validation specialist - process validation (pv) in borehamwood

posted
job type
permanent
salary
£ 40,000 per year
apply now

job details

posted
location
borehamwood, hertfordshire
job category
pharmaceutical
job type
permanent
salary
£ 40,000 per year
reference number
VS_PV
phone
0208 957 2606
apply now

job description

Roles : Validation Specialist - Process Validation (PV)

Hours : 9-5

Pay : £40k - £55k + Up to £2k pa Bonus

Benefits : 25 days holiday + Bank Holiday, Pension up to 6% Matched , life assurance , free parking

Location : BPL, Dagger Lane, WD6 3BX

BPL is based in Elstree, Hertfordshire the enclosed secure campus is surrounded in natural beauty, greenery, lakes and wildlife. A truly wonderful working environment, along with an extremely supportive team.

Working within a niche sector within the pharmaceutical industry, this opportunity will give the successful candidate a chance to develop themselves and learn new skills that could see them enjoy a highly successful career.

BPL has a significant annual and longer-term investment plan to optimise existing production and processes, and dramatically increase production capacity over the next 3-5 years , the Validation team form a key part of this programme.

Roles and Responsibilities :

As part of the Validation team, you will be taking ownership of all aspects of service delivery which relate to equipment commissioning, qualification and validation within your remit. You will be ensuring compliance with all applicable (EHS and GxP) regulatory and internal Quality standards and industry best practice. You will need to be committed to, and passionate about providing a reliable and compliant service to meet and exceed the customer's needs. This is a customer-facing role, and as such the ability to form relationships across the organisation is essential for success.

Essential Skills :



* Must have worked within a in Process Validation (PV) environment.
* In depth knowledge of the requirements and expectations of Process Validation when applied to aseptically produced products.
* In depth knowledge of the requirements and expectations of Process Media Simulation when applied to aseptically produced products.
* Experienced in the application of risk based methodologies/continued process verification in order to maintain the validated state.
* Practical hands-on experience of executing Process Validation.
* You understand, can clearly explain and would be able to train others in Process Validation.
* Collective responsibility for the ongoing compliance of all assets at the Elstree, Hertfordshire facility within your remit, ensuring that the equipment meets regulatory requirements at all times with a target of zero impact to routine operations.
* Maintain an ongoing dialogue with Validation Management to ensure validation resources are effectively deployed to meet dynamic and competing business priorities.
* Support the implementation validation strategies that allow the work to be executed by the most appropriate personnel (internal and external) whilst maintaining standards.
* Highlight risks to product quality, patient safety and/or data integrity throughout the validation lifecycle so that they are understood, transparent and can be managed through the application of a quality risk management approach.

Please apply today or call Ben on 02089572606 for more information

skills

validation, environment, gmp, gdp, pharma, blood, plasma, Process, VA, validation,