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Analytical Chemist / Sample Coordinator

Publicatie datum
Werkgebied Oldenzaal
Aantal uren per week 32 - 40 uur p/w
Opleidings niveau HBO/WO

Job description

As part of the expansion of our Analytical Laboratory with the implementation of QC analysis under GMP, we are looking for an enthusiastic and motivated Analytical Chemist who likes to play a coordinating role in the planning of our QC analyzes. Do you have these coordinating skills, and do you want to join our analytical team? Then read further…..

The organization

Nanomi is leader in the field of microsphere and nanoparticle development of long-acting release injectables. The company is located in the green surroundings of Oldenzaal and is a subsidiary of Lupin ltd. The Nanomi team is young and internationally oriented. The working atmosphere is informal and dynamic, with personal development and humor as important pillars.

The analytical laboratory plays an important role in the quality control of our products. This includes both QC analyses under GMP and routine analyses to support our R&D activities. As Analytical Chemist / Sample Coordinator you will have an important coordinating role in the planning and execution of the analyses. It’s essential to maintain good contact with Project Management about QC analyses and with Process and Formulation engineers regarding R&D analyses. Furthermore, you will contribute in the execution of release and stability testing of our products. Next to that, you support product development; as a team we do our job as efficient and effective as possible. The analytical techniques you work on are diverse, for example HPLC, GC, KF, DSC and determination of characteristics of our products like syringeability and injectability.

Responsibilities

  • Coordinates of sample receipt and sample storage of GMP samples.
  • Plans and coordinates of QC analyses for release and stability testing.
  • Plans and coordinates of routine analyses of R&D production.
  • Executes QC analysis for release and stability testing of GMP batches.
  • Executes routine analytical techniques according to procedures and protocols on (stability) samples to support product development.
  • Executes method transfer, verification and validation activities.
  • Records analytical results into lab books, Test Data Sheets or data systems to obtain (graphical) overviews ready for interpretation.
  • Checks and reports whether assay controls and samples are conform expectations.
  • Executes data interpretation and trend analysis.
  • Proposes and implements improvements of procedures on the analytical laboratory, including technical, logistical and EHS procedures.
  • Keeps assigned equipment in good working order and compliance with respect to maintenance and qualified status.
  • Writes and updates Standard Operating Procedures for assigned instruments and equipment.

Functional contacts

You have functional internal contact with engineers, chemists, scientists and project management to exchange information on samples, results and the daily planning of the related work.

Profile

  • Knowledge: comparable to BSc (HLO) in analytics.
  • Experience: 5 to 8 years of industrial experience in the field of analytical chemistry of (bio-) pharmaceuticals, food or biomaterials. Experience in HPLC and GMP is preferred.
  • Skills: Proven coordinating and planning skills, keeping the overview, administrative skills,
  • Competences: Result-oriented, accurate, team player, handy, pro-active and agile attitude.

Interested? Please contact us! We are happy to receive your CV and motivation letter

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Publicatie datum
Werkgebied Oldenzaal
Aantal uren per week 32 - 40 uur p/w
Opleidings niveau HBO/WO

Nanomi B.V.
Zutphenstraat 51
7575 EJ Oldenzaal
The Netherlands

T: +31 8 800 40 800
E: hr@nanomi.com