Quality control inspectors Work, Jobs in Turnhouse, Edh (with Salaries)

Specialist Quality Control
NextPharma GmbH —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Data analysis skills
Validation Technician
AliveDx —Penicuik
- Full-time
- Computer literacy
- Continuous improvement
- Organisational skills
- Annual leave
QA Assistant
J K Thomson —Musselburgh
- From £26,436.80 a year
- Full-time
- Computer literacy
- Writing skills
- Quality control
- Free parking
Quick apply
QA Technician
SGS —Livingston
- Up to £32,000 a year
- Full-time
- Quality control
- Data entry
- Annual leave
Quick apply
4d
Infection Prevention & Control Auditor
NHS Scotland —Newbridge
- £34,544 - £43,039 a year
- Travel
- Organisational skills
- Communication skills
8d
Quality Inspector
Thomson Pettie Ltd —Cumbernauld
- From £12.71 an hour
- Overtime
- Continuous improvement
- Quality control
- Data entry
- Free parking
Quick apply
3d
Food Safety Auditors - (Global)
LRQA group —Edinburgh
QC Inspector
Ritchie Precision —Motherwell
- £28,500 - £35,500 a year
- Full-time
- Quality control
- In-person
- Communication skills
- Free parking
Quick apply
12d
Warehouse Operative - Checker
gategroup —Edinburgh
- £12.70 an hour
- Overtime
- Free parking
- Annual leave
Quick apply
Advanced NDT Technician
Glacier Energy —Inverkeithing
- Full-time
- Analysis skills
- Travel
Quick apply
Manufacturing Technician
Leonardo UK Ltd —Edinburgh
- £31,000 - £35,500 a year
- Full-time
- Hybrid work
- Quality control
- Flexible schedule
- Referral programme
5d
Multi NDT Technician (Temporary Ad Hoc Scopes)
Oceaneering —Rosyth
- £23 - £25 an hour
- Overtime
- Hotel
- Quality control
QA/QC Inspector
Proclad Group —Glenrothes
- Overtime
- Microsoft Word
- Quality control
- Communication skills
Seafood Auditor - Global (ASC, BAP, MSC COC & MSC)
LRQA group —Edinburgh
- English
QA/QC Inspector
Proclad —Glenrothes
- Overtime
- Microsoft Word
- Quality control
- Communication skills
CMM Programmer UCMMPG
Oil States Industries (UK) Ltd —Whitburn
- Quality control
- Communication skills
Quick apply
Seafood Auditor - Global
LRQA group —Edinburgh
- English
NDT Technician
Proclad —Glenrothes
- Full-time
- Computer literacy
- Computer skills
Welding Inspector
NAVANTIA UK —Methil
- Full-time
- IT
- Communication skills
Quick apply
NDT Technician
Proclad Group —Glenrothes
- Full-time
- Computer literacy
- Computer skills

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Specialist Quality Control

NextPharma GmbH -
Livingston

Apply Now

Job details

Full-time

Qualifications

Microsoft Word
Report writing
GLP
Report generation
Analytical chemistry
Computer literacy
Data analysis skills
Quality control within general manufacturing industry
Microsoft Office Suite
Email software
Quality control
Pharmaceutical industry setting experience
Instrumentation calibration
Communication skills

Full job description

Location:
Livingston, GB, EH53 0TH

#job-location.job-location-inline { display: inline; }
Job Function: Quality Control
Anticipated Start Date: 01/08/2026
Job Type: Full-Time
Are you looking for...

an exciting professional challenge?

We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,300 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.

Job Purpose:
To support the production of both development and market finished products under GMP conditions in all areas of quality control and calibration.

Key responsibilities and accountabilities:
Work as part of a team alongside Production and other analytical departments including development and stability.
Actively involved in performing analytical activities to determine fitness for purpose of starting materials, intermediate and finished products
Technically competent in analytical activities (e.g., pharmacopeial wet chemistry, HPLC, GC, Dissolution) for QC testing of raw materials, packaging components and finished products. All activities to be performed under current cGMP, In house SOP’s and/or pharmacopoeia
Perform sampling of starting materials, packaging components and finished products
Perform cleaning verification analysis to assure suitability of Production equipment for subsequent use
Support calibration of key analytical equipment and measuring devices used in or on production equipment
Comply with company health and safety procedures.

Personality:
Results oriented with a positive outlook and clear focus on high quality output: Solid planning and organizational ability; Reliable, tolerant, and dependable: Comfortable dealing with senior managers and customers: Enjoy working in a fast, stimulating environment. Goal-oriented: Able to work under pressure and meet deadlines; Excellent communication/ presentation skills. Able to get on with others and be a team player but equally comfortable working independently.

Personal Situation

Flexible and able to work extended hours when required.

Specific Job Skills:
Required:
Relevant qualification, HNC/HND/Science Degree or Equivalent
An understanding of drug development and manufacturing processes
Demonstrated technical competence of the technical and practical skills involved in analytical activities to prescribed quality standards
Skilled in analytical techniques e.g., HPLC, Dissolution, Gas Chromatography, and wet chemistry techniques
Able to communicate well with others, both laboratory and non-laboratory based
Able to work with minimal supervision.
Good understanding of quality control, SOP and GMP adherence

Desired:
Have a broad knowledge with and experience of working within a cGMP/GLP environment.
Experience of working within a pharmaceutical or biotechnology industry
Ability to work to key regulatory and compliance requirements
Experience of quality control within a pharmaceutical environment
Experience of Chromeleon software
Experience of data reporting and checking data within a QC environment
Understand and demonstrate a pragmatic approach to problem solving with GMP constraints.

Computer skills: Must be competent in the use of MS Office, particularly Excel and Word,
e-mail and internet. Previous use of chromatographic acquisition software is desired but not essential.

Literacy and Numeracy: Must be competent in writing reports both for internal use and for customers. Must be competent in the interpretation of analytical data.

Business Presentation Skills: Must be an excellent face-to-face and telephone communicator.

It's time for your next chapter:
We look forward to receiving your application.

Apply Now

Refine Your Search

quality control inspectors jobs in turnhouse, edh

Specialist Quality Control

Validation Technician

QA Assistant

QA Technician

Infection Prevention & Control Auditor

Quality Inspector

Food Safety Auditors - (Global)

QC Inspector

Warehouse Operative - Checker

Advanced NDT Technician

Manufacturing Technician

Multi NDT Technician (Temporary Ad Hoc Scopes)

QA/QC Inspector

Seafood Auditor - Global (ASC, BAP, MSC COC & MSC)

QA/QC Inspector

CMM Programmer UCMMPG

Seafood Auditor - Global

NDT Technician

Welding Inspector

NDT Technician

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