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Bioanalytical Data Reviewer

72% Flex
Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

BSc with PhD, 5-6 yrs exp, HPLC exposure, Experience in regulated cGMP environment, protein methods.

Key responsabilities:

  • Ensure accurate results of scientific test procedures
  • Review data and write up results accurately and confidentially
  • Perform analytical testing and update documentation as required
Resillion Netherlands  logo
Resillion Netherlands SME https://www.eurofins-cybersecurity.com/
51 - 200 Employees
See more Resillion Netherlands offers

Job description

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Your missions

Company Description

Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

In 2018, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 47 countries, employing about 45.000 staff.

Job Description

Consider joining Eurofins BPT where people are the most important element in our business.  Eurofins BPT is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide.

Eurofins BPT are currently recruiting a Data Reviewer Senior Analyst/Scientist for our Biopharmaceutical department based in Dungarvan Co. Waterford. 

Hybrid role offering 2 days working from home, once fully trained (approx 3 months) 

The purpose of this job is mainly the data review of scientific test procedures used on client samples ensuring that accurate results have been produced. This person will also work to develop any ancillary procedures associated with the processes used; ensuring customer samples are completed within their required specifications.


• Responsible for reviewing data, analytical procedures and appropriate documentation to the relevant regulatory standard.
•    Responsible for the review of specific technological projects and writing up the results of these projects accurately, confidentially and on time for the clients.
•    Senior Analysts are permitted to sign all technical documents within the company once their training in this task is successfully completed.  This includes laboratory reports, SOPs, protocols, investigation reports and any other documentation issued.
•    This person will perform analytical testing when not engaged in review activities. 
•    This person will ensure that all documentation is completed on time, accurately and legibly.
•    Responsible for updating any relevant documentation as required.
•    Responsible for handling any customer related queries where necessary and liaising with their team to problem solve these queries if needed.
•    Keep their training records up to date and to initiate training as per their training plan where possible when free from work.
•    Deputise for line management as required during periods of Team Leader absence.
•    Adhere to all company standards in the area of safety, housekeeping and quality, notifying management of any discrepancies.
•    Ensure that customers’ requirements are fully met and in so doing be flexible to work in any area of the business as is required.
•    Identify any opportunities for improvement of quality and service and work with the team to implement continuous improvement.
 

Qualifications
  • BSc with PhD nice to have for this role with HPLC exposure and Biologic courses ideally, 5-6 years industry exp.
  • HPLC and capillary electrophoresis experience is essential
  • Experience of protein  methods (SDS-PAGE, Western blot, IEF, CE,) is desirable.
  • Experience of working in a regulated cGMP environment is essential.
  • Strong technical writing, presentation and trouble shooting skills essential.
  • Ability to work independently within a team-based environment.

Additional Information

Additional Company Benefits

Addition holiday leave

Birthday day (after one year)

Attendance award

Free tea & coffee

Training & Developent

Study support

Free parking

Death in Service

Sports & Social

Corporate Social responsibility day

Salary & bonus reviewed annually

Paid Sick Leave

Finder’s Fee

Recognition Program

Contributory Pension (Depending on length of service/role)

Health Insurance (Depending on length of service/role)

Income Protection (Depending on length of service/role)

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Soft Skills

  • Attention to Detail
  • Time Management
  • Problem Solving
  • Interpersonal Skills

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