Regulatory affairs manager Work, Jobs in Stanwell, Sry (with Salaries)

Quality Assurance Officer
Medreich Plc —Feltham
- £32,000 - £35,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Free parking
- Annual leave
Quick apply
6d
Regulatory Affairs Manager UK&I
Medtronic —Watford
- £71,760 - £107,640 a year
- Full-time
- Analysis skills
- Project management
- Organisational skills
Regulatory Affairs Manager
Reckitt —Slough
- Management
- Communication skills
- Employee assistance programme
- Life insurance
Regulatory Affairs Manager
pladis —Chiswick Park Station
- Full-time
Senior Regulatory Affairs Manager (UK/Ireland)
Perrigo —London
- Hybrid work
- In-person
- Leadership
6d
Senior Manager/Associate Director, Government and Regulatory Affairs
Access Partnership —London
- Hybrid work
Quick apply
5d
Regulatory Affairs Associate/Manager
Transpire BIO Inc. —London
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Senior Manager Medical Information
Vertex Pharmaceuticals —Paddington
- Full-time
- Remote
- Analysis skills
- Bachelor's degree
- In-person
Head of Medical Affairs, UK
Genmab —London
- £123,800 - £185,700 a year
- Full-time
- Doctoral degree
- English
- Leadership
- Annual leave
Senior Regulatory Affairs Manager
Elanco —Hook
- Full-time
- English
- Master's degree
- Leadership
Regulatory Manager - Pharmaceuticals
University College London Hospitals NHS Foundation Trust —London
- £66,274 - £73,496 a year
- Full-time
Regulatory / Compliance Manager
Sigma Consulting Group —London
- £50,000 a month
- Full-time
- Hybrid work
- Contracts
- AI
- Communication skills
Quick apply
Corporate Affairs Manager
NextStep —London
- £70,000 - £90,000 a year
- Full-time
- Hybrid work
- Communication skills
Quick apply
Regulatory Affairs Manager
Vodafone —London
- Full-time
- Analysis skills
- Leadership
- Communication skills
- Annual leave
GB Sr. Manager, Regulatory Affairs - Europe
The Bountiful Company —London
- Bachelor's degree
- Leadership
- Communication skills
Quick apply
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
HCIB Regulatory Affairs Senior Manager (MSS)
HSBC Global Services Limited —London
- Full-time
- Financial services
7h
Compliance and Risk Manager
ExpandJO Business Solutions Ltd. —Watford
- £7,600 - £8,333 a month
- Full-time
- Analysis skills
- In-person
Quick apply
HCIB Regulatory Affairs Senior Manager (CIB)
HSBC Global Services Limited —London
- Full-time
- Financial services
7h
Senior Manager, PV Process Quality Lead
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- Microsoft Office
- Bachelor's degree
- Travel
12d

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regulatory affairs manager jobs near stanwell, sry

Quality Assurance Officer

Medreich Plc -
Feltham

Quick apply

Job details

Full-time
£32,000 - £35,000 a year
6 days ago

Benefits

Free parking
Casual dress
Cycle to work scheme
Annual leave
Flexitime
Company pension
Flexible schedule
Life insurance
On-site parking

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Computer literacy
English
Quality management
Microsoft Office
Master's degree
Analysis skills
Quality assurance
Bachelor's degree
Organisational skills
Communication skills
FDA regulations
Time management

Full job description

Medreich plc

Location: Feltham, TW13 7HF

Quality Assurance Officer

Medreich is an established pharmaceutical company based in Feltham. Medreich Plc pride ourselves on being an employer who is passionate about our employees and their development and wellbeing.

Job Role

The Quality Assurance Officer shall support Quality Management System (QMS) activities and ensure compliance with applicable GMP requirements. The role involves handling deviations, change controls, complaints, batch release documentation review, and coordination with internal and external stakeholders to maintain compliance and product quality standards.

Key Responsibilities:

Quality Management System (QMS)

Knowledge on Change Controls, Deviations, CAPAs, and Product Quality Complaints.

Participate in investigations and follow-up of quality events.

Track QMS activities to ensure timely closure and compliance with defined timelines.

Support preparation of quality metrics and trend reports.

Batch Release Activities:

Support QPs for batch release activities in accordance with approved procedures.

Documentation and Compliance:

Prepare SOPs (Standard Operating Procedures), protocols, reports, and quality documents.

Ensure GMP documentation practices are followed.

Support internal audits, self-inspections, and regulatory inspection readiness activities.

Communication and Coordination:

Coordinate with Manufacturing, QC, Regulatory Affairs, Supply Chain, and Contract Manufacturing Organizations (CMOs).

Follow up on quality-related actions and provide timely updates to stakeholders.

Required Knowledge:

Basic knowledge of GMP requirements (EU GMP, WHO GMP, PIC/S, or US FDA regulations).

Understanding of Change Control, Deviation Management, CAPA, Complaints Handling, and Batch Release processes.

Knowledge of Good Documentation Practices (GDP) and Data Integrity principles.

Skills and Competencies:

Excellent verbal and written communication skills.

English language proficiency (speaking, reading, and writing).

Strong attention to detail and documentation review skills.

Ability to work independently and within cross-functional teams.

Excellent organisational and time management skills.

Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).

Wide knowledge of products and processes used in the manufacture of medicines.

Undertaking any other duties, either for this department or any other department within the business, which may be requested by the Line Manager, for which training and/or an explanation has been provided and understood.

The right candidate will also have:

2-3 years of working knowledge within a QA role in the pharmaceutical industry.
An enthusiastic, confident, and self-motivated personality and the ability to quickly contribute to the culture and way of working.
Computer literate and numerate.
Ability to work in a team environment.
Ability to work under pressure and meet deadlines.
Able to work in autonomy and demonstrate engagement and ability to use initiative.
Able to share experience and good practices with team members.
Observing and complying with company SOP's & Health and Safety Policies.
Contribute to any other related tasks as and when required

Salary & Benefits

· Salary £32,000-£35,000 depending on experience.

· Annual bonus (non-contractual, subject to company and individual performance)

· Pension scheme (up to 10% employer contribution)

· Life insurance

· 25 days annual leave

· Cycle to work Scheme

· Free parking on Site

· Flexible hours to be agreed with Line Manager

· One day working from home per week on completion of successful probation period.

Job Type: Full-time

Pay: £32,000.00-£35,000.00 per year

Benefits:

Casual dress
Company pension
Cycle to work scheme
Flexitime
Free parking
Life insurance
On-site parking

Ability to commute/relocate:

Feltham TW13: reliably commute or plan to relocate before starting work (required)

Application question(s):

Have you worked in the pharmaceutical industry?

Education:

Bachelor's (preferred)

Experience:

QA: 2 years (required)

Language:

English (required)

Work authorisation:

United Kingdom (required)

Work Location: In person

Quick apply

Refine Your Search

regulatory affairs manager jobs in stanwell, sry

Quality Assurance Officer

Regulatory Affairs Manager UK&I

Regulatory Affairs Manager

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Senior Regulatory Affairs Manager (UK/Ireland)

Senior Manager/Associate Director, Government and Regulatory Affairs

Regulatory Affairs Associate/Manager

Senior Manager Medical Information

Head of Medical Affairs, UK

Senior Regulatory Affairs Manager

Regulatory Manager - Pharmaceuticals

Regulatory / Compliance Manager

Corporate Affairs Manager

Regulatory Affairs Manager

GB Sr. Manager, Regulatory Affairs - Europe

Senior Regulatory Affairs Specialist

HCIB Regulatory Affairs Senior Manager (MSS)

Compliance and Risk Manager

HCIB Regulatory Affairs Senior Manager (CIB)

Senior Manager, PV Process Quality Lead

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