Quality Assurance Scientist

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality

Kymos

We are an innovative and fast-growing CRO offering you the opportunity to develop your career in an excellent working environment. Kymos Group is a scientific-technical services company directed to companies of the chemical-pharmaceutical and veterinary sector.

KYMOS offers a wide range of analytical services in Medicinal Chemistry to optimize the research, the development and the quality control for innovative, generic and biological drug substances and drug products from the preclinical stage to market.

KYMOS also has an extensive experience in developing and validating bioanalytical methods and sample analysis in any biological matrix using the latest technology. Mass spectrometry and immunology laboratories are available to carry out small molecule and biologic projects.

KYMOS is also an international group, Kymos Group, with sites in Italy, PHARMAPROGRESS and in Germany, PROLYTIC.

Job description

We are hiring a Quality Assurance Scientist for our GMP area of Quality Assurance.

The QA Scientist will be assigned the following responsibilities:

Participate in the implementation and improvement of quality
Supervise and approve the necessary documentation to carry out the analytics.
Give the necessary support in the release of lots.
Satisfy our clients' needs in matters related to quality
Write procedures and reports, as well as assess deviations from established quality standards and change controls.
Evaluate corrective actions, deviations and claims.
Guarantee compliance with regulatory requirements to the health authorities.

Requirements

We are looking for a candidate with a Pharmacy Degree or Chemistry Degree and with 2 years of experience in a Quality Assurance Department in the Pharmaceutical Industry.

The candidate should have knowledge of Quality Control Techniques, Analytics and Pharmaceutical Production and comply with GMP regulations.

A high level of English, both written and spoken is required for this position

Benefits

Why should you work with us?

You will become part of a young and dynamic team in a fast growing CRO
The company has and interesting working schedule with flexibility in arrival and departure times and intensive schedule on Friday
Our headquarters is located in an amazing place at the foothill of Collserola Park, the green lung of Barcelona.
We encourage challenges and autonomy, so you will have possibilities of learning and growing

Job closed

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality

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