Pharmaceutical Technologist works in a team with the Procurement Officer and reports to the Procurement & Logistics Manager. The incumbent will be responsible of performing tasks related to pharmaceutical drugs and provide a variety of warehousing and stock management responsibilities, which include receiving of goods, storage and distribution of goods.
    The Pharmaceutical Technologist will be required to liaise and work closely with the P&L Team to ensure that the core objectives of MSK are achieved. The position is fulltime and will report to the P&L Manager.
    Key Responsibilities
    The position will be 50% based at the SO and 50% of time spent in the field stores/Pharmacies
    This job has two key responsibilities:
    Pharmaceutical Technologist
    Activities Include:-

    Ensures all drugs requested and purchased are approved by QAM team and in line with MSI Global regulations for purchase of drugs

    A member of the Standard Product List Committee and overall responsibility for Quality of products received and dispatched in MSK
    Update Q-TRACK communicate any deviations to the laid out standard
    To assure that the drugs supplies are as per the Standard Product List and informing Deputy Director Quality Assurance and the Deputy Director Procurement of any changes.
    To receive and check incoming Medical products and supplies (from suppliers and other organization) and ensure quality and standards of the medical products and supplies.
    Conducting random checks on quality of drugs and participate in sampling process of products for pharmacovigilance purposes.
    To monitor drugs’ expiry date and minimum medical stock level in order to protect the supply rupture and report findings to Deputy Director Procurement.
    Auditing medical items, supplies and commodities procurement plans sent by field teams
    Management, Support and implementation Q-Track with LSO.

    Offer technical support in forecasting and quantification of medical supplies to all service delivery leads.

    Advice different teams on quantification of needs monthly/quarterly basis and help them forecast based on the consumption trends for each team.
    Coordinate the distribution of medicines and medical supplies to all service points in a timely and effective manner while maintaining quality of the supplies i.e. Cold chain
    Support the implementation of good storage practices in all stores/Pharmacies within MSK e.g establish re-order levels, sorting of items, arrangement of stores, temperature tracking and FEFO arrangements
    Stores and Warehousing

    The Activities include:

    Coordination of receipt of goods, verifies the documents against goods delivered, and makes sure the suppliers sign the relevant documents.
    Verifies receipts against purchase orders, processes customer returns on a daily basis
    Maintain inbound receiving records.
    Assists in shipping of goods, receiving, stocking, storing, and inventory of materials. Assist the Inventory Control staff with receiving corrections.
    Manage all courier and delivery services between SO and field teams
    To ensure proper storage of medicines by standard warehouse running documents and procedures and to locate the drugs by categorized lay-out
    To maintain medical storage space clean and tidy stacking of boxes and set correct room temperature and level of moisture by keeping daily track records and maintaining the warehouse cold chain.
    To arrange picking, sorting and packing of Medical Products for distribution to various destination.
    Overseeing stock holding management to ensure protection and safe storage

    The activities include:

    Ensuring availability and updated bin cards in all stores handling medical supplies.
    Keep records of serious untoward incidents e.g. drug errors, poor quality, expired drugs as requested by Program Pharmacist
    Lead weekly and monthly support office cycle counts and reports
    Maintains records, searching for and compiling information and data; responding to routine request with answers by phone, in person, or by correspondence.
    Maintains cleanliness of the warehouses, goods and materials in them and keeps the equipments in good working order
    Checks periodically and make sure that the needed materials are in necessary quantity and quality.
    Ensures proper labelling and shelving of the warehouses.
    Timely distribution of goods

    The activities include:

    Coordination of dispatch of goods in the warehouse through the appointed currier service provider.
    Run and distribute department reports and correspondence for warehouses and distribution.
    Ensures distribution forms, requisitions, purchase orders forms and packaging slips are completed accurately.
    Assist with packing and pick slips, and log tracking.
    Support MSK Centres with stock Management and reporting
    Lead and report monthly stock counts
    Train staff on re-order levels and management
    Train staff on importance on FIFO to avoid supplies expiring at the stores
    Line manage the Assistant ware house officer.

    Knowledge, Skills and Attitudes
    Qualifications:

    Bachelor’s degree in Procurement, Logistics or any other relevant discipline.
    Diploma in Pharmacy from accredited institutions by Pharmacy and Poisons Board
    Enrolled Pharmaceutical Technologist with Pharmacy and Poisons Board
    Minimum of three (3) years post training experience in the same position
    At least a Diploma or an equivalent combination of education and experience in warehouse and stores management preferably with a medical store.
    The Candidate should have experience working with any ERP system.

    Skills and Experience:

    Minimum 3 years working in the same capacity in a busy organisation especially INGO.
    Proven experience in Warehouse management and stock control.
    Computer Literate
    Good communication skills
    Knowledge of drugs and their indications, contra indications, dosing, side effects and proper administration
    Knowledge of clinical operations and procedures
    Ability to train other assigned staff as necessary
    Ability to maintain quality, safety, and/or infection control standards
    Experience in medical or health sector an added advantage
    Analytical solving skills
    Attention to detail and high level of accuracy
    Effective organizational skills
    Good computer skills.
    Excellent report writing skills.
    Security and safety minded.

    Attitude / Motivation:
    Successful performance at MSI is not simply defined in terms of ‘what’ people achieve, but equally is about ‘how’ people go about their jobs and the impact that they have on others. There are 13 key behaviours that MSI encourages in all employees and they are defined below:
    Initiative
    Thinking ahead and taking action to make the most of opportunities by finding the optimum solution
    Innovative
    Thinking creatively and outside of the box so that ideas generated create a positive outcome
    Effective Communication
    Communicating through active listening and good questioning techniques, using appropriate body language, ensuring information is clear and concise.
    Responsive
    Being responsive to changing priorities and demands
    Working Efficiently
    Planning, prioritising and organising work to ensure work is accurate and deadlines are met
    Sharing Information
    Sharing information and knowledge whilst maintaining confidentiality
    Focus on Learning
    Taking responsibility for keeping knowledge and skills updated and for seeking opportunities to develop further
    Commitment
    Awareness and understanding of goals, vision and values and how your role impacts on this and going the extra mile to meet role requirements
    Driven
    Drive and determination to deliver results
    Accountable
    Taking responsibility for appropriate decisions that you make, and the actions and behaviour you demonstrate
    Embracing Change
    Openness to embracing change within the organisation and being able to adjust plans/activities accordingly
    Motivated
    Motivation towards achieving quality results to maximise potential
    Team Player
    Working as part of a team by being supportive, flexible and showing respect for each other

  • Regulatory Affairs Manager 

Regulatory Affairs Executive

    Regulatory Affairs Manager Regulatory Affairs Executive

    Job Purpose Statement:

    To translate the Pharma (Rx) business objectives into an actionable regulatory affairs strategy so as to ensure that our standards in respect to regulatory conformance and business continuity are maintained.
    To add value to business by ensuring timely submissions and approvals for new products in WCA markets as well as maintenance of registered licences in alignment with local regulations and corporate.
    Ensure Regulatory compliance by support and compliance to the QMS system

    Essential Job Responsibilities:

    Development and coordination of regulatory strategies with the support of the Head of Regulatory for regulatory submissions in WCA and collaboration with the HRA to simplify and improve existing regulatory processes, systems and techniques for the markets supported, to achieve the business objectives.
    Ensure timely submissions and approvals of applications according to regulatory plan and strategy, ensuring continuity of supply and regulatory compliance.
    Management of Regulatory projects to support new initiatives as appropriate to the business.
    Ensure alignment of the regulatory registration submission strategy to commercial strategies and work effectively with key stakeholders and 3rd party service providers.to achieve the desired regulatory outcomes.
    Liaise with Regulatory Authorities and provide appropriate answers on matters relating to Regulatory approvals/queries for our Products.
    Ensure alignment of registered details with original dossiers and corporate databases, maintenance of and compliance with Regulatory Databases (OPAL, REQUIRE, GRACE)
    Support the artwork control process to ensure changes and approval are done in time to avoid product stock out or delays in supplies.
    Management of tender activities in relevant markets (as applicable)
    Monitor and keep in touch with changes in the regulatory environments. Provide intelligence to local stakeholders and central team on changes in regulatory environment in the region.
    Working with industry associations to strategically position our values and address any issues that would affect the business.
    Support and ensure compliance to the QMS/QRM processes within Regulatory (written standard maintenance/compliance, regulatory issue management, risk management, management monitoring (L1 Audit), deviation handling, CAPA management, training, 3P oversight). Provide regulatory support to GMP inspections as required.

    Competencies: (Expertise and Knowledge)
    Knowledge & Application
    The level of technical knowledge required for the role is applied for assessment of the regulatory files, submission of right first-time dossiers to Regulatory Authorities, communication with global and local stakeholders.
    Examples:

    Preparation of registration dossier according to local regulations
    Preparation of SmPC and PIL and coordination of their drafts with global and local stakeholders
    Communication with Authorities (submission of official requests, providing answers for Authorities’ request)
    Communication with regulatory third-party service providers to ensure the company objectives are met

    Problem Solving and Innovation
    Works across multiple markets in complex regulatory environment with high unpredictability of regulatory decisions, not yet fully established regulations (evolving in maturity), lack of transparency and dialogue with Regulatory Authorities, different interpretation and application of regulations/guidelines.
    Works in one of the most critical areas in terms of compliance to ensure:

    Patients have access to products with minimal possible interruption of supplies because of changing regulatory requirements and
    Supplied products are compliant with registered details, so there is no risk for patients’ safety or our reputation;
    Risk of mistakes in products information is managed properly to minimize impact of regulatory related mistakes on business.

    Works in one of fast-changing areas where changes are caused by external factors (regulatory requirements and practices), business needs to be aligned for each single country and in line with central procedures of compliance and product improvements. Needs to have the ability to make evaluative judgement.
    Works through local regulatory service providers to provide the regulatory support required in market (i.e. appointments, submissions, follow up, response to queries, regulatory intelligence & advocacy)
    Interaction
    The role involves interaction with multiple stakeholders internally and externally and requires excellent communication, collaboration and negotiation skills:
    Internally

    Country level: LOCs Quality, Medical, Logistics and Distribution, Legal, Commercial
    Regional: Regional Regulatory Affairs
    Global level: Global Regulatory Affairs, GMS

    Externally

    Regulatory Authorities
    3rd party service providers
    Pharmaceutical Trade Associations

    The communication needs to be clear, specific and consistent across all stakeholders both internal and external. It needs to be adapted to manage the diversity, harness the commitment & contribution of stakeholders internally and externally and collaborative to deliver the goal for the organization.
    Multi-Cultural Awareness
    The role involves interacting with multiple countries with racial/ethnic diversity as well as variance in socio-economic environment.
    These factors need to be considered while working on regulatory strategy as well as interacting with internal and external stakeholders since alignment with the country’s and state authorities’ vision is essential for regulatory strategy or advocacy initiatives to be successful.
    Therefore, the role holder should have the:

    Ability to write and speak in English and French: Intermediate/upper-intermediate level;
    Ability to work within diverse cultures and differing levels of organizational maturity;
    High degree of comfort and positive engagement working as a member of a multifunctional and multicultural team
    Constant search for Innovation, contributing with passion, and performance achieved with Integrity
    Ability for multitasking, quick adaptation, agility and ability to make decisions/influence outcomes that include assessment of the potential impact, attention to detail.

    Impact
    Impacts business targets ensuring all new submissions, regulatory variations and renewals are agreed with logistics, commercial teams and in the countries, so they have minimal impact on supplies.
    Influences on continuous product supply by ensuring alignment of registered details with original dossiers in multiple countries in WCA (as assigned) and working through third party service providers to achieve desired outcomes as per plan.
    Impact on compliance (in complex/dynamic regulatory environment) ensuring that the standards of governance and oversight are applied, and that risks and issues are appropriately managed
    Basic Requirements:

    Bachelor’s Degree. Pharmacy or appropriate scientific degree
    Minimum 3 years Regulatory Experience in the industry. Good working knowledge of regulations, current industry practices, and experience with seeking out, interpretation and application of regulatory guidance.
    Excellent communication influencing and negotiation skills
    Masters or PhD (would be an added advantage)
    Qualification in project management (would be an added advantage)

    go to method of application »

  • Regulatory Specialist

    Regulatory Specialist

    The Position
    Do you perform best where change is daily and the unexpected is a routine? Do you wish to make a difference?. If yes, you have an opportunity to be part of the Novo Nordisk Middle Africa Regulatory Affairs team, which is responsible for effective execution of Novo Nordisk regulatory strategies across countries in Africa.
    Yes, we are looking for a “Regulatory Specialist” based in Nairobi (Kenya).
    Responsibilities
    Securing regulatory approval of new products (NDA), Maintain registration for existing products in due time, Ensure the flow of local regulatory process across the region, Coordinate and supervise regulatory applications related to product Life Cycle Management (LCM), Develop and update labelling in compliance with the local regulatory requirements, Ensure regulatory compliance in promotional material according to local legislation and Standard Operation Procedures (SOPs), Monitor the current regulations and updates across countries in Africa that are potentially impacting Novo Nordisk & ensure timely implementation.Assist in implementation of Novo Nordisk Quality Management System (QMS), ensuring product quality, focus on business critical issues that may have an impact on license to operate, ensure inspection readiness and assist in Pharmacovigilance activities across Middle Africa.
    You have a proactive and solution oriented approach to the challenges with logical reasoning, Adaptable and flexible with ability to multi task and deliver results, Good negotiation, collaboration and stakeholder management skills and a Good team player.
    Qualifications
    We expect you to hold a Bachelor of Pharmacy, BSc degree (e.g. in Pharmacy or pharmaceutical related studies). You are fluent in written English and French languages. You have minimum 3 years of experience in pharmaceutical industry, 2 (two) year experience in the Regulatory as a RA associate. You have the knowledge of local regulations and regional legislation across countries in Africa. If you have working knowledge in the area of Quality Assurance and Pharmacovigilance it will be an advantage.Working at Novo Nordisk
    At Novo Nordisk, we strive for excellence. You share the same passion and commitment as our employees in our journey to make a difference to patients’ lives. In exchange, we offer you the chance of a lifetime to work with extraordinary talent and benefit from unmatched opportunities for professional and personal development.
    Contact
    If you are interested in the challenging and rewarding position posted above, please apply via www.novonordisk.com/jobs. CVs sent to e-mail account will not be taken into consideration; only the applications received at the jobs site are reviewed.
    Millions rely on us
    To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.

  • Pharmacist

    Pharmacist

    Job Description

    Educate patients about medications to raise sense of autonomy and reduce non-compliance and complications
    Participate in formulating the interdisciplinary plan of care
    Provide technical and clinical information and communicate results of monitoring activities to patients, nurses and physicians as required regarding the contents, utilization, therapeutic actions, possible adverse reactions or interactions of drugs.
    Actively supporting the development, education & training of colleagues; building pharmacy capability of store teams

  • Pharmacist 

Medical Officers

    Pharmacist Medical Officers

    Job Responsibilities

    Coordinate delivery of pharmaceutical services, for both inpatient and outpatient;
    Management of patients/clients requiring specialized pharmaceutical services;
    Supervision of pharmaceutical technologists and support staff deployed in the pharmacy department;
    Conduct routine trainings to brief clinicians on updates related to pharmaceutical products and information;
    Coordinate pharma-covigillance activities and ensure patient safety is guaranteed; and
    Any other related duties as may be assigned.

    Requirements

    Holder of Bachelor of Pharmacy degree;
    Valid practicing license and a letter of Good Standing from the Pharmacy and Poisons board;
    Successfully undertook one year of internship;
    A certificate in health commodity management is an added advantage; and
    Be computer literate.

    General Conditions

    Must be a Kenya citizen;
    Fulfills expectations of Chapter Six of the Constitution of Kenya on Leadership and Integrity.

    Apply for the job and must attach photocopies of the following documents in support of your application:

    National Identity Card;
    Academic Certificates (from Primary to the highest level attained), Professional Certificates and Curriculum
    Vitae that includes three referees;
    Clearance Certificate from the Ethics and Anti-Corruption Commission;
    Certificate of Good Conduct Directorate of Criminal Investigation);
    Tax Clearance Certificate from KRA;
    Credit Reference Bureau Certificate; and
    Clearance Certificate from HELB.

    go to method of application »

  • Regulatory Affairs Manager – Export

    Regulatory Affairs Manager – Export

    Job description
    Your Responsibilities
    Job Purpose Statement

    To translate the Pharma (Rx) business objectives into an actionable regulatory affairs strategy so as to ensure that GSK standards in respect to regulatory conformance and business continuity are maintained.
    To add value to business by ensuring timely submissions and approvals for new products in WCA markets as well as maintenance of registered licences in alignment with local regulations and corporate.
    Ensure Regulatory compliance by support and compliance to the QMS system

    Key Responsibilities

    Development and coordination of regulatory strategies with the support of the Head of Regulatory for regulatory submissions in WCA and collaboration with the HRA to simplify and improve existing regulatory processes, systems and techniques for the markets supported, to achieve the business objectives.
    Ensure timely submissions and approvals of applications according to regulatory plan and strategy, ensuring continuity of supply and regulatory compliance.
    Management of Regulatory projects to support new initiatives as appropriate to the business.
    Ensure alignment of the regulatory registration submission strategy to commercial strategies and work effectively with key stakeholders and 3rd party service providers.to achieve the desired regulatory outcomes.
    Liaise with Regulatory Authorities and provide appropriate answers on matters relating to Regulatory approvals/queries for GSK Products.
    Ensure alignment of registered details with original dossiers and corporate databases, maintenance of and compliance with Regulatory Databases (OPAL, REQUIRE, GRACE)
    Support the artwork control process to ensure changes and approval are done in time to avoid product stock out or delays in supplies.
    Management of tender activities in relevant markets (as applicable)
    Monitor and keep in touch with changes in the regulatory environments. Provide intelligence to local stakeholders and central team on changes in regulatory environment in the region.
    Working with industry associations to strategically position GSK values and address any issues that would affect the business.
    Support and ensure compliance to the QMS/QRM processes within Regulatory (written standard maintenance/compliance, regulatory issue management, risk management, management monitoring (L1 Audit), deviation handling, CAPA management, training, 3P oversight). Provide regulatory support to GMP inspections as required.

    Competencies (Expertise and Knowledge)
    Knowledge & Application
    The level of technical knowledge required for the role is applied for assessment of the regulatory files, submission of right first-time dossiers to Regulatory Authorities, communication with global and local stakeholders.
    Examples

    Preparation of registration dossier according to local regulations
    Preparation of SmPC and PIL and coordination of their drafts with global and local stakeholders
    Communication with Authorities (submission of official requests, providing answers for Authorities’ request)
    Communication with regulatory third-party service providers to ensure the company objectives are met

    Problem Solving and Innovation

    Works across multiple markets in complex regulatory environment with high unpredictability of regulatory decisions, not yet fully established regulations (evolving in maturity), lack of transparency and dialogue with Regulatory Authorities, different interpretation and application of regulations/guidelines.
    Works in one of the most critical areas in terms of compliance to ensure
    Patients have access to products with minimal possible interruption of supplies because of changing regulatory requirements and GSK continuous improvement of products;Supplied products are compliant with registered details, so there is no risk for patients’ safety or GSK reputation;Risk of mistakes in products information is managed properly to minimize impact of regulatory related mistakes on business.
    Works in one of fast-changing areas where changes are caused by external factors (regulatory requirements and practices), business needs to be aligned for each single country and in line with central procedures of compliance and product improvements. Needs to have the ability to make evaluative judgement.
    Works through local regulatory service providers to provide the regulatory support required in market (i.e. appointments, submissions, follow up, response to queries, regulatory intelligence & advocacy)

    Interaction
    The role involves interaction with multiple stakeholders internally and externally and requires excellent communication, collaboration and negotiation skills
    Internally

    Country level LOCs Quality, Medical, Logistics and Distribution, Legal, Commercial
    Regional Regional Regulatory Affairs
    Global level Global Regulatory Affairs, GMS

    Externally

    Regulatory Authorities
    3rd party service providers
    Pharmaceutical Trade Associations

    The communication needs to be clear, specific and consistent across all stakeholders both internal and external. It needs to be adapted to manage the diversity, harness the commitment & contribution of stakeholders internally and externally and collaborative to deliver the goal for the organization.
    Multi-Cultural Awareness
    The role involves interacting with multiple countries with racial/ethnic diversity as well as variance in socio-economic environment. These factors need to be considered while working on regulatory strategy as well as interacting with internal and external stakeholders since alignment with the country’s and state authorities’ vision is essential for regulatory strategy or advocacy initiatives to be successful.
    Therefore, the role holder should have the

    Ability to write and speak in English and French Intermediate/upper-intermediate level;
    Ability to work within diverse cultures and differing levels of organizational maturity;
    High degree of comfort and positive engagement working as a member of a multifunctional and multicultural team
    Constant search for Innovation, contributing with passion, and performance achieved with Integrity
    Ability for multitasking, quick adaptation, agility and ability to make decisions/influence outcomes that include assessment of the potential impact, attention to detail.

    Impact

    Impacts business targets ensuring all new submissions, regulatory variations and renewals are agreed with logistics, commercial teams and in the countries, so they have minimal impact on supplies.
    Influences on continuous product supply by ensuring alignment of registered details with original dossiers in multiple countries in WCA (as assigned) and working through third party service providers to achieve desired outcomes as per plan.
    Impact on compliance (in complex/dynamic regulatory environment) ensuring that the standards of governance and oversight are applied, and that risks and issues are appropriately managed.

    Why You?

    Bachelor’s Degree. Pharmacy or appropriate scientific degree
    Minimum 3 years Regulatory Experience in the industry. Good working knowledge of regulations, current industry practices, and experience with seeking out, interpretation and application of regulatory guidance.
    Excellent communication influencing and negotiation skill
    Masters or PhD (would be an added advantage)
    Qualification in project management (would be an added advantage)

  • Pharmaceutical Technologist 

Pharmacy Assistant

    Pharmaceutical Technologist Pharmacy Assistant

    Job Details
    As a growing Retail Pharmacy entity with envisioned Branch extension and current branch in Kitengela, on the Outskirts of Nairobi, we are looking to recruit a Pharmaceutical Technologist who is a result oriented, self-driven and dynamic individual to share in the company’s ideals and vision and contribute to its growth.Reporting directly to the Pharmacist in charge the incumbent shall be responsible for the day to day running of the pharmacy with the following duties and responsibilities:

    Dispensing of prescriptions, Patient counseling and counter- prescribing to optimize the Pharmacy Sales.
    Making Extemporaneous Preparations, and technical supervision of Pharmacy Assistant/s as required.
    Stock control and Inventory Management including monitoring of expiries, with good working Knowledge of Phamacore-Inventory/Financial management system.
    Short listing items sold for ordering, conducting stock counts as and when required by the management and receiving deliveries from suppliers.
    Maintaining cleanliness of the Pharmacy and all storage areas and conforming to good storage practices.
    Providing inventory, Sales and Cash collection reports to the management as needed.
    Keeping appropriate patient records and doing follow ups to ensure optimal pharmaceutical care and treatment outcomes, and ensuring storage of prescription records for Two years as required by Cap 244 of the Kenyan laws.
    Performing Blood Glucose Monitoring, Blood Pressure check, Weight and BMI Check and providing the required advice on medicines and doing the necessary referrals.
    Sale of Medical Aids, Self testing Kits and Medical Equipment and training of patients on their use.
    Sale of Vaccines, Insulin and other cold chain products and ensuring optimal cold chain maintenance until use by the end consumer. Also provision of technical advice on cold chain management to clients.
    Participating in Health Promotion and Marketing initiatives organized by the Pharmacy.
    Performing any other duties as may be required by the management.

    Minimum Qualifications/Education Requirements:

    A Diploma in Pharmacy/Pharmaceutical Technology from a recognized Institution
    Enrollment Certificate from Kenya’s Pharmacy & Poisons Board
    Valid Practice license (if currently employed)

    Work Experience:

    A minimum of One Year Post Enrollment Experience in a busy Retail Pharmacy.
    Good Working knowledge of Phamacore-inventory management System and other data bases.

    go to method of application »

  • Pharmaceutical Technologist

    Pharmaceutical Technologist

    Supervises/Oversees: None
    Key Responsibilities and Duties:

    Provide advice for non-prescription medications.
    Monitor drugs and other medical supplies levels and initiate the procurement process.
    Take inventory and track medication and supply orders.
    Keep records of all drug stocks ordered, drugs issued to clients and stocks remaining.
    Arrange drugs in the required manner.
    Establish and maintain good relationships with customers which includes clinics, doctors, hospitals and other institutions
    Monitor storage conditions i.e. expiry status and security of the pharmaceuticals
    Any other duties that may be assigned from time to time.

    Requirements:

    Must be registered with the Pharmacy and Poison Board
    Degree/ Diploma holder from a recognized institution.
    Original Professional and academic certificates with up to date license
    At least 2 years of working experience in a similar position
    Strong negotiation and customer care skills