Production Pharmacist

IBN AL BAYTAR HIKMA Sidi Thabet, Ariana Publiée le 4 octobre 2026
Expirée

Détails de l'annonce

Référence

246127

Date de publication

4 octobre 2026

Type de contrat

CDI

Lieu de travail

Sidi Thabet, Ariana, Tunisie

Expérience requise

Entre 2 et 5 ans

Niveau d'études

Doctorat

Salaire proposé

Non communiqué

Disponibilité

Plein temps

Langues

Arabe Français Anglais

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Description de l'annonce

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.

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. 

Description:

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 Responsibilities

  • Supervise and coordinate daily pharmaceutical production operations.
  • Ensure compliance with GMP, company procedures, and regulatory requirements.
  • 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.

Qualifications & 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.
  • Excellent problem-solving, communication, and leadership skills.
  • 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