Specialist – Raw Materials

Job title: Specialist – Raw Materials

Company: Julphar

Job description: Description

Job Ref. ID: 50495

Job Title: Specialist – Raw Materials



Work Location: UAE (RAK head office)

Job Type: Specialist

Employment Type: Full Time Employment (Un-limited Contract)

Job Description:

Purpose: Specialist – the role holder is responsible to adhere with cGMP principles, GLP and to maintain ‎them in effective manner. ‎ In this role you’re responsible for analysis, investigations and update SOP. Responsible to maintain ‎the quality of the materials, evaluate the products through internal specifications and processes. ‎Conduct investigation to identify any inconsistencies and malfunctions. A specialist must have ‎excellent communication skills, as well as be detail-oriented to identify areas of improvement and ‎ensure process compliance.‎

Key responsibilities & Accountability: • Accountable to adhere with cGMP principles and to maintain them in effective manner • Responsible for chemical analysis according to approved specifications, test methods and ‎other quality procedures and perform related calculations efficiently and review quality ‎related metrics done by analysts.‎ • Responsible for the follow up the correct application of test methods and ensure accuracy ‎in implementation various procedures.‎ • Explains and executes the SOPs and other written procedures and ensure their right ‎practice.‎ • Uses different laboratory equipment and have control over their function and cleanliness ‎to achieve various analytical goals. ‎ • Follows and ensures GLP, GMP and safety procedures and maintain hygienic conditions in ‎lab.‎ • Prepares volumetric and/or test solutions as required through the analysis.‎ • Maintains records and ensure proper documentation of the analysis and enter data on ‎SAP.‎ • Responsible for the release all starting materials and finished products as well as ‎intermediate and bulk product.‎ • Provide support to Quality Assurance in complaint investigation.‎ • Responsible for updating raw material testing specification to comply with purchase ‎requirements.‎ • Responsible for preparation of analytical control documents • Responsible for the analysis of complaint samples and process validation samples • Conduct quality control new staff training and hear/suggest feasible methods to improve ‎efficiency and output • Responsible to follow by literature studies the scientist development within the field of ‎quality control • Apart from above, the works assigned by Team Leader / Manager and support colleagues ‎whenever necessary ‎


– Education • ‎4 years Bachelor Degree in Science/Pharmacy or equivalent field.‎

– Experience: • At least 5-6 years’ experience in Quality Management in similar organization in pharma / ‎Health care / Medical Industry.‎ • Must be experienced in managing complex and sensitive operational challenges.‎

– Training:

Key Competencies: • In terms of competency you are highly result oriented with strong sense of accountability ‎& ownership.‎ • High on process compliance with strong attention to details.‎ • Good communication, interpersonal and collaboration skills.‎ • Ability to understand new learnings and implant in workplace.‎ • Must be a resourceful problem solvers and must possess strong ability to work effectively ‎under pressure with excellent time and task management.‎ • Motivated, highly organized, focused, and hardworking.‎ • Possess the ability to develop and maintain an effective working relationship with internal ‎and external sections, function as team player and comply with company policies.‎

Technical Competencies: • Strong command in English (communicating, writing and speaking) and Arabic is preferred.‎ • Proficient in MS Office (MS Excel and MS Word, etc.).‎ • Strong Knowledge in cGMP, & GDP principles.‎

Expected salary:

Location: United Arab Emirates

Job date: Wed, 02 Mar 2022 23:35:58 GMT

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