Product support Work, Jobs in Virginia Water, 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
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Montana Bakery —Slough
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Learning & Communications Coordinator
Tropic Skincare —Croydon
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- Monday to Friday
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Sales & Events Supervisor
Foxhills Club & Resort —Chertsey
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Pigment —London
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Quality Assurance Officer

Medreich Plc -
Feltham

Quick apply

Job details

Full-time
£32,000 - £35,000 a year
7 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

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