Sr. QA Technician; 2nd Shift

Second Shift (Afternoons)

Able to lift 40 lbs. without assistance, Office, Standing for full shift

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

As a Sr. Quality Assurance Technician, you will play a pivotal role in the overarching success of the Quality Operations team. The QA Operation team reviews and monitors all clinical labeling documentation, as well as performs final quality release of all clinical labels manufactured in our Bohemia, NY facility. With the support of department leadership, you will support the team by ensuring that all batch record documentation (a real time record of everything that is manufactured) has been verified and that products meet the form, fit, and function requirements of our clients to safely and successfully serve their patients’ needs.

You will also support the packing of clinical labels to ensure safety.

• Perform real-time verification of job documentation to ensure accuracy and completeness with a 24-hour turnaround time.

• Categorize and log all work performed in accordance with local procedures and regulatory requirements.

• Organize and maintain all batch records in clinical labeling custody including on-site storage and final archival.

• Perform pack out of clinical labels to ensure safe delivery to client/packaging sites.

• Participate in the PPI program by actively performing JDI and assisting with GEMBA

High school diploma or equivalent required.

• Minimum of 2 years of work experience in QA or QC or related field is required

• Required:
  
  Experience in a cGMP environment

• Strong understanding of quality assurance principles and practices:
  Possesses a comprehensive knowledge of quality assurance principles, methodologies, and best practices. Understands inspection techniques, and relevant paperwork procedures. Familiar with quality control tools and able to interpret and analyze data effectively.

• Attention to detail and accuracy:
  Pays close attention to detail and maintains accuracy. Possesses a meticulous approach to their work, ensures that all documentation is completed with precision including the ability to identify and document deviations or non-conformities accurately, as well as the skill to spot potential quality issues and take appropriate actions.

• Effective communication and documentation skills:
  Possesses excellent communication skills, both written and verbal. Communicates' findings, observations, and recommendations clearly and concisely to colleagues, supervisors, and other stakeholders. Accurately records and maintains detailed reports, logbooks, and other quality control records. Ensures proper traceability and facilitates effective communication within the organization.

• Communication
  
  Skills:
  
  Strong verbal and written communication skills for reporting and collaboration.

• Technical
  
  Skills:
  
  Proficiency with QA tools, software testing frameworks, and methodologies.

• Time Management:
  Efficiently managing time to meet deadlines and project milestones.

• Multitasking:
  Ability to handle multiple projects and tasks…