Quality Assurance Senior Specialist
Posted on Sep 21, 2024 by Cambridge Isotope Laboratories, Inc.
Xenia, OH
Other
Immediate Start
Annual Salary
Full-Time
Cambridge Isotope Separations (CIS) has an outstanding opportunity for an experienced Quality Assurance Senior Specialist based onsite in our Xenia, OH location. CIS is the world leader in the separation of 13C and 18O and is a subsidiary of Cambridge Isotope Laboratories (CIL) in Massachusetts, the world’s leading producer of stable isotopes and stable isotope-labeled compounds. CIL separates both 13C and 18O at its Xenia, Ohio, facility and has the world’s largest production capacity for both 13C and 18O. CIL also has the only large capacity nongovernmental D2O (Deuterium Oxide) enrichment columns in the world located at its CIS facility.
Summary:
Primary responsibility of the GMP Quality Assurance Senior Specialist is to work as a team member to uphold compliance and maintenance of the Company’s cGMP (Current Good Manufacturing Practices) and Quality systems to in-house and/or external specifications, standards, and regulations. Helps to establish quality standards for products and processes and suggest modifications to prevent defects in components or final products. Works closely with cross-functional teams to identify and mitigate quality risks. Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Work is performed primarily in an administrative office environment.
Responsibilities:
Responsibilities include, but are not limited to:
Oversight and maintenance of various Quality Systems (e.g. CAPA, Deviation, Supplier Management, Customer Complaints, biennial review, internal/external auditing, etc.)
Conduct root cause analysis for defects, non-conformities, or other quality failures and report approval
Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary
Act as an administrator of CIS’s electronic Quality Management System (eQMS)
Perform document writing/revisions, document/data review/approval, change control coordination/approval, continuous improvements, and other duties as needed
Design/implement quality assurance protocols, procedures, and methods for evaluating the performance of processes, equipment, and finished products
Author/review various reports (e.g. annual product reviews, annual deviation/CAPA/EM reports)
Lead and/or actively participate in internal/external/supplier audits, risk management programs, and project meetings, as needed
Act as Team Leader in the absence of Team Leader/Supervisor/Manager to subordinate employees
Perform other duties as needed including, but no limited to:
Raw material documentation review and release
Batch record review and release of finished products
Perform room/line clearances
Revision and creation of documents, including SOP’s and forms
Label review and final inspection
Create batch records, logbooks and controlled forms
Initiation, tracking, review, final distribution, and reconciliation of GMP documents
Review of facility/utility monitoring data
Requirements
Bachelor’s degree in chemistry/sciences or quality assurance/management; equivalent applicable industry experience may be substituted for the degree requirement.
Minimum of 8 years of experience in a cGMP Quality, regulatory, and/or chemical manufacturing environment, with increasing responsibilities and independence
Experience with GMP Quality Assurance and knowledge and experience with ICH Q7A is preferred
Applied knowledge of GMP principles across quality disciplines, including but not limited to: Batch Record Review, Change Control, Training, Investigations, CAPA, Supplier Qualification, Process Validation/Qualification
Competencies: Technical expertise, Problem-solving skills, Leadership skills
Ability to identify and seek needed information/Research skills
Excellent interpersonal, verbal and written communication skills
Attention to detail, organizational skills, ability to multitask and follow tasks through to completion. Work independently and in a team environment
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
CIL is an EEO/Affirmative Action employer.
Learn more about us on our website:
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website:
Summary:
Primary responsibility of the GMP Quality Assurance Senior Specialist is to work as a team member to uphold compliance and maintenance of the Company’s cGMP (Current Good Manufacturing Practices) and Quality systems to in-house and/or external specifications, standards, and regulations. Helps to establish quality standards for products and processes and suggest modifications to prevent defects in components or final products. Works closely with cross-functional teams to identify and mitigate quality risks. Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Work is performed primarily in an administrative office environment.
Responsibilities:
Responsibilities include, but are not limited to:
Oversight and maintenance of various Quality Systems (e.g. CAPA, Deviation, Supplier Management, Customer Complaints, biennial review, internal/external auditing, etc.)
Conduct root cause analysis for defects, non-conformities, or other quality failures and report approval
Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary
Act as an administrator of CIS’s electronic Quality Management System (eQMS)
Perform document writing/revisions, document/data review/approval, change control coordination/approval, continuous improvements, and other duties as needed
Design/implement quality assurance protocols, procedures, and methods for evaluating the performance of processes, equipment, and finished products
Author/review various reports (e.g. annual product reviews, annual deviation/CAPA/EM reports)
Lead and/or actively participate in internal/external/supplier audits, risk management programs, and project meetings, as needed
Act as Team Leader in the absence of Team Leader/Supervisor/Manager to subordinate employees
Perform other duties as needed including, but no limited to:
Raw material documentation review and release
Batch record review and release of finished products
Perform room/line clearances
Revision and creation of documents, including SOP’s and forms
Label review and final inspection
Create batch records, logbooks and controlled forms
Initiation, tracking, review, final distribution, and reconciliation of GMP documents
Review of facility/utility monitoring data
Requirements
Bachelor’s degree in chemistry/sciences or quality assurance/management; equivalent applicable industry experience may be substituted for the degree requirement.
Minimum of 8 years of experience in a cGMP Quality, regulatory, and/or chemical manufacturing environment, with increasing responsibilities and independence
Experience with GMP Quality Assurance and knowledge and experience with ICH Q7A is preferred
Applied knowledge of GMP principles across quality disciplines, including but not limited to: Batch Record Review, Change Control, Training, Investigations, CAPA, Supplier Qualification, Process Validation/Qualification
Competencies: Technical expertise, Problem-solving skills, Leadership skills
Ability to identify and seek needed information/Research skills
Excellent interpersonal, verbal and written communication skills
Attention to detail, organizational skills, ability to multitask and follow tasks through to completion. Work independently and in a team environment
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
CIL is an EEO/Affirmative Action employer.
Learn more about us on our website:
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website:
Reference: 202105891
https://jobs.careeraddict.com/post/95494942
Quality Assurance Senior Specialist
Posted on Sep 21, 2024 by Cambridge Isotope Laboratories, Inc.
Xenia, OH
Other
Immediate Start
Annual Salary
Full-Time
Cambridge Isotope Separations (CIS) has an outstanding opportunity for an experienced Quality Assurance Senior Specialist based onsite in our Xenia, OH location. CIS is the world leader in the separation of 13C and 18O and is a subsidiary of Cambridge Isotope Laboratories (CIL) in Massachusetts, the world’s leading producer of stable isotopes and stable isotope-labeled compounds. CIL separates both 13C and 18O at its Xenia, Ohio, facility and has the world’s largest production capacity for both 13C and 18O. CIL also has the only large capacity nongovernmental D2O (Deuterium Oxide) enrichment columns in the world located at its CIS facility.
Summary:
Primary responsibility of the GMP Quality Assurance Senior Specialist is to work as a team member to uphold compliance and maintenance of the Company’s cGMP (Current Good Manufacturing Practices) and Quality systems to in-house and/or external specifications, standards, and regulations. Helps to establish quality standards for products and processes and suggest modifications to prevent defects in components or final products. Works closely with cross-functional teams to identify and mitigate quality risks. Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Work is performed primarily in an administrative office environment.
Responsibilities:
Responsibilities include, but are not limited to:
Oversight and maintenance of various Quality Systems (e.g. CAPA, Deviation, Supplier Management, Customer Complaints, biennial review, internal/external auditing, etc.)
Conduct root cause analysis for defects, non-conformities, or other quality failures and report approval
Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary
Act as an administrator of CIS’s electronic Quality Management System (eQMS)
Perform document writing/revisions, document/data review/approval, change control coordination/approval, continuous improvements, and other duties as needed
Design/implement quality assurance protocols, procedures, and methods for evaluating the performance of processes, equipment, and finished products
Author/review various reports (e.g. annual product reviews, annual deviation/CAPA/EM reports)
Lead and/or actively participate in internal/external/supplier audits, risk management programs, and project meetings, as needed
Act as Team Leader in the absence of Team Leader/Supervisor/Manager to subordinate employees
Perform other duties as needed including, but no limited to:
Raw material documentation review and release
Batch record review and release of finished products
Perform room/line clearances
Revision and creation of documents, including SOP’s and forms
Label review and final inspection
Create batch records, logbooks and controlled forms
Initiation, tracking, review, final distribution, and reconciliation of GMP documents
Review of facility/utility monitoring data
Requirements
Bachelor’s degree in chemistry/sciences or quality assurance/management; equivalent applicable industry experience may be substituted for the degree requirement.
Minimum of 8 years of experience in a cGMP Quality, regulatory, and/or chemical manufacturing environment, with increasing responsibilities and independence
Experience with GMP Quality Assurance and knowledge and experience with ICH Q7A is preferred
Applied knowledge of GMP principles across quality disciplines, including but not limited to: Batch Record Review, Change Control, Training, Investigations, CAPA, Supplier Qualification, Process Validation/Qualification
Competencies: Technical expertise, Problem-solving skills, Leadership skills
Ability to identify and seek needed information/Research skills
Excellent interpersonal, verbal and written communication skills
Attention to detail, organizational skills, ability to multitask and follow tasks through to completion. Work independently and in a team environment
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
CIL is an EEO/Affirmative Action employer.
Learn more about us on our website:
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website:
Summary:
Primary responsibility of the GMP Quality Assurance Senior Specialist is to work as a team member to uphold compliance and maintenance of the Company’s cGMP (Current Good Manufacturing Practices) and Quality systems to in-house and/or external specifications, standards, and regulations. Helps to establish quality standards for products and processes and suggest modifications to prevent defects in components or final products. Works closely with cross-functional teams to identify and mitigate quality risks. Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Work is performed primarily in an administrative office environment.
Responsibilities:
Responsibilities include, but are not limited to:
Oversight and maintenance of various Quality Systems (e.g. CAPA, Deviation, Supplier Management, Customer Complaints, biennial review, internal/external auditing, etc.)
Conduct root cause analysis for defects, non-conformities, or other quality failures and report approval
Perform analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary
Act as an administrator of CIS’s electronic Quality Management System (eQMS)
Perform document writing/revisions, document/data review/approval, change control coordination/approval, continuous improvements, and other duties as needed
Design/implement quality assurance protocols, procedures, and methods for evaluating the performance of processes, equipment, and finished products
Author/review various reports (e.g. annual product reviews, annual deviation/CAPA/EM reports)
Lead and/or actively participate in internal/external/supplier audits, risk management programs, and project meetings, as needed
Act as Team Leader in the absence of Team Leader/Supervisor/Manager to subordinate employees
Perform other duties as needed including, but no limited to:
Raw material documentation review and release
Batch record review and release of finished products
Perform room/line clearances
Revision and creation of documents, including SOP’s and forms
Label review and final inspection
Create batch records, logbooks and controlled forms
Initiation, tracking, review, final distribution, and reconciliation of GMP documents
Review of facility/utility monitoring data
Requirements
Bachelor’s degree in chemistry/sciences or quality assurance/management; equivalent applicable industry experience may be substituted for the degree requirement.
Minimum of 8 years of experience in a cGMP Quality, regulatory, and/or chemical manufacturing environment, with increasing responsibilities and independence
Experience with GMP Quality Assurance and knowledge and experience with ICH Q7A is preferred
Applied knowledge of GMP principles across quality disciplines, including but not limited to: Batch Record Review, Change Control, Training, Investigations, CAPA, Supplier Qualification, Process Validation/Qualification
Competencies: Technical expertise, Problem-solving skills, Leadership skills
Ability to identify and seek needed information/Research skills
Excellent interpersonal, verbal and written communication skills
Attention to detail, organizational skills, ability to multitask and follow tasks through to completion. Work independently and in a team environment
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
CIL is an EEO/Affirmative Action employer.
Learn more about us on our website:
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website:
Reference: 202105891
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