Pharmaceutical Work, Jobs in Central Region, Sct (with Salaries)

Regulatory and Quality Associate
Cross Healthcare Ltd —Stirling
- From £12.71 an hour
- Weekend availability
- Microsoft Word
- Bachelor's degree
- Quality control
Quick apply
5d
Laboratory Support
SGS —Glasgow
- Full-time
- Laboratory experience
- Annual leave
Quick apply
4d
Clinical Project Coordinator
BDD Pharma —Glasgow
- £27,000 - £29,000 a year
- Full-time
- Hybrid work
- No experience needed
- SharePoint
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
4d
Molecular Biology QC Analyst
SGS —Glasgow
- From £25,000 a year
- Full-time
- Laboratory experience
- Quality control
- Communication skills
- Annual leave
Quick apply
3d
Quality Analyst
Kerry —Clackmannanshire
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Quality control
Experienced Regulatory Submissions Coordinator
Medpace, Inc. —Stirling
- Full-time
- Bachelor's degree
- In-person
- Communication skills
- Annual leave
- Work from home
QC Micro Tech
Piramal Healthcare UK Limited —Grangemouth
9d
QC Technician- Days
Piramal Pharma Solutions Inc. —Grangemouth
- Bachelor's degree
- Continuous improvement
- Quality control
9d
Regulatory Submissions (Study Start-up) Manager
Medpace, Inc. —Stirling
- Full-time
- In-person
- Leadership
- Communication skills
- Annual leave
- Work from home
5d
Molecular Biology Scientist
SGS —Glasgow
- From £30,000 a year
- Full-time
- Data analysis skills
- Laboratory experience
- Communication skills
- Annual leave
Quick apply
3d
Medical Writer
ApotheCom —Glasgow
- Hybrid work
- Writing skills
- Annual leave
- Work from home
2d
Manufacturing Technician
Piramal Healthcare UK Limited —Grangemouth
- Weekend availability
- Computer literacy
- Continuous improvement
- Computer skills
9d
Junior Project Engineer
M Group —Grangemouth
- £32,000 a year
- Overtime
- Engineering
- Travel
- Annual leave
- Employee assistance programme
Protein Scientist
Piramal Healthcare UK Limited —Grangemouth
- Manufacturing
4d
QA Compliance Officer
Piramal Healthcare UK Limited —Grangemouth
- Microsoft Powerpoint
- Microsoft Word
- Business
3d
Senior Medical Writer
Nucleus Global —Glasgow
- Hybrid work
- Work from home
- Life insurance
Pharmacy Support Worker - Pharmacy
NHS Scotland —Glasgow
- £29,103 - £31,409 a year
- Part-time
- English
- Supervising experience
- Mentoring
- Annual leave
- Employee assistance programme
3d
Process and Project Engineer
Kerry —Clackmannanshire
- Full-time
- Engineering
- Data analysis skills
- Continuous improvement
Senior Manufacturing Technician
Piramal Healthcare UK Limited —Grangemouth
- Mentoring
- Communication skills
Contamination Control Manager
Piramal Healthcare UK Limited —Grangemouth
- Engineering
- Master's degree
- Bachelor's degree

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Regulatory and Quality Associate

Cross Healthcare Ltd -
Stirling

Quick apply

Job details

Permanent | Full-time | Zero hours contract
From £12.71 an hour
5 days ago

Benefits

Company pension
On-site parking

Qualifications

Microsoft Word
Quality management change control procedures
Quality control within general manufacturing industry
Quality assurance
Bachelor's degree
Quality control
Organisational skills
Multidisciplinary collaboration
Pharmaceutical industry setting experience
EU Good Distribution Practice (GDP)
Communication skills

Full job description

About Us

Cross Healthcare is a trusted specialist in the wholesale and repackaging of branded and generic pharmaceuticals. We supply high-quality products at competitive prices to customers across the UK, Europe and worldwide.

Our global import and export operations are supported by a licensed pharmaceutical repackaging facility, enabling medicines to be prepared for parallel trade. We are committed to maintaining the highest standards of quality and regulatory compliance, while building strong relationships with customers, suppliers and partners.

The Role

We're looking for a Regulatory & Quality Associate to join our growing Regulatory and Quality team. This is a varied and rewarding role that combines responsibilities across Regulatory Affairs and Quality Assurance, offering an excellent opportunity to build a career within the pharmaceutical industry.
You'll help ensure our products remain fully compliant with MHRA requirements while supporting the quality processes that underpin our licensed repackaging operations. The role is ideal for someone with exceptional attention to detail who enjoys working in a structured, fast-paced and highly regulated environment, and offers exposure to pharmaceutical licensing, artwork management, GMP/GDP compliance and quality systems.

What you'll be doing

Your responsibilities will include:

Supporting the preparation and maintenance of pharmaceutical product licences.
Creating and maintaining Bills of Material, Master Reference Files, and regulatory records.
Reviewing and approving artwork, labels and printed packaging materials.
Creating and maintaining label templates using BarTender software.
Performing goods-in, print room, and in-process quality checks.
Reviewing batch documentation and preparing batches for Qualified Person (QP) certification.
Raising and assisting with Change Controls, Deviations and CAPAs.
Maintaining quality records, logs, training records and controlled documentation.
Working closely with Production, Commercial and other departments to ensure efficient operations.
Ensuring compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and company procedures.

What we're looking for

The successful candidate will have:

Exceptional attention to detail.
Ability to work accurately in a highly regulated environment.
Excellent written and verbal communication skills.
Strong organisational skills and the ability to manage multiple tasks.
Good IT skills, including Microsoft Word and Excel.
The ability to work both independently and as part of a team.
A proactive, flexible approach and willingness to learn.

Previous experience within pharmaceuticals, Quality Assurance or Regulatory Affairs would be advantageous but is not essential, as full training will be provided for the right candidate.

In return, we offer

Company pension
On-site parking
Ongoing training and development
The opportunity to develop a long-term career within the pharmaceutical industry
A supportive and collaborative working environment

There may occasionally be a requirement to work additional hours, including weekends, to meet business needs.
If you're looking to develop a career in the pharmaceutical industry and enjoy working in a role where quality, accuracy and attention to detail are essential, we'd love to hear from you.

Pay: From £12.71 per hour

Benefits:

Company pension
On-site parking

Work Location: In person

Quick apply

Refine Your Search

pharmaceutical jobs in central region, sct

Regulatory and Quality Associate

Laboratory Support

Clinical Project Coordinator

Molecular Biology QC Analyst

Quality Analyst

Experienced Regulatory Submissions Coordinator

QC Micro Tech

QC Technician- Days

Regulatory Submissions (Study Start-up) Manager

Molecular Biology Scientist

Medical Writer

Manufacturing Technician

Junior Project Engineer

Protein Scientist

QA Compliance Officer

Senior Medical Writer

Pharmacy Support Worker - Pharmacy

Process and Project Engineer

Senior Manufacturing Technician

Contamination Control Manager

I want to receive the latest job alerts for pharmaceutical in central region, sct

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