Project Manager Biologics

at  Anabiotec

8000 Bruges, West-Vlaanderen, Belgium -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate21 Nov, 2024Not Specified23 Aug, 2024N/AGood communication skillsNoNo
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Description:

WHY JOIN ANABIOTEC?

anacura, a family-owned, growing center of excellence in healthcare with over 250 employees consists of 3 independent laboratories: Labo Nuytinck, active in medical analytics and AnaBioTec and OHMX.bio, active in drug development. The labs have their main activities in a state-of-art anacura building set in a green environment near Ghent, Belgium.
AnaBioTec provides analytical services for characterization, assay development and quality assessment of novel and established medicines, ranging from synthetic molecules and biologics, to cell & gene therapies. With more than 20 years of experience we proudly contribute to these medicines of tomorrow by helping our customers to accelerate their drug development journey. We support startups, biotech as well as large pharma companies worldwide from pre-clinical drug development, through clinical phases I, II, III all the way to commercial drugs. We take proud in our flexibility, diligence and science thereby operating as an extension of our clients with tailored resources and pro-active, science driven advice. To achieve all this, AnaBioTec is set-up as a workspace with open doors where all our employees are encouraged to continuously improve & grow, are taken care of as valuable assets and are welcomed to actively contribute to the goals of AnaBioTec.
In our journey of continued growth, we are looking for a (m/f/x):

Responsibilities:

  • As a project manager you are the single point of contact for our pharma/biotech customers.
  • You advise the customer in the analytical part of their drug development. You translate their needs into laboratory assignments and make estimates of the workload.
  • You actively maintain knowledge of current regulatory requirements and serve as a subject matter expert (SME) in regulatory or customer’s audits.
  • You manage analytical method development, phase appropriate validation and release/stability testing (writing, set-up, review, data management) for developmental and commercial compounds.
  • You actively work together with your fellow project managers, scientists and group leads to kick-off, execute and finalize the projects in accordance with customer expectations.
  • You are responsible for the interpretation of the results and reporting to the clients.
  • You closely follow working methods and procedures and you are able to proactively detect issues and propose mitigations.
  • You will be lead or participate in internal projects as part of our continuous improvement company culture.
  • Finally, you keep your scientific knowledge up-to-date through literature and attendance at scientific seminars.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

8000 Bruges, Belgium