Qc Finished Products Supervisor

6 days ago

مصر, Egypt Multicare Egypt for Pharmaceutical Industries Full time

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 +21 years of prominent existence in the local market and has almost +66 products marketed and more to come through the pipelines. Multicare Egypt for Pharmaceutical Industries is the manufacturing facility of Pharmacare for Trading Agency, which located at the Industrial Zone - New Cairo and its HQ at New Cairo as well close by the facility. 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 Supervisor per the following details:

- **Location **: New Cairo, Industrial Zone, Third Settlement
- **Reporting**: Finished Products Section Head
- **Grade**: qC01/qC03

**Purpose**:
Successful incumbent will be responsible for conducting different types of tests and analysis further to finish products in a timely manner for in-process and finished products to ensure products specifications fulfil the prevailing standards governed by Regulatory and GMP practice.

**A.Essential Duties and Responsibilities**:

- Analyze finished products assuring strict compliance with standards prior to the release and report results with conformity statement
- Perform physical testing and chemical analysis of different pharmaceutical dosage forms including Tablets and Capsules
- Adhere to the approved controlled standard operating procedures and work instructions of finished product specifications and test methods whilst testing performing
- Test system modifications in order to get ready for new process implementations and introduce databases of known test deficiencies
- Maintain the quality control approved control records related to the daily work and adhere to the governing record-retention and archiving policy
- Calibrate instruments according to work instructions to ensure compliance to standards
- Fully abide by the instructions of Environmental, Health and Safety in handling all job related tasks and activities
- Drive day-to-day operation of QC laboratory, including management and scheduling of laboratory personnel to meet the need of manufacturing schedule
- Perform wet and instrumental analysis (HPLC, UV Spectrophotometer, Viscometer, Titro-processor, pH meter, Balance, ovens, Centrifuge, Dissolution tester, Disintegration tester, Hardness tester, Friability tester)of bulk, in-process and finished products
- Work in a testing environment, assess products, check quality and accuracy, and create tests scripts
- Report and participate in investigation of any NCR with assigned cross functional committee as appropriate
- Create and/or review the Certificate of Analysis (Test Notes) presented to the MoH
- Quality Management, as required, may assign and require other duties and responsibilities not previously mentioned above
- Facilitates a culture of “speaking up” and ensuring all cGMP compliance activities are followed
- Support regulatory inspections and audits
- Coach, mentor and develop the QC Analysts reporting to him/her

**B. Job Requirements**:

- 3-5 Years post-graduate pharmaceutical manufacturing experience preferably in Quality Control Dept.
- Experience of same role at reputable Pharmaceutical companies
- 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 preferably at different functional areas like Production, QC, QA, etc among them most work experience desired at Quality Control Supervisory role

**D. Education Requirements**:
A degree in Pharmacy is ESSENTIAL. Related post-graduate qualification is highly desired (GMP, TQM, etc)

**E.Competencies and Behaviors**:

- Indisputable leadership capabilities
- Strategic thinking and planning skills
- Excellent written and verbal skills in English
- Ability to handle simultaneously parallel task with quality delivery

**What we offer*

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