Qc Finished Product Senior Specialist

3 days ago

مصر, Egypt Multicare Egypt for Pharmaceutical Industries Full time

**Previous work experience at the capacity of QC-FP role is ESSENTIAL**

**---------------------------------------------------------------------------------------------------------------------------------------------------**

**MultiCare** Egypt for Pharmaceutical Industries is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, gender identity or expression, age disability, or other characteristics protected by prevailing regulations, practice or customs/traditions.

**MultiCare** is a well-established Pharmaceutical Company with diversified scope in both manufacturing and marketing of pharmaceutical products, supplements, cosmetics and medical devices. **MultiCare** has +22 years of prominent existence in the local market and has almost +69 products marketed and more to come through the pipelines. **MultiCare** Egypt for Pharmaceutical Industries is the manufacturing facility which located at the Industrial Zone - New Cairo and its HQ is close by the facility as well in New Cairo. We are one of the fast growing Pharmaceutical Companies in the market which has strong ambition and aspiration to be one of the key players not only in Egypt but also within the region.

Our international alliances are effective in different countries, including Saudi Arabia, United Arab of Emirates, India and New Zealand with future aspiration to extend more business associations and affiliations in near future to further markets. Recently Multicare Poland has been launched which will be the entry port of the business to the European Union (EU).

**Vacancy**:
For the Quality Control Function, we are hiring a QC Finished Products Senior Specialist per the following details:
**Location**: New Cairo, Industrial Zone, Third Settlement
**Reporting**: QC FP Supervisor
**Grade**: qCfp 01/qCfp 03

**Purpose**:
The position holder is responsible for analyzing chemical tests for in-process and finished products in a timely manner. In addition to performing all stability testing. The analyst will also research potential deficiencies and work with production and engineers in order to provide solutions. He will work under a defined SOP and guidelines that need to be fulfilled

**A.Essential Duties and Responsibilities**:

- Analyze finished products entering finished products lab to comply with standards before release, reporting results with conformity statement
- Prepare chemical reagents used in analysis
- Responsible for any deviations in analysis from methods.
- Prepare trend analysis reports for any activity done in the quality control department like water system to get the reports ready by the end of the year.
- Write all SOP’s in quality control in order to have all quality control activities and instruments updated and effective
- Verify ,Validate Methods and perform Specific laboratory activities
- Perform wet and instrumental analysis (HPLC, UV Spectrophotometer, Viscometer, Titroprocessor, pH meter, Balance, ovens, Centrifuge, Dissolution tester, Disintegration tester, Hardness tester, Friability tester)of Bulk, in-process and finished products
- Perform physical testing and chemical analysis of different pharmaceutical dosage forms( tablets, capsules ,drops and syrups)
- Prepare and standardizes volumetric solutions, reagents, dissolution media and buffers
- Calibrate instruments according to work instructions to ensure compliance to standards
- Participate in validation of facilities and manufacturing processes to ensure compliance to standards.
- Follows the approved controlled standard operating procedures and work instructions of finished product specifications and test methods during test performing
- Follows the instructions of environmental, Health and Safety
- Maintain the quality control approved control records related to the daily work
- Provide progress reports in relation to process tests and execute test case scenarios to the FP Supervisor

**B. Job Requirements**:

- 1-2 Year post-graduate pharmaceutical manufacturing experience handling the same role at sound Pharmaceutical Organizations
- Ability to work autonomically or a member of diversified cross
- functional teams
- Ability to prioritize activities, to make difficult decisions to ensure efficient use of resources and address critical issues impacting the business

**C. Knowledge**:
Pharmaceutical manufacturing understanding (GMP, TQM, Policies and SOPs, etc)

D. **Education Requirements**:
Life-Science graduate

**E.Competencies and Behaviors**:

- Ability to prioritize tasks and meet set timelines
- Handling of simultaneous tasks with quality delivery
- Average written and verbal skills in English
- Flexibility to work autonomically or as member of cross-functional team

**What we offer**:
With us, there are always opportunities to break new ground. We empower you to fulfill your ambitions, and our diverse businesses offer various career moves to seek new horizons. We tru

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