Jobs and Careers
BR
Pharmaceutical Quality Assurance Specialist (ZR_24998_JOB)
BruntWorkUKRemotepart_timeVerifiedPosted 9 Jul 2025
About the role
This is a remote position.
Schedule:- Flexible hours based on project needs - 20 hours per week
- Client time zone: UK/London (BST/GMT)
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 benefits and taxes. The professional fees are at hourly rates, and the rate depends on your performance in the application process.
ZR_24998_JOB
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s
Similar roles
VP, Pharmaceutical Quality
Dyne Therapeutics
Waltham
Quality Culture Program Lead — Pharmaceutical (Hybrid — Indianapolis, IN) Contract with Possible Extension
Pharmavise Corporation
IndianapolisRemote
Virtual Remote-Inside Pharmaceutical Sales Representative- EST
Amplity Health
Florida, United StatesRemote