Pharma Document Controller - DMS Specialist (12-Month)

Pharma Document Controller - DMS Specialist (12-Month)

Full-Time 30000 - 40000 Β£ / year (est.) No working from home possible
QCS Staffing

At a Glance

  • Tasks: Manage and organise documents in a high-tech system for the pharma industry.
  • Company: Join a leading staffing agency with a focus on the pharmaceutical sector.
  • Benefits: Gain valuable experience, competitive pay, and potential career advancement.
  • Other info: 12-month contract with opportunities to learn and grow in a dynamic environment.
  • Why this job: Be part of a crucial team ensuring compliance and quality in healthcare.
  • Qualifications: Experience in pharma/biotech, knowledge of cGMP/GXP, and MS Office skills.

The predicted salary is between 30000 - 40000 Β£ per year.

QCS Staffing is seeking a Document Controller for a 12-month contract in Liverpool. This role involves supporting global document administration within the electronic Document Management System, managing both paper and electronic records.

The ideal candidate will have extensive experience in the pharmaceutical or biotech industry, knowledge of cGMP/GXP standards, and proficiency in MS Office. Strong attention to detail and excellent communication skills are also essential.

Pharma Document Controller - DMS Specialist (12-Month) employer: QCS Staffing

At QCS Staffing, we pride ourselves on being an excellent employer by fostering a collaborative and innovative work culture that values each team member's contributions. Located in the vibrant city of Liverpool, we offer competitive benefits, opportunities for professional growth within the pharmaceutical sector, and a supportive environment that encourages continuous learning and development. Join us to be part of a dynamic team dedicated to excellence in document management and compliance.

QCS Staffing

Contact Details:

QCS Staffing Recruitment Team

We think you need these skills to ace Pharma Document Controller - DMS Specialist (12-Month)

Document Management
cGMP/GXP Standards
MS Office Proficiency
Attention to Detail
Communication Skills
Pharmaceutical Industry Experience
Biotech Industry Experience