Associate Scientist, Formulation Development at Hikma Pharmaceuticals PLC

Staoueli, Algiers, Algeria -

Full Time

Start Date

Immediate

Expiry Date

18 Jul, 26

Salary

0.0

Posted On

20 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical skills, Problem-solving, Tech transfer, Pharmaceutical development, Validation, Project management, Communication, Teamwork, SAP, GMP, Quality assurance, Documentation, EHS compliance, Feasibility studies, Stability testing

Industry

Description

Location: Algiers, Algeria Job Type: Full-time 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 Associate Scientist, Formulation Development 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. Main Responsibilities: Execute tech transfer, development, and validation projects from feasibility study through to stability batch placement, ensuring adherence to timelines and budgets Monitor project progress closely and ensure all activities are completed according to plan Propose solutions to technical challenges related to development and tech transfer activities Prepare and manage all required documentation from project initiation to registration file submission Conduct investigations in case of issues arising during tech transfer or development phases Collaborate with central and local teams from feasibility study to validation batch execution Ensure effective cross-functional collaboration to support smooth project execution Execute and follow up on SAP-related tasks Ensure confidentiality of all R&D projects Maintain compliance with EHS (Environment, Health & Safety) and quality standards Support continuous and efficient execution of all R&D projects from start to finish Perform other related duties as assigned by management Required Skills: Strong analytical and problem-solving skills Ability to manage multiple projects and meet deadlines Good knowledge of pharmaceutical development and tech transfer processes Effective communication and teamwork skills Basic knowledge of SAP systems is an advantage Understanding of GMP and quality requirements Academic Background and Knowledge: Degree in Pharmacy or Engineering (Biology, Chemistry, or Process Engineering) Bachelor’s degree in pharmacy or a related scientific field (master’s degree is preferred) 0–2 years of experience in the pharmaceutical industry, preferably in R&D and/or Production Knowledge of pharmaceutical development, validation, and tech transfer processes

Responsibilities

The Associate Scientist will execute tech transfer, development, and validation projects while ensuring adherence to timelines and quality standards. They are responsible for preparing project documentation, conducting investigations, and collaborating across functional teams to support R&D objectives.