Senior Specialist Solid Dose Validation/Pharmacist Jobs in UAE at Julphar

Title: Senior Specialist Solid Dose Validation/Pharmacist

Company: Julphar

Location: UAE

Type: Full Time

Category: Pharmaceutical

Location: Ras Al-Khaimah


Senior Specialist Solid Dose Validation (Pharmacist) Division: QA Operations Country: UNITED ARAB EMIRATES Work


UAE (RAK head office) Job Type: Senior Specialist Solid Dose Validation (Pharmacist)

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

Job Description:


Maintain oversight of the process of Solid dose product(s) assigned End to End (from raw material to ‎packaging) throughout the commercial life cycle starting tech transfer to product discontinuation.‎ Key responsibilities & Accountability:

Key Responsibilities& Key Result Areas
• Ensure effective and full implementation of GMP related requirements to Solid dose products ‎validation practices
• Comply with Julphar information security and policies
• Comply with Data integrity, privacy declarations and procedures ‎
• Create/Update protocols as per relevant Non sterile VMP
• Execute VMP activities related to Solid equipment Qualification, Cleaning & Process Validations ‎
• Providing CAPA for relevant departments from validation reporting to close identified gaps
• Participate as SME in all deviations relevant to Solid batches and contribute in identification of root ‎cause and identification of CAPA
• Contribute in Technical Risk Assessments for process improvements
• Maintain all system inspection ready & presenting Validation reports to internal & external audits ‎
• Escalate of any schedule predicted delays, validation outcome issues in a timely manner for Team ‎leader & Management decision making
• Actively participate & value add in continuous improvement initiatives.‎
• Support the CAPA implementation and monitoring its effectiveness
• Conduct & support for On – Job training wherever needed


– Education
• Master Degree in (Bio)
Pharmacy or related other science (e.g. process technology, Chemistry)‎

• A minimum of 6 years of relevant experience in biopharmaceutical and/or Solid dose industry (preferably ‎in a sterile environment)‎
• Must have background in Biotech QC testing data review/ trending
• Must have background in Solid QC testing data review/ trending
• Must have hands on experience in the manufacturing of tablets, hard gel capsules, Oral suspension, ‎
• Minimum 2+ years’ Experience in FBD technologies
• Minimum 2+ years’ Experience in Compaction technologies
• Preferable experience in Minitab – Training:


• High on communication and collaboration , having an ability to manage multiple stakeholders at a ‎time
• In terms of competency, you are highly result oriented with strong sense of accountability & ‎ownership.‎
• Must be able to manage tasks and priorities and easily adapt to changing situations. ‎
• Good command in English (Communicating, writing and speaking)‎
• Good prioritizing skills and being able to make a just decision also in case of (time) pressure
• Flexible learning abilities
• Excellent root cause analysis capabilities, Innovative abilities, creative, strong drive to improve
• Must be highly organized, self-motivated to learn new things and implement them in building or updating ‎quality system for Pharmaceuticals ‎ Technical


• Excellent knowledge of cGMP and strong focus on clients and quality/compliance;‎
• Data Analytics/ Experience in Statistical Process Control Job


Senior Specialist Solid Dose Validation (Pharmacist) Division: QA Operations Country: UNITED ARAB EMIR…


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