Total 5 quality assurance control job vacancies in cork 01

• pengumpulan sampel beton
• pengujian kekuatan tekan
• analisis komposisi material beton.

1 . Memastikan bahan baku, seperti kelapa, air, dan komponen lain yang digunakan, sesuai dengan standar kualitas yang ditentukan

2 . Melakukan pengujian fisik dan kimia terhadap bahan baku (misalnya pH, kebersihan, turbidity, dll.)

3 . Mengawasi setiap tahap proses pengolahan santan dan air kelapa untuk memastikan konsistensi kualitas

4 . Memastikan suhu, tekanan, waktu proses, dan parameter lainnya sesuai dengan standar

5 . Melakukan sampling secara berkala untuk diuji di laboratorium

6 . Mencatat hasil monitoring dan pengujian dalam laporan yang sistematis

7 . Memastikan seluruh fasilitas produksi, alat, dan mesin selalu bersih dan higienis sesuai standar sanitasi industri makanan

8 . Melakukan inspeksi kebersihan secara berkala pada ruang produksi dan peralatan

9 . Mengidentifikasi produk yang tidak memenuhi standar kualitas dan memastikan tindakan korektif segera diambil (misalnya menghentikan produksi sementara, mengulang proses, atau menghentikan distribusi produk yang tidak layak)

10 . Memastikan alat-alat pengujian di laboratorium selalu dikalibrasi dan berfungsi dengan baik untuk menghindari kesalahan pengujian

11 . Memastikan proses produksi dan produk akhir aman untuk dikonsumsi

12 . Melakukan sampling produk secara berkala selama proses produksi untuk diuji kualitasnya

13 . Mengimplementasikan dan mematuhi sistem manajemen mutu seperti BRC, ISO, HACCP, atau GMP

14 . Memastikan standar mutu diterapkan dalam setiap aspek produksi dan distribusi

• Minimal lulusan SMA/SMK
• Memiliki pengalaman kerja di bidang manufaktur minimal 1 tahun (pengalaman di
• Bisa menggunakan alat ukur
• Good attitude, jujur, pekerja keras dan bersedia bekerja dalam tekanan
• Bersedia bekerja sistem shift

QUALITY ENGINEER

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

Alcon is the global leader in eye care, dedicated to helping people see brilliantly. With our 70-plus-year heritage, we are the largest eye-care device company in the world – with complementary businesses in Surgical and Vision Care. Being a truly global company, we work in over 70 countries and serve patients in more than 140 countries.

As A Quality Engineer you will plan, conduct and provide direction on all quality engineering activities. You will apply comprehensive and diverse knowledge of engineering principles and practices within broad assignment areas. You may coordinate and direct activities of quality engineers and other quality engineering staff.  You are responsible for development of assigned staff. In this role, a typical day will include:

• Utilize Quality Engineering principles and problem-solving skills to improve and maintain products/processes that are aligned with the overall Quality and Business vision while ensuring production build schedule attainment.
• Lead and manage investigations providing formal structured approach to identify root causes, establish corrective actions and execute prevention plans in products and/or processes.
• Employ appropriate risk management to prevent unanticipated failure modes and improve capability of processes.
• Ensures effective quality strategies are created for the validation of equipment, test methods and processes as well as master validation plans and risk management documentation in accordance with regulatory requirements and internal Alcon requirements.
• Utilize Quality Engineering tools and practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
• Reviews Analytical Methods and Specifications, Validation Protocols, Deviations, Investigations, Impact Assessments, and other forms of Quality documentation as assigned.

WHAT YOU’LL BRING TO ALCON:

• 4+ years’ experience in a relevant role
• Knowledge of FDA, medical device, GMP and validation requirements.
• Experience in Equipment and process validations.
• Knowledge of Statistics
• Skills: Project management, problem solving, statistical analysis and word processing.
• People management experience.
• Report writing expertise and highly developed people skills Ability to coach and drive performance and values and behaviors.
• Diploma in Business, Science or Engineering.

ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

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Senior Quality Project Engineer

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

Alcon is the global leader in eye care, dedicated to helping people see brilliantly. With our 70-plus-year heritage, we are the largest eye-care device company in the world – with complementary businesses in Surgical and Vision Care. Being a truly global company, we work in over 70 countries and serve patients in more than 140 countries.

We are currently recruiting for a Senior Quality Project Engineer to join our team here in Cork. You research process technologies and process control improvements for site implementation. They apply comprehensive and diverse knowledge of engineering principles and practices for Quality focused process controls improvements. They use specialist knowledge and leadership in leading the execution of these improvement activities. A typical day in this role will include;

• Utilize Quality Engineering principles and problem-solving skills to improve and maintain processes that are aligned with the overall Quality and Business vision while ensuring production build schedule attainment.
• Responsible for introducing and validating new process control projects from design through completion and in compliance with regulatory requirements.
• Work with automation solution providers to specify, design and implement solutions if necessary. Responsible for supporting and improving existing process controls through process analysis and the application of engineering principles.
• Employ appropriate risk management to prevent unanticipated failure modes.
• Ensures effective quality strategies are created for the validation of equipment, test methods and processes as well as risk management documentation in accordance with regulatory requirements and internal Alcon requirements.
• Responsible for project management & planning and for liaising with other departments/plants affected by these projects. Also for reporting project status to management and highlighting areas of concern early. Responsible for ensuring all projects are completed to agreed timelines and within budget. Also that all work adheres to H&S and environmental requirements.
• Author/Reviews Test Methods, Specifications, Validation Protocols, Deviations, Investigations, Impact Assessments and other forms of Quality documentation as assigned.
• Perform an active role in further development of the quality management system and drive continuous improvement and innovation from a quality perspective.
• Actively participate in external audits by Notified Bodies and Health Authorities as subject matter expert for areas of responsibility.

What You Will Bring To Alcon:

• Third level qualification in a Business or Engineering Discipline
• As minimum 5-10 years in a medical device or pharmaceutical environment
• Preferred 5 years’ experience in Medical Device or Pharmaceutical industry with a Bachelors degree in a technical discipline
• Knowledge of FDA, medical device, GMP and validation requirements.
• Experience in Equipment and process validations.
• Excellent Project management problem solving & analytical ability.
• Attention to detail with excellent organizational skills.
• Knowledge of Line Clearance and Product Segregation requirements Report writing expertise and highly developed people skills.                                      

How You Can Thrive At Alcon

• A competitive salary package with fixed salary, bonus, pension and health insurance
• A flexible work environment with competent and committed colleagues. We enjoy working together in a good and respectful manner, and we celebrate our common successes
• See your career like never before with focused growth and development opportunities                                 

Alcon Careers

See your impact at www.alcon.com/careers

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ATTENTION: Current Alcon Employee/Contingent Worker

If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.

Find Jobs for Employees

Find Jobs for Contingent Worker