Incoming QA Manufacturing Inspector
At Alcon, we are driven by the meaningful work we do to help our patients 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.
Responsibilities
Perform in-process QA including IQA, MRB, Operator Certification, and Compliance Audits.
Inspect manufacturing raw materials and components to assure compliance to specifications.
Proofread packaging and labeling components.
Coordinate raw material chemical, microbiological and functional testing.
Maintain material/component status and release to inventory using material management software.
Maintain inspection records.
Prepare and administer certification tests.
Perform non-conforming material review and report results.
Maintain area and equipment in a clean, orderly manner.
Observe and report deviations from Good Manufacturing Practices and/or procedures during compliance audits.
Ensure familiarity with production processes.
Identify and issue non-conformities associated with equipment, material, or product failing to meet specifications.
Investigate and identify root cause of non-conformities, providing corrective and preventive actions.
Disposition QNs/DCTs as necessary and administer the MRB process.
Track data and perform basic data entry and elementary mathematical evaluation, e.g., average and deviation range.
Evaluate sampling plans and recommend reduction based on statistical analysis of historic data.
Maintain accurate and organized inspection and QA project records.
Prepare files for document retention.
Maintain updated procedures and specifications.
Support validation, process improvement work, and new material introduction.
Perform other related duties assigned by the manager or supervisor.
Maintain knowledge of applicable SOPs and inspection plans and ensure personnel training.
Ensure continual Quality System compliance by adhering to regulatory and Alcon QS requirements.
Use appropriate root cause analysis tools when leading NCE investigations, if applicable.
Qualifications
Minimum: Leaving Certificate or equivalent, or Certificate or Diploma in a quality-related field.
Minimum: 1 year in a quality/technical or manufacturing role.
Preferred: 2 years experience in medical device or pharmaceutical industry QA.
Strong organizational ability and attention to detail.
Adaptable and capable of moving quickly between tasks.
Good understanding of Good Manufacturing Practices and quality systems.
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.
Opportunities for focused growth and development.
Work in a respectful and collaborative culture.
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