Senior Associate Micro EM

Job Title: Senior Associate Micro EM Recruiter: Neha Malik

Contract type: 12-month Fixed Term Contract

The Role:

Our client is a Multinational Technology Service center with the most innovative technology, ranging from ERP systems to data analytics and digital

This role will support qualification of a new production facility by writing qualification documents, SOPs, trend reports The current expectation is to work days, however there maybe a request to go on shift at a later date in order to support performance qualification of the new

Join us! There has never been a better time to do your lifes best work!

Requirements

Key Responsibilities:

Specific Job Duties:

• Lead QC Technical documentation projects as an individual
  
• Accountable for timely completion of projects within the technical writing
  
• Collaborate with internal resources and business partners to support project requirements and ensure project
  
• Work in accordance with cGMP and GLP
  
• Ensure consistent and good documentation practices are
  
• Creation, review, and update of documentation, , Laboratory Technical Protocols and Reports, Standard Operating Procedures, and Analytical
  
• Translating complex topics into clear, concise, and understandable topics is
  
• Review standards for documentation types, structure, and assembly so that content is organized logically with the end reader in
  
• Maintain Documents in the document management
  
• Technically strong background in microbiology and aseptic
  
• Experience in LIMS, Change Control, Track wise, SAP and CDOCS an
  
• Flexibility the EM role often encounters changing priorities on a daily
  
• Support QC Specialist with risk assessments/procedures for new
  
• Working with the project team to ensure we have sufficient resources and equipment for the
  
• Completing qualification works for the new isolator, media
  
• Reading & review of EM
  
• Execution of EM PQ of new facility
  

Experience and Qualification:

• Bachelors degree in a science
  
• Biopharmaceutical QC experience in Environmental Monitoring
  
• Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products
  
• Experience in technical
  Experience working in an aseptic clean
  Proficient in the use of LIMS & LMES
  

Benefits

Benefits:

• Benefit from Independent Solution s ethical principles!
  
• Pre-interview preparation before attending the interview and help to use STAR technology to answer the questions.
  
• While placed on client sites you will be an integral part of our team, gaining support and access to the knowledge and experience of our cross-functional Life Science team.
  
• We offer attractive rates - competitive margins compared to our
  
• Payment on time and in
  
• We are recognized as approved suppliers to leading key pharmaceutical and medical device
  

You must have the right to work in Ireland for this

If you have the above skills & experience, please contact or apply at

Independent solutions provide End to End solutions to the life sciences and we are expertise in Bio-Tech, Biopharma, and medical We are the sole source of exceptional Project managers,