641 Biomedical Field Service Engineer jobs in Derry, NH

Pace Analytical Life Sciences

Salem, NH 03079

Minimum of 2-3 years of experience in a microbiology role within a sterile fill finish manufacturing environment.
Develop and validate microbiological methods in compliance with regulatory guidelines.
Perform endotoxin, bioburden and particulate matter testing.
Ensure compliance with GMP, GLP, and other regulatory requirements.
Investigate and resolve any microbiological quality issues or deviations.
Collaborate with cross-functional teams to support product development and manufacturing processes.
Perform routine and non-routine microbiological testing of raw materials, in-process samples, and finished products.
Bachelor's or Master's degree in Microbiology, Biology, or a related field.
Proficiency in microbiological techniques such as aseptic techniques, microbial enumeration, and endotoxin testing.
Strong understanding of GMP, GLP, and regulatory requirements.
Conduct environmental monitoring of the manufacturing facility, including air, surface, and personnel monitoring.
Document and review test results accurately and promptly.
Maintain and calibrate laboratory equipment and instruments.

L3Harris Technologies

Wilmington, MA 01887

L3Harris Technologies

Wilmington, MA 01887

L3Harris Technologies Careers

Wilmington, MA 01887

US Navy

Manchester, NH 03101

Adecco

Boxborough, MA 01719

Ability to perform acceptance and performance testing to ensure compliance with specifications
Ability to read and interpret engineering drawings and documentation
Strong problem-solving, organizational, and time-management skills
Experience in mechanical assembly and testing

Hologic

Londonderry, NH 03053

Perform process validations and improvement suggestions
Maintain and present daily management board
Minimum of 3 years of manufacturing experience including assembly, testing, and shipping of products
High School Diploma or equivalent
Review non-conforming materials for accuracy
Operate, test, calibrate and repair production equipment, products and related subassemblies as required per specifications and document results with operations and engineering
Ability to work overtime to meet production schedule as needed
Work on special projects as requested
Able to work in a team environment
Must follow all applicable FDA regulations and ISO requirements
Comply with 6S
Report failures via NCR process
Ability to work in a controlled Clean Room environment (if applicable)
Conduct inventory transactions
Ensure calibrated equipment is within specification