IBN AL BAYTAR HIKMAفرصة مهنية
فرصة عمل

مطلوب Production صيدلي

Location: Sidi Thabet Job Type: CDI About Us For over 45 years، Hikma Pharmaceuticals has been putting better health within reach، every day، by creating high-quality medicines and making them accessible to tho…

الموقع
تونس
النشر
2026-09-27

تفاصيل الوظيفة

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Location: Sidi Thabet Job Type: CDI About Us For over 45 years، Hikma Pharmaceuticals has been putting better health within reach، every day، by creating high-quality medicines and making them accessible to those who need them

Requirements & Qualifications

  • Ensure compliance with GMP، company procedures، and regulatory requirements
  • Excellent problem-solving، communication، and leadership skills
  • Ensure compliance with GMP، company procedures، and regulatory requirements.
  • Excellent problem-solving، communication، and leadership skills.

We are helping to shape a healthier world that enriches all our communities، and our global team of 9، 500+ empowered employees are central to this mission

As a trusted and reliable partner of over 800 high-quality generics، specialty and branded pharmaceutical products، we are driven to improve access to medicine

Through our 29 manufacturing plants، 9 R&D centers across the MENA، North America and Europe، our footprint allows us to play a critical role in serving patients

We are looking for a talented Production Pharmacist to join us

At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop، wellbeing is prioritised and our inclusive approach values contributions from all

We’re seeking candidates who embody our values: Innovative، driven to keep learning، Caring، genuinely compassionate in their work، and Collaborative، eager to solve problems together

If you want to be part of a team that cares about impact، this is the place for you.

Key

Supervise and coordinate daily pharmaceutical production operations

Review and approve batch manufacturing records and production documentation

Monitor production processes to ensure product quality and operational efficiency

Investigate production deviations and implement corrective and preventive actions (CAPA)

Collaborate with Quality Assurance، Quality Control، Engineering، and Supply Chain teams

Ensure proper utilization of equipment، facilities، and manpower

Participate in process validation، qualification، and continuous improvement initiatives

Support audits and regulatory inspections

Train and coach production personnel on GMP and operational procedures.

& Experience Degree in Pharmacy

Registered Pharmacist with a valid professional license (where applicable)

Minimum of 3 years of experience in pharmaceutical manufacturing/production

Strong knowledge of GMP، pharmaceutical regulations، and quality systems

Experience in sterile، non-sterile، solid dosage، or injectable manufacturing is an advantage

Proficiency in Microsoft Office and pharmaceutical production systems

Key Competencies Leadership and team management Attention to detail Quality and compliance focus Analytical thinking Decision-making and problem-solving Continuous improvement mindset

Location: Sidi Thabet

Job Type: CDI

About Us

For over 45 years، Hikma Pharmaceuticals has been putting better health within reach، every day، by creating high-quality medicines and making them accessible to those who need them

We are helping to shape a healthier world that enriches all our communities، and our global team of 9، 500+ empowered employees are central to this mission.

Through our 29 manufacturing plants، 9 R&D centers across the MENA، North America and Europe، our footprint allows us to play a critical role in serving patients.

We’re seeking candidates who embody our values: Innovative، driven to keep learning، Caring، genuinely compassionate in their work، and Collaborative، eager to solve problems together.

Supervise and coordinate daily pharmaceutical production operations.

Review and approve batch manufacturing records and production documentation.

Monitor production processes to ensure product quality and operational efficiency.

Investigate production deviations and implement corrective and preventive actions (CAPA).

Collaborate with Quality Assurance، Quality Control، Engineering، and Supply Chain teams.

Ensure proper utilization of equipment، facilities، and manpower.

Participate in process validation، qualification، and continuous improvement initiatives.

Support audits and regulatory inspections.

& Experience

Degree in Pharmacy.

Registered Pharmacist with a valid professional license (where applicable).

Minimum of 3 years of experience in pharmaceutical manufacturing/production.

Strong knowledge of GMP، pharmaceutical regulations، and quality systems.

Experience in sterile، non-sterile، solid dosage، or injectable manufacturing is an advantage.

Proficiency in Microsoft Office and pharmaceutical production systems.

Key Competencies

Leadership and team management

Attention to detail

Quality and compliance focus

Analytical thinking

Decision-making and problem-solving

Continuous improvement mindset

خطوتك التالية

ابدأ التقديم بثقة

انتهت فترة التواصل المباشر لهذا الإعلان؛ يمكنك مراجعة الوظائف المشابهة.

التقديم والتواصل

انتهت فترة التواصل المباشر

مرّ أكثر من 30 يومًا على نشر الإعلان؛ لذلك تم إخفاء وسائل التواصل والتقديم المباشر كما في الموقع السابق.

الإعلان قديم
جاهزية التقديم

هل هذه الوظيفة مناسبة لك؟

راجع النقاط السريعة قبل الضغط على التقديم لتحسين فرصك.

الموقع واضح اسأل عن الراتب الوصف متاح
قبل التقديم

قدّم بطريقة أوضح تزيد فرص الرد

اكتب رسالة مختصرة توضّح خبرتك وسبب مناسبتك للوظيفة.

  1. راجع الموقع والراتب والمتطلبات الأساسية.
  2. جهّز رسالة قصيرة مرتبطة بالوظيفة وخبرتك.
  3. قدّم من خلال زر التقديم أو وسيلة التواصل المتاحة.
الخطوة التالية

سجّل الدخول للتقديم بدون تكرار بياناتك

الحساب يساعدك على حفظ الوظائف، تتبع حالة الطلب، واستخدام سيرتك الذاتية في التقديم بسرعة.

  • جهّز رسالة مختصرة توضّح خبرتك المناسبة للوظيفة.
  • أكمل السيرة الذاتية لتظهر بشكل أفضل لصاحب العمل.
حالة التقديم المباشر

انتهت فترة التقديم والتواصل

تُخفى أزرار التقديم وبيانات التواصل بعد مرور المدة المعتمدة، مع إبقاء تفاصيل الإعلان والوظائف المشابهة.

الإبلاغ عن الإعلان

استخدم هذا النموذج إذا كان الإعلان غير صحيح أو يحتوي على بيانات مضللة أو محتوى غير مناسب.

سجّل الدخول للإبلاغ عن الإعلان

تسجيل الدخول يساعد فريق المراجعة على متابعة البلاغ والتواصل معك عند الحاجة.

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