Hikma Pharmaceuticals

Analyst, Pharmaceutical Development (m/f) - On-site, Morocco

L'Oriental

CDI / Temps pleinSur siteLicence / Bac+3Qualité / HSEPharmaceutique

L’essentiel du poste

Résumé par Postule AI

Analyst role in Pharmaceutical Development at Hikma's Morocco location, working on-site. The position centres on analytical lab work, method validation and stability testing, GXP and cGMP compliance, documentation and CAPA support, and acting as primary contact for related sites. A bachelor's degree in chemical engineering, chemistry or similar is required, along with lab experience, SOP discipline, teamwork and problem-solving skills.

Vos missions

  • Stay updated with regulatory and quality standards, GXP compliance evolutions and best practices worldwide.
  • Perform method validation, verification, transfer and stability sample analytical work, including reports and CoAs.
  • Handle requests, labelling and management of process validation batches and stability samples for new filings.
  • Support management of critical documents and CAPA, and prepare quality management and audit reviews.
  • Act as primary contact for related sites to support introduction of assigned products.
  • Remain up to date on all analytical techniques required.

Profil recherché

  • You hold a bachelor's degree in chemical engineering, chemistry or a similar field
  • You have experience working in an analytical lab environment under cGMP requirements
  • You are comfortable following SOPs and policies and troubleshooting lab equipment and software
  • You enjoy teamwork and solving problems while prioritizing tasks

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About Hikma

Founded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people in need. Hikma continues to innovate daily to transform the lives of the millions of people it serves.

In the late 1980s, Hikma extended beyond the Middle East and acquired land in Portugal to build a sterile factory for injectable pharmaceutical products. Today, in Portugal, Hikma has more than 1,000 employees and 3 factories producing injectable medicines.

Role Overview

Hikma intends to recruit an Analyst, Pharmaceutical Development (m/f) to join the Pharmaceutical Development team. This is an on-site position.

Main Responsibilities

  • Stay updated with regulatory and quality standards, GXP compliance evolutions and best practices where needed worldwide.
  • Perform required method validation, verification, transfer and stability sample analytical work, including generating reports and filling CoAs.
  • Handle requests, labelling and management of assigned product process validation batches and stability samples for new geographical and presentation filings.
  • Support the management of critical documents and CAPA, and prepare quality management and audit reviews.
  • Act as primary contact for related sites to support the introduction of assigned products.
  • Remain up to date on all analytical techniques required.

Profile

  • Bachelor's degree in chemical engineering, chemistry or similar.
  • Demonstrated knowledge of working in an analytical lab environment and of cGMPs, with the ability to follow SOPs and policies.
  • Demonstrated ability to perform required analytical techniques and to operate and troubleshoot associated equipment and software.
  • Capability to work with others as part of a team, with good problem-solving skills to make necessary adjustments and prioritize tasks.

We Offer

  • Direct contract with Hikma
  • Competitive salary aligned with the role
  • Life insurance
  • Health insurance extended to student children (up to age 24)
  • Annual performance bonus
  • Real growth opportunities

If you think this is a good opportunity for your professional career, join us and contribute to Better Health, within everyone's reach, every day.

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