Job description
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.
Detailed Job Description
- To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.
- Responsible to carry-out chemical and physical analysis of Simi Finished /Raw Material / Stability.
- Responsible for the operation of various QC equipment (depending on the section he is working)
- Responsible for recording all working data
- Entering data of analysis on SAP
- Ensure Final Products adhere to all specifications and regulations.
- To ensure the analysis is performed correctly as per applicable procedures
- To involve and support external and internal audits and to close the audit observations on time.
- Responsible for handling of Quality management system actions like CAPAs, AMS and Change controls using Ample logic system.
- To follow and ensure data integrity and good documentation practices are implemented in the QC labs.
- To follow Standard Operating Procedures (SOPs) strictly
- Assist in trouble shooting and solving problems that may come up in the day-to-day operation of the department.
- Helps supervisors/Designate in assigned tasks.
Core Competency
- Highly oriented with strong sense of accountability & ownership.
- Has Strong communication, interpersonal and problem-solving skills.
- Business acumen partnered with a dedication to legality.
- Must be able to manage tasks and priorities and easily adapt to changing situations.
- Highly disciplined and must be organized, self-motivated to learn new learnings and implement them at workplace.
- Proficient in HPLC, GC, UV-Vis spectrophotometry, and other analytical techniques.
- Deep knowledge of GMP, GLP, and regulatory guidelines (USP, EP, BP).
- Skilled in analytical method validation and transfer.
- Experienced in dissolution testing and assay analysis.
- Strong understanding of data integrity principles and ALCOA+ compliance.
- Accurate documentation and review of laboratory records and test reports.
- Effective communication with cross-functional teams (QA, production, R&D).
- Strong attention to detail and commitment to continuous improvement.
- Execute daily operations in compliance with EMS and EHS standards, using appropriate PPE and safe practices.
- Identify, reduce, and prevent environmental impacts and operational risks.
- Contribute to EHS activities, audits, and continual improvement initiatives.
Qualification/Functional Knowledge
- Bachelor’s degree in pharmacy/science.
- Proficient with computer software application.
- Minimum 3-6 years’ experience in the same field.
We value people from different backgrounds. Could this be your story?
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