Regulatory Writer, Manufacturing Science and Technology (MSAT)

at  Novo Nordisk

Bagsværd, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate20 Nov, 2024Not Specified06 Nov, 2024N/APharmaceutical Industry,English,Excel,Continuous Improvement,Chemistry,It,WritingNoNo
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Description:

Regulatory Writer, Manufacturing Science and Technology (MSAT)
Category: Manufacturing
Location:Bagsværd, Capital Region of Denmark, DK
Are you passionate about writing and ready to make a meaningful impact in regulatory submissions? Do you bring experience within API manufacturing processes or the regulatory field, excelling in a role with a clear purpose and direct impact on Novo Nordisk’s ability to deliver to patients?
If you share our drive to make a difference in the production of API products, then join us today in Product Supply (PS) API MSAT Project Office department!

QUALIFICATIONS

To succeed in this role, we imagine you:

  • Hold a MSc. degree in Pharmacy, Chemistry, Engineering, or a similar field
  • Bring a passion for writing, coupled with a keen eye for details
  • Have practical experience in the pharmaceutical industry, regulatory sector, or health authorities, with a focus on writing or reviewing regulatory documents
  • Excel at organizing and prioritizing your tasks effectively
  • Display full proficiency in both spoken and written English

It would be considered as a strong advantage if you have experience with the manufacturing of API’s.
On a personal level, you have a structured and detail-oriented approach to everything you do. You take pride in delivering high-quality documents and to do so, you build and create a network to improve your knowledge and skills. While you thrive working on your own, you also effectively collaborate with various departments across the area. You are proactive and curious, bringing a can-do attitude and a mindset based on continuous improvement.

Responsibilities:

  • Hold a MSc. degree in Pharmacy, Chemistry, Engineering, or a similar field
  • Bring a passion for writing, coupled with a keen eye for details
  • Have practical experience in the pharmaceutical industry, regulatory sector, or health authorities, with a focus on writing or reviewing regulatory documents
  • Excel at organizing and prioritizing your tasks effectively
  • Display full proficiency in both spoken and written Englis


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Content, Journalism, Clinical Pharmacy

Graduate

Chemistry, Engineering

Proficient

1

Bagsværd, Denmark