Eurofins: Lead Auditor- Healthcare — Gujrat, PB, India

About Eurofins

Eurofins provides analytical testing and laboratory services across life sciences and other industries. Its work includes assessing food, water, pharmaceutical and cosmetic products for qualities such as safety, authenticity, composition and accurate labelling. The employer also describes activities in genomics, clinical-study support, biopharmaceutical development and manufacturing, and diagnostic testing. Scientific methods and dependable information are central to this business, supported by the technology and operational functions used to deliver laboratory services.

The position and its setting

Eurofins lists Lead Auditor- Healthcare in Gujrat, PB, India, under reference REF48514J. The details below separate the work described by the employer from essential conditions, preferred experience and practical preparation advice.

• Department: Quality Assurance
• Employment type: Full-time
• Employer listing date: 7 September 2023
• Legal Entity: CIN021 - Eurofins Assurance India Private Limited
• Contract Type: Permanent
• Business Lines: Other Business Line
• Brands: Eurofins India Assurance

Responsibilities and work described

• Carry out audits at suppliers in accordance with the reference regulations, Eurofins Sisthema procedures and specific customer requests
• Draft audit reports within agreed timelines
• DESCRIPTION OF THE ACTIVITIES
• Macro Areas of Activity
• Pre-audit
• Management of pre-audit documents
• Preparation of the audit agenda
• Collaboration in travel preparation
• Audit
• Research / execution: the audit
• Post-audit
• Drafting of audit reports and audit comments
• Drafting amended documents following customer request
• Evaluation of the CAPA plan
• CROSS-FUNCTIONAL (INTERNAL AND ETERNAL) RELATIONS
• Roles and Areas with which links are held

Essential requirements and candidate background

• Scientific degree (preferably Pharmacy, Chemistry and Pharmaceutical Technology, Chemistry)
• Technical Audit Report Writing skills are mandatory
• Previous
• Experience: minimum 10 plus years in the field of pharmaceuticals, medical devices and / or cosmetics (QA, Regulatory Affairs, QC, Consulting)
• Conducting at least 10 supplier audits and/or internal audits
• Knowledge of- EU GMP part I & II, ISO 9001, ISO 13485, ISO 15378, ISO 22716,CFR21 part 210,211, EU GDP, IPEC guidelines, English language level C, Microsoft Office
• Specific technical practical skills (know-how) - Conducting Audits of Quality Management Systems
• Transversal skills-
• Attention to order and Quality Self-control
• Autonomy Analytical capacity
• Customer and result orientation Confidentiality
• Compliance with planned timelines

Location, schedule and contract conditions

• Work arrangement: On-site
• Advertised location: Gujrat, PB, India

Pay and application dates

A verified salary figure is not established in this article. An online estimate for another Lead Auditor- Healthcare vacancy is not an offer for reference REF48514J; use the employer’s own pay disclosure and recruitment communication.

A closing date is not confirmed in this article. Check the current employer page before submitting: an undated posting can change or be withdrawn.

How to apply to Eurofins

Applications follow the official employer page linked below.

Open the official Eurofins posting below and match the title and reference REF48514J.

Compare your qualifications and experience with the essential conditions for the Gujrat, PB, India position, then read the preferred criteria separately.

Prepare an accurate CV and the supporting items requested in that employer’s application. Provide only information and documents you are authorised to share.

Use the employer’s application option, complete the required fields and review the submission. Retain the acknowledgement when one is provided. Job Alerts World does not receive the application.

Practical preparation: GMP

GMP references concern work performed within a controlled manufacturing or quality environment. In an application, explain your actual involvement with procedures, records, deviations or other controls relevant to the post.

Relevant skills

• MS Office
• GMP
• ISO
• audit
• compliance
• sales
• regulatory affairs
• chemistry
• pharmacy