Pharmaceutical Quality Assurance Specialist (ZR_23563_JOB)

Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

Minimum 5 years of experience in quality assurance within the life sciences industry., Proven experience in pharmaceutical or clinical research organizations., Strong background in quality auditing and compliance., Excellent attention to detail and superior English communication skills..

Key responsibilities:

  • Design and implement comprehensive quality control processes for clinical research projects.
  • Conduct thorough quality assurance audits to maintain compliance standards.
  • Review and enhance documentation systems to ensure alignment with quality requirements.
  • Collaborate with team members to ensure adherence to quality standards.

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BruntWork Human Resources, Staffing & Recruiting SME https://www.bruntworkcareers.co/
501 - 1000 Employees
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Job description

This is a remote position.

Job Highlights:

  • Contract type: Independent Contractor
  • Schedule:Flexible hours based on project needs - 20 hours per week

Client Time zone: UK/London time zone

 

Client Overview

Join an innovative leader in the clinical research industry that provides cutting-edge endpoint solutions for pharmaceutical companies and clinical research organizations conducting critical trials. This growing company is at the forefront of ensuring quality and compliance in clinical research, working with some of the biggest names in the industry.


Job Description

As a Quality Assurance Consultant, you’ll play a pivotal role in shaping and maintaining quality standards across clinical research initiatives. This position offers the unique opportunity to contribute to the development and implementation of quality control processes that directly impact the success of clinical trials. You’ll work with a dynamic team, leveraging your expertise to ensure excellence in endpoint-solutions while maintaining compliance with industry standards.


Responsibilities
  • Design and implement comprehensive quality control processes for clinical research projects
  • Conduct thorough quality assurance audits to maintain compliance standards
  • Review and enhance documentation systems to ensure alignment with quality requirements
  • Provide strategic oversight of quality assurance processes across multiple projects
  • Collaborate with team members to ensure adherence to quality standards
  • Develop and maintain quality assurance tracking systems
  • Create and implement quality improvement initiatives

Requirements
  • Minimum 5 years of experience in quality assurance within the life sciences industry
  • Proven experience in pharmaceutical or clinical research organizations
  • Strong background in quality auditing and compliance
  • Excellent attention to detail and analytical skills
  • Superior English communication abilities, both written and verbal
  • Demonstrated ability to work independently and drive initiatives
  • Corporate experience in clinical research or pharmaceutical industry
  • Experience with major clinical research organizations
  • Proven track record of implementing quality control systems
  • Strong documentation and reporting skills

Benefits
Independent Contractor Perks:
  • Permanent Work from home
  • Immediate Hiring
  • Steady Freelance Job

Please note that since this is a permanent work-from-home position and an “Independent Contractor” arrangement, the candidates must have their own computer and internet connection. They will handle their own benefits and taxes. The professional fees are on hourly rates and the rate depends on your performance in the application process.


ZR_23563_JOB



Required profile

Experience

Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Quality Control
  • Quality Assurance
  • Communication
  • Analytical Skills
  • Detail Oriented

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