Eurofins Advinus Job Vacancy | Quality Assurance

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About Eurofins Advinus:

Eurofins Advinus is a premier contract research, development, and manufacturing organization (CRDMO) serving diverse industries to help advance their R&D programs within defined timelines with the highest level of quality. With 30+ years of GLP experience, we have a proven track record of successfully delivering many integrated and stand-alone projects to meet our partner’s requirements. We offer a complete suite of drug discovery and development services. Our drug discovery services include medicinal and synthetic chemistry, ADMET/DMPK, and Discovery Biology across various therapeutic areas. Our preclinical development services include process development, DMPK, and safety assessment for developing full CMC & Pharmtox packages towards IND submissions. Our team has immense experience with NDA-enabling studies.

Eurofins Advinus supports drug substance requirements from multi-kilogram to multi-ton scale for preclinical toxicology studies, clinical trials, and commercial manufacturing. We manufacture RSMs, advanced intermediates, APIs, and NCEs. We provide a seamless transition from candidate selection to commercialization. In the last 5 years, we have completed 100+ GMP campaigns. For the Agrochemical sector, Eurofins Advinus offers product development services to support global regulatory submissions. We have successfully executed studies following all international guidelines.

We offer a wide range of field and lab trials to the manufacturers of Agricultural inputs, like pesticides, biopesticides, and fertilisation.

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About Eurofins Advinus Job Vacancies:

Hello Connections,
We are Hiring for Quality Assurance Executive for our company Eurofins Spectro Analytical Lab Pvt Ltd.

Location & Experience
Delhi/Greater Noida- Chemistry or Mechanical background with Min one year of technical Experience.
Mumbai- Chemistry or Mechanical background with 3 to 5 years of technical Experience (with Preference if he/she has handled QA work also)

Job Responsibility :
1.    Knowledge of Quality Management Systems as per ISO/IEC 17025:2017
2.    To prepare & control documents and to ensure the lab is using the latest version of documents in the lab.
3.    Handled external assessments.
4.    Review of processes like; root cause investigation for Complaints, negative feedbacks, non-confirming work, Follow up of corrective action and continuous monitoring for effective implementation.
5.    Preparation of PT/ILC/IQC plans and coordination. Review of results and initiation of Interlaboratory comparison programs, evaluation of Z scores.
6.    Coordinating with customers for complaint closure and feedback.
7. Cross-functional coordination and follow-up with internal team to timely closure of projects.
8.    Keeping track of training calendars
9.    Conducting internal and process audits as per regulatory requirements, customer requirements & internal requirements etc.
10. Knowledge of MS Office (MS Word, Powerpoint, Excel etc)

Interested Candidates can share their candidature at [email protected]