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Senior Validation Specialist

Job LocationLiverpool
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent , full-time

Job Description

Responsibilities:Development/Improvement activities:- Serve as SME to support Site/Global projects- Proactively identifies scope for improvement or development based on knowledge of short to mid-term business needs- Leads and develops a strategy, plans and manages projects for method development or improvement as identified- Makes data supported decisions on project progression; uses technical expertise to overcome analytical issues- Documents project work as detailed lab book records or under technical protocols and reports as appropriate- Disseminates project findings/status updates at regular meetings/ forums within Global AS&T- Represents as an interface between AS&T and Key stakeholders (QC, MS&T, Regulatory Affairs, QA)Operations Support:- Participates in lab work-load planning with the wider team- Performs tests in accordance with established methods and properly documents test results- Provides guidance/mentorship/training to other lab staff as required- Evaluates performance of analytical instruments and equipment and recommends new acquisition or replacements- Authors protocols and reports for suitability studies and investigations to support testing and compliance issues- Ensures laboratory instruments are maintained in a qualified status, calibrated and properly maintained and documentation complies with cGMP standards- Assists and maintains standard operating procedures (SOPs), risk assessment and other documentation as necessary- Documents quality issues and performance measures for management reviewQualifications:- Bachelor’s degree in a relevant scientific discipline (Chemistry, Biochemistry.) with over 5 years’ experience- A recognized expert in Biochemistry methods (SDS-PAGE/CE)- Experience of working in pharmaceuticals, particularly biologics / Influenza- Experience of assay development and validation- Assay lifecycle from proof of concept to registration- Desirable to have experience of process or product characterization using a variety orthogonal methodsPLEASE NOTE THIS IS A 6 MONTH FTCDifferent qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.#LI-MS1Our BenefitsCSL Seqirus is committed to attracting and retaining world-class employees who are valued for their contributions to achieving business objectives. Learn more about some of the benefits you can participate in when you join CSL Seqirus.About CSL Seqirus CSL Seqirus is part of CSL Limited (ASX: CSL). As one of the largest influenza vaccine providers in the world, CSL Seqirus is a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. Learn moreabout CSL Seqirus.We want Seqirus to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL Seqirus.Do work that matters at CSL Seqirus!Watch our ‘On the Front Line’ video to learn more about CSL Seqirus

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