Process Inspector - Press Manufacturing - 3rd Shift

In Process Inspector - Press Manufacturing - 3rd Shift page is loaded## In Process Inspector - Press Manufacturing - 3rd Shift remote type:
Fully Onsite locations:
Bohemia, New York, USAtime type:
Full time posted on:
Posted Todayjob requisition :
R
- ** Work Schedule
** Third Shift (Nights)
** Environmental Conditions
** Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Warehouse, Will work with hazardous/toxic materials
** Job Description
**** Pay Range: $22-$24*
* ** 3rd Shift 11:00pm - 07:30am
**** QC Technician II (In Process Inspector - Press Manufacturing)
** 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.##

** Location/Division Specific Information:
** Clinical Labeling Services, part of the Clinical Trials Division, located in Bohemia, New York provides leading clinical label design, production and management services for the pharmaceutical and biotechnology industry. Our advanced inspection software, full in-house print capabilities, and proprietary translation and regulatory approval system are designed to reduce overall clinical trial label cycle times

The QC Technician II plays a crucial role in ensuring the quality and accuracy of labeling materials used in clinical trials. They are responsible for conducting inspections to verify compliance with regulatory requirements and internal standards. Their attention to detail and adherence to quality control procedures significantly impact the overall efficiency and safety of the manufacturing process## A Day in the Life:

Conduct thorough inspections:
Responsible for performing inspections and tests on raw materials, in-process samples (startups), and finished products. Follows established protocols and applies various analytical techniques to ensure compliance with quality standards and regulatory requirements.

Document and report findings:
Accurately records and documents all inspection and test results. Effectively communicating findings is crucial for maintaining traceability and facilitating corrective actions.

Ensuring adherence to quality control procedures:
Ensures that all quality control procedures and protocols are followed consistently including monitoring and verifying compliance with standard operating procedures (SOPs), safety guidelines, and regulatory requirements#
*
* Education:

** High school diploma or equivalent required.#
** Experience**:

* Required:

Minimum of 1 year of work experience in QA or QC or related field
* Preferred:
Experience in a cGMP environment#
** Knowledge, Skills, Abilities:
*** Strong understanding of quality control principles and practices:
Possesses a comprehensive knowledge of quality control principles, methodologies, and standard processes. Understands inspection techniques, and relevant paperwork procedures. Familiar with quality control tools and able to interpret and analyse 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 inspections, tests, and documentation are 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.…