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Salary
≈ $23k – $53k per year (Estimated)
Location
In office (Sintra)
Seniority
Junior · 5+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 22, 2026. First seen by Alion on Oct 18, 2026.

Overview
Company
Impact
Profile match
Headquartered in London, United Kingdom, Hikma Pharmaceuticals is a multinational pharmaceutical company specializing in the development, manufacturing, and distribution of generic, specialty, and branded medicines. Operating across three core business segments - Injectables, Generics, and Branded products - the company provides an extensive portfolio spanning critical therapeutic areas such as anti-infectives, cardiovascular therapies, oncology, and pain management. With widespread manufacturing infrastructure and commercial operations across North America, the Middle East and North Africa (MENA), and Europe, it supplies hospitals, healthcare systems, and retail pharmacies globally with affordable, high-quality treatments.

Founded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people in need. Based on very solid foundations, we continue to innovate daily and find practical solutions to transform the lives of the millions of people we serve.

At the end of the 1980s, we extended ours beyond the Middle East and acquired land in Portugal for the construction of a sterile factory for injectable pharmaceutical products. This was an important turning point for the company, and our first step into a new region. Today, in Portugal, we have more than 1000 employees and 3 factories for the production of injectable medicines.

Hikma intends to recruit an Associate Manager, Quality Compliance - (m/f) to integrate theQuality Compliance - Corporate department reporting directly to the Sr. Director, Quality Compliance

Main Responsibilities:

  • Lead the coordination, approach and execution of audits for injectable, oral, laboratory, Data Integrity manufacturing processes and contract manufacturing organizations (CMOs).
  • Ensure compliance of Hikma injectable and oral sites with Hikma rules and policies 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, timely completion and communication with Hikma Quality Management.
  • Provide guidance to concerned Hikma employees on injectable, oral, laboratory, Data Integrity and CMO manufacturing processes to ensure that applicable international standards and specifications are followed.
  • Investigate problems and assess deviations related to the concerned manufacturing processes, recommending the necessary corrective actions.
  • Implement internal quality auditing, subsidiary audit and follow-up audit programmers, ensuring that Hikma sites maintain cGMP compliance and that health and safety regulations are followed during audits.
  • Provide technical and administrative support to under-license and new partner projects, including supplier qualification, system upgrades, gap analysis and support before, during and after authority audits up to product registration.
  • Prepare periodic reports and documentation, support process standardization, participate in third-party or authority audits and perform other duties assigned by the direct supervisor.

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: Performs moderately difficult tasks using job-related applications, Microsoft Office applications and other relevant programs, and uses internet functions effectively.
  • Data analysis: Performs complex data analysis using multi-sourced data and prepares reports presenting the results through professional graphs, charts and other visual aids.
  • Documentation and recording information: Applies and uses various techniques to document and record information in written or electronic formats.
  • English language: Demonstrates mastery of the language, with near-native ability to read, understand and write extremely difficult or abstract prose and use a wide range of vocabulary, idioms, colloquialisms and slang.
  • Government relations: Represents the company externally within the government sector and develops and maintains good rapport with its employees.
  • Laws and legislations: Possesses knowledge of the laws and legislations of several countries where Hikma operates, including the MENA region, USA and Europe.
  • Project management: Ability to manage projects through effective planning, implementation, monitoring and completion, while ensuring the best use of 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

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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