About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

The Compliance Officer will be responsible for providing management and day to day support to the Company’s overall Compliance activities

across all business units and functions ensuring that risks and controls from project inception to support within their business unit are

identified, prioritized, effectively managed, and monitored. Additionally, this role should work within the business unit to ensure Company

follows the required internal and external compliance standards and delivers a reduction in the overall risk profile.


RESPONSIBILITIES AND TASKS :

  1. Corporate Governance Compliance ( including Operations, Regulatory and Policy Framework ):
    • Contribute to maintenance of the Business Unit delivery and operational frameworks (Activities, deliverables, roles, and responsibilities) and ensure alignment to country regulations.
    • Ensure Company activities align with Egypt Regulatory requirements and liaise with commercial/marketing to ensure proper implementation of the regulations.
    • Contribute to ensuring the Company is keeping up to date with regulatory and legal requirements through a pro-active knowledge management program in alignment with legal function.
    • Ensure the Company and all its BU and functions adhere to its Bylaws, charters. Policies and authority levels.
    • Support tracking and managing all CAPAs across BU, department and functions and escalate to top management and audit committee any significant gaps and findings.
  2. Corporate Governance Compliance
    • Ensure that the Company complies and adheres to all required regulatory filling and keeps up-to-date corporate registry and official documents.
    • Ensuring that policies and SOPs are in place to ensure proper management and tracking of regulatory filling and disclosures including capital market authority requirements.
  3. Risk Management
    • Contribute to identification and initiation of Risk mitigation projects to address significant risks impacting the Company
    • Facilitate risk identification and risk discussions within BU, both operational risk, regulatory and strategic risk
    • Assist the Management to make risk informed decisions through a comprehensive Risk Dashboard
    • Raise and approve (where necessary) Policy Exceptions and significant Risks
    • Input into, review and enforce compliance within Policies and Standards as required within Business Unit
    • Ensure emerging risks are identified and escalated appropriately and in a timely manner
    • Perform GRC requirements within third party framework
    • Ensure awareness of process and report suspected breach
    • Provide training and education program to ensure ongoing awareness on new and updated Policies and Standards within the Company
  4. Audit Support
    • Contribute to ensuring Business Unit is ready to host external inspections from regulatory bodies
    • Support management of overall Business Unit inspection readiness activities and CAPAs in liaison with the business
    • Report status on CAPA’s to Business Unit RMCB
  5. Policy Formation
    • Create, review, and approve policy, standards, procedures, guidance, and training for compliance with relevant legislation and SOP Requirements.
    • Support reviews of the commercial and marketing activities to make sure it complies with legislation and specifies any required changes within their Business Unit
  6. Education:
    • Bachelor’s Degree in Pharmaceutical, Accounting, Law, preferably MA in business related field
  7. Experience:
    • 7-10 years’ experience in Compliance and Risk Management At least 8-10 years’ experience preferably pharmaceutical industry.
  8. Skills:
    • Ability to meet assigned deadlines.
    • Excellent communication and interpersonal skills.
    • Good Negotiation skills.
    • Highly detail oriented and organized in work.
    • Familiar with rules and regulations for export of commodities internally and externally.
    • Excellent project management skills to manage own project and tasks.
    • Fluent in English & Arabic.
  9. Working Conditions:
    • For non-(Administrative/ clerical) jobs.

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

Implement optimization process for the supply chain and planning department


RESPONSIBILITIES AND TASKS :

    • Participate in the development of the supply chain strategy for the organization.
    • Coordinate the process of supply/demand forecasting, inventory utilization, and on time delivery.
    • Support continuous quality improvement of the APIs and excipient required for production
    • Planning delivery timetables
    • Ensuring stores have enough stock
    • Making sure suppliers have enough stock to meet demand
    • Overseeing the ordering and packaging process
    • Monitoring stock levels
  1. Education:
    • Bachelor’s degree in pharmaceutical science
  2. Experience:
    • 1-3 years supply chain in pharmaceutical company
  3. Skills:
    • Very Good communication skills.
    • A strong sense of ethics.
    • Integrity, Services and accountability
    • Commitment to quality.
    • Time management.
    • Tech knowledge (Microsoft App advanced knowledge)

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

The Taxes manager Manager will oversee the activities of Company Taxes. Developing, implementing, and maintaining a system of Taxes

according to Egyptian laws and taxes regulations.


RESPONSIBILITIES AND TASKS :

    • Delivering a full range of tax services in compliance with laws and regulations within timeframe.
    • Building relationships and interacting with clients to provide excellent planning, consulting and expertise.
    • Providing innovative tax planning and reviewing all kinds of tax returns.
    • Identify and mitigate tax risks.
    • Manage tax provision and tax compliance process.
    • Improve processes by developing or implementing best practices.
    • Manage and coordinate tax audits.
    • Maintain tax balances on general ledger to be confirmed with Tax Authority records.
    • Prepare all tax papers in regular basis and handle all information data requests by Tax Inspectors.
  1. Education:
    • Bachelor degree of Faculty of commerce Accounting section
    • Post-graduate degree is preferred. (CPA – CMA – ESAA)
  2. Experience:
    • 10 to 15 Years of experience included at least 5 years in big four firms.
  3. Skills:
    • Excellent verbal and written communication skills.
    • Excellent organizational skills.
    • Excellent time management skills with a proven ability to meet deadlines.
    • Strong analytical and problem-solving skills.
    • Proficient with Microsoft Office Suite or related software.

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

Develop, implement, and maintain the bulk and finished product sample analysis, according to specification & method of analysis and in

compliance with regulatory requirements.

Monitor analytical activities during quality studies like process validation, cleaning validation and hold time studies.


DIMENSIONS:

    • Physical and chemical analysis of bulk and finished product samples.
    • Review and check the analysis results. Reporting the data using statistical tools with interpretation of the results.
    • Monitor and check analysis work related to quality assurance studies.
    • Prepare and review the relevant quality control documents.

RESPONSIBILITIES AND TASKS :

    • Perform physical testing and chemical analysis of different pharmaceutical dosage forms.
    • Prepare and standardizes volumetric solutions, reagents, dissolution media and buffers.
    • Follows the controlled standard operating procedures and work instructions of finished product specifications and test methods during analysis process.
    • Maintain the quality control approved control records related to the daily work.
    • Issues and signs test certificates.
    • Report and participate in investigation of any OOS case or NCR.
    • Review, Check & follow up all results of bulk, semi-finished & finished product.
    • Prepare and write the relevant quality control documents as specifications, analytical monographs, sampling processes and technical instructions.
    • Training the analysts & Subordinates.
    • Implementation of good documentation practices ( GDP ) and good laboratory practices (GLP) in Qc labs.
    • Follow up and review subordinates.
    • Handling & control of lab equipment during lab activities.
    • Calibration of all analytical instruments in Quality Control Lab.
    • Recording the activities in the operation and instrument logbooks
    • Aware and follow safety measures in the lab.
    • Participating in APR analysis by trending QC data
  1. Education:
    • Bachelor of Science, or pharmacy.
  2. Experience:
    • 3 – 5 years
  3. Skills:
    • Good manners.
    • Work under pressure.
    • Problem solving & Logic thinking.
    • An Organized person.
    • Teamwork.
    • Has ability to improve & is able to learn.
    • Good Communication skills.
    • Basic Quality tools.
    • Soft Skills (Time Management, Team Building)
  4. Working Conditions:
    • For non-(Administrative/ clerical) jobs.

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

Quality Assurance Documentation senior will be responsible for assisting in the implementation and maintenance of the Quality Management

System (QMS) by coordinating the revision, review, and approval of Batch Manufacturing Record (BMR), Batch Packaging Report (BPR), SOPs and other GMP documents ensuring compliance with applicable domestic standards and regulations.


DIMENSIONS:

    • Preparation for external audits and Follow audit findings investigation.
    • Vendor qualification and conducting the vendor audits.
    • Document and record control.
    • Issuance and reviewing of QA documents.
    • Revision of batch records, certificate of analysis, method of analysis, specifications, etc…

RESPONSIBILITIES AND TASKS :

    • Develop procedures to ensure that Quality System documents are originated, changed, reviewed, distributed, archived and periodically reviewed using systems that are efficient and meet all regulatory requirements.
    • Develop and maintains systems that effectively archive and retrieve quality records assigned to the Document Control, including external standards, technical reports, etc.
    • Ensure that the Document Control systems used at all company sites are harmonized where appropriate.
    • Updates and maintains Quality Assurance Operations logs and databases and generating metrics as needed
    • Follow up the registration requirements (samples, certificates, specifications, methods of analysis) for the registration department.
    • Creation, update & issue batch records required for production – Filling & Packaging.
    • Prepare periodic summaries of document and record control activities, including the analysis of the types of changed documents, change order cycle times.
    • Responsible for Preparation, Review, Control and Revision of Standard Operating Procedure.
    • Preparation, Review and Control of Formats and all documents.
    • Responsible for training program.
    • Responsible for Preparation, Review, Control and Revision of head files Like (Site Master File, Quality Manual).
    • Responsible for Preparation, Review, Control and Revision of Analysis Worksheets.
    • Responsible for Preparation, Review, Approval, Control and Revision of Specifications and Standard Test Procedures.
    • Participates in internal audits and supporting external audits
    • Responsible for Batch Release process.
    • Responsible for reconciliation of documents.
    • Responsible for batch record revision after retrieval from production.
  1. Education:
    • Bachelor of pharmacy or science
  2. Experience:
    • (3-5) year of experience.
  3. Skills:
    • computer knowledge,
    • English language is good
    • Good in Microsoft excel & word and soft skills

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

This position is responsible for assisting with Quality Assurance tasks and managing company documents while also ensuring their accuracy,

quality and integrity. Adheres to record retention policies, safeguard information and retrieve data more effectively


DIMENSIONS:

    • Issue and follow up CAPA, Deviation, incident and change control documents.
    • Annual product review (APR) data collection and analysis.
    • Preparation of Common Technical Documents (CTD) files for Pharmaceutical and Nutraceuticals products.
    • Participate in internal audit program and vendor qualification audits.
    • Stoppage of any process where Quality measurements or GMP is not conducted.

RESPONSIBILITIES AND TASKS :

    • Preparation of CTD files according to ICH guidelines.
    • Expertise proficiency with software tools and matrices for CTD submission.
    • Provide the regulatory reviews of customer complaints and defining the regulatory responsibility.
    • Conducting internal audit for production department, engineering, warehouse, etc..
    • Perform the intermediate and finished product and on-line inspections.
    • Regular check of RH (%), P and temperature in different production areas.
    • Reporting any deviation happened in production area.
    • Handling of returned drug products.
    • Responsible for Annual product review data collection.
    • Coordinate / Support Change Controls as needed.
    • Write, review and approve Policies, Standard Operating Procedures (SOPs) and associated processes/guidelines.
    • Coordinate activities associated with event resolution and CAPAs with a focus on organizing and attending cross-functional meetings to lead/facilitate investigations and to provide updates on discrepancy investigations; publish notes and action items from meetings; provide support to the investigation process and follow-up to assure timely discrepancy closure.
    • Perform independent quality evaluation of deviation reports including root cause analysis cause/preventive action identification, CAPA effectiveness check and trending.
    • Ensure that inspection and audit responses are completed from initiation to closure
    • Support activities to evaluate regulatory compliance
    • SOP writing/revision
    • Participate in the internal audit program, vendor qualification audits,
    • Initiate, Review and approve deviations, CAPAs, change controls.
    • Revise and issuing the SOP's for all the departments
    • Check in-process testing done by production technicians by performing testing, reviewing test data, and writing investigations according to SOPs and GMPs.
  1. Education:
    • Bachelor of pharmacy or science
  2. Experience:
    • (3-5) year of experience.
    • Experience in preparation of Common Technical Documents (CTD) files for Pharmaceutical and Nutraceuticals products.
  3. Skills:
    • computer knowledge,
    • English language is good
    • Good in Microsoft excel & word and soft skills

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

To provide an efficient administration service to the Quality Department. This may include such tasks as scanning, filing, archiving and retrieval,

ordering stationery. To ensure all administration databases and tracking tools are up to date and correct.


DIMENSIONS:

    • Document and record control.
    • Issuance of QA documents.

RESPONSIBILITIES AND TASKS :

    • Responsible for the organization of records
    • Performs a variety of administrative and office support activities
    • Distributing documents
    • Performs data entry and maintains databases
    • Responsible for preparation, Photocopying of all controlled and Uncontrolled Copies of Master documents.
    • Responsible for Issuance Standard Operating Procedure.
    • Responsible for training program.
    • Responsible for Scanning quality assurance document.
    • Responsible for Issuance of Analysis Worksheets.
    • Responsible for Issuance of Specifications and Standard Test Procedures.
    • Responsible for storage & archiving of all documents after retrieval.
    • Responsible for Issuance of registers and formats.
    • Responsible for Issuance of Batch Manufacturing Record (BMR) and Batch Packaging Report (BPR) for production
  1. Education:
    • Bachelor's Degree
  2. Experience:
    • (1-3) year of experience.
  3. Skills:
    • computer knowledge,
    • English language is good
    • Good in Microsoft excel & word

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

The Quality Assurance (QA) Manager will oversee the activity of the quality assurance department and staff,developing, implementing, and

maintaining a system of quality and reliability testing for the organization's products and/or development processes.


RESPONSIBILITIES AND TASKS :

    • Lead the efforts of QA personnel responsible for the testing, investigations, and method transfer activities to ensure compliance with all regulatory requirements, company policies, values, and goals.
    • Develops, implements, and manages processes to ensure that products meet required specifications for quality, function, and reliability prior to delivery.
    • Provide leadership for lot release, incoming quality, manufacturing, and labs investigations, change control and corrective and preventative action review/approval, manufacturing support, record review/approval, and ongoing projects support (if any).
    • Identifies and sets appropriate quality standards and parameters for products.
    • Communicates quality standards and parameters to QA team, product development team, and other appropriate staff.
    • Coordinates product testing processes
    • Identifies and analyzes issues, bugs, defects, and other problems, particularly when problems recur in multiple products; recommends and facilitates solutions to these issues.
    • Reviews client, customer, and user feedback.
    • Maintains compliance with international, local, and organizational laws, regulations, guidelines, and policies.
    • Performs other duties as assigned.
    • Supervisory Responsibilities:
      • Hires and trains quality assurance staff
      • Oversees the daily workflow and schedules of the department.
      • Conducts performance evaluations that are timely and constructive.
  1. DIMENSIONS:

    The section provides numerical data marking the scope of the job.

    List the significant quantities on which the job has direct or indirect impact

    • Financial
      • Annual expense budget, operating cost (including equipment), projects costs …
    • Non-Financial:
      • No. of staff, no. of programs…
  2. WORK CONTACTS:

    Define the main contacts required to achieve the scope of the job:

    • Whom to be contacted? (level) managerial.
    • Department’s managers (QC, Warehouse, Production, etc…).
    • How frequent? Daily or when required
    • Purpose of contacts? Feedback about work progress, updates and or obstacles.
    • Differentiate between internal and external contacts. Internal contacts.
    • Internal:
      • Department’s managers (QC, Warehouse, Production, etc…).
      • Contacts Daily or when required.
      • Purpose of contacts: Feedback about work progress, updates and or obstacles.
    • External:
      • Distributing companies responsible.
      • Contacts if there is customer complaints or product recall.
  3. Education:
    • Bachelor degree of Pharmaceutical Science.
    • Post-graduate QMS degree is preferred.
  4. Experience:
    • 10 Years and fields of experience.
  5. Skills:
    • Excellent verbal and written communication skills.
    • Excellent organizational skills
    • Excellent time management skills with a proven ability to meet deadlines
    • Strong analytical and problem-solving skills.
    • Strong supervisory and leadership skills.
    • Proficient with Microsoft Office Suite or related software
  6. Working Conditions:
    • For non-(Administrative/ clerical) jobs

About the Company :

NERHADOU is Ranked among the top 50 leading corporates for 6 consecutive years out of 1200 Pharmaceutical Corporates in Egypt in terms of

Market Share of Pharmaceutical Products’ Domestic Sales (2019) . Nerhadou is the Nutraceutical & Pharmaceutical market leader in the Middle

East & Africa, while being acknowledged among the top 10 leading corporates in the Egyptian pharmaceutical industry.


JOB PURPOSE :

The executive assistant will be responsible for managing the schedules and communications of the deputy CEO. HE/SHE will be responsible for

prioritizing mails and phone calls and arrange meetings and business events.


RESPONSIBILITIES AND TASKS :

    • Manage the calendar and appointments.
    • Set up business meetings and events.
    • Responsible for EMAILS, and presentations.
    • Organize and maintain the office filling system.
    • Prepare reports as assigned.
    • Travel and accommodation arrangements.
    • Attend meetings and Take minutes.
    • Handle confidential documents ensuring they remain secure.
    • Maintain electronic and manual records ensuring the information is stored and easily accessed.
  1. DIMENSIONS:

    The section provides numerical data marking the scope of the job.

    List the significant quantities on which the job has direct or indirect impact

    • Financial
      • NA
    • Non-Financial:
      • NA
  2. WORK CONTACTS:

    Define the main contacts required to achieve the scope of the job:

    • Internal:
      • Internal stakeholders
    • External:
      • Any other
  3. Education:
    • BSC business Administration or any relevant field
  4. Experience:
    • 3-5 years in similar position preferably in pharmaceutical field
  5. Skills:
    • Very good in Micro soft office (Word – excel – power point).
    • Very good command of English reading and writing.
    • Very Good communication skills.
    • Excellent organization skills.
    • Integrity and confidentiality.
    • Can work under pressure in a timely and accurately manner.
  6. Working Conditions:
    • Office based.

Interested applicants should send their CV to ( Job@nerhadou.com ) and mention the position subject line