Validation Officer

5 months ago


Hove, United Kingdom Custom Pharma Services Full time

Job Advert

**We have an exciting opportunity for a Validation Officer to join our team based in Hove, to implement current validations and to create validation documentations to ensure all processes, equipment, cleaning methodologies, utilities/facilities, computer, analytical methods are validated**

**About Custom Pharma Services (CPS)**

Custom Pharma Services is located in Brighton, UK since 1979 and is a full-service contract development and manufacturing organisation (CDMO) providing services tailored to your needs, no matter how niche or complex. Custom covers the full spectrum of activities from development through commercial manufacturing for both clinical and commercial use. Specialising in Oral Solid Dosage forms with the ability to handle highly potent drugs and poorly bioavailable compounds Custom really is your one stop resource. With direct access to highly skilled experts offering a partnership approach Custom Pharma Services truly has a molecule first mentality, managing all projects with the end in mind. Custom Can

Custom Pharma Services is an Investors in People Silver accredited workplace where teamwork and support is encouraged, and where every individual is valued and supported to achieve their full potential because if you can, then Custom Can

**What you will be doing;**
- Effectively managing / executing validation projects and providing commissioning, qualification and validation (CQV) support to new and ongoing projects across site.
- Ensuring that the validation activities are performed in accordance with company policy and legislative requirements.
- Composing and reviewing all validation documentation associated with processes, equipment, methods, utilities/ facilities and computer systems.
- Providing QA input to various other projects on site as required in the maintenance of company Quality Systems with respect to validation, and compliance or as deemed necessary by Quality Assurance Management.
- Participating in the developments and technical transfer of new products as required.
- Supporting QA compliance activities.
- Degree level qualifications in an Engineering/Science discipline, or equivalent or
- Lower level qualification in addition to validation experience
- Experience in the pharmaceutical industry preferably with some exposure to validation
- A thorough understanding of Good Manufacturing Practice
- Strong teamwork and interpersonal skills
- Good communication, planning and organisational skills
- Computer literate, competent in Microsoft Word and Excel
- Strong documentation skills and system compliance
- Good problem solving skills
- Computer literacy.
- High levels of attention to detail.

**Our benefits package includes**:

- Rising holiday allowance to 26 days holiday plus UK bank holidays
- Group personal pension scheme
- Annual profit related company and individual bonus payment based on successful performance
- Life assurance at twice annual salary
- Health Plan with Simply Health including access to a GP or Counselling Services 24/7, money back on prescriptions, optical, dental and physiotherapy
- Ride to work scheme
- Subsidised Gym Membership
- Discount Shopping Portal
- Enhanced Maternity / Paternity Pay
- Employee Referral Scheme bonus of £1,000
- Values based awards
- Free hot drinks vending

**Applicants must have the right to work in the UK without requiring sponsorship, we do not hold a sponsorship licence.**

**Strictly no agencies please.


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