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Job role: As a Validation Engineer you will be accountable for validating/qualifying the systems, equipment and utilities used in the development and clinical manufacture of a range of solid dosage forms. An individual contributor role that applies technical, control system and engineering knowledge to the design and validation of new equipment, systems and utilities within the solid dose manufacturing area in Sandwich. The role will also include some safety and management of the full asset lifecycle. You will help to design robust manufacturing solutions and demonstrate systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. Colleague will work closely with operational and technical teams within department to validate equipment, utilities and systems. Colleague will be expected to interact with Global Workplace Solutions, Quality Assurance and Environmental Health and Safety to assist the manufacture of solid oral dosage forms for clinical supply. Organisational Relationships: Department: Drug Product Manufacturing Group, Drug Product Supply, Pharmaceutical Sciences Small Molecule (PSSM) Reports to: SDM Validation and Technical Support Lead Liaises with: Key stakeholders in DPS, DPD, PGS, GWS, Quality, Safety and external subject matter experts Resources controlled: Role will typically operate as an individual contributor at a local level contributing to department and cross group activities and input to cross department initiatives. Role will be a recognised SME in certain aspects of either equipment, facility or system validation. Requirements: Ideally educated to degree level in Chemical, bio-medical, bio-engineering, mechanical engineering or equivalent however candidates with a formal engineering qualification i.e. BTEC Level 4, HND / HNC or equivalent with 1-3 years pharmaceutical industry experience will also be considered. . Working knowledge of equipment, facility and utility asset lifecycle management from initial design and procurement through to validation and operational use. Awareness of GAMP 5 regulations. Awareness of computerized systems validation and CFR21 Pt 11 Comprehension of facility design and associated building management systems. Suitable knowledge of engineering operations including, instruments, controls and mechanical aspects of manufacturing equipment and associated services. A working knowledge of GMP and demonstrated understanding of compliance and quality management including change control and data integrity. Experience of Safe Systems of Work and risk assessment tools used in both Quality & Safety areas beneficial. Evidence of planning and organizational skills in the project management of operational aspects of capital projects. Good interpersonal, organisational and communication skills (both oral and written) and demonstrated skills in team matrix working. Proven ability to deliver technical reports and presentations. Knowledge of solid dose manufacturing techniques is desirable. Knowledge of cleaning validation program, cleaning processes used in solid oral dose and cleaning regulations Job Description: Schedules and executes validations/qualifications per Standard Operating Procedures (SOPs), protocols and regulatory guidelines. Coordinates and conveys all testing with affected functional groups and evaluates test results. Executes validation activities to include Change Control initiation, protocol preparation, scheduling, Factory Acceptance Testing, protocol execution, data review and final report generation. Accountable for completion of fully system lifecycle activities associated with equipment, utilities or facilities from project initiation through maintenance of the validated state to retirement / redesignation. Participate in development / improvements to the validation program as needed to remain current with cGMPs and industry standards. Participates on teams assembled to specify, install, validate, troubleshoot and maintain systems and equipment. Participates in deviation investigations to identify root causes and define corrective and/or preventative actions (CA/PA). Participate and present data in Regulatory Agency, Customer, Corporate and Internal audits when necessary. Assist and execute cleaning validation program as required. Other duties include, but are not limited to: Aid with additional focus area: Automation, Facility Support, Process Development, Capital Projects Assist in ensuring future equipment meet the technical requirements of the operation. Contribute to the selection and integration of new equipment and services, ensuring validation, quality requirements and the process capability of the equipment is in line with pre-defined needs. Assist and develop equipment/services robustness and manage the risks and impact of failure. Manage minor projects which include all operational and financial aspects. Drive quality, safety and continuous improvement related activities. Deliver training and assist to ensure efficient use and deployment of equipment. Provide immediate troubleshooting and manufacturing assistance during manufacturing operations. Work Location Assignment: On Premise #LI-PFE Purpose Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. Digital Transformation Strategy One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience. Flexibility We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation! Equal Employment Opportunity We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees. DisAbility Confident We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here! Engineering #LI-PFE