(manufacturing qa) Work, Jobs in Wishaw, Nlk (with Salaries)

Specialist Quality Control
NextPharma GmbH —Livingston
- Full-time
- Microsoft Word
- Computer literacy
- Data analysis skills
Quality Manager (Manufacturing QA)
NHS Scotland —Edinburgh
- £65,125 - £70,303 a year
- Hybrid work
- Master's degree
- Bachelor's degree
- Quality control
3d
QA Technician
SGS —Livingston
- Up to £32,000 a year
- Full-time
- Quality control
- Data entry
- Annual leave
Quick apply
11d
Quality Inspector
Thomson Pettie Ltd —Cumbernauld
- From £12.71 an hour
- Overtime
- Continuous improvement
- Quality control
- Data entry
- Free parking
Quick apply
10d
QA Technician II
Thermo Fisher Scientific —Paisley
- Full-time
- Microsoft Word
- Continuous improvement
- Quality control
- Annual leave
- Referral programme
Regulatory and Quality Associate
Cross Healthcare Ltd —Stirling
- From £12.71 an hour
- Weekend availability
- Microsoft Word
- Bachelor's degree
- Quality control
Quick apply
10d
Quality Assurance Manager- Backshift
Albert Bartlett —Airdrie
- Full-time
- Continuous improvement
- Team management
- Quality control
- Free parking
Quick apply
5d
Manager, Quality Assurance
LGC Biosearch Technologies —Bellshill
- Full-time
- Analysis skills
- Bachelor's degree
- Continuous improvement
- Employee assistance programme
- Employee discount
Quick apply
QA Compliance Officer
Piramal Healthcare UK Limited —Grangemouth
- Microsoft Powerpoint
- Microsoft Word
- Business
9d
Quality Control Lab Manager
Thermo Fisher Scientific —Paisley
- Full-time
- Project management
- Bachelor's degree
- Continuous improvement
7d
Customer Quality Engineer
Peak International Group —Renfrew
- £0.01 a year
- Continuous improvement
- Organisational skills
Quick apply
Customer Quality Engineer
Peak Scientific —Glasgow
- Continuous improvement
- Organisational skills
Quality Assurance Engineer
Spire —Glasgow
- Hybrid work
- Schematics
- Engineering
- Continuous improvement
- Employee stock purchase plan
- Annual leave
Quality Assurance Engineer
Spire Global —Glasgow
- Hybrid work
- Schematics
- Engineering
- Continuous improvement
- Employee stock purchase plan
- Annual leave

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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

(manufacturing qa) jobs in wishaw, nlk

Specialist Quality Control

Quality Manager (Manufacturing QA)

QA Technician

Quality Inspector

QA Technician II

Regulatory and Quality Associate

Quality Assurance Manager- Backshift

Manager, Quality Assurance

QA Compliance Officer

Quality Control Lab Manager

Customer Quality Engineer

Customer Quality Engineer

Quality Assurance Engineer

Quality Assurance Engineer

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