Alcon

eye care

QAManufacturingInspector-WeekendShift

$0–0k Cork, Ireland FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“QA Manufacturing Inspector - Weekend Shift at Alcon. Skills: Product Release, Compliance Audits, Non-Conforming Event (NCE) investigation, Data tracking and trending. Perform final product release of all manufactured products. Review DHR for completeness”

What You'll Achieve.

Ensure product is released in a timely and compliant manner; Ensure continual Quality System (QS) compliance

Industry & Context.

eye care
Problems you'll solve

Investigate and Identify root cause of non-conformities; Provide corrective/preventive actions; root cause analysis

Eligibility Requirements

Weekend Shift

What They're Looking For.

Must Have

1 year in Quality/Technical or Manufacturing role, Leaving Cert or equivalent

Nice to Have

Certificate or Diploma in a Quality related field, 2 years experience in Medical Device or Pharmaceutical industry

What You'll Do.

Perform final product release of all manufactured products

Review DHR for completeness

Prepare and administer Certification Tests

Review reject samples and assist in initiating training guidelines

Perform reject review on cosmetic rejects and report results

Maintain area and equipment in a clean

Observe and report deviations from Good Manufacturing Practices

Ensure familiarity with production processes

Complete Surveillance Audits and walkthroughs of Production areas

Identify and Issue non-conformities

Investigate and Identify root cause of non-conformities

Provide corrective/preventive actions

Disposition QN’s as necessary

Perform basic data entry and elementary mathematical evaluation

Help in evaluating sampling plans

Recommend sampling plan reduction based on statistical analysis

Maintain accurate and organized files

Prepare files for document retention

Maintain updated procedures and specifications

Support validation and process improvement work

Perform other related duties as assigned

Perform some laboratory testing duties

Maintain knowledge of and make revisions to applicable SOP’s

Ensure area personnel are trained on SOP’s and Inspection Plans

Ensure continual Quality System (QS) compliance

Adhere to established and evolving Regulatory and Alcon QS requirements

Ensure that appropriate root cause analysis tools are used

How You'll Work.

Team & Collaboration

Work with competent and committed colleagues; Enjoy working together in a good and respectful manner

Process & Methodology

process improvement work

Full Job Description

**QA Manufacturing Inspector - Weekend Shift** 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. The QA Inspector is responsible for final product release of all manufactured products, Operator Certification, Compliance Audits & QA Surveillance Audits. Ensure product is released in a timely and compliant manner. **A typical day to day would be to:** * Product Release - Product Release of all manufactured products. DHR review for completeness. Preparation and administration of Certification Tests. Perform review on reject samples and assist in initiating training guidelines. Perform reject review on cosmetic rejects and report results. Maintain area and equipment in a clean, orderly manner at all times. Observe and report on any/all deviations from Good Manufacturing Practices and/or procedures citied during compliance audits. Ensure familiarity with production processes. Complete Surveillance Audits and walkthrough of Production areas. * Non-Conforming Event (NCE) - Identify and Issue non-conformities as required. Investigate and Identify root cause of non-conformities and provide corrective/preventive actions. Disposition QN’s as necessary. * Data tracking and trending - Perform basic data entry and elementary mathematical evaluation of data (e.g., average, deviation range. Help in evaluating sampling plans and recommend reduction based on statistical analysis of historic data. * Documentation - Maintain accurate and organized files for, DHR/BHRs, and/or QA projects. Prepare files for document retention as needed. Maintain updated procedures and spec

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