Validation Officer
| Posting date: | 26 June 2025 |
|---|---|
| Hours: | Full time |
| Closing date: | 26 July 2025 |
| Location: | DE24 8SW |
| Remote working: | On-site only |
| Company: | Riverside Medical Packaging |
| Job type: | Permanent |
| Job reference: |
Summary
Riverside is looking to recruit a full time Validation Officer to work with the validations
team. The ideal candidate will be computer literate with a high standard of knowledge of
GMP practices, experience of document control and able to identify ideas for
continuous improvement. The candidate must be able to demonstrate exceptional
organisational and timekeeping skills, the ability to communicate well at all levels and
display an analytical approach to problem solving.
OBJECTIVE
To be responsible for all aspects of day-to-day validation throughout the Company,
meeting scheduled requirements in line with quality, cost and safety standards.
MAIN TASKS
1. To manage the day-to-day running of the Validations department/staff in line
with the business requirements as defined by the department lead.
2. To ensure that DQ, IQ, OQ and PQ are carried out on all machinery and subsequent
tooling.
3. To ensure that all packaging validations are planned and carried out in line with
production and customer requirements
4. To ensure that comprehensive validation reports are created and issued for the
relevant files
5. To work in conjunction with project and quality team to ensure that all new
validation work is carried out to ensure that all deadlines are met.
6. To strive to achieve validation sales in line with forecasts.
7. Presenting departmental reports and validation project progress to the
department lead at regular intervals.
8. Ensure all quality systems and procedures are utilised to achieve and improve
good manufacturing practice (GMP).
9. To contribute towards maintaining, promoting and developing high health and
safety standards and to carry out all duties and specific responsibilities.
10. To facilitate the development of an open and productive culture where people
take pride and responsibility in what they do.
11. To continually inform and involve all relevant personnel of information
necessary to ensure alignment of current and future objectives.
12. To identify training needs and ensure adequate training and development is carried
out with self and staff at all levels.
13. In line with company objectives, work towards the utilisation of Lean
Manufacturing techniques.
14. To carry out any other relevant tasks as may be required by circumstances or
are requested by the Company.
We are committed to equality and diversity. We therefore consider employment
applications from all internal applications.
If you would like to apply for this role, please email your cover letter and CV to
hr@riversidemedical.co.uk by 30th June 2025.
Please note that applications submitted without a cover letter will not be considered.
team. The ideal candidate will be computer literate with a high standard of knowledge of
GMP practices, experience of document control and able to identify ideas for
continuous improvement. The candidate must be able to demonstrate exceptional
organisational and timekeeping skills, the ability to communicate well at all levels and
display an analytical approach to problem solving.
OBJECTIVE
To be responsible for all aspects of day-to-day validation throughout the Company,
meeting scheduled requirements in line with quality, cost and safety standards.
MAIN TASKS
1. To manage the day-to-day running of the Validations department/staff in line
with the business requirements as defined by the department lead.
2. To ensure that DQ, IQ, OQ and PQ are carried out on all machinery and subsequent
tooling.
3. To ensure that all packaging validations are planned and carried out in line with
production and customer requirements
4. To ensure that comprehensive validation reports are created and issued for the
relevant files
5. To work in conjunction with project and quality team to ensure that all new
validation work is carried out to ensure that all deadlines are met.
6. To strive to achieve validation sales in line with forecasts.
7. Presenting departmental reports and validation project progress to the
department lead at regular intervals.
8. Ensure all quality systems and procedures are utilised to achieve and improve
good manufacturing practice (GMP).
9. To contribute towards maintaining, promoting and developing high health and
safety standards and to carry out all duties and specific responsibilities.
10. To facilitate the development of an open and productive culture where people
take pride and responsibility in what they do.
11. To continually inform and involve all relevant personnel of information
necessary to ensure alignment of current and future objectives.
12. To identify training needs and ensure adequate training and development is carried
out with self and staff at all levels.
13. In line with company objectives, work towards the utilisation of Lean
Manufacturing techniques.
14. To carry out any other relevant tasks as may be required by circumstances or
are requested by the Company.
We are committed to equality and diversity. We therefore consider employment
applications from all internal applications.
If you would like to apply for this role, please email your cover letter and CV to
hr@riversidemedical.co.uk by 30th June 2025.
Please note that applications submitted without a cover letter will not be considered.