Quality Control Manager

**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 close by the facility at New Cairo as well. 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).

**QC Manager Vacancy**:
**MultiCare** Egypt for Pharmaceutical Industries is seeking for a Quality Control Manager as per the following details:

- **Designation**: QC Manager
- **Location**: 3rd Settlement, New Cairo, Kattamia (Industrial Area), Cairo
- **Reporting**: Quality Director
- **Grade**: qCm01/qCm03

**Job Purpose**:
We are hiring a Quality Control Manager to lead the function at Multicare to entail setting and implementing internal/external quality requirements to ensure Multicare's products meet standard quality expectations as per the prevailing authorities' guidelines, internal policies and associated Standard Operating Procedures (SOP)

**A. Essential Duties and Responsibilities**:

- One of the big tickets of the role is the responsibility for ensuring manufactured products meet set standards of quality, reliability and performance
- Lead the QC Team handling Raw Materials, Microbiology and Finished Products towards meeting/exceeding the functional/business set objectives
- Develop, coach, mentor Quality Control members to ensure readiness of a second line ready to pursue further own career at Multicare
- Motivate and inspire the QC Team enhance the productivity and ensure retention of talents
- Drive the sustainable on-going process of continuous improvement of the Quality Control function by challenging the status-quo and device/suggest recommendations to strengthen capabilities and efficiency of the team
- Review current Quality Control practices and device a full-fledged self-inspection auditing process (L1) as a key mechanism and toll for the ongoing continuous improvement and development strategy
- From QC perspective, ensure manufacturing processes comply with local and global standards of production
- Cross-functional interaction with counterparts' function at the site; QA, Production, Regulatory, WH, etc through effective communication to ensure quality is the key theme of all activities performed
- Oversee the recruit and training of QC personnel to ensure an effective work unit and continuous team development
- Focal point of contact for QC function and assist/facilitate external quality auditors as of the QC responsibility
- Maintain proper records and documentation of quality tests and other quality-related activities through following the practice and governing guidelines of Documentation Retention Policy
- Collect and compile relevant quality statistical data to be presented to internal or external affiliates
- Assess performance and identify any areas of improvement, recommend and implement actions to enhance them
- Liaise with other managers and concerned to provide training, tools and techniques to enable others to achieve quality standards
- Ensure cGMP and TQM and vis-à-vis system and guidelines are embedded /instilled in the day-to-day practice of the QC tasks

**B. Qualification/Knowledge/Experience**:
Level of Education:

- Pharmacy graduate preferably with related post-graduate QMS degree or

Experience:

- Track record of leading the QC function at sound pharmaceutical organizations

Language:

- Excellent verbal, written and interpersonal communication skills. English fluency essential

IT Literacy:

- MS-Office

**C. Competencies and Behaviors**:

- Leading by example to be role model for others
- Balance between people and task orientation
- Ability to inspire and motivate subordinates
- Team developer
- The drive for self-development, the ability to collaborate, and an action-oriented work ethic
- Excellent written and verbal skills in English
- Ability to handle simultaneously paral