QA Engineering

WHAT WERE LOOKING FOR:

• Bachelors degree or above majoring in Chemical Engineering Materials Science Pharmacy or related fields.
• ISO9001Familiar with ISO9001 quality management system requirements.
• GMP ISO13485 Familiar with GMP requirement or ISO13485 system or drug packaging materials requirement.

CERTIFICATIONS:

CET -4

EXPERIENCE:

• 1At least 1 year work experience in QMS.

THOSE NECESSARY TO PERFORM THE JOB COMPETENTLY:

• Experience in quality management of single-use product is preferred.
• Experience in QMS related to medical devices pharmaceutical packaging materials and drugs is preferred.
• Internal auditor is preferred.

PREFERRED QUALIFICATIONS:

• OfficeExcelPPTWordProficient in Office suite (Excel PPT Word).
• Have experience in quality management system.
• Solid written and verbal communication skills.
• Have certain data analyze ability.
• CET-4Good English reading and writing skills passed CET-4 or above.
• Has good communication and teamwork skills and a strong sense of responsibility.

HOW YOU WILL THRIVE AND CREATE AN IMPACT:

• Assist the manager of quality department to establish the document management system and implement the management of the formulation review revision distribution recovery storage and destruction of documents.
• ETQManage quality system documents and records and implement management of the formulation review revision issuance retrieval storage and destruction of documents and records; The process of managing quality system documents and records in ETQ.
• ERPResponsible for the release of materials and products reviewing inspection records of materials intermediate products semi-finished products and finished products ensuring that raw materials packaging materials intermediate products products to be packaged and finished products meet requirements and quality standards and completing ERP system operations.
• Responsible for preparing monthly and annual quality reports.
• Responsible for the management of archives and calibration of measuring instruments.
• CAPAResponsible for organizing and tracking deviations changes CAPA The completion status and results of the disposal of non-conforming products.
• Assist in supervising the on-site quality management of the company and conducting supervision and inspection of the companys site.
• Complete other tasks assigned by the leader.

Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

Why Avantor

Dare to go further in your career. Join our global team of 14000 associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

The work we do changes peoples lives for the better. It brings new patient treatments and therapies to market giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his moms voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents learn new skills and grow your career at Avantor.

We are committed to helping you on this journey through our diverse equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!

EEO Statement:

We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex gender identity sexual orientation race color religious creed national origin physical or mental disability protected Veteran status or any other characteristic protected by federal state/province or local law.

If you need a reasonable accommodation for any part of the employment process please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

3rd party non-solicitation policy:

By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor or by failing to comply with the Avantor recruitment process you forfeit any fee on the submitted candidates regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation