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 role is to ensure purity of research and GMP materials.Responsibilities:*Maintain, clean, and sterilize manufacturing equipment.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:*Organization*Attention to detail*DocumentationEducation:High SchoolExperience:0-1 yearsQualifications:*High school diploma or general education degree (GED); or one to three months related experience and/or training*Experience working in a GMP facility or pharmaceutical environment is preferred 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 ensure purity of research and GMP materials.Responsibilities:*Maintain, clean, and sterilize manufacturing equipment.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:*Organization*Attention to detail*DocumentationEducation:High SchoolExperience:0-1 yearsQualifications:*High school diploma or general education degree (GED); or one to three months related experience and/or training*Experience working in a GMP facility or pharmaceutical environment is preferred 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 ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:*Review all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. 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 ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:*Review all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. 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.
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