Hikma Pharmaceuticals

Associate Manager, Quality Compliance (Corporate)

L'Oriental

CDI / Temps pleinSur site10+ ansMaster / Bac+5AnglaisQualité / HSEPharmaceutique

L’essentiel du poste

Résumé par Postule AI

Hikma Pharmaceuticals is hiring an Associate Manager, Quality Compliance for its Corporate department, reporting to the Sr. Director, Quality Compliance. The role coordinates audits across injectable, oral, laboratory, Data Integrity and CMO manufacturing, ensures cGMP compliance, and drives CAPA follow-up. It requires a science degree, quality auditing certification, 10 years of related experience (5 supervisory) and pharmaceutical manufacturing experience. The position is on-site in Morocco.

Vos missions

  • Lead the coordination and execution of audits across injectable, oral, laboratory and Data Integrity manufacturing processes and CMOs.
  • Ensure compliance of Hikma injectable and oral sites through internal audits and periodic checks against SOPs and standards.
  • Follow up observations from Hikma and third parties, including CAPA plan implementation and communication with Hikma Quality Management.
  • Investigate problems and assess deviations in manufacturing processes, recommending necessary corrective actions.
  • Implement internal quality, subsidiary and follow-up audit programs, ensuring cGMP compliance during audits.
  • Provide technical and administrative support to under-license and new partner projects, up to product registration.

Profil recherché

  • You have a pharmaceutical quality background, especially in oral and injectable manufacturing.
  • You have supervisory experience and a quality auditing certification such as ASQ or ISO 9001.
  • You are comfortable leading audits, investigating deviations and following up CAPA actions.
  • You combine strong data analysis and reporting skills with near-native English.

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Associate Manager, Quality Compliance (Corporate)

Hikma is recruiting an Associate Manager, Quality Compliance to join the Quality Compliance - Corporate department. The role reports directly to the Sr. Director, Quality Compliance and is based on-site in Hay Al Hikma II, Oriental, Morocco.

About Hikma

Founded by Samih Darwazah over 40 years ago in Jordan, Hikma aims to provide affordable, quality medicines to people in need. In Portugal, the company has more than 1,000 employees and 3 factories producing injectable medicines.

Main Responsibilities

  • Lead the coordination, approach and execution of audits for injectable, oral, laboratory, Data Integrity manufacturing processes and CMOs.
  • Ensure compliance of Hikma injectable and oral sites through internal audits and periodic checks against applicable standards, specifications and SOPs.
  • Follow up observations raised by Hikma and third parties, including CAPA plan implementation and communication with Hikma Quality Management.
  • Provide guidance on manufacturing processes to ensure applicable international standards and specifications are followed.
  • Investigate problems and assess deviations, recommending necessary corrective actions.
  • Implement internal quality, subsidiary and follow-up audit programs, ensuring cGMP compliance and health and safety regulations during audits.
  • Provide technical and administrative support to under-license and new partner projects, including supplier qualification and authority audits up to product registration.
  • Prepare periodic reports and documentation, support process standardization and participate in third-party or authority audits.

Profile

  • B.Sc. degree in Chemistry, Biology, Microbiology, Chemical Engineering or equivalent.
  • M.Sc. degree in Total Quality Management or equivalent.
  • Quality auditing certification, such as ASQ, ISO 9001 or equivalent.
  • 10 years of experience in a related position, including at least 5 years in a supervisory position.
  • Experience in the pharmaceutical industry, including oral and injectable manufacturing.
  • Computer skills: Microsoft Office and job-related applications, with effective use of internet functions.
  • Data analysis: Complex data analysis using multi-sourced data, with results presented through professional graphs and charts.
  • Documentation and recording information: Documenting information in written or electronic formats.
  • English language: Near-native ability to read, understand and write complex prose.
  • Government relations: Represents the company externally within the government sector and maintains good rapport with employees.
  • Laws and legislations: Knowledge of laws and legislations of several countries where Hikma operates, including MENA, USA and Europe.
  • Project management: Planning, implementation, monitoring and completion of projects, managing time, human resources and budget.

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

Join us and contribute to Better Health, within everyone's reach, every day.

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