Team lead (QA-Engineering oversight)

Julphar; Ras Al Khaimah; On-site; AED 200,000 - 300,000; Full time

Job summary

A leading pharmaceutical company in Ras Al Khaimah seeks an experienced Engineering Manager. The role focuses on ensuring compliance with engineering standards, overseeing QMS activities, and driving continuous improvement. Ideal candidates will possess a Bachelor's degree in Engineering, at least 8-9 years of relevant experience, and strong communication skills. Join us to make a significant impact in pharmaceutical quality assurance.

Qualifications

• Minimum 8-9 years of relevant experience.
• At least 7 years in the pharmaceutical/healthcare industry.
• Strong knowledge of pharmaceutical business.

Responsibilities

• Ensure compliance with cGMP principles.
• Monitor engineering QMS activities.
• Review engineering SOPs related to quality management.

Skills

Result-oriented

Attention to detail

Strong communication skills

Interpersonal skills

Problem-solving

Organizational skills

Education

Bachelor's degree in Electrical/Mechanical/Mechatronics Engineering

Master's degree (a plus)

Tools

MS Office (Excel, Word)

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

• Responsible to adhere with the cGMP principles and maintains them in effective manner. Adhere to engineering procedures, ensures compliance to the system, and supervise team members for the same.
• To monitor all the 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 team for deviation management process.
• Ensure that all engineering related documentation comply with cGMP guidelines.
• Create continuous improvement framework for engineering compliance.
• Review of comparison sheets and ensure all new URS for systems and equipment’s are in compliance with GMP guidelines.
• Responsible for approving qualification procedures for new equipment and ensure that procedures comply with standards.
• Responsible for reviewing all engineering SOPs which is related to quality management.
• To be engaged in new projects.
• Monitor overall equipment effectiveness and find ways for further improvements.
• Identify deficiencies in skills and work to improve individual’s capabilities through coaching, development and training.
• Maintain and promote a teamwork environment with effective and clear communication amongst colleague.

Core Competency

• In terms of competency, you are highly result oriented with strong sense of accountability & ownership.
• High on process compliance with strong attention to details.
• Has the understanding on how to align resources and guide others to achieve desired results.
• Must have a solution centric mind to understand issues and solve them within a stipulated time frame, ability to understand new issues quickly and make decisions.
• Strong technical knowledge with strong implementation.
• Strong communication, interpersonal and collaboration skills.
• You must have excellent understanding of Pharmaceutical Business with strong Planning skills.
• Ability to prioritize, multi-task and work effectively under pressure to meet deadlines.
• Must be organized professional, self-motivated to learn new things and implement them at workplace

Qualification/Functional Knowledge

• Minimum 8-9 years Bachelor in electrical/ Mechanical /Mechatronics Engineering/ any discipline in same field.
• Master degree is a plus.
• At least 7 years’ experience in similar organization in pharm / Health care / Medical Industry.
• Proven track record in systems initiation and KPI design
• Should have handled a similar position for a better fitment in this role.
• Excellent command in English (Communicating, writing and speaking).
• Excellent in MS Office (MS Excel and MS Word, etc.).

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