Overview:
Do you have a degree in Engineering/Science or extensive experience working in a Validation role within the Pharmaceutical/healthcare industry? We are looking for a Validation Officer to join our Aseptic Services team to support with planning, executing and maintaining validation activities. The role is 37.5 hours per week Monday-Friday, 7.5 hours between the hours of 8am - 6pm and it will be based in Runcorn.
Fresenius Kabi is a global healthcare company that specialises in lifesaving medicines and technologies for infusion, transfusion and clinical nutrition. The company's products and services are used to help care for critically and chronically ill patients.
Responsibilities:
Draft, review and improve validation documentation
Execute all validation activities relating to facilities, processes, cleaning, and equipment, ensuring that all validation is performed in compliance to cGxp
Planning and scheduling validation activities to maintain validation status
Maintain compliance with Data Integrity Regulations and GAMP standards
Investigate the root cause(s) of non-conformances and identify and ensure implementation of corrective / preventive actions to reduce non-conformances
Support manufacturing and other operations in the development, implementation and maintenance of GxP standards
Provide technical support to production to maintain GxP and production efficiency
Complete risk assessments as required to ensure that the production equipment and production facilities comply with the relevant GxP and HSE guidelines
Collate, review and interpret data from the QMS process
Perform trend analysis of data and generate trend analysis reports and implement effective corrective measures as required
Maintain an awareness of developments in the field of validation to ensure a continued provision of an up-to-date service, providing guidance and training
Occasionally work outside of hours
Qualifications:
Minimum of a Degree in engineering/science subject or extensive experience of working in a validation role within the pharmaceutical/healthcare related industry
Experience and knowledge of cGMP and regulatory requirements for areas of expertise
Experience of manufacture of sterile medicinal products
Experience in thermal mapping and small instrument/systems (balances, pumps) is an advantage
Clean room experience at least to Grade C is an advantage
BenefitsNo rota'd weekend working and no night shifts
Contributory Pension Scheme (rises with service)
Role specific tailored training and development plan
Life Insurance (4 x salary, death in service)
25 days holiday (rises to 35 after 5 years service) and ability to buy/sell holidays
Healthcare cashback scheme (including dental, optical & alternative therapies)
Maternity, Paternity and Adoption Leave
Professional fees paid
Bike to work scheme
Long Service Awards
Employee Assistance Programme
Free onsite parking and subsidised canteen
Blue Light Card
Company funded family days out
We are proud to foster a workplace free from discrimination. Diversity of experience, perspectives, and background create a better work environment and better products. Whatever your identity, we will give your application fair consideration.
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