Bausch + LombNYSE: BLCO: Manufacturing and selling contact lenses and eye health products.
3+ YOEHigh school diploma and 3+ years in a pharmaceutical, FDA-regulated, or related facility; quality experience preferred; requires SOP comprehension, independent work, detail, and critical thinking.
Johns Hopkins Health System: Provides clinical care, medical research, and health education services.
Bachelor's in health/biological/nursing/public health, clinical research coordination experience, knowledge of GCP/FDA/IRB, strong organization and communication skills.
CONMEDNYSE: CNMD: Manufacturer of surgical instruments and patient monitoring medical devices.
7+ YOEBachelor's in Engineering/Operations/Life Sciences; 7+ years PM in regulated industry; knowledge of FDA Design Controls, ISO 13485, ISO 14971, and validation.
BayCare Health System: Operates non-profit hospitals and outpatient healthcare facilities in Florida.
3+ YOESupervise regulatory team, manage IRB and FDA submissions, register trials on ClinicalTrials.gov; requires 3 years research regulatory submissions experience and a bachelor's degree.
TakedaTokyo Stock Exchange / New York Stock Exchange: 4502 / TAK: Researches, develops, and manufactures prescription pharmaceutical medicines.
2+ YOERequires an LPN or LVN license, CPR and AED certification, basic IV therapy qualification, FDA-approved training, and two years of clinical or hospital experience.
ACGME: Accredits graduate medical education programs and institutions in America.
1+ YOEFluent English/Spanish,1+ year HR experience (manufacturing/logistics preferred),HRIS experience,knowledge of GMP/FDA a plus,strong organization and confidentiality.
CSLASX: CSL: Global biotechnology developing and manufacturing protein-based therapies and vaccines.
1+ YOEPerforms venipuncture and plasmapheresis, monitors donors and equipment, documents incidents, follows SOPs and FDA guidelines; high school diploma and ~12 months medical experience preferred.
Alliance Clinical Network: Operates medical research sites for Phase I-IV clinical trials.
Coordinate clinical research activities, assist with screening, informed consent, data collection, specimen handling, and regulatory compliance; knowledge of GCP/HIPAA/FDA/IATA preferred.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint
OneBlood: Provides blood collection and distribution services to hospitals.
Performs phlebotomy and donor collection procedures, obtains medical history and vitals, provides customer service, and follows FDA/AABB policies; high school diploma or equivalent required.
OneBlood: Non-profit blood collection and distribution organization.
Performs phlebotomy and donor collection, obtains medical history and vitals, follows FDA and AABB standards, high school diploma required, basic computer and customer service skills.
IntegerNYSE: ITGR: Manufactures medical devices and components for global healthcare companies.
5+ YOEBachelor's in engineering,5+ years progressive engineering experience,knowledge of QMS/FDA regulations,Six Sigma and problem-solving methodologies,project leadership and strong written/oral communication.
Quality Management System (QMS), U.S. Food and Drug Administration (FDA), Integer Production System, SiOP, 5S, 6-Sigma, 8D, RCA, Ishikawa, Kepner-Tregoe, PMP
West Pharmaceutical ServicesNYSE: WST: Manufactures packaging and delivery systems for injectable medicines.
3+ YOERequires high school diploma or GED, 3+ years of progressive maintenance experience, electrical and PLC troubleshooting, automation and project management experience, FDA regulations knowledge, and schematic interpretation.
CSLASX: CSL: Global biotechnology producing plasma-derived and recombinant therapies.
1+ YOEHigh school diploma or equivalent required; 12 months of medical or healthcare experience preferred. Must follow SOPs, FDA, HSE, and OSHA requirements and operate plasma collection equipment.
Personal Digital Assistant (PDA), electronic donor information management system, Standard Operating Procedures (SOPs), Food and Drug Administration (FDA), Health Safety & Environmental (HSE), Occupational Safety and Health Administration (OSHA)
Formulated Solutions: Contract development and manufacturing for consumer healthcare and pharmaceuticals.
3+ YOE2+ MgmtLead blending/compounding operations in a GMP environment, ensure cGMP/FDA compliance, supervise staff, troubleshoot processes, maintain documentation; able to lift 50 lb and work flexible schedules.
Microsoft Word, Microsoft Excel, Microsoft Outlook, ERP/MRP systems, Electronic Batch Record systems
McKessonNYSE: MCK: Distributes pharmaceuticals and provides healthcare technology and medical supplies.
4+ YOE4+ years relevant experience in regulated pharmaceutical distribution or quality; bachelor’s in scientific/technical/quality field or equivalent; knowledge of cGMP, DSCSA, FDA regs; strong communication and analytical skills.
Quality Assurance Inspector, PM, Deli Kitchen - Lakeland
Lakeland, Florida, United States
$20-$27/hrOnsiteFull Time
Publix: Operates a chain of employee-owned supermarkets and pharmacies.
Ensure GMP and FDA/USDA compliance, perform temperature and product checks, collect samples, use MS Word/Excel/Outlook, be 18+, able to work rotating shifts, nights, weekends, and holidays.
Microsoft Word, Microsoft Excel, Microsoft Outlook
LonzaSIX Swiss Exchange: LONN: Manufactures medicines and provides development services for healthcare companies.
5+ YOEBachelor's degree preferred, 5+ years supporting enterprise/document/QMS systems in regulated environments; skills in system configuration, data migration, workflow design, and applying FDA/cGMP requirements; strong communication.
Documentum, TrackWise, Microsoft SharePoint, LIMS, Empower
Kedrion Biopharma: Collects and fractionates blood plasma to produce rare disease therapies.
1+ Mgmt1+ year supervisory experience preferred; bachelor’s degree preferred; knowledge of FDA/CLIA/cGMP regulations; proficiency with Microsoft Office and data entry; ability to manage staffing, compliance, and cold storage operations.
B & M Precision: A medical device contract manufacturer producing surgical-grade components with a focus on quality and continuous improvement.
5+ YOE5+ years quality/inspection experience in regulated manufacturing, knowledge of ISO 13485 and FDA 21 CFR Part 820, document control experience, GR&R and metrology skills, MS Office proficiency.
Micro-Vu, Keyence, Optical Comparators, MS Office Suite, Adobe Visio, Microsoft PowerPoint, Microsoft Excel, PivotTables, VLOOKUP