Quality assurance pharmaceutical Work, Jobs in London (with Salaries)

Quality Assurance Executive (Pharmaceutical Manufacturing)
Bova Specials UK Limited —London
- £35,000 - £40,000 a year
- Full-time
- Computer literacy
- Maths
- Bachelor's degree
- Referral programme
Quick apply
9d
Quality Control Analyst
ACE Laboratories Ltd —London
- £26,500 - £28,000 a year
- Full-time
- Writing skills
- Laboratory experience
- Quality control
- Free parking
Quick apply
Quality Control Officer
Vitabiotics —London
- Full-time
- Hybrid work
- Bachelor's degree
- Continuous improvement
- No degree
- Free parking
- Annual leave
Quick apply
QA Associate
hVIVO Services Limited —London
- Administrative experience
Product Quality Assurance Technician
DiaSorin —Dartford
- Full-time
- Quality control
- Organisational skills
- Communication skills
Senior Quality Control Analyst
ACE Laboratories Ltd —London
- £28,000 - £32,500 a year
- Full-time
- Writing skills
- Laboratory experience
- Quality control
- Free parking
Quick apply
Quality Analyst
London North West University Healthcare NHS Trust —London
- £33,262 - £36,027 a year
- Full-time
- Quality control
- Hospice
- Teaching
Quick apply
1d
QA/GMP Compliance Expert
British Compliance Institute —London
- Continuous improvement
- Quality control
- Contracts
- Flexible schedule
Quality Officer
Alliance Healthcare —Woking
- Full-time
- Hybrid work
- Continuous improvement
- No degree
Quality Operations Manager
Vitabiotics —London
- Full-time
- Hybrid work
- Writing skills
- Bachelor's degree
- Continuous improvement
- Free parking
- Annual leave
Quick apply
7d
Quality Manager - GCP (with GMP awareness)
Ellipses Pharma —London
- Travel
- Communication skills
Team Leader for Industrial Quality Control (Pharmaceuticals)
Bova Specials UK Limited —London
- £35,000 - £37,000 a year
- Full-time
- Computer literacy
- Maths
- Continuous improvement
- Referral programme
Quick apply
7d
Senior Quality Auditor - Steriles
Advanz Pharma —London
- Hybrid work
- Communication skills
- Employee assistance programme
QA Auditor
hVIVO Services Limited —London
- In-person
- Communication skills
Quality Release Specialist
Clinigen —Byfleet
- Full-time
- Continuous improvement
- Computer skills
- Employee assistance programme
- Employee discount
Quick apply
2d
Quality Lab Manager
Tropic Skincare —Croydon
- £45,000 - £50,000 a year
- Monday to Friday
- Hybrid work
- Engineering
- Bachelor's degree
- Continuous improvement
- Employee assistance programme
- Employee discount
Quick apply
12d
Head of Computerized Systems Quality Assurance & Validation
IXICO —London
- Full-time
- Hybrid work
- Machine learning
- AI
- Communication skills
- Annual leave
- Employee assistance programme
12d
Associate Quality Lead
Roche —Welwyn
- English
- Bachelor's degree
- Continuous improvement
Senior Process Quality Excellence Specialist
UCB —Slough
- English
- Analysis skills
- Bachelor's degree
2d
Director QA, GMP External Operations Cell and Genetic Therapies - VCGT
Vertex Pharmaceuticals —Paddington
- Full-time
- Master's degree
- Bachelor's degree
- Continuous improvement

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Quality Assurance Executive (Pharmaceutical Manufacturing)

Bova Specials UK Limited
London

Quick apply

Job details

Permanent | Full-time
£35,000 - £40,000 a year
9 days ago

Benefits

Cycle to work scheme
Company pension
Company events
Private medical insurance
Referral programme

Qualifications

Document control
Non-conformance investigation
Computer literacy
Quality management change control procedures
Quality control within general manufacturing industry
Internal department liaison
Maths
Quality assurance
Bachelor's degree
Organisational skills
Technical writing
Environmental monitoring
Computer skills
NVQ
Training & development
Phone etiquette
Document management
Communication skills
Internal quality assurance
Time management

Full job description

Operational Relationships:

Responsible to QA/Quality Manager

Report to Quality Assurance Manager

Qualifications: Educated to science bachelor’s degree level or equivalent knowledge/expertise in the field.

Experience: 2-3 years within a relevant Sr.QA Officer role.

Main Duties & Responsibilities

This job description gives a general outline of the duties of the post and is not intended to be an inflexible or finite list. It may therefore be varied so that changing needs of the service can be met, in consultation with the post holder.

Role Responsibilities

Batch release

1. Review batch documentation and verify records are in compliance with GMP, validation records and relevant associated documentation to release the product for use

2. To inspect the finished product for compliance to relevant specifications

3. To review all relevant in process tests results and QC data relating to the batch

4. To document the batch release process in compliance with GMP

5. To escalate any rejected batches to senior management

Documentation

1. To comply with the organisation’s Documentation Policy.

2. To generate and maintain documentation ensuring contemporaneously completion and in a clear written language.

3. To maintain the documentation control system in accordance with cGMP and company SOP

4. Generate, review and approve batch manufacturing records (Worksheets, etc).

5. Generate and maintenance of technical documents i.e. master batch documentation, validation documentations, specification documents, standard operating procedure and technical agreements.

Quality Management System

1. Work with the quality management system to ensure compliance to regulations.

2. Coordinate, write and review quality exception reports, corrective and preventive actions (CAPA), change controls, customer complaints and quality investigations.

3. Facilitate timely follow up and closure of deviations, change controls and corrective and preventive actions (CAPA).

4. Write and review quality reports.

5. Tracking of documents and validation activities.

6. Ensure compliance to cGMP standards and provide support to the quality management operations.

7. Review of site environmental monitoring programs.

8. Monitor and maintain all quality system process to identify improvement opportunities.

Training

1. To draft and execute training materials for all BOVA UK staff members.

2. To maintain all training records and review training files on periodic basis.

3. Perform periodic peer observations of various team members for critical process steps and report your observations to department managers.

4. To participate in training programs for quality assurance staff.

General skill Set required by Bova UK:

1. Minimum education to a degree or NVQ 3 level in Science related discipline or equivalent;

2. Demonstrate an ability to read and interpret documents which relate to health & safety and regulations, operating and maintenance instructions, and procedure manuals;

3. Demonstrate an ability to calculate basic and advanced figures which may include, but are not limited to, discounts, solutions strengths, concentrations, proportions, percentages, weights and volumes;

4. Must demonstrate an understanding of the importance of time management, following instructions and organisational skills;

5. Must possess exemplary computer skills and knowledge and be able to adapt to and learn any new computer software that may need be implemented;

6. Have an ability to follow complex, multistep procedures and processes

7. Must be able to execute the physical demands required for this role including manual handling of equipment and materials;

8. Must demonstrate a willingness to work with chemicals in knowledge of potential side effects, and must ensure that all staff follow the procedures to ensure safe handling of hazardous chemicals;

9. Must demonstrate an ability to conduct complex procedures in an environment in which the noise level may be moderate, and be accurate and prompt;

10. Must demonstrate an ability to perform repetitive work within a busy manufacturing environment

11. Must have professional telephone etiquette skills for communicating with customers and suppliers

12. Must demonstrate excellent communication skills with other staff, suppliers and customers

13. Must be able to work on a multi-departmental level within the organisation to accomplish the overall business goals

14. Respond to correspondence (phone, email, mail or other) in a timely and efficient manner;

15. Other reasonable duties as assigned by senior management on an ad hoc basis.

Job Types: Full-time, Permanent

Pay: £35,000.00-£40,000.00 per year

Benefits:

Company events
Company pension
Cycle to work scheme
Private medical insurance
Referral programme

Application question(s):

Do you have an understanding of Sterile and non-sterile pharmaceutical operations?

Education:

Bachelor's (required)

Experience:

being a Senior QA Officer in a pharmaceutical environment.: 2 years (required)
CAPA, Deviations, change controls, doc management, OOS/OOT: 2 years (required)
Reviewing batch docs and verify they are compliant with GMP: 2 years (required)

Work Location: In person

Quick apply

Refine Your Search

quality assurance pharmaceutical jobs in london

Quality Assurance Executive (Pharmaceutical Manufacturing)

Quality Control Analyst

Quality Control Officer

QA Associate

Product Quality Assurance Technician

Senior Quality Control Analyst

Quality Analyst

QA/GMP Compliance Expert

Quality Officer

Quality Operations Manager

Quality Manager - GCP (with GMP awareness)

Team Leader for Industrial Quality Control (Pharmaceuticals)

Senior Quality Auditor - Steriles

QA Auditor

Quality Release Specialist

Quality Lab Manager

Head of Computerized Systems Quality Assurance & Validation

Associate Quality Lead

Senior Process Quality Excellence Specialist

Director QA, GMP External Operations Cell and Genetic Therapies - VCGT

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