Production Supervisor - Solid Dosage Forms

Egypt - Cairo

Job description

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 +23 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 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).

VACANCY:

MultiCare Egypt for Pharmaceutical Industries is seeking a professional caliber to join the Production Team at the facility as Production Supervisor as per the following details :

  • Designation: Production Supervisor
  • Location: Industrial Zone, third Settlement , New Cairo
  • Grade: pS01/pS02
  • Reporting to : Production Manager

Job Purpose:

The Production Supervisor ensures the execution of all pertinent production phases in compliance with the requirements of the GMPs supervising the activities carried out by the personnel of the Production Department. The Production Supervisor is responsible for the planning of Production Department (drug production in sterile lines and packaging area

A. Essential Duties and Responsibilities:

  • Oversee work teams within the production area to lead the technical resources of the team
  • You will be relied on to solve complex problems within your area of expertise
  • Convey instructions and production schedules in accomplishing a variety of tasks, such as meeting quality, accountability, security, productivity and safety requirements. You will ensure that all activities are completed based on Standard Operating Procedures, batch records, Current Good Manufacturing Practices and plant procedures
  • Manage multiple projects and ongoing work activities within a team
  • Responsible for effective leadership of team which includes managing the daily operation ensuring that applicable safety guidelines policies are followed
  • Ensure compliance with all regulators and company requirements
  • Participate in equipment failure investigations to determine root causes and propose solutions, process operational improvements
  • Assure appropriate communication and implementation of corrective/preventive actions to avoid reoccurrence
  • Responsible for counseling colleagues to assure proper development for their success, and to provide corrective action when necessary
  • Execute the production preparation process in order to match the production flow process
  • Supervise different production processes
  • Follow up the delivery of the product step by step in order to facilitate the internal operation
  • Verify the methods of dressing, behavioral standards, and flow of materials in compliance with internal procedures
  • Execute and supervise the compilation of the Batch Record of the products and logbooks of the equipment in real time and in accordance with GMP requirements
  • Revise Production Plan on the bases of change requested by different authorized stakeholders
  • Verify the correct compilation of batch product records, logbooks, and worksheets
  • Report to the function manager of any anomaly / deviation detected during any processing phase of its own relevance
  • Supervise the activities carried out by the personnel of the Production Department in relation to the various organizational positions
  • Collaborate with the Production Manager with the aim of ensuring the achievement of production objectives consistent with the GMP (quantity, mix, costs) through the verification of the correct application of the planning of the activities
  • Maintain and control the equipment / plants of competence, in accordance with the requirements of the procedures
  • Share a daily plan to assigned department for analysis of the products

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 trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!

For the selected candidates, we offer a superb working environment and a challenging atmosphere.

You can also look forward to a competitive salary and benefits package with room for talents and potential candidates to sharpen and advance their career forward supported by exposure, learning and development opportunities.

Job Type: Full-time


B. Qualification/Knowledge/Experience:Level of education: Life Science DegreeExperience: 3-5 years previous experience of similar role is mandated preferably in Solid Dosage Forms Production Lines - Multinational experience is an advantageLanguage :English proficiency is mandatedIT Literacy: Professional MS-Office knowledgeC. Competencies and Behaviors:Professional communication skills both written and oralAbility to work under sustainable pressure and handling of simultaneous tasks to meet timelineStrong planning and organization capabilitiesAbility to influence, convince and persuadeStrong sense of accountability and autonomyMust be flexible and adaptable to changeProven record of problem-solving, decision-making skills and application of process improvement tools
Post date: Today
Publisher: Wuzzuf .com
Post date: Today
Publisher: Wuzzuf .com