8 Responsible Pharmacist jobs in South Africa

Faircape Group owns and operates six premier retirement villages across the Western Cape. Among these, Tokai Estate and Heritage Manor host our growing Sub-Acute Care and Rehabilitation Centres , where we provide restorative care to patients recovering from Medical, Neurological, Orthopaedic, Surgical, and Respite conditions.

In addition to sub-acute services, we also support our long-term care facilities by providing comprehensive pharmaceutical services, including the dispensing of blister packs to residents across our retirement villages.

Our goal is to bridge the gap between hospital and home, supporting recovery in a structured, therapeutic environment. We work within a high-functioning multidisciplinary team (MDT) of doctors, nurses, therapists, and allied health professionals committed to excellent patient outcomes.

We are seeking a Responsible Pharmacist to join our team. The successful candidate will play a key role in growing our pharmacy services, ensuring compliance, and delivering high-quality pharmaceutical care across both sub-acute and long-term care environments.

What We Offer:

• Collaborative Environment – Work with an MDT of doctors, nurses, and therapists.
• Quarterly Performance Bonuses – Recognition for strong leadership and impact.
• Long Service Leave – Rewarding commitment and loyalty.
• Discounted ISP Packages – Affordable internet connectivity.

If you are passionate about healthcare, thrive in fast-paced environments, and want to make a difference in both short-term recovery and long-term care, apply now to join our team.

Duties include but are not limited to:

• Dispensing of any medicine on authorised prescriptions (in-patients and out-patients)
• Evaluation of a patient's medicine-related needs, ensuring safe medication distribution and provide advice to any person with regard to the use of medicine
• Preparation or packaging of any medicine or scheduled substance or the supervision thereof
• Prescription monitoring to ensure that prescribing and administration of medicines are monitored regularly and to ensure compliance is adhered to
• Ensure billing of any items issued is completed and up to date (including in-patient and out-patient accounts)
• Ensuring medical aid authorization of chronic medication for out-patients has been received
• Report on medication discrepancies/ errors, and adverse drug reactions
• Ensure that the Good Pharmacy Practice guidelines and pharmacy procedures are adhered to.
• Assessing and updating current policies and procedures
• Provide regular feedback to management with regard to any new developments or concerns within the pharmacy
• Train and provide support to pharmacist staff
• Ensuring continuous professional development by means of the pharmacy quality
• Attend regular MDT meetings

Requirements Qualifications - BPharm and SAPC registered with relevant experience.

Experience and Knowledge -

• Proven experience as a Responsible Pharmacist
• Medication Management experience
• Propharm and Clinic Manager experience would be advantageous
• Hospital experience will be advantageous.
• Able to carry out all dispensing activities as per SAPC.

Skills and Attributes

• Strong understanding of pharmacology, drug interactions, dosages and pharmaceutical sciences
• Regulatory compliance
• Good understanding of the private healthcare industry and its challenges
• Excellent leadership and decision-making skills
• Ability to multitask and work efficiently under pressure
• Excellent attention to detail
• Ethical integrity
• Understand great patient care.
• Strong interpersonal skills and professional communication.
• Computer proficiency
• Professional and focused
• Well presented and professional.
• Business Acumen

Specific Requirements:

• Clear health record
• Clear criminal record
• Clear credit record
• Two Written references

Working Hours - Monday to Friday from 09h00 to 18h00 and 4 hours alternative weekends per month (10:00-15:00) We offer a lucrative salary, based on experience, qualification, skills and attributes

To see more about Faircape and what we have to offer go and look at our informative website - Tokai Estate Healthcare Website

Should you not receive a response within 2 weeks of applying, please consider your application unsuccessful.

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Faircape Group owns and operates six premier retirement villages across the Western Cape. Among these, Tokai Estate and Heritage Manor host our growing Sub-Acute Care and Rehabilitation Centres , where we provide restorative care to patients recovering from Medical, Neurological, Orthopaedic, Surgical, and Respite conditions. In addition to sub-acute services, we also support our long-term care facilities by providing comprehensive pharmaceutical services, including the dispensing of blister packs to residents across our retirement villages. Our goal is to bridge the gap between hospital and home, supporting recovery in a structured, therapeutic environment. We work within a high-functioning multidisciplinary team (MDT) of doctors, nurses, therapists, and allied health professionals committed to excellent patient outcomes. We are seeking a Responsible Pharmacist to join our team in Tokai Estate within the Southern Suburbs. The successful candidate will play a key role in growing our pharmacy services, ensuring compliance, and delivering high-quality pharmaceutical care across both sub-acute and long-term care environments. What We Offer: Collaborative Environment Work with an MDT of doctors, nurses, and therapists. Quarterly Performance Bonuses Recognition for strong leadership and impact. Long Service Leave Rewarding commitment and loyalty. Discounted ISP Packages Affordable internet connectivity. If you are passionate about healthcare, thrive in fast-paced environments, and want to make a difference in both short-term recovery and long-term care, apply now to join our team. Duties include but are not limited to: Dispensing of any medicine on authorised prescriptions (in-patients and out-patients) Evaluation of a patient's medicine-related needs, ensuring safe medication distribution and provide advice to any person with regard to the use of medicine Preparation or packaging of any medicine or scheduled substance or the supervision thereof Prescription monitoring to ensure that prescribing and administration of medicines are monitored regularly and to ensure compliance is adhered to Ensure billing of any items issued is completed and up to date (including in-patient and out-patient accounts) Ensuring medical aid authorization of chronic medication for out-patients has been received Report on medication discrepancies/ errors, and adverse drug reactions Ensure that the Good Pharmacy Practice guidelines and pharmacy procedures are adhered to. Assessing and updating current policies and procedures Provide regular feedback to management with regard to any new developments or concerns within the pharmacy Train and provide support to pharmacist staff Ensuring continuous professional development by means of the pharmacy quality Attend regular MDT meetings Requirements Qualifications - BPharm and SAPC registered with relevant experience. Experience and Knowledge - Proven experience as a Responsible Pharmacist Medication Management experience Propharm and Clinic Manager experience would be advantageous Hospital experience will be advantageous. Able to carry out all dispensing activities as per SAPC. Skills and Attributes Strong understanding of pharmacology, drug interactions, dosages and pharmaceutical sciences Regulatory compliance Good understanding of the private healthcare industry and its challenges Excellent leadership and decision-making skills Ability to multitask and work efficiently under pressure Excellent attention to detail Ethical integrity Understand great patient care. Strong interpersonal skills and professional communication. Computer proficiency Professional and focused Well presented and professional. Business Acumen Specific Requirements: Clear health record Clear criminal record Clear credit record Two Written references Working Hours - Monday to Friday from 09h00 to 18h00 and 4 hours alternative weekends per month (10:00-15:00) We offer a lucrative salary, based on experience, qualification, skills and attributes To see more about Faircape and what we have to offer go and look at our informative website - Tokai Estate Healthcare Website Should you not receive a response within 2 weeks of applying, please consider your application unsuccessful.

Ensuring compliance with all the provisions of the Act 101 of 1965; Pharmacy Act, Act 53 of 1973 and all regulations and guidelines pertaining to the Wholesale license for medicinal products and Good Wholesaling/Distribution and Good Housekeeping Practices and Good Pharmacy Practice. Supervision of purchasing, acquiring, importing, keeping, possessing, using, releasing, storage, packaging, supplying or selling of any medicine or schedule substance or the supervision thereof.

·    Compliance to national regulatory requirements (Act 101 of 1965; Pharmacy Act 53 of 1973, SAHPRA, PICS/WHO guidelines and OHS act) with respect to Quality Management Systems and current Good Distribution & Wholesaling Practices (cGDP/GWP).
·    Establish an effective quality management system to support the Adcock Ingram Healthcare SAHPRA Licence.
·    Ensure Standard Operating Procedures (SOP’s) are initiated, reviewed, approved and implemented
·    Ensure that quality systems are implemented and comply with SAHPRA Guidelines.
·    Review and approve Validation protocols and reports ensuring compliance with cGDP/GWP requirements.
·    Maintain a satisfactory service level to Logistics Distribution.
·    Lead quality review meetings with the involvement of the AIL RP and Managing Director to assess the effectiveness and applicability of the quality systems.
·    Escalate non-compliance of the quality systems immediately to Executive Management where necessary and assist in addressing the non-compliance.
·    Perform performance assessments of all direct reports against agreed objectives.
·    Product Release (based on Applicant release)
·    Audits (preparation and correcting any non-conformances found) and CAPA initiation and close-out
·    Deviations and Non-conformance raising, monitoring and close-out. Raise, maintain and monitor deviations, non-conformances and CAPA’s.
·    Supply and maintain S5 & S6 stock and Registers.
·    Supply and maintain section 21 items.
·    Assist with stock take.
·    Dedicated storage area management (Damages, Quarantine, Returns, Cold Store & Schedule Stores).
·    Management of reverse logistics (RETURNS).
·    Pharmacovigilance reporting.
·    Receipt, fine checking and sampling of 3rd party stock.
·    Deputise the Responsible Pharmacist (RP) by performing all RP duties and accepting responsibility as stand in RP in the absence of the RP.
·    Assisting the Responsible Pharmacist (RP) where required.
·    Performing duties, tasks and reasonable instructions as delegated by the Responsible Pharmacist.
·    Key holder to critical keys required for daily operations.
·    After hours, call out in case of fridge failure or emergencies.
·    Risk Assessments, initiate and lead Risk Assessment meetings with various personnel to understand occurrences and trends in quality, operations and distribution.
·    Personal interaction in all critical regulatory interactions with SAHPRA; DOH and SAPC.
·    Foster good working relationships with the health authorities, principals and internal customers.
·    Participate in Marketing, Supply chain; Regulatory and Quality Assurance cross-functional teams.
·    Inform all Pharmacists of Adcock Ingram Healthcare about current developments in the legislation and other developments regarding compliance with current Distribution Practices.
·    Approve technical records and training.
·    Ensure correct handling of recalled and quarantined stock.
·    Ensure timely handling and reporting product complaints from within the warehouse or from external customers.
·    Ensure continuous supervision of the wholesale or distributor pharmacy.
·    Take corrective measures in respect of deficiencies noted regarding inspection reports of council or third-party audits conducted.
·    In addition to the general responsibilities:
·    Ensure that unauthorized people do not obtain access to pharmaceutical products in the wholesale or distributor pharmacy premises outside of normal trading hours.
·    Establish policies and procedures for the employees of the wholesale and distributor pharmacy regarding the acts performed and services provided in the wholesale pharmacy
·    Ensure the safe and effective storage and keeping of pharmaceutical products in the wholesale and distributor pharmacy under his/her direct personal supervision
·    Ensure correct and effective record keeping of the purchase, sale, possession, storage, safekeeping and return of pharmaceutical products.
·    Ensure that the following registrations, recordings and licence are current and in place:
·    The registration of the Pharmacist with the Pharmacy Council in accordance with the provisions of Section 14 of the Pharmacy Act.
·    The premises licence of the wholesale or distributor pharmacy issued by the Director-General, Department of Health, in accordance with the provisions of Section 22(1) of the Pharmacy Act.
·    The recording of the premises license of the wholesale or distributor pharmacy at the Pharmacy Council in accordance with Section 22(2) of the Pharmacy Act, read together with Regulation 8(5) of the “Regulations relating to Ownership and Licensing of Pharmacies”; and
·    Assisting the RP to ensure that contracts (Service Level Agreements/ Technical Agreements) exist between service providers and principles stipulating where all responsibilities lie.
·    To ensure that all employees are conversant with the system laid down for use and following the STANDARD OPERATING PROCEDURES.
·    That the specified quality is maintained during storage and transport.
·    To ensure that all logs are completed by the distribution / warehousing facility e.g. temperature control, cleaning, maintenance etc.
·    To ensure that disposal or destruction of medicines is correctly and regularly performed under proper control so as not to be a health hazard.
·    To ensure that an adequate pest control program is in place at the distribution facility, using acceptable food grade bait, and to ensure that precautions are taken to ensure that product contamination does not occur.
·    To ensure that self-inspection audits are performed and any deviations followed up.
·    To ensure that goods on arrival at the distribution facility are placed in quarantine, sampled for retesting after importation, and retained in quarantine until formally released where applicable.
·    To update batch status to the market according to correct procedure.
·    To check all relevant documentation to formally release final packed product for distribution where applicable.
·    To ensure GDP/GWP training is provided to all employees on an annual basis.

***Closing Date 15 August 2025***
 
 
 
 

• Bachelor’s degree in pharmacy (BPharm)
• Active member with SAPC.
• Computer Literacy in MS Office
< i>2-3 years’ relevant experience within a pharmaceutical distribution/wholesale environment would be an advantage.
• E perience in Quality Management Systems would be an advantage.
• Or cle R12 experience would be an advantage

Fine Chemicals requires the services of a Responsible Pharmacist & QA Manager. To qualify for these positions the most suitable candidates must fulfill the following requirements

JOB SPECIFICATIONS:

• Minimum requirement BPharm Degree
• A minimum of 3-5 years of Manufacturing and Quality experience is needed
• A minimum of 5-10 years of Management experience in Pharmaceutical, API, or medical device manufacturing facilities.
• Must have 3-5 years of Management/Supervisory experience
• Must be registered with the Pharmacy Council
• Must have completed Internship & Community Service
• Must have experience in validation processes and requirements
• Must have internal and overseas vendor auditing experience.
• Sound knowledge of GMP regulations (European, US, UK, WHO, PICS).
• Knowledge of other pharmaceutical and scientific standards (ICH, Pharmacopoeia etc.)
• Knowledge and understanding of Quality Management Systems in pharmaceutical and related industries.
• Must have had exposure to international pharmaceutical practices.
• Knowledge of engineering systems as relates to utilities and equipment in facilities.
• Sound knowledge of manufacturing products and processes.
• Knowledge of packaging technology is an advantage.
• Microbiological experience would be advantageous
• Product registration experience would advantageous
• Computer proficiency in MS Office and SAP.

BASIC JOB FUNCTIONS (Brief Summary)

• SAHPRA Permit Applications
• Obtaining the necessary permits for import and export of Specified Schedule 5 and Schedule Substances.
• Host customer and regulatory audits on behalf of Fine Chemicals.
• Technical, supply, and quality agreements are completed accurately and timeously.
• Ensure annual renewal takes place with the South African Pharmacy Council (SAPC)
• Ensure that Management Review (QSMR)of the Quality System is conducted periodically.
• Suitable systems exist for the management of SOPs, change control, deviations are investigated and resolved, CAPA is raised where appropriate, and review and approval of all quality-related documents.
• Systems are managed to ensure compliance with standards in QSMR meetings.
• Establish policies and procedures concerning acts performed and services provided in the company relating to scheduled substance.
• Ensure that there is an effective system for the release/rejection of all APIs/intermediates for use outside the control of FCC.
• To ensure legal compliance to all Acts, i.e. the Pharmacy Act (Act No 53 of 1974, as amended) and the Medicines and Related Substance Control Act (Act 101 of 1965, as amended)
• To carry out the duties of a Responsible Pharmacist in accordance with Regulations 28 of the Pharmacy Act
• To act responsibly in the practice of pharmacist in accordance with operational requirements of the business
• Initiate, compose, implement, and regularly update all documentation related to the Quality Unit.
• Train appropriate personnel in SOP’s and other relevant areas.
li >Administer and conduct internal audits.
• Participate in the batch release process by ensuring adherence of products to GMP guidelines.
• Manage and maintain the Quality Management System.
• Manage and control staff and other resources as required to meet the objectives of the Quality Unit and FCC.
• Adhere to and promote compliance with H&S regulations.
• Conduct supplier audits and participate in vendor management processes.

PERSONAL ATTRIBUTES (Brief Summary)

• Good organizational skills, proven leadership skills, and self-driven.
• Exceptional attention to detail and accuracy.
• Excellent report writing and document reviewing skills.
• Uncompromising individual integrity and work ethic.
• Exercise interpersonal skills, communication, training, and problem-solving skills to optimize team performance.
• Demonstrate initiative and apply advanced concepts
• Proven leadership skills, self-driven and motivated. 

Suitably qualified applicants are invited to submit their CV’s online on or before the specified date. Preference will be given to applicants from designated groups in accordance with laws governing employment equity, where such laws are applicable to the Aspen entity that will employ the successful candidate. If you have not heard from the HR department within 30 days of this advert closing, please consider your application unsuccessful.

Responsible Pharmacist

The Responsible Pharmacist is to ensure that all pharmaceutical and related activities undertaken and/or under consideration are according to licenses and legislation as well as any corporate guidelines. The suitable candidate will take full responsibility for all pharmaceutical actions taking place in the Sterile Manufacturing unit and are compliant according to national / international cGMP Guidelines, and will be based in Midrand, Gauteng.

Duties & Responsibilities

Regulatory and Licence Compliance

• To liaise with the SAPC in terms of statutory compliance and to ensure Good Manufacturing Practice and Good Pharmacy Practice in the Sterile Manufacturing Unit.
• To undertake the overall administration of the pharmacy business, as described in Section 25(1) of the Pharmacy Act of 1974.
• Responsible to SAHPRA for compliance with the requirements of the Medicines and Related Substances Act, 1965 (Act 101 of 1965).
• To liaise with SAHPRA in terms of regulatory compliance, registration of medicine and final product, pharmacovigilance, and complaints.
• Ensure GMP and Good Laboratory Practice (GLP) compliance from suppliers and contracted laboratories.
• Ensure that persons being employed at the company and who provide services forming part of the scope of pharmacy practice of a pharmacist are appropriately registered with the South African Pharmacy Council.
• Notify the Pharmacy Council immediately upon receiving knowledge that his/her services as responsible pharmacist have been or will be terminated.
• Take corrective measures in respect of deficiencies with regard to inspection reports of the Pharmacy Council or in terms of the Medicines Act.
• Ensure that a letter of authorisation to communicate with Council, signed by the GM/CEO, be submitted to SAHPRA.
• Control the manufacturing or distribution of medicines, scheduled substances or medical devices in terms of the provisions of the Medicines Act, 1965.
• Be part of the decision-making process affecting the pharmacy business.
• Does not introduce or carry out any instruction or order of management with regards to the pharmacy business of the pharmacy owner which could amount to a contravention of legislation applicable to such pharmacy business.
• Ensure that the directors of the company comply with all the conditions of ownership of such a pharmacy business.
• Ensure that no person is appointed to perform any act falling outside the scope of practice of the category in which such person is registered or which he/she is not authorised to perform in terms of the Pharmacy Act, 1974 (Act 53 of 1974).
• Report in writing any non-compliance with the Pharmacy Act to the management of such pharmacy business and furnish Pharmacy Council with a copy thereof.
• Ensure continuous registration of the pharmacy with the statutory bodies.
• To facilitate programmes of Continuing Professional Development for all pharmacists.
• To ensure regulatory compliance with respect to procurement, storage, distribution and correct disposal of all medicinal and medical products.
• To co-ordinate training (if applicable) of Pharmacist Assistant with an accredited Service Provider for all admixing and supportive staff.
• To assess and approve all customers for compliance with statutory and regulatory requirements.
• To purchase and maintain the latest up to date Reference Books as stipulated by SAPC.
• Ensures that all activities undertaken or proposed to be undertaken are in compliance with legislated requirements and in compliance with corporate guidelines.
• Implement corrective action from SAHPRA and/or Pharmacy Council inspections and or corporate audits.

Quality Compliance

• To review Quarterly Risk Reports.
• To oversee the implementation of a Quality Management System.
• To oversee the SOP process and approve all written procedures pertaining to the scope of practise of a pharmacist as set out in Act 53 of 1974.
• To oversee that processes needed for the Quality Management System are established, implemented and maintained.
• To oversee annual Management Reviews.
• To manage all product complaints by ensuring that they are reported on in-house database on time and to follow up regularly with respect to responses to such complaints.
• To oversee the preparation of Product Quality Reviews (PQR) of all final products.
• To ensure that Quality agreements are in place with all suppliers of product and critical services.
• To oversee inspections of all suppliers of product and services which have an impact on Quality.
• To oversee the assessment of all distributors and transporters for compliance as per SLA with the service provider.
• To promote the awareness of customer requirements throughout the company.
• To establish a culture of continuous training within the company and to ensure proper documentation of such training.
• To ensure that Technical Agreements are in place with all suppliers and distribution companies.

Sterile Product and Facility Compliance

• To manage and ensure smooth functioning of the Aseptic Services Unit, ensuring compliance to cGMP and specific requirements of SAHPRA as stated in the License to Manufacture.
• Ensure correct use and maintenance of all ASU equipment.
• Conduct periodic research on products being mixed in the ASU with respect to validation of Processes, Stability and other components.
• Ensure adherence to occupational health and safety requirements.

Staff Management and Training

• Ensure co-operation between quality and production staff.
• Ensure personnel have the correct education, training and experience to perform the assigned function.
• Assess staff competency as well as co-ordinate and facilitate training of staff.
• Implement disciplinary action where required.
• Oversee training of cGMP and other compliance training for all new and existing staff as required.
• Ensure a robust training system is in place that ensures compliance with cGMP.

Budgets

• Manage Capex, expense and CASH-flow budgets.
• Endeavour to achieve annual budgets and production target.

General

• To represent the company at various Professional Associations e.g. ISPE, PDA, PSSA, SAAPRA, SAAHIP, SAAPI.

Stock Control

• Oversee the stock control process.
• Ensure monthly cycle counts are performed.
• Ensure annual stock take is performed in line with Head Office requirements.
• Ensure adequate stock levels are maintained.

Production

• Will be responsible for the final release of all products produced inside the ASU.
• Implementing of best practices, designed to develop and improve manufacturing efficiency.
• Oversee all the production processes inside the ASU.
• Assist in conducting audit activities to ensure compliance with all licence conditions and GMP rules and regulations.

Desired Experience & Qualification

• B.Pharm Degree
• Management training

Desired Work Experience

• At least five years’ experience in Pharmaceutical industry.
• Two to three years management level experience with experience in leading and managing a Quality team and/or Production team, with proven track record.
• Management of Projects within the pharmaceutical industry advantage.

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Responsible Pharmacist SAPC Warehousing East Rand

Manage and maintain the pharmaceutical operations in accordance with SAHPRA, SAPC, company, and client requirements. Oversee the quality management system (QMS) documentation, records, processes, and procedures.

Minimum requirements :

• Matric / Grade 12
• Qualified and registered pharmacist with ISO 9001 knowledge
• Minimum 2-3 years experience with ISO 9001 Quality Systems Management and auditing
• Valid SA driver's license and own vehicle
• Willing to work after hours if necessary
• Warehousing experience is beneficial

Job description : General

• Maintain certification against ISO 9001 and relevant pharmaceutical licenses
• Implement, manage, and maintain procedures for a successful QMS system
• Manage corrective and preventive actions (CAPAs) from audits
• Compile QMS reports and provide feedback to management
• Identify corrective actions and opportunities for improvement
• Promote awareness of the QMS within the business
• Set up and facilitate QMS meetings
• Maintain QMS documentation and filing
• Prepare and schedule management review meetings
• Perform administrative tasks and general housekeeping

Pharmaceuticals

• Must be registered as a pharmacist with SAPC
• Liaise with SAPC for compliance and licensing
• Ensure proper handling, storage, and distribution of pharmaceutical products
• Control access to scheduled products and ensure delivery only to licensed entities
• Maintain contracts and SLAs with third-party distributors and service providers
• Ensure all clients possess necessary licenses and registrations
• Ensure regulatory compliance in procurement, storage, and disposal of medicinal and medical products
• Maintain storage control and documentation for Schedule 5 and 6 products
• Purchase and keep reference books as stipulated by SAPC
• Sample imported products and keep retention samples as per instructions
• Assess third-party distributors and transporters for compliance
• Report improvement needs to management
• Act as Pharmacovigilance Responsible Person and manage ADR reporting
• Oversee pharmaceutical warehouse operations, including inventory control and stock management
• Ensure occupational health and safety compliance
• Document any out-of-limit situations and report to QA
• Ensure personnel working in storage areas are properly trained
• Control access to restricted storage areas
• Maintain accurate records of pharmaceutical receipt, storage, and transfer
• Participate in CPD programs and ensure pharmacist coverage in the absence of the Responsible Pharmacist
• Ensure availability of reference sources as per regulations

Training

• Plan, schedule, and conduct QMS training sessions
• Manage training records according to company procedures

Audits

• Plan and conduct internal quality audits
• Manage audit follow-ups and corrective actions
• Coordinate with regulatory bodies on audit schedules and requirements
• Manage and prepare for customer audits

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Introduction

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 Regulatory Responsible Pharmacist!

Duties & Responsibilities

As their new Regulatory Responsible Pharmacist, here’s what you’ll do:

• Operationally be involved with all aspects of the distribution processes and quality issues of the total organization.
• Responsible for the coordination and management of review, updating, compilation and submission of CTD dossiers to SAHPRA.
• Overall responsibility to ensure that ALL operations are conducted according to the requirements of The Medicines and Related Substances Act (Act 101 of 1965), as amended, and The Pharmacy Act (Act 53 of 1974), as amended, as well as in accordance with the requirements of any other related legislation including Medical Device Regulation (2016) and ISO standards applied i.e., ISO 13485.
• Act as a Responsible Pharmacist for the company including the warehouse and the applicant.
• The Responsible Pharmacist shall be responsible to The Pharmacy Council for any act performed by or on behalf of the company.

Desired Experience & Qualification

What you will need:

• A minimum of 5 years experience as a Regulatory Responsible Pharmacist from the Pharmaceutical/Medical/FMCG Manufacturing industry essential
• Matric plus BPharm Registered with SAPC
• Regulatory Affairs experience a must have
• Warehousing and Distribution experience
• In depth knowledge of Regulations, Acts, and Guidelines
• SAHPRA experience a MUST HAVE!

Interested?

Start an AFFAIR with this company and apply now !

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