Job Openings

Below is a list of current job openings at Synergy Bioscience. Please click on an opening in the list to view details and apply.

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TitleLocationDepartmentJob Related Skills
Business Development ManagerDallas, TXSalesB2B Sales, Business Development, CRM Software, Lead Generation, Microsoft Office (Word, Excel, ..etc.), Sales
QA Consultant - Pharmaceutical ExperienceHoustonClient ServicesBiocompatibility, CAPA, Design Control, FDA Regulations, Quality Assurance
BiochemistDallas, TXOperationsAmino Acids Characterization, Analytical Chemisty, CLIA Experience, Chemistry / Immunoassay Analyzer, FDA Regulations, Protocol / Technical Report Writing, SOP Writing, Technical Writing, Test Method Validation, Therapeutic Protein Characterization
Business Dev. ManagerNorth CarolinaSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Dev. ManagerNew JeresySalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Dev. ManagerBostonSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Dev. ManagerAustinSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Dev. ManagerChicagoSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Dev. ManagerSan FranciscoSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerSan FranciscoSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerSan DiegoSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerDallas, TXSalesB2B Sales, Business Development, CRM Software, Microsoft Office (Word, Excel, ..etc.)
Business Development ManagerNew JeresySalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerAustinSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerDallas, TXMarketingB2B Sales, Business Development, CRM Software, Microsoft Office (Word, Excel, ..etc.), Sales
Business Development ManagerBostonSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerChicagoSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
Business Development ManagerDallas, TXSalesBusiness Development
Business Development ManagerDallas, TXSalesBusiness Development, Sales
Business Development ManagerNorth CarolinaSalesAnalytical Chemisty, B2B Sales, Business Development, Pharmaceutical Development, Sales
CAPA ConsultantHoustonClient Services21 CFR 803, 21 CFR Part 11, 510K, Auditing, CAPA, Data Analysis, Data Integrity, Design Control, Design History File - DHF, Design of Experiment - DOE, EP Compendial Test Methods, EU Annex 11, FDA Audit Experience, FDA Audit Remediation, FDA Regulations, FMEA / PFMEA, Human Factors Engineering
cGMP AuditorDallas, TXOperationsAuditing, FDA Audit Remediation, FDA Regulations
ChemistDallas, TXOperationsAnalytical Chemisty, Pharmaceutical Development, Protocol / Technical Report Writing, Stability Studies, Test Method Validation
Cleaning Validation ConsultantDallas, TXClient ServicesBiocompatibility, FDA Regulations
Data Integrity / CSV ConsultantHoustonClient Services21 CFR Part 11, Computer System Validation, Data Integrity, EU Annex 11, FMEA / PFMEA, GAMP 5, ISO 13485, Validation
Medical Device - Design Control Senior ConsultantDallas, TXClient Services510K, Biocompatibility, Design Control, FDA Audit Remediation, FDA Regulations, Human Factors Engineering, Medical Devices Experience, Process Improvement, Protocol / Technical Report Writing, Risk Management, SOP Writing, Validation
Medical Device 510K Filing SpecialistDallas, TXClient Services510K, FDA Regulations, ISO 13485, Medical Devices Experience, Warning Letters Remediations
Medical Device Senior ConsultantDallas, TXClient Services21 CFR 803, 21 CFR Part 11, 510K, Auditing, CAPA, Data Analysis, Data Integrity, Design Control, Design History File - DHF, Design of Experiment - DOE, EP Compendial Test Methods, EU Annex 11, FDA Audit Experience, FDA Audit Remediation, FDA Regulations, FMEA / PFMEA, Human Factors Engineering
Pharmaceutical GMP QA SpecialistDallas, TXOperationsAuditing, Batch Review, CAPA, Computer System Validation, Data Integrity, FDA Audit Experience, FDA Regulations, IQ/OQ/PQ, Microsoft Office (Word, Excel, ..etc.), Quality Assurance, Regulatory Compliance, SOP Writing, Supplier Quality Management
Pharmaceutical R&D ScientistDallas, TXOperationsPharmaceutical Development
Post-Market Surveillance SpecialistN/AClient ServicesMDR, Medical Devices Experience, Post Market Surveillance
Process Validation Engineer - Medical DeviceDallas, TXClient ServicesFDA Regulations, IQ/OQ/PQ, Medical Devices Experience, Protocol / Technical Report Writing, Quality Assurance, Regulatory Compliance, Validation
QA Consultant - Pharma ExperienceDallas, TXClient ServicesBiocompatibility, Design Control, FDA Regulations
Quality Assurance SpecialistDallas, TXOperationsFDA Audit Remediation, Warning Letters Remediations
Senior ChemistDallas, TXOperationsAnalytical Chemisty, FDA Regulations, Technical Writing
Senior Digital Marketing SpecialistDallas, TXMarketingBusiness Development, Digital Marketing
Senior MicrobiologistDallas, TXOperationsAntimicrobial Effectiveness Testing (Chapter, EP Compendial Test Methods, FDA Regulations, JP Compendial Test Methods, Microbial Enumeration Testing, Microbiology, Protocol / Technical Report Writing, SOP Writing, Sterility Testing, Test Method Validation, Testing for Specified Organisms, USP Compendial Test Methods, Validation
Senior QA/RA Specialist Dallas, TXOperations21 CFR Part 11, Auditing, CAPA, Data Integrity, FDA Audit Remediation, FDA Regulations, ICH Guidelines, ISO 13485, Microbiology, Quality Assurance, Regulatory Compliance, Risk Management, Supplier Quality Management, USP Compendial Test Methods
Senior Regulatory Affairs ConsultantDallas, TXClient Services21 CFR 803, 21 CFR Part 11, 510K, Auditing, Data Analysis, Data Integrity, Design Control, Design History File - DHF, Design of Experiment - DOE, EP Compendial Test Methods, EU Annex 11, FDA Audit Experience, FDA Audit Remediation, FDA Regulations, FMEA / PFMEA
Software Quality Assurance EngineerDallas, TXClient ServicesDesign Control, Medical Devices Experience, Quality Assurance, Risk Management, SOP Writing, Validation
Sr. Regulatory Affairs ConsultantDallas, TXClient ServicesN/A
Supplier Quality SpecialistN/AClient ServicesCAPA, Design of Experiment - DOE, FDA Regulations, ISO 13485, ISO 14971, Medical Device Class 1, Medical Device Class 2, Medical Device Class 3, Medical Devices Experience, SOP Writing, Supplier Quality Management, Validation
Showing 1 - 42 of 42

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