Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:*Oversee employees.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*Excellent written and oral communication skills.*Ability to work in a clean room environment for extended periods of time.*Ability to wear and work in PPE.Education:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:*Oversee employees.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*Excellent written and oral communication skills.*Ability to work in a clean room environment for extended periods of time.*Ability to wear and work in PPE.Education:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this position is assay assessment, development, implementation, and validation for use evaluating human biologic drug products manufactured in a cGMP lab. Must be up to date on all methods for QC testing. Set-up, organization, and day to day operations of a QC laboratory.Responsibilities:*Must be able to organize all accumulated data*Keep notebooks up to date and signed*Write protocols for test method validation*Write development reports, validation, and all other relevant technical reports*Write SOPs, testing records, protocols*Responsible for in-process testing*Responsible for release testing*Responsible for stability testing. *Responsible for Method Qualification and Validation.*Must be able to Qualify USP/compendia methods*Responsible for transfer of assays, test method validation, and qualification of new equipment.Working hours: 8:00 AM - 5:00 PMSkills:*Gel electrophoresis*ELISA assays'*HPLC Analysis of Plasmid iso-forms*qPCR gene expression and genomic *Mammalian cell culture and transfection*Wet Chemistry* Experience with Spectramax, qPCR software, HPLC software, Gel imaging software.Education:BachelorsExperience:4-7 yearsQualifications:*Life Sciences Bachelor's degree and 3+ years of relevant experience in molecular biology, microbiology, or chemistry. *2-5 years of assay development experience.*Experience with qPCR is required*Experience with chromatography, gel electrolysis, and microbiology techniques *Method development and optimization in a cGMP environment www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this position is assay assessment, development, implementation, and validation for use evaluating human biologic drug products manufactured in a cGMP lab. Must be up to date on all methods for QC testing. Set-up, organization, and day to day operations of a QC laboratory.Responsibilities:*Must be able to organize all accumulated data*Keep notebooks up to date and signed*Write protocols for test method validation*Write development reports, validation, and all other relevant technical reports*Write SOPs, testing records, protocols*Responsible for in-process testing*Responsible for release testing*Responsible for stability testing. *Responsible for Method Qualification and Validation.*Must be able to Qualify USP/compendia methods*Responsible for transfer of assays, test method validation, and qualification of new equipment.Working hours: 8:00 AM - 5:00 PMSkills:*Gel electrophoresis*ELISA assays'*HPLC Analysis of Plasmid iso-forms*qPCR gene expression and genomic *Mammalian cell culture and transfection*Wet Chemistry* Experience with Spectramax, qPCR software, HPLC software, Gel imaging software.Education:BachelorsExperience:4-7 yearsQualifications:*Life Sciences Bachelor's degree and 3+ years of relevant experience in molecular biology, microbiology, or chemistry. *2-5 years of assay development experience.*Experience with qPCR is required*Experience with chromatography, gel electrolysis, and microbiology techniques *Method development and optimization in a cGMP environment www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
Spherion Staffing has partnered with FUJIFILM Diosynth Biotechnologies to recruit for this role. This is an exciting opportunity to be a part of the cutting-edge project of COVID-19 vaccine production. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department, working in various manufacturing operations such as vaccine and therapeutic production.Responsibilities:- Opportunity to work with protein purification, various filtration systems, and cell cultivation- Operation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.- Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records, training provided- Responsible for learning and applying current Good Manufacturing PracticeWorking hours: 6:00 AM - 6:00 PM (Various Shifts Available)Skills:- Excellent oral and written communication skills, interpersonal and organizational skills.- Ability to receive training in various filtration and analytical techniques- Good self-discipline and attention to detail.- Must be able to work flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary. - Must be able to work alternative shift hours and weekends as required.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:- Must express strong interest in a career preferably in Chemistry, Biology, Life Sciences or related fieldThe physical demands described here are representative of those that must be met by an employee tosuccessfully perform the essential functions of this job. Reasonable accommodations may be made toenable individuals with disabilities to perform the essential functions. While performing the duties ofthis job, the employee is regularly required to:- Experience prolonged standing, bending, stooping, twisting, and stretching.- Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.- Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves- Lift and/or move 25-50 pounds frequently.- Attendance is mandatory.Additional working conditions & physical requirements for some positions:- No make-up or jewelry can be worn when working in the clean room environment.- Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply and a recruiter will reach out to schedule an interview after reviewing your application!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
Spherion Staffing has partnered with FUJIFILM Diosynth Biotechnologies to recruit for this role. This is an exciting opportunity to be a part of the cutting-edge project of COVID-19 vaccine production. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department, working in various manufacturing operations such as vaccine and therapeutic production.Responsibilities:- Opportunity to work with protein purification, various filtration systems, and cell cultivation- Operation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.- Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records, training provided- Responsible for learning and applying current Good Manufacturing PracticeWorking hours: 6:00 AM - 6:00 PM (Various Shifts Available)Skills:- Excellent oral and written communication skills, interpersonal and organizational skills.- Ability to receive training in various filtration and analytical techniques- Good self-discipline and attention to detail.- Must be able to work flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary. - Must be able to work alternative shift hours and weekends as required.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:- Must express strong interest in a career preferably in Chemistry, Biology, Life Sciences or related fieldThe physical demands described here are representative of those that must be met by an employee tosuccessfully perform the essential functions of this job. Reasonable accommodations may be made toenable individuals with disabilities to perform the essential functions. While performing the duties ofthis job, the employee is regularly required to:- Experience prolonged standing, bending, stooping, twisting, and stretching.- Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.- Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves- Lift and/or move 25-50 pounds frequently.- Attendance is mandatory.Additional working conditions & physical requirements for some positions:- No make-up or jewelry can be worn when working in the clean room environment.- Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply and a recruiter will reach out to schedule an interview after reviewing your application!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.