Scientist, Analytical Sciences (QC Analytical)

at  Pharmaron

Liverpool L24, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate17 Jul, 2024Not Specified18 Apr, 2024N/AGene Therapy,Testing,Regulatory Guidelines,Industrial Experience,Analytical Skills,Management Skills,Pharmaceutical Industry,Immunoassays,Molecular Biology,Sequencing,Communication Skills,Electrophoresis,Equipment Qualification,Analytical SciencesNoNo
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Description:

Responsibilities:

Key roles and responsibilities:

  • Support Project leads on delivery of internal and Client-based work packages through the planning, design, delivery and reporting of activities within the QC analytical laboratories to meet project timelines in line with policies and procedures.
  • Ensure maintenance of stock reagents and consumables and laboratory housekeeping for all work performed.
  • The preparation and execution of a range of documentation including but not limited to development reports, operating procedures, phase appropriate validation, analytical proformas and test records in a timely manner with a right first-time mind set.
  • Drive 5S and operational excellence initiatives as a means for continuous improvement to ensure that department is a high-performing team.
  • Lead on the delivery and validation of new capital equipment items and train others in procedures, techniques, equipment, and technologies to increase Biologics QC analytical capabilities.
  • Analyse any data to a high standard and ensure that protocols and procedures are delivered with a high attention to detail.
  • Lead on associated QMS including but not limited to Non-Conformances, CAPA’s, Out of Specification and Change Controls.
  • Complete all laboratory or batch related documentation in a timely and compliant manner, participating in reviews of the documentation to obtain quality sign off when necessary.
  • Subject matter expert in areas relating to QC analytical, including but not limited to Biological GMP analytical testing for separation and plate-based analytics.
  • Set exemplary standards within the laboratory and facility in compliance with Development, Quality and EHS Policies and Procedures

Our Company: “We are a dynamic, fast-growing company, with an enviable reputation for leading edge science, offering contract research services to some of the world’s leading pharmaceutical companies, solving what were believed to be unsolvable scientific challenges”.We believe in our ability to relentlessly push forward the boundaries of scientific excellence, delivering solutions for our clients, always operating ethically and with integrity. We take pride in our professionalism and commitment to always deliver our very best work.We are based in the vibrant city of Liverpool with a world class R&D and manufacturing facility that offers a complete end to end development service. Our 80,000 sq. ft facility houses an established Biologics Department that consists of Analytical and Process Sciences. Our Liverpool site has a remarkable 20 Year Track Record in Biologics Development, which now offer A Fully Integrated Gene Therapy Drug Substance Solution in our state of the art cGMP facility purpose designed for viral vectors with onsite plasmid DNA and renowned analytical capabilities for release and characterisation.

  • We offer a competitive salary and a progressive and comprehensive suite of employee benefits
  • We offer state of the art working environment in our modern Liverpool site
  • We offer the opportunity for growth and development and will support funding for relevant training and development programme


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

Liverpool L24, United Kingdom