Shift Quality Oversight Specialist at GSK
Montrose DD10 8EA, , United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

09 Nov, 25

Salary

0.0

Posted On

10 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Communication Skills, Coaching, Pharmaceutical Manufacturing, Teams, Deviation Management, Mentoring, Manufacturing Processes

Industry

Pharmaceuticals

Description

Site Name: UK - Angus - Montrose
Posted Date: Aug 8 2025
Are you ready to help deliver quality that makes a difference? At GSK, we are united by our mission to improve lives through our innovative pharmaceutical products. Join us as a Shift Quality Oversight Specialist and take on a pivotal role in ensuring patient safety and product quality while driving a proactive quality culture.

BASIC QUALIFICATIONS

  • A scientific qualification (HNC, HND, BSc, BEng) or significant experience in quality/compliance within pharmaceutical manufacturing.
  • Proven experience in deviation management, coaching and mentoring, and continuous improvement initiatives.
  • Strong knowledge of QMS, cGMP principles, and API manufacturing processes.
  • Excellent communication skills to engage teams across all levels.

PREFERRED QUALIFICATIONS

  • Experience in non-sterile microbiology and delivering change management projects.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

As a Shift Quality Oversight Specialist, you will:

  • Be the first line of contact for quality issue management, offering rapid response and timely interventions across GMP areas like production, warehouse, utilities, and laboratories.
  • Ensure compliance with GMP standards, procedures, and inspection readiness through independent checks and proactive oversight.
  • Perform quality process confirmations and maintain adherence to ALCOA+ principles for documentation and records.
  • Foster a Quality Starts With Me (QSWM) culture through coaching, mentoring, and emphasizing the importance of compliance for patient safety.
  • Provide oversight of equipment cleaning, inspection activities, and support batch release processes for smooth, compliant material flow.
  • Participate in activities related to non-sterile microbiology, including water/environmental monitoring and deviation management.
  • Role model GSK’s Global Production System (GPS) standards and contribute to change management initiatives and continuous improvement.
Loading...