QA and EHS Associate

at  Sartorius

Nottingham, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Sep, 2024Not Specified18 Jun, 2024N/AGood communication skillsNoNo
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Description:

We are looking for a Quality and Environmental Health and Safety Associate to join our team in Nottingham. You will have a BSc in Life Sciences, biotechnology, biology, molecular biology etc. and/or strong experience in administrative duties working within the pharmaceutical or biotechnology industry.
We are looking for a QA and EHS Associate for the QA and EHS department at Sartorius Albumedix Ltd. In this role, you will be responsible for reviewing documentations related to manufacturing, QC worksheets and environmental health and safety including administrative duties to ensure meeting quality standards and compliance.
The team consists of 5 professionals, and we are looking forward to shaping the future with you.
This position is available full – time. It is an onsite role in central Nottingham and the site is easy to get to, being a short walk from the train station and tram stop.

READY TO JOIN SARTORIUS?

About Sartorius
Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide.
We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving your application.

Responsibilities:

  • On a daily basis you will manage shared QA activities including but not limited to, review BMRs (batch manufacturing records), QC worksheets, batch release, paperwork related to deviations, change controls whilst following SOPs and GMP regulations
  • You will carry out activities related to EHS i.e.: COSHH assessments, near miss accident reports, taking minutes at Health and Safety meetings, write reports
  • Support customer and internal audits, supplier evaluation, product quality review
  • Use eQMS (DocCompliance) for administrative activities and provide support in further implementation activities for the system
  • Carry out training in QA and EHS issues
  • You will work closely with other departments i.e.: manufacturing, QC, EHS, R&D


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Software Testing, Clinical Pharmacy

Graduate

Proficient

1

Nottingham, United Kingdom