
evelo
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CountryHosted in Canada
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Traffic rank#366,931 Site Rank
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Site age22 yrs old
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Traffic rank
#366,931
#366,931
Site age
22 yrs
22 yrs
Location
Canada
Canada
Newest job postings for evelo
via Geebo
posted_at: 3 days agoschedule_type: Full-timesalary: 20–28 an hour
Evelo Biosciences, Inc. (Nasdaq:
EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of an interdisciplinary team. Evelo's... vision is to improve the lives of patients with serious
Evelo Biosciences, Inc. (Nasdaq:
EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of an interdisciplinary team. Evelo's... vision is to improve the lives of patients with serious diseases through the development of a broadly applicable new modality of medicines. Humans have evolved over millennia with the microbes in and on our bodies. These microbes play a vital role in developing and directing immune and biological responses. Evelo is harnessing the therapeutic potential of specific strains of naturally occurring microbes and developing them as a new class of medicines, monoclonal microbials. We have validated that orally delivered monoclonal microbials modulate immunological and biological effects throughout the body after initial interactions with human cells in the gut. Evelo is pioneering the development of this new class of medicine for the treatment of autoimmune, immunoinflammatory, metabolic, neurological, neuroinflammatory diseases and cancer. This is an outstanding opportunity to join a fast-paced company in a new exciting field of medicine. As a member of the Evelo team, you will be a vital part of helping to shape Evelo's vision:
in transforming therapies through a new modality of medicines. We are seeking a dedicated Senior Downstream Process Development Engineer who is interested in joining a highly dynamic and intellectually challenging team. This position will offer a tremendous opportunity to gain experience in design and scale-up of novel processes. In addition, this role will engage in critical collaborations with our manufacturing, microbiology, immunology, and bioinformatics teams. The successful candidate will be innovative, thrive in an intense and dynamic environment, and use his/her creative and imaginative problem-solving skills to help bring new products to patients. Primary
Responsibilities:
Manage operations and serve as functional area technical expert to support downstream purification and recovery process development activities including centrifugation, depth filtration, tangential flow filtration, chromatography, lyophilization, and spray drying. Lead downstream process development and scaling up activities at laboratory and pilot plant for company's product candidates. Communicate goals of lab processing. Maintain lab organization and records. Perform assays on products, process intermediates, and experimental samples using biotechnical strategies. Conduct range finding studies for improved filtration methods, chromatography steps, and lyophilization. Measure the integrity of filters and verified results to lie within the acceptable range for manufacturing scale. Conduct hands on trouble shooting, process feasibility and process optimization experiments in relation to downstream purification and recovery processes. Develop purification methods to purify various product related impurities to assist product characterization. Assist developed downstream process tech transfer to pilot and GMP manufacturing sites and support pilot and GMP production activities including technical review of development report, tech transfer document, batch records, SOPs, raw material release and production process report. Prepare technical reports and documents to support IND and BLA filing as needed. Desired Skills &
Qualifications:
Strong knowledge of chromatography and membrane purification including affinity, ion exchange, hydrophobic interaction and mixed mode chromatographic separation, and harvest and ultrafiltration/diafiltration (UFDF) membrane processes. Knowledge of drying process development including lyophilization and spray drying. Extensive hands on experience of column packing, AKTA/Unicorn operation and chromatographic purification process development. Operation knowledge and hands on experience of membrane separation process development including depth filtration harvest and UFDF processes. Knowledge and experience with manufacturing production under cGMP regulation. Industry experience with tech transfer and process scaling up in related to downstream purification process. Strong planning and communication skills in a dynamic project environment. Technical support experience in CMO project and communication with external customers is desired. Education &
Experience:
Ph.D. with more than 5 years of biotech industry experience, or M.S with over 8 years of biotech industrial experience directly related to job description or B.S with over 10 years direct biotech industry experience and successful track record. Extensive experience of downstream purification process development, process scale up from lab scale to manufacturing process for production. Experience with tech transfer process from process development to GMP manufacturing site. Understand GMP regulation and FDA/EMA guidance on manufacturing process for biologics. Goal oriented team player with excellent communication skills. Bioengineering knowledge and experience in developing downstream purification process for manufacturing production. Experience in developing high concentration UFDF process. Experience with supporting CMO projects and communication with external customers is a plus.
Salary Range:
$100K -- $150K
Minimum Qualification
Process ManagementEstimated Salary: $20 to $28 per hour based on qualifications Show more details...
EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of an interdisciplinary team. Evelo's... vision is to improve the lives of patients with serious diseases through the development of a broadly applicable new modality of medicines. Humans have evolved over millennia with the microbes in and on our bodies. These microbes play a vital role in developing and directing immune and biological responses. Evelo is harnessing the therapeutic potential of specific strains of naturally occurring microbes and developing them as a new class of medicines, monoclonal microbials. We have validated that orally delivered monoclonal microbials modulate immunological and biological effects throughout the body after initial interactions with human cells in the gut. Evelo is pioneering the development of this new class of medicine for the treatment of autoimmune, immunoinflammatory, metabolic, neurological, neuroinflammatory diseases and cancer. This is an outstanding opportunity to join a fast-paced company in a new exciting field of medicine. As a member of the Evelo team, you will be a vital part of helping to shape Evelo's vision:
in transforming therapies through a new modality of medicines. We are seeking a dedicated Senior Downstream Process Development Engineer who is interested in joining a highly dynamic and intellectually challenging team. This position will offer a tremendous opportunity to gain experience in design and scale-up of novel processes. In addition, this role will engage in critical collaborations with our manufacturing, microbiology, immunology, and bioinformatics teams. The successful candidate will be innovative, thrive in an intense and dynamic environment, and use his/her creative and imaginative problem-solving skills to help bring new products to patients. Primary
Responsibilities:
Manage operations and serve as functional area technical expert to support downstream purification and recovery process development activities including centrifugation, depth filtration, tangential flow filtration, chromatography, lyophilization, and spray drying. Lead downstream process development and scaling up activities at laboratory and pilot plant for company's product candidates. Communicate goals of lab processing. Maintain lab organization and records. Perform assays on products, process intermediates, and experimental samples using biotechnical strategies. Conduct range finding studies for improved filtration methods, chromatography steps, and lyophilization. Measure the integrity of filters and verified results to lie within the acceptable range for manufacturing scale. Conduct hands on trouble shooting, process feasibility and process optimization experiments in relation to downstream purification and recovery processes. Develop purification methods to purify various product related impurities to assist product characterization. Assist developed downstream process tech transfer to pilot and GMP manufacturing sites and support pilot and GMP production activities including technical review of development report, tech transfer document, batch records, SOPs, raw material release and production process report. Prepare technical reports and documents to support IND and BLA filing as needed. Desired Skills &
Qualifications:
Strong knowledge of chromatography and membrane purification including affinity, ion exchange, hydrophobic interaction and mixed mode chromatographic separation, and harvest and ultrafiltration/diafiltration (UFDF) membrane processes. Knowledge of drying process development including lyophilization and spray drying. Extensive hands on experience of column packing, AKTA/Unicorn operation and chromatographic purification process development. Operation knowledge and hands on experience of membrane separation process development including depth filtration harvest and UFDF processes. Knowledge and experience with manufacturing production under cGMP regulation. Industry experience with tech transfer and process scaling up in related to downstream purification process. Strong planning and communication skills in a dynamic project environment. Technical support experience in CMO project and communication with external customers is desired. Education &
Experience:
Ph.D. with more than 5 years of biotech industry experience, or M.S with over 8 years of biotech industrial experience directly related to job description or B.S with over 10 years direct biotech industry experience and successful track record. Extensive experience of downstream purification process development, process scale up from lab scale to manufacturing process for production. Experience with tech transfer process from process development to GMP manufacturing site. Understand GMP regulation and FDA/EMA guidance on manufacturing process for biologics. Goal oriented team player with excellent communication skills. Bioengineering knowledge and experience in developing downstream purification process for manufacturing production. Experience in developing high concentration UFDF process. Experience with supporting CMO projects and communication with external customers is a plus.
Salary Range:
$100K -- $150K
Minimum Qualification
Process ManagementEstimated Salary: $20 to $28 per hour based on qualifications Show more details...
via Cambridge, MA - Geebo
posted_at: 3 days agoschedule_type: Full-timesalary: 20–28 an hour
Evelo Biosciences (Nasdaq:
EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry, is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of growing team. Primary
Responsibilities:
Working with the accounting team on general ledger activities,
Evelo Biosciences (Nasdaq:
EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry, is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of growing team. Primary
Responsibilities:
Working with the accounting team on general ledger activities, and supporting monthly/quarterly close, reporting, and internal controls. General Ledger & Risk Compliance Assist the Assistant Controller with close activities including, but not limited to, reconciling balance sheet accounts and preparing excel schedules in support of the month/quarter end close Assist with the quarter end audit by providing support and answering auditor queries in a timely manner Perform tie-out of quarterly SEC filings and assist with support as necessary and preparation of financial statements and footnotes Support... the Assistant Controller with the company's compliance activities relating to SOX controls, such as capital expenditure forms Support the finance team with other reconciliations and schedule preparation, such as corporate credit card reconciliation, weekly cash tracking and 12-week cash forecast preparation, bank reconciliation, etc Oversee processing of equity award activity, calculation of stock compensation expense, and preparation of equity disclosure. Reporting, A/P, System and other Govern finance master data update (e.g. rolls up for department, project and GL account) in NetSuite, Adaptive, Coupa, etc; validate data interface across various financial systems Coordinate with HR, accounting and FP&A to reconcile headcount information, update headcount reporting model, and prepare month end headcount report Track capital and IT related PO and invoices, update FP&A tracking schedule on a monthly basis Responsible for collecting new vendor forms and creation of vendors in accounting and purchasing systems Prepare annual 1099 tax forms for consultants Manage the company's finance shared inbox ensuring queries are communicated to the finance team as needed Support the administrative function in the company's purchasing system
Qualifications:
Bachelor's degree in Accounting/Finance. Early-mid stage biotechnology /Pharmaceutical a strong plus 5-7 years of relevant experience Finance with a preference to public company environments Some payroll experience required but full training will be provided Detail oriented, highly organized and analytical Proven ability to develop relationships within the business and working collaboratively with both internal and external teams a must Netsuite and/or Coupa / Expensify software experience a plus Ability to work in a fast-paced environment and desire to learn and grow
Salary Range:
$80K -- $100K
Minimum Qualification
AccountingEstimated Salary: $20 to $28 per hour based on qualifications Show more details...
EVLO) a biotechnology company developing a new modality of orally delivered, systemically acting biologics that could disrupt the industry, is looking for a highly motivated individual who is energized by the prospect of working in a clinical stage company, has a strong desire to learn, and wishes to be an integral member of growing team. Primary
Responsibilities:
Working with the accounting team on general ledger activities, and supporting monthly/quarterly close, reporting, and internal controls. General Ledger & Risk Compliance Assist the Assistant Controller with close activities including, but not limited to, reconciling balance sheet accounts and preparing excel schedules in support of the month/quarter end close Assist with the quarter end audit by providing support and answering auditor queries in a timely manner Perform tie-out of quarterly SEC filings and assist with support as necessary and preparation of financial statements and footnotes Support... the Assistant Controller with the company's compliance activities relating to SOX controls, such as capital expenditure forms Support the finance team with other reconciliations and schedule preparation, such as corporate credit card reconciliation, weekly cash tracking and 12-week cash forecast preparation, bank reconciliation, etc Oversee processing of equity award activity, calculation of stock compensation expense, and preparation of equity disclosure. Reporting, A/P, System and other Govern finance master data update (e.g. rolls up for department, project and GL account) in NetSuite, Adaptive, Coupa, etc; validate data interface across various financial systems Coordinate with HR, accounting and FP&A to reconcile headcount information, update headcount reporting model, and prepare month end headcount report Track capital and IT related PO and invoices, update FP&A tracking schedule on a monthly basis Responsible for collecting new vendor forms and creation of vendors in accounting and purchasing systems Prepare annual 1099 tax forms for consultants Manage the company's finance shared inbox ensuring queries are communicated to the finance team as needed Support the administrative function in the company's purchasing system
Qualifications:
Bachelor's degree in Accounting/Finance. Early-mid stage biotechnology /Pharmaceutical a strong plus 5-7 years of relevant experience Finance with a preference to public company environments Some payroll experience required but full training will be provided Detail oriented, highly organized and analytical Proven ability to develop relationships within the business and working collaboratively with both internal and external teams a must Netsuite and/or Coupa / Expensify software experience a plus Ability to work in a fast-paced environment and desire to learn and grow
Salary Range:
$80K -- $100K
Minimum Qualification
AccountingEstimated Salary: $20 to $28 per hour based on qualifications Show more details...
via Cambridge, MA - Geebo
posted_at: 2 days agoschedule_type: Full-timesalary: 20–28 an hour
This is an outstanding leadership opportunity to join a fast-paced company in a new exciting field of medicine. Evelo Biosciences is dedicated to improving the lives of patients globally through the development of monoclonal microbials. As a member of the Evelo team, you will be a vital part of helping to shape Evelo's vision:
transforming therapies through a new modality of medicines. We are... seeking a Head of Formulation Development who is interested
This is an outstanding leadership opportunity to join a fast-paced company in a new exciting field of medicine. Evelo Biosciences is dedicated to improving the lives of patients globally through the development of monoclonal microbials. As a member of the Evelo team, you will be a vital part of helping to shape Evelo's vision:
transforming therapies through a new modality of medicines. We are... seeking a Head of Formulation Development who is interested in joining a highly dynamic and intellectually challenging team. This leadership role will afford a qualified candidate an opportunity to work in an innovative, fast paced environment and shape Evelo's vision to bring new products to patients. Reporting into the VP-Head of Process Development, the successful candidate will be responsible for establishing and leading Evelo's drug product development function and strategy. As a member of the Process Development Leadership team, this leadership role will afford a qualified candidate the opportunity to work in an innovative, fast-paced environment and shape Evelo's global vision to bring a new modality of products to patients. We are seeking a proven leader, to drive the strategy, development, scale-up, and execution of oral solid-dosage form processes supporting early and late-stage process development, internal R&D and global manufacturing. This individual will lead the Drug Product development team, including pre-formulation, formulation, scale-up and manufacture for a new class of orally-delivered biological medicines. The scope spans the development of novel early-stage processes and formulations, and the late-stage translation to commercialization of our lead products. With a proven track record of late-stage development and commercialization in complex biologic products, the ideal candidate will be leading and growing the drug product function in the development and optimization of a new biological product modality spanning pilot-scale, pivotal, and commercial batch manufacturing. They will also be responsible for the overall drug product programs, development of the team and function, authoring/reviewing technical and manufacturing reports and regulatory submissions such as IND, IMPD, BLA. Primary
Responsibilities:
Define and execute overall strategies for drug product development within Evelo Build and mentor a strong technical team and function. Lead and oversee all facets of formulation development and drug delivery internally and through the management of CMOs and CROs Provide technical leadership of technology transfers and drug product GMP clinical manufacturing Author CMC related sections for regulatory filings and development reports Deliver technological innovation in drug product process, formulation development and drug delivery Partner with the CMC development teams to successfully deliver the program objectives Desired Skills &
Qualifications:
A self-starter and strategic thinker with a demonstrated ability to drive results and lead innovation. Proven ability to drive technical strategy, as well as, lead and influence cross-functional teams. Successful in developing and broadly communicating cross-functional technical strategy and direction in support of CMC deliverables Outstanding track record of collaboration, stakeholder relationship management, and influencing key decision makers. Demonstrated understanding of industry trends, practices, techniques, and standards which impact the business and can translate that knowledge into action plans. Strong analytical skills and ability to distill key information from various data sources. Demonstrated technical project management and/or project leadership experience Proven ability to operate with a high level of ambiguity, while making sound and timely decisions based on project priorities and risk assessments. Demonstrated experience in leading and mentoring talent. Excellent communication skills - written and verbal. Ability to travel up to 30% Education &
Experience:
The successful candidate will have a MS/Ph. D in Chemical Engineering, Pharmaceutical Sciences, Pharmacy, Biochemistry, Materials Science, or related field. Minimum of 12 years of experience in oral-solid dosage formulation and development. Previous experience with biologics and/or bacteria products is a plus. Substantial experience in supporting drug product development from early clinical to commercial launch. Broad understanding of Drug Development and critical functional interfaces. Recognized as an expert in product and formulation development, scale-up, tech transfer, and manufacturing support. Significant technical project management and/or project leadership experience Ability to travel up to 30% About Evelo Evelo Biosciences is dedicated to improving the lives of patients globally through the development of a new modality of medicines - monoclonal microbials. Monoclonal microbials are orally delivered medicines that modulate systemic immunology and biology through direct interactions with human cells in the gut. These new medicines are broadly applicable across many diseases - including autoimmune, immunoinflammatory, metabolic, neurological, neuroinflammatory diseases and cancer. Monoclonal microbials have the potential to fundamentally change traditional models of drug discovery and development. By finding and selecting naturally occurring monoclonal microbials with defined therapeutic effects, Evelo can improve the speed, cost and success of drug discovery and development. Evelo's platform enables pharmacological intervention at all stages of disease with naturally occurring, safe and effective monoclonal microbials. Evelo currently has product four candidates in development:
EDP1815, EDP1867, EDP1622 and EDP2939 for the treatment of inflammatory diseases including psoriasis, atopic dermatitis, and COVID-19, and EDP1503 for the treatment of cancer. Evelo is advancing additional product candidates in other disease areas. For more information, please visit www.evelobio.com and engage with Evelo on LinkedIn. Notice:
Roles that take place fully on-site/in office will require Covid-19 vaccination. Please note that this role is a fully on-site role in our Cambridge, MA office.
Salary Range:
$200K -- $250K
Minimum Qualification
Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications Show more details...
transforming therapies through a new modality of medicines. We are... seeking a Head of Formulation Development who is interested in joining a highly dynamic and intellectually challenging team. This leadership role will afford a qualified candidate an opportunity to work in an innovative, fast paced environment and shape Evelo's vision to bring new products to patients. Reporting into the VP-Head of Process Development, the successful candidate will be responsible for establishing and leading Evelo's drug product development function and strategy. As a member of the Process Development Leadership team, this leadership role will afford a qualified candidate the opportunity to work in an innovative, fast-paced environment and shape Evelo's global vision to bring a new modality of products to patients. We are seeking a proven leader, to drive the strategy, development, scale-up, and execution of oral solid-dosage form processes supporting early and late-stage process development, internal R&D and global manufacturing. This individual will lead the Drug Product development team, including pre-formulation, formulation, scale-up and manufacture for a new class of orally-delivered biological medicines. The scope spans the development of novel early-stage processes and formulations, and the late-stage translation to commercialization of our lead products. With a proven track record of late-stage development and commercialization in complex biologic products, the ideal candidate will be leading and growing the drug product function in the development and optimization of a new biological product modality spanning pilot-scale, pivotal, and commercial batch manufacturing. They will also be responsible for the overall drug product programs, development of the team and function, authoring/reviewing technical and manufacturing reports and regulatory submissions such as IND, IMPD, BLA. Primary
Responsibilities:
Define and execute overall strategies for drug product development within Evelo Build and mentor a strong technical team and function. Lead and oversee all facets of formulation development and drug delivery internally and through the management of CMOs and CROs Provide technical leadership of technology transfers and drug product GMP clinical manufacturing Author CMC related sections for regulatory filings and development reports Deliver technological innovation in drug product process, formulation development and drug delivery Partner with the CMC development teams to successfully deliver the program objectives Desired Skills &
Qualifications:
A self-starter and strategic thinker with a demonstrated ability to drive results and lead innovation. Proven ability to drive technical strategy, as well as, lead and influence cross-functional teams. Successful in developing and broadly communicating cross-functional technical strategy and direction in support of CMC deliverables Outstanding track record of collaboration, stakeholder relationship management, and influencing key decision makers. Demonstrated understanding of industry trends, practices, techniques, and standards which impact the business and can translate that knowledge into action plans. Strong analytical skills and ability to distill key information from various data sources. Demonstrated technical project management and/or project leadership experience Proven ability to operate with a high level of ambiguity, while making sound and timely decisions based on project priorities and risk assessments. Demonstrated experience in leading and mentoring talent. Excellent communication skills - written and verbal. Ability to travel up to 30% Education &
Experience:
The successful candidate will have a MS/Ph. D in Chemical Engineering, Pharmaceutical Sciences, Pharmacy, Biochemistry, Materials Science, or related field. Minimum of 12 years of experience in oral-solid dosage formulation and development. Previous experience with biologics and/or bacteria products is a plus. Substantial experience in supporting drug product development from early clinical to commercial launch. Broad understanding of Drug Development and critical functional interfaces. Recognized as an expert in product and formulation development, scale-up, tech transfer, and manufacturing support. Significant technical project management and/or project leadership experience Ability to travel up to 30% About Evelo Evelo Biosciences is dedicated to improving the lives of patients globally through the development of a new modality of medicines - monoclonal microbials. Monoclonal microbials are orally delivered medicines that modulate systemic immunology and biology through direct interactions with human cells in the gut. These new medicines are broadly applicable across many diseases - including autoimmune, immunoinflammatory, metabolic, neurological, neuroinflammatory diseases and cancer. Monoclonal microbials have the potential to fundamentally change traditional models of drug discovery and development. By finding and selecting naturally occurring monoclonal microbials with defined therapeutic effects, Evelo can improve the speed, cost and success of drug discovery and development. Evelo's platform enables pharmacological intervention at all stages of disease with naturally occurring, safe and effective monoclonal microbials. Evelo currently has product four candidates in development:
EDP1815, EDP1867, EDP1622 and EDP2939 for the treatment of inflammatory diseases including psoriasis, atopic dermatitis, and COVID-19, and EDP1503 for the treatment of cancer. Evelo is advancing additional product candidates in other disease areas. For more information, please visit www.evelobio.com and engage with Evelo on LinkedIn. Notice:
Roles that take place fully on-site/in office will require Covid-19 vaccination. Please note that this role is a fully on-site role in our Cambridge, MA office.
Salary Range:
$200K -- $250K
Minimum Qualification
Life SciencesEstimated Salary: $20 to $28 per hour based on qualifications Show more details...
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