Senior Quality Assurance Specialist at Verbatim Pharma

London, Essex - England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

10 Nov, 26

Salary

55000.0

Posted On

01 Oct, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Industry

Pharmaceutical Manufacturing

Description

What the role will look likeSupport the effective operation and continued development of the pharmaceutical quality system.
Provide hands-on QA guidance across clinical trial sourcing, supply and distribution activities.
Review quality documentation and help ensure that processes are applied consistently.
Work closely with operational and commercial colleagues to resolve quality-related questions.
Help identify quality risks and support proportionate, practical solutions.
Contribute to quality reviews, improvement initiatives and team checkpoints.
Provide coaching and mentoring to colleagues within the quality function.
Promote a strong quality culture across a lean, entrepreneurial organisation.

You will bring:Recent, direct experience within clinical trial supply chains.
At least three to four years of core Quality Assurance experience.
Experience gained within a clinical trial supply organisation, specialist pharmaceutical wholesaler, or medium-sized CMO or CDMO.
A practical understanding of the quality requirements associated with the sourcing, handling and distribution of medicines.
The ability to apply quality principles in a bespoke, lower-volume and high-value environment.
Confidence working autonomously while remaining approachable and collaborative.
The judgement and communication skills needed to guide and mentor colleagues.
A pragmatic, detail-focused approach, with the flexibility to operate effectively in a growing specialist business.
General GDP, logistics or manufacturing experience will be valuable, but applicants will need demonstrable clinical supply exposure to succeed in this position.

Responsibilities

What the role will look likeSupport the effective operation and continued development of the pharmaceutical quality system.
Provide hands-on QA guidance across clinical trial sourcing, supply and distribution activities.
Review quality documentation and help ensure that processes are applied consistently.
Work closely with operational and commercial colleagues to resolve quality-related questions.
Help identify quality risks and support proportionate, practical solutions.
Contribute to quality reviews, improvement initiatives and team checkpoints.
Provide coaching and mentoring to colleagues within the quality function.
Promote a strong quality culture across a lean, entrepreneurial organisation.

You will bring:Recent, direct experience within clinical trial supply chains.
At least three to four years of core Quality Assurance experience.
Experience gained within a clinical trial supply organisation, specialist pharmaceutical wholesaler, or medium-sized CMO or CDMO.
A practical understanding of the quality requirements associated with the sourcing, handling and distribution of medicines.
The ability to apply quality principles in a bespoke, lower-volume and high-value environment.
Confidence working autonomously while remaining approachable and collaborative.
The judgement and communication skills needed to guide and mentor colleagues.
A pragmatic, detail-focused approach, with the flexibility to operate effectively in a growing specialist business.
General GDP, logistics or manufacturing experience will be valuable, but applicants will need demonstrable clinical supply exposure to succeed in this position.