Julphar Pharmaceuticals PLC is a joint venture between Gulf Pharmaceuticals Industries (Julphar) U.A.E and MEDTECH Ethiopia, which is involved in the manufacturing of LIFE SAVING Drugs for the local Ethiopian market use as well as for export. Julphar is looking for new candidates with big ambitions, potentials and commitment to improve the quality of life for our end customers. 

Job information and Candidate specification

Position Title : Junior Quality Assurance Pharmacist

Division : Quality Assurance 

Reporting to : Quality Assurance Manager

Junior QA Pharmacist is responsible for carrying out/ participating in various QA Operations: Documentation, Internal Auditing, Product Quality Review, Validation/ Qualification of process/ Equipment/ Method, and Training activities within the organization.

Main Responsibilities:

Under the guidance of the QA Manager, The Jr.QA Pharmacist shall carry out the following duties:

• Reviewing of batch processing records received from IPQA-supervisor, before transferring to the QA Associate Manager. 

• Notify any error observed during review of batch documents and coordinate with production and packaging department for rectifying mistakes. 

• Preparation, review, and issuance of new/ existing Batch processing documents.

• Carryout daily/ weekly inspection along with senior QA staffs for cGMP compliance gap assessment in the company.

• Record non-compliances and notify department of the recorded non-compliance observations and follow up the correction. 

• Prepare a summary report of the observed non-compliance to the QA/QC Manager.

• Participate in periodic self-inspections conducted in the company and follow up of the implementation and closeout of the audit observations. 

• Responsible for receiving, logging, assessing, and follow-up of the closing of initiated CAPA (Corrective and Preventive Action) and retaining the documents related to it.   

• Review all documents (Standard Operating Procedures and technical documents) for correctness and compliance prior to further review by QA Associate Manager. 

• Responsible for receiving, reviewing, controlling, handling, and distribution of all Julphar Pharmaceuticals PLC. (Ethiopia) SOPs and technical documents.

• Responsible for documents archiving and retrieval of supersedes documents. 

• Review all annually manufactured products by Julphar Pharmaceuticals Plc. (Ethiopia) and prepare Product Quality Review (PQR) document for each product. 

• Follow-up the conduction of training by departments as per their respective approved training calendar and archive training related documents. 

• Participate in the execution of both validation and qualification activities; document compilation, review, and follow-up. 

• Check stability study data for any OOS or OOT and make sure the necessary action is taken.

• Compile and document finalized stability study records and prepare report. 

• Prepare and review an approved vendor list for APIs, inactive raw materials and packaging materials. 

• Performs other duties (where explanation provided and understood) that concern the department in accordance with the instruction issued by the Quality Assurance Manager.

Employment type: Permanent

Number Required: One 

Place of Assignment: Addis Ababa

Salary: As per the Company Scale            

Posting Date: August 04, 2025

Closing Date: August 10, 2025

Job Requirements

Job Requirements (Education and work experience): 

• Bachelor’s degree in pharmacy, 

• No work experience is required 

Skills required: 

• Good interpersonal skill 

• Good communication skills

• Proactive and commitment for outcome

• Have good knowledge about current Good Manufacturing Practice.

How To Apply

Interested applicants who meet the above requirements are requested to submit their CVs and all supportive documents in a Single Pdf Format through julpharethiopia@gmail.com until August 10, 2025

Job Requirements BSc Degree in Pharmacy or in a related field of study Duties and Responsibilities: - Reviewing of batch processing records received from IPQA-supervisor, before transferring to the QA Associate Manager.  - Reviewing of batch processing records received from IPQA-supervisor, before transferring to the QA Associate Manager.  - Preparation, review, and issuance of new/ existing Batch processing documents. - Carryout daily/ weekly inspection along with senior QA staffs for cGMP compliance gap assessment in the company. How to Apply Submit your application, updated CV and supporting credentials via email: julpharethiopia@gmail.com