Specialist - Product Lifecycle

Overview

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism. Our core values:
Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents, create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.

We value people from different backgrounds. Could this be your story? Apply today or visit  to read more about us and the journey of Julphar

• Prepare, review, and oversee process and cleaning validation documentation and execution activities for Sterile Facilities, including Liquid Injectables, Lyophilized products, and Sterile Powder Filling.
• Conduct process validation for various dosage forms such as Oral Solid Dosage (Tablets, Capsules, PPS), Oral Liquids (Syrups, Suspensions, Oral Drops), and Semi-Solids (Ointments, Creams, Suppositories).
• Manage process validation activities for API biological drug substances and sterile products.
• Demonstrate familiarity with filter validation requirements in sterile areas.
• Design and execute Aseptic Process Simulation (APS) studies, including preparation of related protocols and reports.
• Lead the visual inspection qualification process.
• Manage shipping validation activities for cold chain products.
• Oversee cleaning validation activities, including dirty equipment hold-time studies.
• Review and support Change Controls, CAPAs, and Deviations associated with qualification and validation activities.
• Act as Quality General in EQMS to complete actions related to qualification and validation.
• Monitor and verify CAPA effectiveness related to validation activities.

• Strong results orientation with a high level of accountability and ownership.
• Ability to prioritize, multitask, and perform effectively under pressure to meet deadlines.
• Excellent communication, interpersonal, and collaboration skills.
• Highly disciplined, organized, and self-motivated to learn and implement new practices.
• Proven technical expertise in qualification and validation within sterile and biotech facilities.
• Strong implementation skills with adaptability to changing business requirements.
• Ability to work effectively in cross-functional environments, collaborating with internal and external stakeholders.
• Strong capability to communicate technical, scientific, and regulatory information clearly—both verbally and in writing.

• Education:
  
  Bachelor’s degree in Pharmacy or Science.
• Experience:
  
  Minimum 3–5 years of relevant experience in qualification and validation within the pharmaceutical/biotech industry.
• Hands-on experience with regulatory audits (SFDA, WHO, EU, USFDA).
• Strong working knowledge of QMS systems such as Agile, Veeva Vault, Track Wise, and Ample Logic.
• Excellent computer proficiency and command of English (written and spoken).
• Demonstrated problem-solving and team coordination skills.
• Solid understanding of cGMP principles and Risk Assessment methodologies.