At Julphar, we are on a journey of culture transformation, and 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 with the compassion and commitment of our employees.
Detailed Job Description
- Responsible for adhering to cGMP principles and maintaining them effectively. Adhere to engineering procedures, ensure compliance to the system, and supervise team members for the same.
- Monitor all engineering QMS activities on Ample Logic, e.g., deviation handling, CAPA, change control, etc.
- Act as QM for all external area engineering deviations and CAPA management.
- Participate in cross-functional teams for deviation management processes.
- Ensure that all engineering-related documentation complies with cGMP guidelines.
- Create a continuous improvement framework for engineering compliance.
- Review comparison sheets and ensure all new URS for systems and equipment are in compliance with GMP guidelines.
- Approve qualification procedures for new equipment and ensure procedures comply with standards.
- Review all engineering SOPs related to quality management.
- Engage in new projects.
- Monitor overall equipment effectiveness and seek ways for further improvements.
- Identify skill deficiencies and work to improve individual capabilities through coaching, development, and training.
- Maintain and promote a teamwork environment with effective and clear communication among colleagues.
Core Competencies
- You are highly result-oriented with a strong sense of accountability and ownership.
- High process compliance with strong attention to detail.
- Understanding how to align resources and guide others to achieve desired results.
- Solution-centric mindset to understand and resolve issues within stipulated timeframes.
- Strong technical knowledge with effective implementation skills.
- Excellent communication, interpersonal, and collaboration skills.
- Good understanding of the pharmaceutical business with strong planning skills.
- Ability to prioritize, multitask, and work effectively under pressure to meet deadlines.
- Organized, self-motivated professional eager to learn and implement new skills.
Qualifications and Functional Knowledge
- Minimum 8-9 years in electrical, mechanical, mechatronics engineering, or related fields.
- A master's degree is a plus.
- At least 7 years’ experience in a similar organization within the pharmaceutical, healthcare, or medical industry.
- Proven track record in system initiation and KPI design.
- Experience in a similar position is preferred.
- Excellent command of English (speaking, writing, and communication).
- Proficiency in MS Office (Excel, Word, etc.).
We value people from diverse backgrounds. Could this be your story? Apply today or visit www.Julphar.net to learn more about us and our journey.