| Job alert | Jobs 111 - 120 of 19158 |
Business Development Manager- Electronics Manufacturing
Spartronics
–
Cleveland, OH
100000.0-125000.0 per year
... Knowledge of EMS related certifications such as ISO 9001, AS9100, 21-CFR820, FDA/QSR Registered Class I, II, and III, ISO 9001, ISO 13485, ISO Class 8, RoHS and REACH, MDSAP, ANSI ESD S20.20, IPC-A-610, IPC-A-620- Helpful Technical, Engineering, or ... - Jun 06
Quality Compliance Manager
NeilMed Pharmaceuticals
–
Santa Rosa, CA, 95402
POSITION PURPOSE The purpose of this position is to ensure compliance with established standards and agency guidelines such as ISO 13485:2016, Health Canada, and US FDA by providing direction to QA/QC team members to maintain and improve quality ... - May 24
Copy Editor, Pharmaceutical Marketing Services
Deerfield – Agency of Brand®
–
Conshohocken, PA, 19429
... attitude toward acquiring knowledge and honing skills Knowledge of AMA editorial style guidelines preferred Understanding of FDA regulations as it impacts the MLR submission process Using applications: Microsoft Office At Deerfield, we are dedicated ... - May 23
1st Shift Assistant Team Leader
HANSEN FOODS WISCONSIN LLC
–
Bellevue, WI, 54311
... Ability to learn all applicable USDA, FDA, and OSHA regulations applicable to Hansen's operation 5. Maintain a safe work environment and oversee quality from start to finish to ensure we meet our customer expectations. 6. Excellent verbal and ... - Jun 04
Compounding Assistant
Fragrance Manufacturing
–
Allentown, PA, 18109
... Verifying item numbers, lot numbers, and weights on FDA mixes (acting as the “2nd signature”). Complies with all required PPE. Demonstrates reliability and dependability by consistently maintaining good attendance. Follows supervisor/manager ... - Jun 05
Quality Consultant SME Pharma Medical Devices
Excellis Health
–
New Hope, PA, 18938
... Understanding and interpreting the FDA regulations for both Pharmaceutical and Medical Device products including those for developing, filing/approving, manufacturing, labeling, packaging, testing, storing and distributing the products Understanding ... - May 28
Quality Consultant SME Pharma Medical Devices
Excellis Health
–
San Francisco, CA, 94104
... Understanding and interpreting the FDA regulations for both Pharmaceutical and Medical Device products including those for developing, filing/approving, manufacturing, labeling, packaging, testing, storing and distributing the products Understanding ... - May 26
QA Technician - Incoming
Xtant Medical Holdings Inc
–
Belgrade, MT, 59714
... May assist in the development and maintenance of Document Control and Record Control systems that meet FDA, AATB, and ISO standards and regulations. Assist in the completion and retention of documentation pertaining to SOPs. Understand the ... - Jun 05
Senior Supplier Quality Engineer
InfraredX, Inc.
–
Bedford, MA, 01730
... Maintains supplier quality records in accordance with FDA/GMP and EU MDR requirements. Coordinate review of supplier change requests with cross-functional team, including evaluation of change, implementation planning, and approval. Assist with ... - May 24
Clinical Research Manager
Michigan Institute of Urology
–
Troy, MI, 48084
... Ensures all studies are conducted to FDA regulations and, GCP guidelines Develops, implements, and evaluates department policies, goals, and objectives. Ensures study start up documents are submitted to ethics committee and sponsor in timely manner. ... - Jun 02