Jobot
This Jobot Job is hosted by:
Juan CorreaAre you a fit? Easy Apply now by clicking the Quick Apply button and sending us your resume.
Salary:
$80,000 - $100,000 per yearA bit about us:
We develop innovative gene therapies to treat cancer and prolong patient survival.
We synergistically kill tumors while activating the immune system to fight the patient's cancer, combined with the integration of novel companion diagnostics positions us on the cutting edge of cancer immunotherapies and emerging clinical-stage cancer companies.
Why join us? 401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Life insuranceJob DetailsGeneral Job Description/Team Overview:
As part of a talented and multi-disciplinary team advancing an exciting new approach to genetherapy drug discovery, development, and manufacturing, the successful candidate will supportthe QC operations and work in a laboratory environment under the direction of the QC Manager.
The candidate will be setting up, validating, and executing assays for analysis and release ofretroviral gene therapy products and raw materials.
The position will involve working withanalytical instrumentation (i.
e.
, ddPCR, PCR, high-throughput automated fluorescence andluminescence systems, robotic nucleic acid and protein extraction system, FTIR, particle analyzer,osmometer), as well as a variety of chemical and biological assays, and reporting results.
Thecandidate will interact with R&D, process development, production, quality, and technical teams,as well as contract labs on analytical testing projects.
The level will be determined based upon thecandidate's education, skills, and/or related experience.
Primary Duties and Responsibilities (include but are not limited to):
? Perform assigned testing in a timely and organized manner in compliance with theapplicable GLP, cGMP, safety, and environmental regulations, as well as company policiesand procedures.
? Test raw materials, in-process samples, finished products, and validation and stabilitysamples to ensure conformity to standards and specifications.
? Work with retroviral gene therapy products and associated assays (ddPCR, PCR, cell-basedpotency assays, virus infection, and proliferation assays, ELISA, kinetics, SDS PAGE,agarose gel, western blot, etc.
).
? Lead analytical method development/optimization/qualification and stability studyprojects.
? Operate, calibrate, troubleshoot and maintain analytical equipment.
Assist in laboratoryequipment qualifications (IQ, OQ, PQ, and MQ).
? Serve as subject matter expert for assigned assays.
Job Description:
Senior QC Analyst? Evaluate and implement new techniques and technologies.
? Draft Standard Operating Procedures (SOPs), analytical technical reports, methodvalidation, and stability protocols and reports.
Conduct literature searches to identifysuitable methods.
? Train junior analysts in new procedures and basic to complex laboratory troubleshootingtechniques.
? Support investigations to determine the root cause of deviations and out ofspecification/trend results and implement appropriate corrective and preventative actionsin a timely manner.
? Maintain organized, accurate, and complete laboratory notebooks and records.
? Assist in general upkeep of laboratory and maintain a clean work environment.
? Perform other duties as assigned.
Required
Qualifications:
? Bachelor's or Master's (preferred) degree in Chemistry, Biochemistry, BiologicalSciences, or related field with a minimum of 4 to 6 years analytical laboratory experiencein the industry (biotech/pharma company).
? Must be proficient in mammalian cell culture and aseptic techniques, cell-based assay,PCR, ELISA, gel electrophoresis, FTIR, and wet chemistry.
Knowledge of retroviral genetherapy assays and techniques is a plus.
? Strong ability in troubleshooting and problem solving with methods and instrumentation.
? Familiar with current GLP/cGMP, FDA, ICH, USP, and ISO regulations and guidelines,laboratory documentation, safety, and environmental requirements.
? Time management skills to optimize the analysis process and perform multiple tasks at thesame time.
? Advanced level of written and verbal communication skills with the ability to readtechnical procedures and governmental regulations and guidelines.
Able to write reports,and required quality control documentation.
? Support quality and continuous improvement processes.
Willing to complete continuededucation coursework, training, or certification in quality control laboratory skills to fulfillassigned duties, as necessary.
? Able to understand statistics and statistical software to interpret experimental results.
Job Description:
Senior QC Analyst? Able to stand prolonged periods and lift 30 lbs.
? General knowledge of Federal and State regulatory requirements in a GxP environment.
? Proficient in computer skills including Microsoft Office (Word, Excel, PowerPoint) andothers as applicable.
? Excellent organization skills with attention to detail and accurate record keeping.
? High degree of discretion dealing with confidential information.
? Ability and willingness to work flexible hours when needed.
? Demonstrated ability to work independently and in a team environment.
? Excellent written, verbal, and interpersonal communication skills.
? Eligible to work in the U.
S.
Interested in hearing more? Easy Apply now by clicking the Quick Apply button.
Benefits:
401K, Employee Events, Employee Referral Program, Flexible Schedules, Free Food and Coffee, Game Rooms, Life Insurance, Maternity/Paternity Paid Leave, Medical, Dental and Vision, On Site Cafeteria, Paid Holidays, Paid sick days, Parking , Performance bonus, Professional Development, Retirement / Pension Plans, Vacation/paid time off, Work From HomeAbout the Company:
Jobot Company Size:
500 to 999 employeesIndustry:
Biotechnology/PharmaceuticalsFounded:
2018Website:
https:
//jobot.
com/.
Estimated Salary: $20 to $28 per hour based on qualifications.
Juan CorreaAre you a fit? Easy Apply now by clicking the Quick Apply button and sending us your resume.
Salary:
$80,000 - $100,000 per yearA bit about us:
We develop innovative gene therapies to treat cancer and prolong patient survival.
We synergistically kill tumors while activating the immune system to fight the patient's cancer, combined with the integration of novel companion diagnostics positions us on the cutting edge of cancer immunotherapies and emerging clinical-stage cancer companies.
Why join us? 401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Life insuranceJob DetailsGeneral Job Description/Team Overview:
As part of a talented and multi-disciplinary team advancing an exciting new approach to genetherapy drug discovery, development, and manufacturing, the successful candidate will supportthe QC operations and work in a laboratory environment under the direction of the QC Manager.
The candidate will be setting up, validating, and executing assays for analysis and release ofretroviral gene therapy products and raw materials.
The position will involve working withanalytical instrumentation (i.
e.
, ddPCR, PCR, high-throughput automated fluorescence andluminescence systems, robotic nucleic acid and protein extraction system, FTIR, particle analyzer,osmometer), as well as a variety of chemical and biological assays, and reporting results.
Thecandidate will interact with R&D, process development, production, quality, and technical teams,as well as contract labs on analytical testing projects.
The level will be determined based upon thecandidate's education, skills, and/or related experience.
Primary Duties and Responsibilities (include but are not limited to):
? Perform assigned testing in a timely and organized manner in compliance with theapplicable GLP, cGMP, safety, and environmental regulations, as well as company policiesand procedures.
? Test raw materials, in-process samples, finished products, and validation and stabilitysamples to ensure conformity to standards and specifications.
? Work with retroviral gene therapy products and associated assays (ddPCR, PCR, cell-basedpotency assays, virus infection, and proliferation assays, ELISA, kinetics, SDS PAGE,agarose gel, western blot, etc.
).
? Lead analytical method development/optimization/qualification and stability studyprojects.
? Operate, calibrate, troubleshoot and maintain analytical equipment.
Assist in laboratoryequipment qualifications (IQ, OQ, PQ, and MQ).
? Serve as subject matter expert for assigned assays.
Job Description:
Senior QC Analyst? Evaluate and implement new techniques and technologies.
? Draft Standard Operating Procedures (SOPs), analytical technical reports, methodvalidation, and stability protocols and reports.
Conduct literature searches to identifysuitable methods.
? Train junior analysts in new procedures and basic to complex laboratory troubleshootingtechniques.
? Support investigations to determine the root cause of deviations and out ofspecification/trend results and implement appropriate corrective and preventative actionsin a timely manner.
? Maintain organized, accurate, and complete laboratory notebooks and records.
? Assist in general upkeep of laboratory and maintain a clean work environment.
? Perform other duties as assigned.
Required
Qualifications:
? Bachelor's or Master's (preferred) degree in Chemistry, Biochemistry, BiologicalSciences, or related field with a minimum of 4 to 6 years analytical laboratory experiencein the industry (biotech/pharma company).
? Must be proficient in mammalian cell culture and aseptic techniques, cell-based assay,PCR, ELISA, gel electrophoresis, FTIR, and wet chemistry.
Knowledge of retroviral genetherapy assays and techniques is a plus.
? Strong ability in troubleshooting and problem solving with methods and instrumentation.
? Familiar with current GLP/cGMP, FDA, ICH, USP, and ISO regulations and guidelines,laboratory documentation, safety, and environmental requirements.
? Time management skills to optimize the analysis process and perform multiple tasks at thesame time.
? Advanced level of written and verbal communication skills with the ability to readtechnical procedures and governmental regulations and guidelines.
Able to write reports,and required quality control documentation.
? Support quality and continuous improvement processes.
Willing to complete continuededucation coursework, training, or certification in quality control laboratory skills to fulfillassigned duties, as necessary.
? Able to understand statistics and statistical software to interpret experimental results.
Job Description:
Senior QC Analyst? Able to stand prolonged periods and lift 30 lbs.
? General knowledge of Federal and State regulatory requirements in a GxP environment.
? Proficient in computer skills including Microsoft Office (Word, Excel, PowerPoint) andothers as applicable.
? Excellent organization skills with attention to detail and accurate record keeping.
? High degree of discretion dealing with confidential information.
? Ability and willingness to work flexible hours when needed.
? Demonstrated ability to work independently and in a team environment.
? Excellent written, verbal, and interpersonal communication skills.
? Eligible to work in the U.
S.
Interested in hearing more? Easy Apply now by clicking the Quick Apply button.
Benefits:
401K, Employee Events, Employee Referral Program, Flexible Schedules, Free Food and Coffee, Game Rooms, Life Insurance, Maternity/Paternity Paid Leave, Medical, Dental and Vision, On Site Cafeteria, Paid Holidays, Paid sick days, Parking , Performance bonus, Professional Development, Retirement / Pension Plans, Vacation/paid time off, Work From HomeAbout the Company:
Jobot Company Size:
500 to 999 employeesIndustry:
Biotechnology/PharmaceuticalsFounded:
2018Website:
https:
//jobot.
com/.
Estimated Salary: $20 to $28 per hour based on qualifications.
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