QC Reviewer - FSP, client dedicated

Thermo Fisher Scientific; Stevenage; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global contract research organization seeks a QC Reviewer to support workflows with data management in a pharmaceutical environment. The role involves stringent data verification, fostering strong relationships with partners, and ensuring compliance with quality standards. If you have a scientific background and attention to detail, apply to enhance therapeutic delivery for urgent health needs.

Qualifications

• Previous experience in a pharmaceutical manufacturing environment.
• Knowledge of GMP/GxP regulations.
• Proactive attitude with willingness to learn and adapt.

Responsibilities

• Verify data matches across source and raw data.
• Identify data inconsistencies and manage corrections.
• Provide consolidated tables from multiple data sources.

Skills

Attention to detail

Communication Skills

Data Verification

Data Management

Education

BSc/MSc in a Scientific Discipline

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our clients to make the world healthier, safer, and cleaner.

Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.

The role of QC Reviewer will ideally be based fully, or partially, at our client's site in Stevenage however remote working may be considered.

As a QC Reviewer within our client dedicated team you will provide data management in support of key workflows which includes data checking and CMC Statistics data management

Responsibilities:

• Verify data in the BYOD data product matches data in source systems

• Verify data in source documents matches data matches raw data

• Identify gaps where data inconsistencies are identified

• Manage the data associated with CMC statistics workflows

• Provide consolidated tables generated from multiple data sources

• Communicate any discrepancies with the parties involved and take steps to correct them in a timely manner.

• Performing a check of the current data to ensure that it is accurate, consistent, and reflects its intended purpose.

• Assesses procedures for accuracy, simplicity, and practicality and influences changes as appropriate

• Builds and maintains good working relationships with internal and external partners

• Manages issues and risks identified in area of responsibility

The successful candidate will have

• BSc/MSc in a Scientific Discipline

• Previous experience in a pharmaceutical manufacturing environment

• Previous experience in a comparable role, including prior experience with data review, data verification and data management

• Knowledge of GMP/GxP regulations

• Strong attention to detail with a focus on quality

• Fluency in Enlgish with strong communication skills (oral and written)

• Proactive attitude with willingness to learn and adapt to meet business needs

Our 4i Values:

Integrity – Innovation – Intensity – Involvement

If you resonate with our 4i values above, and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the world’s most urgent health needs, submit your application – we’d love to hear from you!