Quality Assurance Scientist


  • Location: Frankfurt am Main (Germany)
  • Sector: Pharmaceutical and biopharmaceutical
  • Vacancies: 1
  • Discipline: R&D

PROLYTIC

KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, Germany and Denmark and a Liaison office in South Korea, offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have been successfully inspected by EMA, FDA, and ANVISA.

KYMOS GROUP is devoted in providing high quality and added value services to its partners and it is highly oriented to innovation, offering services of research, development and quality control in many different fields such as small molecules, proteins, antibodies, nucleic acids, and advanced therapies.

KYMOS GROUP has a young and dynamic staff of more than 330 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.

PROLYTIC is a scientific and technical service company that caters to biotechnology and pharmaceutical companies. We offer a broad range of analytical services in the fields of bioanalysis, pharmacokinetics, pharmaceutical analytics, and RNA/DNA analysis, covering the entire process from preclinical and clinical development to the commercialization of various active pharmaceutical ingredients (APIs).

 

 

Job description

We are hiring a Quality Assurance Scientist to incorporate to our team. The person will be assigned the following responsibilities:

 

  • Coordinate the GMP area of Quality Assurance. 
  • Provide regulatory & technical expertise with respect to laboratory quality systems and procedures.
  • Conduct and participate in audits to meet quality requirements.
  • Supervise and approve the necessary documentation to carry out the analytics.
  • 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, Chemistry or related 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 comply with GMP regulations.

Knowledge of GLP regulations will be a plus. 

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

 

Job closed

  • Location: Frankfurt am Main (Germany)
  • Sector: Pharmaceutical and biopharmaceutical
  • Vacancies: 1
  • Discipline: R&D