The Quality Control Technician monitors adherence to policies and procedures to ensure that quality standards are met from raw material receipt through shipment of finishedproducts. They are responsible for following Standard Operating Procedures to ensure compliance to the cGMP requirements in OTC and Medical Device manufacturing. In addition, they provide regular feedback to the Operations Manager, Laboratory Manager, and other team members to ensure full understanding and compliance with defined protocols.Responsibilities:-Quality control analyses for in-process manufacturing operations-Quality control analyses required for release of incoming raw materials-Quality control analyses required for release of finished goods-Analysis of products undergoing stability-Participation in Validation activities (Method Validation, Process Validation, Cleaning Validation, etc.)-Maintenance of a calibration schedule for facility instruments and equipment (scales, pH meters, spectrophotometers, etc.)Working hours: 8:00 AM - 5:00 PMSkills:-Maintenance of a well-kept laboratory notebook-Generation of Quality System documentation such as: Quality Incoming Inspection forms, Certificates of Analysis, and Deviations-Reporting observed OOS results to the Laboratory Manager and participating in resulting investigations.Education:AssociateExperience:1-4 yearsQualifications:Minimum A.A. or A.S. in Chemistry, Biology, Biotechnology, or related scientific discipline, or 2 years of laboratory experience-Experience with organoleptic, titrimetric, spectrophotometric, andviscometric technique and instrumentation preferred-cGMP experience is a plus-Good verbal and written communication skills-Good organizational skills-Knowledgeable in Microsoft Office Suite (Word and Excel minimum) Please consider and apply today. Wonderful opportunity for the educated and experienced lab QC Technician.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. 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.
The Quality Control Technician monitors adherence to policies and procedures to ensure that quality standards are met from raw material receipt through shipment of finishedproducts. They are responsible for following Standard Operating Procedures to ensure compliance to the cGMP requirements in OTC and Medical Device manufacturing. In addition, they provide regular feedback to the Operations Manager, Laboratory Manager, and other team members to ensure full understanding and compliance with defined protocols.Responsibilities:-Quality control analyses for in-process manufacturing operations-Quality control analyses required for release of incoming raw materials-Quality control analyses required for release of finished goods-Analysis of products undergoing stability-Participation in Validation activities (Method Validation, Process Validation, Cleaning Validation, etc.)-Maintenance of a calibration schedule for facility instruments and equipment (scales, pH meters, spectrophotometers, etc.)Working hours: 8:00 AM - 5:00 PMSkills:-Maintenance of a well-kept laboratory notebook-Generation of Quality System documentation such as: Quality Incoming Inspection forms, Certificates of Analysis, and Deviations-Reporting observed OOS results to the Laboratory Manager and participating in resulting investigations.Education:AssociateExperience:1-4 yearsQualifications:Minimum A.A. or A.S. in Chemistry, Biology, Biotechnology, or related scientific discipline, or 2 years of laboratory experience-Experience with organoleptic, titrimetric, spectrophotometric, andviscometric technique and instrumentation preferred-cGMP experience is a plus-Good verbal and written communication skills-Good organizational skills-Knowledgeable in Microsoft Office Suite (Word and Excel minimum) Please consider and apply today. Wonderful opportunity for the educated and experienced lab QC Technician.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. 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.
QA Lab Technician job summary:Local bottler in need of 4 QA Lab Technicians doing lab testing of packaging, labels, water and syrups for a leading international bottling and beverage company. Will be documenting all results into SAP data base. Must have quality and lab experience or laboratory schooling. Must be analytical, attention to detail and computer and data entry skills. Hours are 12 hour rotating shifts working 5:45am-6:15pm for days and 5:45pm-6:15am for nights. Will work 2 days/nights on and 2 days/nights off depending on day or night shift and working every other weekend Fri-Sun. Pay will be $15.25/hr. These are long term temporary positions with the possibility permanent hire.Responsibilities:QA Lab Technician job responsibilities:* Perform quality control tests in the lab as well as on-site when necessary* Recognize and report any food safety issues* Assist with testing and calibrating lab equipment in preparation for specific tasks* Prepare samples prior to shipping them to customers* Perform quality control tests on ingredients, completed products and product samples* Follow all company policies and procedures to ensure product integrity and quality control* Analyze retrieved data and prepare reports for laboratory managementWorking hours: Various Shifts AvailableSkills:QA Lab Tech skills:* Quality and lab exp or schooling* Analytical* Attention to detail* Computer and data entry skillsEducation:AssociateExperience:1-4 yearsQualifications:QA Lab Tech qualifications:* High School diploma or equivalent required; Associate degree a plus* Capable of prioritizing tasks to meet goals and ensure product quality* 1+ years' laboratory experience in food manufacturing environment* Ability to communicate effectively* Attention to detail Please apply onlineSpherion 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.
QA Lab Technician job summary:Local bottler in need of 4 QA Lab Technicians doing lab testing of packaging, labels, water and syrups for a leading international bottling and beverage company. Will be documenting all results into SAP data base. Must have quality and lab experience or laboratory schooling. Must be analytical, attention to detail and computer and data entry skills. Hours are 12 hour rotating shifts working 5:45am-6:15pm for days and 5:45pm-6:15am for nights. Will work 2 days/nights on and 2 days/nights off depending on day or night shift and working every other weekend Fri-Sun. Pay will be $15.25/hr. These are long term temporary positions with the possibility permanent hire.Responsibilities:QA Lab Technician job responsibilities:* Perform quality control tests in the lab as well as on-site when necessary* Recognize and report any food safety issues* Assist with testing and calibrating lab equipment in preparation for specific tasks* Prepare samples prior to shipping them to customers* Perform quality control tests on ingredients, completed products and product samples* Follow all company policies and procedures to ensure product integrity and quality control* Analyze retrieved data and prepare reports for laboratory managementWorking hours: Various Shifts AvailableSkills:QA Lab Tech skills:* Quality and lab exp or schooling* Analytical* Attention to detail* Computer and data entry skillsEducation:AssociateExperience:1-4 yearsQualifications:QA Lab Tech qualifications:* High School diploma or equivalent required; Associate degree a plus* Capable of prioritizing tasks to meet goals and ensure product quality* 1+ years' laboratory experience in food manufacturing environment* Ability to communicate effectively* Attention to detail Please apply onlineSpherion 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 a bio-pharmaceutical industry leader to recruit for this role. The responsibilities for the position include: QC assays, testing, documentation, QC analysis, and validation.Responsibilities:- QC Assays (ELISA Assays, HPLC Analysis of Plasmid iso-forms, Wet Chemistry Techniques)- Testing- Documentation (write protocols for test method validation and Qualifications, write development reports, validation, and other relevant technical reports)- QC Analysis (HPLC software)- Validation (Qualification of USP/compendia methods, Tech transfer of assays, Test Method validation, Qualification of new equipment)Working hours: 12:00 AM - 12:00 PM (Various Shifts Available)Skills:- Assay development experience- Experience with gPCR is a must- Method development and optimization experience in a cGMP environment a plus- Experience with chromatography, gel electrophoresis, and microbiology techniques are preferredEducation:BachelorsExperience:1-4 yearsQualifications:Candidates should have a Bachelor???s or Associate's degree and 3+ years of relevant experience and 2-5 years of assay development experience Apply today at 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 responsibilities for the position include: QC assays, testing, documentation, QC analysis, and validation.Responsibilities:- QC Assays (ELISA Assays, HPLC Analysis of Plasmid iso-forms, Wet Chemistry Techniques)- Testing- Documentation (write protocols for test method validation and Qualifications, write development reports, validation, and other relevant technical reports)- QC Analysis (HPLC software)- Validation (Qualification of USP/compendia methods, Tech transfer of assays, Test Method validation, Qualification of new equipment)Working hours: 12:00 AM - 12:00 PM (Various Shifts Available)Skills:- Assay development experience- Experience with gPCR is a must- Method development and optimization experience in a cGMP environment a plus- Experience with chromatography, gel electrophoresis, and microbiology techniques are preferredEducation:BachelorsExperience:1-4 yearsQualifications:Candidates should have a Bachelor???s or Associate's degree and 3+ years of relevant experience and 2-5 years of assay development experience Apply today at 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- Perform preventative maintenance- Document activities as required for GMP materials- Manage supplies inventoryWorking 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 trainingExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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- Perform preventative maintenance- Document activities as required for GMP materials- Manage supplies inventoryWorking 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 trainingExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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 monitor and organize the Quality Control Lab.Responsibilities:- Quality control of assays- Documentation/administration of data- Write Standard Operating Procedures- Data entry into various software systemsWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to receive training in current Good Manufacturing Practice regulations- Ability to wear and work in PPE- Tech savvyEducation:BachelorsExperience:1-4 yearsQualifications:Bachelor's or Associate's degree or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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 monitor and organize the Quality Control Lab.Responsibilities:- Quality control of assays- Documentation/administration of data- Write Standard Operating Procedures- Data entry into various software systemsWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to receive training in current Good Manufacturing Practice regulations- Ability to wear and work in PPE- Tech savvyEducation:BachelorsExperience:1-4 yearsQualifications:Bachelor's or Associate's degree or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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 manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Prepare solutions to be used in the manufacturing process- Follow validation protocols- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to receive training in current GMP regulations- Ability to wear and work in PPEEducation:BachelorsExperience:4-7 yearsQualifications:Bachelor's or Associate's degree in a science related field or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment Apply today at 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 manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Prepare solutions to be used in the manufacturing process- Follow validation protocols- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to receive training in current GMP regulations- Ability to wear and work in PPEEducation:BachelorsExperience:4-7 yearsQualifications:Bachelor's or Associate's degree in a science related field or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment Apply today at 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 and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.- Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations- Assist in routine internal audits, review deviations and investigations- Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's)Working hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Meticulous organizational skills and demonstrating meticulous documentation and record review practices- Technical writing experienceEducation:BachelorsExperience:1-4 yearsQualifications:- Associate's degree and/or one to three years of relevant experience- Must have previous technical writing experience- Experience working in a GMP facility or pharmaceutical environment is preferred- Experience with microbiology techniques is preferred Apply today at 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 and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.- Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations- Assist in routine internal audits, review deviations and investigations- Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's)Working hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Meticulous organizational skills and demonstrating meticulous documentation and record review practices- Technical writing experienceEducation:BachelorsExperience:1-4 yearsQualifications:- Associate's degree and/or one to three years of relevant experience- Must have previous technical writing experience- Experience working in a GMP facility or pharmaceutical environment is preferred- Experience with microbiology techniques is preferred Apply today at 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 provide software validation and equipment calibration to support manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor?s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today at 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 provide software validation and equipment calibration to support manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor?s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today at 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.
Join the Biotech movement in North Carolina as a Material Coordinator Associate. This position is responsible for performing all warehouse staging, shipping and receiving functions including proper receipt and handling of all materials and items entering the receiving and shipping sectors of the facility essential to plant operations.Responsibilities:1.Uploads, pulls, and moves finished goods, inventoried and non-inventoried materials via manual handling and fork truck operation. Palletizes, stacks, and shrink wraps materials to facilitate warehousing and distribution operations. 2.Inspects and verifies item counts against freight bills, bills of lading, inter-branch, and packing forwarders and samples shipping orders of materials to be shipped.3.Separates, identifies, and receives materials against purchase and credit orders and enters purchase materials receipts via computer data entry/bar code systems for inventory control.4.Moves, transfers, and distributes materials to facilitate plant operations or customer support according to standard operating procedures. Uses computer to inquire on inventory status and via the inventory bar code system program to move and/or transfer inventory by data entry of item, lot, quantity, and location destinations for finished goods and other inventoried materials.5.Performs miscellaneous warehousing functions including cycle counts and providing support to the M&D Team, other plant teams, and customers.Working hours: 3:00 PM - 1:30 AMSkills:*BPCS, ERP or AS400 knowledgeEducation:High SchoolExperience:1-4 yearsQualifications:* 2 - 4 years in manufacturing warehouse environment experience preferred.* Working knowledge of cGMPs, good warehouse procedures including lot, location control, FEFO and FIFO principles.* Good computer skills for accurate data entry, word processing, etc* Forklift certified Apply online then call our office at 919-873-5588.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. 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.
Join the Biotech movement in North Carolina as a Material Coordinator Associate. This position is responsible for performing all warehouse staging, shipping and receiving functions including proper receipt and handling of all materials and items entering the receiving and shipping sectors of the facility essential to plant operations.Responsibilities:1.Uploads, pulls, and moves finished goods, inventoried and non-inventoried materials via manual handling and fork truck operation. Palletizes, stacks, and shrink wraps materials to facilitate warehousing and distribution operations. 2.Inspects and verifies item counts against freight bills, bills of lading, inter-branch, and packing forwarders and samples shipping orders of materials to be shipped.3.Separates, identifies, and receives materials against purchase and credit orders and enters purchase materials receipts via computer data entry/bar code systems for inventory control.4.Moves, transfers, and distributes materials to facilitate plant operations or customer support according to standard operating procedures. Uses computer to inquire on inventory status and via the inventory bar code system program to move and/or transfer inventory by data entry of item, lot, quantity, and location destinations for finished goods and other inventoried materials.5.Performs miscellaneous warehousing functions including cycle counts and providing support to the M&D Team, other plant teams, and customers.Working hours: 3:00 PM - 1:30 AMSkills:*BPCS, ERP or AS400 knowledgeEducation:High SchoolExperience:1-4 yearsQualifications:* 2 - 4 years in manufacturing warehouse environment experience preferred.* Working knowledge of cGMPs, good warehouse procedures including lot, location control, FEFO and FIFO principles.* Good computer skills for accurate data entry, word processing, etc* Forklift certified Apply online then call our office at 919-873-5588.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. 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 provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor???s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today!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. 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 provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor???s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today!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. 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 perform various hydroponic plant production tasks and experiments.Responsibilities:- Produce plants hydroponically under controlled conditions - Seed, transplant, and manage plant lifecycle in pre- and post-infiltration environments- Assist in the management of the seed bank- Prepare nutrient solution and ensure quality by testing samples for proper fertility and pH levels- Maintain all aspects of the plant irrigation system and repair as needed- Properly dispose of plant waste materials- Assist in manufacturing activities as neededWorking hours: Various Shifts AvailableSkills:- Ability to receive training in current Good Manufacturing Practice (cGMP) regulations- Ability to wear and work in PPE- Ability to work in a warm, humid environmentEducation:High SchoolExperience:0-1 yearsQualifications:- HS Diploma required, Associate???s degree in a STEM related field, preferred- At least 1 year of greenhouse/plant production experience- Possess knowledge of hydroponics and plant nutrition- Experience in automation, preferred Apply today!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. 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 perform various hydroponic plant production tasks and experiments.Responsibilities:- Produce plants hydroponically under controlled conditions - Seed, transplant, and manage plant lifecycle in pre- and post-infiltration environments- Assist in the management of the seed bank- Prepare nutrient solution and ensure quality by testing samples for proper fertility and pH levels- Maintain all aspects of the plant irrigation system and repair as needed- Properly dispose of plant waste materials- Assist in manufacturing activities as neededWorking hours: Various Shifts AvailableSkills:- Ability to receive training in current Good Manufacturing Practice (cGMP) regulations- Ability to wear and work in PPE- Ability to work in a warm, humid environmentEducation:High SchoolExperience:0-1 yearsQualifications:- HS Diploma required, Associate???s degree in a STEM related field, preferred- At least 1 year of greenhouse/plant production experience- Possess knowledge of hydroponics and plant nutrition- Experience in automation, preferred Apply today!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. 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 in the manufacturing department, including task delegation- Assist in scaling-up processes- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Ensure team is manufacturing plasmid DNA in accordance with cGMP guidelines- Prepare solutions to be used in the manufacturing process- Execute validation protocols as needed- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PMSkills:- Possess leadership skills- 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 PPEEducation:AssociateExperience:1-4 yearsQualifications:- Bachelor???s or Associate???s degree in a science related field with 3 or more years of cGMP manufacturing experience- Plasmid purification experience, preferred- Knowledge of microbiological techniques, preferred Apply today!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. 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 in the manufacturing department, including task delegation- Assist in scaling-up processes- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Ensure team is manufacturing plasmid DNA in accordance with cGMP guidelines- Prepare solutions to be used in the manufacturing process- Execute validation protocols as needed- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PMSkills:- Possess leadership skills- 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 PPEEducation:AssociateExperience:1-4 yearsQualifications:- Bachelor???s or Associate???s degree in a science related field with 3 or more years of cGMP manufacturing experience- Plasmid purification experience, preferred- Knowledge of microbiological techniques, preferred Apply today!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. 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.