A global job position with an impact:
We are growing and expanding our Manufacturing Site in Mexico! In the job as Quality Control Manager, you will have the opportunity to actively support the organization ensuring that our manufacturing site runs as needed to have the growth expected of the products we make in Mexico, excel in your own daily tasks and responsibilities, and experience a very varied working day in a dynamic.
Required skills:
• Develop, implement, and maintain quality control policies and procedures.
• Provides supervision of the QC Operations ensuring allocation of adequate resources for
Shop floor QC activities.
• Applies expertise in manufacturing QC concepts and business knowledge to act as the
primary point of contact for their team and the first-line escalation point in areas of their
responsibility.
• Leads or support quality improvement initiatives leads to continuous improvements / cost.
• Assignment of training curricula to Quality personnel based on the Job Description and
ensure training is up to date.
• Provides training, coaching, and mentorship to their team and peers as applicable. Works
with their team to identify areas for improvement, reduce blind spots, and give opportunities
for increasing responsibility as appropriate.
• Maintain the quality control objectives in alignment with the objectives of the plant.
• Promotes and supports the implementation of quality, product and process improvement
projects.
• Revises / analyzes if the current products and processes (including performed actions or
decisions) comply with the regulations, such as the QSRs, ISO 13485, etc.
• Serves as Subject Matter Expert in audits and inspections for their area of responsibility.
• Revises and approves the answers to internal and external audit observations ton ensure the
compliance with the internal procedures and applicable regulations
• Establishes and properly maintains the required documentation of quality control activities
• Defines, monitors and administers the budget of the quality control department/cost
• Collaborates with Engineering and with the Operations departments to develop, conduct and
approve validation strategies of products and processes.
• Revises and approves the investigations, bounding, documentation, revision and approval of
the non-conformities (NCRs), preventive and corrective actions (CAPAs), customer
complaints and escalation of quality problems when applies.
Qualifications:
• Bachelor's degree in a related field
• 7+ years of experience working in Quality
• Experience on medical device industry and understanding of cGMP, ISO13485 and CFR part
820.
• Good analytical thinking and problem-solving mindset.
• Ability to work, interact, and communicate effectively with others.
• Effective verbal and written communication skills.
• Experience working in manufacturing environment.
Authority:
• Final release of Ambu A/S and King System products.
• Reject to release the product/lot and escalate any problems to NCR/CAPA
• Reject the release of product/lot, if disagreeing with the disposition of a NCR or CAPA
• Stop manufacturing if production represents a quality risk
• Put product on hold
• Initiate CAPAs and NCRs
• Approve and reject change requests
Work Environment:
This is a manufacturing facility and as a result, employees have the potential to be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration, or other workplace hazards controlled within compliance of current safety and health standards.
How to Apply:
If you are interested in the position, then please apply as soon as possible through our recruitment system. Note that we will invite candidates for interviews on a continuous basis so no need to hesitate. This job ad will be online until May 30, 2025, but once we have found the right candidate, this ad will no longer be online. You can get more information about the job by contacting to marc@ambu.com