GMP Data Reviewers and Chemists
5 days ago
We are seeking highly motivated candidates for various positions throughout our company, including 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, Validation Engineers, Metrology, Report Generation, Sample Log-In Associates, and HVAC Technicians.
Key Responsibilities:- Review and analyze analytical data to ensure accuracy and compliance with regulatory requirements.
- Develop and configure LabWare LIMS systems to meet business needs.
- Manage and maintain document control systems to ensure compliance with regulatory requirements.
- Validate computer systems to ensure they meet regulatory requirements.
- Conduct method development and validation to ensure accuracy and compliance with regulatory requirements.
- Collaborate with cross-functional teams to ensure successful project execution.
- Bachelor's degree in Chemistry or related field.
- Advanced degree in Chemistry or related field preferred.
- Minimum 2 years of experience in 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, Validation Engineers, Metrology, Report Generation, Sample Log-In Associates, and HVAC Technicians.
- Competitive salaries commensurate with experience.
- Excellent benefits package.
- Great potential for career advancement and leadership in a rapidly growing company.
- Subsidized childcare at our newly acquired childcare facility.
We are an equal opportunity employer and welcome applications from diverse candidates.
-
GMP Data Reviewers and Chemists
4 weeks ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full time**Quality Chemical Laboratories (QCL)** is a leading pharmaceutical testing and development laboratory seeking highly motivated professionals to join our team as analytical data reviewers, LabWare LIMS development/configuration/validation specialists, document control associates, computer system validation and data integrity specialists, and scientists with...
-
GMP Production Chemist
3 weeks ago
Wilmington, North Carolina, United States Masis Professional Group Full timeGMP Production Chemist OpportunityMasis Professional Group is seeking a highly skilled GMP Production Chemist to join our team at 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...
-
GMP Data Reviewers
5 days ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeJoin Our Team at Quality Chemical LaboratoriesWe are seeking highly motivated candidates for various positions throughout our 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,...
-
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeJob DescriptionQuality Chemical Laboratories (QCL), a leading pharmaceutical testing and development laboratory, is seeking highly motivated and experienced professionals to fill various roles in analytical data review, LabWare LIMS development, document control, computer system validation, and data integrity.Key Responsibilities:Review and validate...
-
GMP Data Reviewers
5 days ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL) Job OpportunityWe are 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,...
-
GMP Data Reviewers
2 weeks ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL) Job OpportunityWe are 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,...
-
GMP Data Reviewers
5 days ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL) Job OpportunityWe are 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,...
-
GMP Data Reviewers
1 day ago
Wilmington, North Carolina, United States QUALITY CHEMICAL LABORATORIES Full timeQuality Chemical Laboratories (QCL) Job OpportunityWe are 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,...
-
GMP Data Reviewers
2 weeks ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL) Job OpportunityWe are 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,...
-
GMP Production Chemist
3 weeks ago
Wilmington, North Carolina, United States Masis Professional Group Full timeJob Summary:This position is responsible for performing and developing all processes and procedures used in the GMP Clean Rooms for contract manufacturing. The successful candidate will support various departments in managing the Radiochemistry inventory and records, provide technical support to Production, and work with outside customers and clients.Key...
-
Chemist I
2 weeks ago
Wilmington, North Carolina, United States Core Laboratories Full timeJob SummaryWe are seeking a highly skilled Chemist I to join our team at Core Laboratories. As a Chemist I, you will be responsible for performing laboratory tests and analyses to determine chemical or physical characteristics of various substances.Key ResponsibilitiesConduct laboratory tests and analyses to determine chemical or physical characteristics of...
-
Quality Assurance Associate
2 days ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeJob Summary:Quality Chemical Laboratories (QCL) is seeking a highly skilled Quality Assurance Associate to join our team. As a key member of our quality assurance department, you will be responsible for reviewing and approving reports generated from laboratory data, ensuring compliance with Good Manufacturing Practices (GMPs) and Standard Operating...
-
GMP Compliance Engineer
1 month ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Chemical Laboratories (QCL) is a prominent player in the Pharmaceutical testing and manufacturing sector, currently in search of a skilled individual for the role of Validation Engineer. This role, situated within the Manufacturing and Formulations Services division, mandates a Bachelor’s degree or higher in a scientific or engineering field,...
-
Senior Analytical Data Reviewer
3 weeks ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeWe are 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...
-
Production Chemist
3 weeks ago
Wilmington, North Carolina, United States Masis Professional Group Full timeJob Summary:This position plays a crucial role in the production of radiopharmaceuticals, working under the Production Department director to support production by performing GMP radiochemistry processes in a safe, efficient, and timely manner.Key Responsibilities:Support irradiation program through the preparation of targets and radiochemical processing of...
-
Document Review Specialist
5 days ago
Wilmington, North Carolina, United States Quanta Services Full timeDocument Review SpecialistQuanta Services is seeking a highly skilled Document Review Specialist to join our team. As a key member of our team, you will be responsible for reviewing and validating documents to ensure compliance with regulatory requirements.Main Responsibilities:Review and understand CQV and site quality procedures and align with FDB Large...
-
Manufacturing Quality Assurance Specialist
4 weeks ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeJob Summary:Quality Chemical Laboratories (QCL) is seeking a highly skilled Manufacturing Quality Assurance Associate to join our team in the Manufacturing Quality Assurance department. As a key member of our team, you will be responsible for ensuring the quality and compliance of our manufacturing processes and products.Key Responsibilities:Perform GMP...
-
Manufacturing Quality Assurance Specialist
4 weeks ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeJob SummaryQuality Chemical Laboratories (QCL) is seeking a highly skilled Manufacturing Quality Assurance Associate to join our team. As a key member of our Manufacturing Quality Assurance department, you will be responsible for ensuring the quality and compliance of our pharmaceutical products.Key ResponsibilitiesPerform GMP reviews of manufacturing...
-
Quality Assurance Associate
6 days ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Assurance Associate Job DescriptionQuality Chemical Laboratories (QCL) is seeking a detail-oriented Quality Assurance Associate to join our team. As a QA Associate, you will be responsible for reviewing and approving reports generated from laboratory data, ensuring compliance with Good Manufacturing Practices (GMPs) and Standard Operating Procedures...
-
Quality Assurance Associate
1 week ago
Wilmington, North Carolina, United States Quality Chemical Laboratories Full timeQuality Assurance Associate - Report GenerationQuality Chemical Laboratories (QCL) is seeking a qualified candidate for the position of Quality Assurance Associate - Report Generation. The successful candidate will be responsible for reviewing and approving reports generated from laboratory data, ensuring compliance with Good Manufacturing Practices (GMPs)...