We have other current jobs related to this field that you can find below
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Wilmington, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/ validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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Wilmington, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/ validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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Wilmington, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/ validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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Wilmington, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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Wilmington, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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Wilmington, NC, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/ validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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Wilmington, NC, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/ validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in...
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GMP Chemist
3 months ago
Wilmington, United States Masis Professional Group Full timePharmaceutical GMP Chemist Our client is a production facility specializing in the contract manufacturing of radiopharmaceuticals. This new cGMP clean room suite is a 21 CFR 211 compliant, radiopharmaceutical manufacturing facility dedicated to late stage investigational and commercial stage radiopharmaceuticalsDue to growth they are looking to add another...
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GMP Chemist
3 months ago
Wilmington, United States Masis Professional Group Full timePharmaceutical GMP Chemist Our client is a production facility specializing in the contract manufacturing of radiopharmaceuticals. This new cGMP clean room suite is a 21 CFR 211 compliant, radiopharmaceutical manufacturing facility dedicated to late stage investigational and commercial stage radiopharmaceuticalsDue to growth they are looking to add another...
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Production Chemist
2 weeks ago
Wilmington, United States Masis Professional Group Full timeGMP Production ChemistOur client is a production facility specializing in the contract manufacturing of radiopharmaceuticals. This new cGMP clean room suite is a 21 CFR 211 compliant, radiopharmaceutical manufacturing facility dedicated to late stage investigational and commercial stage radiopharmaceuticalsCurrently they are looking to add another GMP...
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Production Chemist
2 weeks ago
Wilmington, United States Masis Professional Group Full timeGMP Production ChemistOur client is a production facility specializing in the contract manufacturing of radiopharmaceuticals. This new cGMP clean room suite is a 21 CFR 211 compliant, radiopharmaceutical manufacturing facility dedicated to late stage investigational and commercial stage radiopharmaceuticalsCurrently they are looking to add another GMP...
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Manufacturing Quality Assurance Associate
1 month ago
Wilmington, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Manufacturing Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department, requires a Bachelor s degree or higher in a scientific or engineering discipline...
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Analytical Chemist II-III
4 weeks ago
Wilmington, United States DelDOT Full timeSummary Statement This is an Analytical Chemist position in the area of Forensic Toxicology. The incumbent reports to the casework Lab Manager I. At the level II position, responsibilities include analysis of complex biological matrices for both postmortem and DUI/other cases; processing and review of batch paperwork; operation, maintenance, and...
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Forensic Analytical Chemist II-III
4 days ago
Wilmington, Delaware, United States DelDOT Full timeOverview This position is for an Analytical Chemist specializing in Forensic Toxicology. The successful candidate will report to the Lab Manager I and will be responsible for a variety of analytical tasks. Key Responsibilities Conduct analysis of intricate biological samples related to forensic cases. Manage and review documentation associated...
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Advanced Analytical Chemist II-III
4 days ago
Wilmington, Delaware, United States DelDOT Full timeOverview This position is for an Analytical Chemist specializing in Forensic Toxicology, reporting directly to the Lab Manager I. The role encompasses a variety of responsibilities at both the II and III levels, focusing on the analysis of intricate biological samples related to various cases. Key Responsibilities Conduct thorough analyses of...
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GMP Radiochemistry Specialist
4 days ago
Wilmington, Delaware, United States Masis Professional Group Full timeGMP RADIOCHEMIST POSITIONMasis Professional Group is seeking a skilled professional for a production facility specializing in the contract manufacturing of radiopharmaceuticals. This state-of-the-art cGMP clean room suite adheres to 21 CFR 211 standards, focusing on late-stage investigational and commercial radiopharmaceuticals.POSITION OVERVIEW: The...
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GMP Radiochemistry Specialist
4 days ago
Wilmington, Delaware, United States Masis Professional Group Full timePOSITION: GMP Radiochemistry SpecialistMasis Professional Group is seeking a dedicated professional for a role in a state-of-the-art facility focused on the contract manufacturing of radiopharmaceuticals. This facility adheres to cGMP standards and is compliant with 21 CFR 211 regulations, specializing in both late-stage investigational and commercial...
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GMP Radiochemistry Specialist
3 days ago
Wilmington, Delaware, United States Masis Professional Group Full timePOSITION: GMP Radiochemistry SpecialistOur client, a leader in the field of radiopharmaceuticals, operates a state-of-the-art production facility dedicated to the contract manufacturing of radiopharmaceuticals. This facility adheres to cGMP standards and is compliant with 21 CFR 211 regulations, focusing on late-stage investigational and commercial...
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GMP Radiochemistry Specialist
4 days ago
Wilmington, Delaware, United States Masis Professional Group Full timeGMP RADIOCHEMISTMasis Professional Group is seeking a skilled professional for a role in a state-of-the-art facility dedicated to the contract manufacturing of radiopharmaceuticals. This facility adheres to cGMP standards and is compliant with 21 CFR 211 regulations, focusing on late-stage investigational and commercial radiopharmaceuticals.POSITION...
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GMP Radiochemistry Specialist
4 days ago
Wilmington, Massachusetts, United States Masis Professional Group Full timeGMP Radiochemistry SpecialistMasis Professional Group is a leading production facility focused on the contract manufacturing of radiopharmaceuticals. Our state-of-the-art cGMP clean room suite adheres to 21 CFR 211 regulations, dedicated to both late-stage investigational and commercial radiopharmaceuticals.We are currently seeking a skilled GMP...
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GMP Data Reviewers, Chemists, Metrology Positions
2 months ago
GMP Data Reviewers, Chemists, Metrology, LabWare, CPU Validation, Stability, Sample Log-In, and Document Control Positions
Quality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, Pharmaceutical Formulation (with knowledge of manufacturing equipment), Metrology, and Sample Log-In Associates.
Special attention is given to candidates with an advanced degree in Chemistry or related science and experience in method development/validation. Special consideration will also be given to experienced GMP data reviewers.
Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking highly motivated candidates for multiple positions throughout the company in the areas of analytical data review, LabWare LIMS development/configuration/validation, Document Control, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, Biotech, Pharmaceutical Formulation and Manufacturing (requires knowledge of manufacturing equipment), Validation Engineers, Metrology, Report Generation, Sample Log-In Associates, and HVAC Technicians. Special attention given to candidates with an advanced degree in Chemistry or related science and experience in method development/validation. Special consideration also given to experienced GMP data reviewers.
QCL offers competitive salaries commensurate with experience and an excellent benefits package, as well as great potential for career advancement and leadership in a rapidly growing company. We now also offer subsidized childcare at our newly acquired childcare facility.
QCL is an equal opportunity employer.