Pharmaceutical Work, Jobs in Radford (with Salaries)

QMS Officer – Production
L M Manufacturing Ltd —Northampton
- £27,000 - £30,000 a year
- Full-time
- Continuous improvement
- In-person
- Communication skills
Quick apply
1d
Quality Officer
HeliosX —Leamington Spa
- Continuous improvement
Quick apply
7d
Quality & Regulatory Co-Ordinator
AAH Pharmaceuticals —Warwick
- Microsoft Word
- Analysis skills
- Continuous improvement
- Employee assistance programme
- Sick pay
Dental Sales Representative
IQVIA —Warwick
- Full-time
- Business development
- Communication skills
- Employee discount
- Gym membership
Sourcing Coordinator
AAH Pharmaceuticals —Warwick
- Communication skills
- Employee assistance programme
- Sick pay
2d
QMS Compliance Executive (12 months FTC)
Aspire Pharma Ltd —Leicester
- Monday to Friday
- Hybrid work
- Microsoft Word
- English
- Quality control
- Employee assistance programme
1d
Dispensing Assistant
Tri-Pharma Ltd —Sutton Coldfield
- From £12.71 an hour
- Full-time
- Customer service
- Data entry
- Organisational skills
- Employee discount
Quick apply
3h
Pharma on-site Operations Supervisor
TVS Supply Chain Solutions —Birmingham
- £30,900 a year
- Full-time
- Hybrid work
- Recruiting
- Computer skills
- In-person
- Health & wellbeing programme
- Employee assistance programme
Quick apply
9d
Warehouse Operative
AAH Pharmaceuticals —Tamworth
- £12.91 - £14.41 an hour
- No experience needed
- Maths
- Employee assistance programme
- Sick pay
12d
Commercial Analyst
AAH Pharmaceuticals —Warwick
- English
- Analysis skills
- Communication skills
- Employee assistance programme
- Sick pay
6d
Virtual Key Account Manager
IQVIA —Birmingham
- Full-time
- Remote
- Work from home
- Employee discount
Scientific Affairs Manager, UK - Birmingham
Rhythm Pharmaceuticals —Birmingham
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills
Operational Compliance Executive
Aspire Pharma Ltd —Leicester
- Monday to Friday
- Hybrid work
- Microsoft Word
- Microsoft Outlook
- English
- Employee assistance programme
1d
Quality Assurance Advisor / Deputy Responsible Person (DRP)
Personal Homecare Pharmacy —Leicester
- £33,000 - £38,000 a year
- Organisational skills
- Communication skills
- Annual leave
- Employee assistance programme
Quick apply
Territory Business Manager
IQVIA —Coventry
- Full-time
- Nursing
- Nursing home
- No degree
5d
GNFR Procurement Manager
AAH Pharmaceuticals —Warwick
- Microsoft Powerpoint
- Computer literacy
- Continuous improvement
- Employee assistance programme
- Sick pay
Junior Buyer - 12 Month FTC
Well Pharmacy —Redditch
- £30,000 a year
- Microsoft Word
- Organisational skills
- Communication skills
- Annual leave
- Employee discount
12d
Hospital Affairs Lead - UK & Ireland (Midlands West)
Rhythm Pharmaceuticals —Birmingham
- Full-time
- CRM software
- Doctoral degree
- Master's degree
Hospital Affairs Lead - UK & Ireland (Midlands East)
Rhythm Pharmaceuticals —Leicester
- Full-time
- CRM software
- Doctoral degree
- Master's degree
Quality Assurance & Health and Safety Advisor
Personal Homecare Pharmacy —Leicester
- £33,000 - £38,000 a year
- Full-time
- Writing skills
- Analysis skills
- Continuous improvement
- Annual leave
- Employee assistance programme
Quick apply

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QMS Officer – Production

L M Manufacturing Ltd -
Northampton

Quick apply

Job details

Full-time
£27,000 - £30,000 a year
1 day ago

Benefits

On-site parking

Qualifications

Non-conformance investigation
Quality management change control procedures
Quality management
Microsoft Office Suite
Continuous improvement
Multidisciplinary collaboration
Pharmaceutical industry setting experience
Root cause analysis
Communication skills
FDA regulations
Time management

Full job description

QMS Officer – Production

Location: Weedon Bec, Northampton, NN7
Department: Production
Reporting to: Head of Production
Job Type: Full-time, Permanent
Work Location: On-site

About LM Manufacturing Limited

LM Manufacturing Limited is a pharmaceutical manufacturer based in Weedon Bec, Northampton and part of the Zydus Group, a global pharmaceutical organisation committed to quality, innovation and patient care.

Our MHRA and FDA-approved manufacturing facility operates to high standards of Good Manufacturing Practice (GMP), quality and regulatory compliance.

As part of our continued growth, we are looking for an experienced QMS Officer – Production to join our team.

About the Role

Reporting to the Head of Production, the QMS Officer will support the effective management and coordination of Quality Management System (QMS) activities within Production.

The role will have hands-on responsibility for investigations, deviations, CAPAs, change controls, SOPs, risk assessments, training coordination and production documentation, ensuring activities are completed accurately and within required timelines.

Key Responsibilities

Prepare, review, initiate, follow up and support the timely closure of investigations, including OOS, OOT, OOE, deviations and market complaints.
Prepare, review, initiate, track and support the closure of change controls.
Prepare, review, initiate, monitor and support the closure of CAPAs.
Prepare and review risk assessments and protocols.
Prepare, review, initiate and maintain Standard Operating Procedures (SOPs).
Coordinate Production QMS activities and ensure actions are appropriately tracked and escalated.
Monitor QMS timelines and proactively follow up with relevant stakeholders to ensure timely completion and closure.
Support site training coordination activities, including training initiation, review, closure and maintenance of appropriate training records.
Ensure cGMP documentation is maintained in accordance with company procedures and the Quality Management System.
Review Batch Manufacturing Records (BMRs) and Batch Packing Records (BPRs).
Review Production QMS documentation, records and logbooks.
Identify and report non-conformances to the Head of Production and relevant Quality personnel.
Work closely with Production, QA and other cross-functional teams to support investigations and QMS activities.
Participate in internal and external training programmes.
Maintain GMP compliance within the working area, including adherence to approved procedures, gowning requirements and site practices.
Support continuous improvement activities within Production.
Perform other duties and responsibilities appropriate to the role as assigned by management.
Comply with all company Health & Safety, Quality and GMP requirements.

Essential Skills & Experience

Relevant experience within the pharmaceutical industry, ideally within Production, Quality Assurance or a QMS-focused role.
Practical working knowledge of pharmaceutical Quality Management Systems.
Hands-on experience with deviations, investigations, CAPA and change control.
Good understanding of cGMP and Good Documentation Practice (GDP).
Experience preparing and reviewing SOPs and controlled documentation.
Ability to investigate issues, identify root causes and support appropriate corrective and preventive actions.
Strong attention to detail with a quality and compliance-focused approach.
Ability to take ownership and responsibility for assigned activities and drive them through to completion.
Ability to work independently and collaboratively within a cross-functional team.
Strong organisational and time-management skills with the ability to manage multiple QMS activities and deadlines.
Good written and verbal communication skills.
Proficient in Microsoft Office applications.
Self-motivated, proactive and able to work effectively within a fast-paced pharmaceutical manufacturing environment.

Desirable

Experience within an MHRA and/or FDA-regulated pharmaceutical manufacturing environment.
Experience reviewing BMRs/BPRs and production documentation.
Experience with root cause analysis and investigation methodologies.
Experience coordinating or maintaining GMP training records.

Why Join LM Manufacturing Limited?

This is an opportunity to join a growing pharmaceutical manufacturing organisation and work closely with Production and Quality teams in a regulated manufacturing environment.

We provide opportunities for training, professional development and career progression as the organisation continues to grow.

LM Manufacturing Limited is an equal opportunities employer. We welcome applications from suitably qualified candidates and are committed to providing an inclusive working environment.

Job Type: Full-time, Permanent
Work Location: In person – Weedon Bec, Northampton, NN7

Pay: £27,000.00-£30,000.00 per year

Benefits:

On-site parking

Application question(s):

Do you have relevant experience working in a pharmaceutical manufacturing environment in a QMS, Production Quality or Quality Assurance role?

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

pharmaceutical jobs in radford

QMS Officer – Production

Quality Officer

Quality & Regulatory Co-Ordinator

Dental Sales Representative

Sourcing Coordinator

QMS Compliance Executive (12 months FTC)

Dispensing Assistant

Pharma on-site Operations Supervisor

Warehouse Operative

Commercial Analyst

Virtual Key Account Manager

Scientific Affairs Manager, UK - Birmingham

Operational Compliance Executive

Quality Assurance Advisor / Deputy Responsible Person (DRP)

Territory Business Manager

GNFR Procurement Manager

Junior Buyer - 12 Month FTC

Hospital Affairs Lead - UK & Ireland (Midlands West)

Hospital Affairs Lead - UK & Ireland (Midlands East)

Quality Assurance & Health and Safety Advisor

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