Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
Environmental Monitoring GMP Specialist
Apex Systems is a large staffing and consulting firm and we are looking for 4 EM GMP Specialists with 2-4 years of experience working in aseptic techniques/clean rooms, working knowledge of GMPs, experience with cell culture for mammalian cells, and some knowledge of Environmental Monitoring to place at our Biotech client.
Client: Innovative Biotech client
Contract/Perm & duration: 4- month contract (possibility of conversion or extension)
Location: Hamilton
The successful candidate that will be selected to support the QC Microbiology Laboratory would be an experienced individual in the field of manufacturing, able to adhere and demonstrate the principles of Good Manufacturing Practices (GMP). The successful candidate will be required to work specifically to maintain the environmental conditions in clean rooms by performing environmental monitoring (EM), as well as associated testing (ie. gram staining, subculturing, organism identification etc) and sample management, including reconciliation and result recording. The successful candidate will demonstrate flexibility within Microbiology team and larger organization, flowing to work priorities, as required. Environmental monitoring (EM) is an enabling function and, as such, this role will support production, and facility needs to ensure business needs are met. Responsibilities: Delivers microbiology-related services including environmental monitoring, sample management, testing, and equipment management. Collaborates with the Production team to support the requirements of sampling to align with the production schedule Maintains the EM program including (but not limited to): ensuring scheduling of all Grade A, B, C and D samples to meet the sample collection frequency requirements as set forth by internal procedures, ensuring samples are read and documentation is submitted in a timely manner Manages sample management to the third-party testing by approved testing partners Performs aseptic gowning qualification and maintains personnel qualifications. Provides in-suite and on-the-floor support for OmniaBio’ s manufacturing teams, where applicable Ensures all EM documentation is complete and available for approval ensuring the highest quality of data integrity are met utilizing good documentation practices (GDP) Assist with maintaining equipment and laboratory cleaning schedules as deemed appropriate by internal governing standard operating procedures (SOPs)
Key Qualifications: Bachelor’s degree in science (bioengineering, chemical engineering, bioprocess, biotechnology, cell biology, microbiology, chemistry, etc.). Microbiology background is preferred. 2-4 years of industry experience in a cell therapy/viral quality department supporting GMP production or similar within the pharmaceutical, medical technologies, biologics or similar industries. Strong understanding of aseptic/sterile environments and technologies. Excellent understanding GMP regulations and good laboratory practices (GLP) and GDP principles.
