Quality Control Analyst jobs at Kelly Services

Our client, a global leader in the pharmaceutical manufacturing industry, is seeking a QC Analyst to join their team! - Pay: $25-30/hr ($25/hr for entry level/recent graduate) - Shift: 1st shift M-F GENERAL DESCRIPTION: The QC Analyst I performs testing of samples submitted to the laboratory in a cGMP compliant manner, as well as according to approved written procedures. The QC Analyst I may be required to write or revise SOPs, analytical procedures, or other analytical documentation at the discretion of quality control supervisory staff. KEY DUTIES: Perform testing in accordance with written procedures (i.e. USP/EP/JP grade) Documentation of laboratory activities including worksheet/notebook entries according to procedures that define laboratory documentation practices. Processing of electronic data using procedures that ensure data integrity and security. Ship samples to contract testing facilities. Entry of test results from contract laboratories Review and countersign (when necessary) logbooks, notebooks, and worksheets for the purpose of verifying compliance with written procedures, good documentation practices, data integrity and accuracy of calculations. Transcribe results onto analysis reports. Perform daily standardization and performance verifications on laboratory equipment. Comply with site-wide procedures including but not limited to change control, documentation, deviation reporting, cGMP compliance, safety, and electronic data security. Identify deviations to written procedures. Disposal of laboratory waste on an as needed basis. Identify and report unsafe conditions within the laboratory. Identify OOS results, atypical results, and atypical laboratory events requiring a laboratory investigation; perform investigative testing. SKILLS/ABILITIES: Ability to perform routine analysis, such as wet chemistry and operate basic laboratory equipment. Understands paperwork review process. Ability to follow written procedures and exhibit excellent documentation practices. Basic laboratory knowledge and skills analytical techniques in wet chemistry/chromatography Practical experience with various types of laboratory instrumentation Troubleshooting skills with analytical methodology and instrumentation. Technical writing skills Employee must be able to pass a vision exam prior to employment and annually thereafter. PERSONAL ATTRIBUTES: Proactively achieves results for the best of the organization. Willingness to learn new things. Ability to function in a small company atmosphere. Ability to cope with a rapidly changing work environment. Commitment to teamwork. Commitment to continuous improvement in all areas. Ability to focus attention to details and ensure high quality work. Ability to work safely; seek out and encourage safe practices Responsible for managing their time, organizing their workload to be efficient, and have good organizational and communication skills EDUCATION AND EXPERIENCE: Bachelors Degree in Chemistry with 0-2 years of laboratory experience. Other fields of specialty in Sciences are also acceptable provided sufficient chemistry coursework is completed. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

We are seeking a highly motivated Entry-Level Quality Control (QC) Analyst to join our Gene Therapy QC Bioassay group. This is an excellent opportunity for recent graduates or individuals early in their careers to gain hands-on experience in a dynamic and cutting-edge environment supporting AAV-based gene therapy programs. The QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing. Responsibilities: Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing. Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents. Support method transfer, qualification of critical reagents, and other assay-related activities. Participate in the review and basic trending of QC data. Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking. Collaborate with internal teams and external partners as part of cross-functional project support. Contribute to investigations and deviation reports under guidance. Qualifications: Bachelor's degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field. Academic or internship experience with mammalian cell culture and/or ELISAs strongly preferred. Familiarity with basic lab techniques and data analysis methods. Enthusiasm for learning and the ability to work both independently and within a team. Strong organizational, communication, and interpersonal skills. Detail-oriented and eager to develop problem-solving skills in a regulated lab environment.

Our client, a global CDMO, offering products and services across the drug development spectrum is looking for a skilled QC Analyst III to join their team in Ventura County, CA! Job Title: QC Analyst III Job type: 6 month contract - hire Pay rate: $37 - $39/ hr. Job Summary: We are seeking a highly skilled and detail-oriented Senior QC Analyst to perform complex analytical testing in support of pharmaceutical product development and manufacturing. The ideal candidate will have advanced experience in chromatography techniques (e.g., HPLC, UPLC, GC), method validation, data analysis, and regulatory compliance. This position plays a critical role in ensuring product quality, supporting investigations, and driving continuous improvement across the QC function. Key Responsibilities: Perform complex analytical testing including Liquid Chromatography (HPLC/UPLC), Gas Chromatography (GC), and other instrumental and wet chemistry techniques. Troubleshoot analytical instruments and resolve method or equipment-related issues. Participate in and assist with test method validations, verifications, and transfers. Evaluate and analyze test data to identify trends, outliers, or potential issues. Support OOS (Out of Specification) and OOT (Out of Trend) investigations, including CAPA (Corrective and Preventive Action) documentation. Coordinate testing activities with external laboratories, including raw material and specialized testing. Execute, author, and review SOPs, test methods, protocols, reports, investigations, change controls, and data summaries. Utilize risk assessment and root cause analysis tools (e.g., 5 Whys, Fishbone) to support investigations and process improvements. Manage aspects of the stability program, including scheduling, testing, and reporting, and investigate aberrant stability results. Qualifications: Bachelor's or Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field. 3-6+ years of relevant experience in a regulated laboratory environment (pharmaceutical, biotech, or similar). Strong technical expertise in HPLC, UPLC, GC, and other analytical techniques. Working knowledge of cGMP regulations, ICH guidelines, and regulatory expectations. Experience with method validation and stability programs preferred. Ability to manage multiple tasks and work independently in a fast-paced environment. Experience with electronic data systems (e.g., Empower, LIMS, TrackWise, MasterControl). Note: This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Job Title: QC Analyst Schedule: Onsite | Sunday-Thursday | 11:00 PM - 7:30 AM The QC Analyst is an entry-level, hands-on laboratory position responsible for performing routine and critical analytical testing to support quality control operations. This role involves the generation, analysis, documentation, and communication of analytical data in compliance with regulatory requirements and standard operating procedures (SOPs). The position supports testing of raw materials, in-process samples, finished products, stability studies, and cleaning validation. This is a temporary-to-hire role with an anticipated conversion around six months. Key Responsibilities Perform accurate, efficient, and high-quality analytical testing in accordance with USP/NF/EP/JP/FCC standards or customer-supplied methods. Typical testing includes, but is not limited to: Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metals, FTIR, HPLC, and GC. Maintain complete, accurate, and compliant written documentation of all analytical work performed. Interpret analytical data and clearly communicate results, deviations, and issues to appropriate personnel. Organize and schedule daily workload to ensure timely completion of testing. Calibrate, operate, and maintain laboratory instruments and equipment. Follow laboratory safety practices, chemical hygiene procedures, and all applicable regulations. Become proficient in all relevant SOPs and test methods. Work effectively in a “flow-to-the-work” team-based environment. Maintain a clean, organized, and safe laboratory workspace in collaboration with other team members. Perform peer reviews of analytical testing and documentation. Write or update SOPs as needed. Adapt to changing priorities and take on additional responsibilities to meet business and quality objectives. Education & Experience Requirements Bachelor's degree in Chemistry, Biology, Chemical Engineering, or Life Sciences with no prior QC experience OR Bachelor's degree in another discipline with relevant experience in a Quality Control laboratory. Required Skills & Qualifications Ability to multitask efficiently in a fast-paced laboratory environment. Strong attention to detail with the ability to deliver accurate results on the first attempt. Ability to work effectively under pressure and meet production deadlines. Effective verbal and written communication skills in English. General knowledge of laboratory equipment and analytical techniques. Basic understanding of laboratory safety and safe handling of chemicals. Proficient computer skills, including Microsoft Word and Excel. Ability to stand for extended periods while performing laboratory testing. Strong teamwork skills and the ability to collaborate across functional groups.

Title: Sterility Assurance Scientist Duration: 6 Month Contract (potential of extension) Responsibilities: The Sterility Assurance Scientist is a technical role that assists in development and implementation of the site's sterility assurance programs and provides technical guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant efficacy. The principal role is a position that develops and implements a technical agenda and is responsible for providing technical leadership for the Parenteral Process Team. The principal role is also expected to serve as a mentor within the TSMS team and engage in upstream and external to site activities related to sterility assurance contamination control strategies are established. Key Objectives/Deliverables • (Associate/Senior) Ensure and provide oversight and technical guidance for sterility assurance programs at the manufacturing floor level. • Lead or provide technical oversight for Provide technical support for activities related to sterility assurance programs including but not limited to: • Airflow Pattern Testing • Environmental Monitoring Performance Qualifications • Aseptic Process Simulations • Cleaning, Sanitization, and Disinfection • Gowning within GMP Classified Areas • Aseptic Processing Techniques • Contamination Control • Assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead or assist in the development and implementation of processes and facility monitoring to ensure effective contamination control strategies are established. • (Senior) Lead/assist with support and/or provide technical expertise for developing the site's contamination control strategy and cleaning and sanitization program/strategy, and disinfectant efficacy strategies. • (Senior) Lead/assist with support and/or provide technical expertise for the facility's cleanroom gowning and aseptic technique strategy/program. • (Principal) Knowledge in pharmaceutical Microbiology, related to microbiological media, microbiological enumeration techniques, and microorganism isolation and identification. • (Principal) Lead/provide technical oversight for one or both the Environmental Monitoring (EM) or Aseptic Process Simulation (APS) program: • (EM) Authoring EM Performance Qualifications (EM PQ) and overseeing the execution. • (EM) Evaluating EM data and authoring EM Trend Reports. • (EM) Assist with identifying facility environmental isolates and how to create and maintain environmental isolated cultures. • (APS) Authoring APS protocols and overseeing the execution. • (APS) Evaluating the APS data, including personnel qualifications, and authoring APS reports. • (APS) Assist with tracking and tending APS to ensure all regulatory requirements and Global Quality Standards are met for each manufacturing line/process. • Apply sterility assurance risk management to evaluate manufacturing processes and associated controls with respect to potential introduction of microbial, endotoxin, and particulate contamination. • Analyze microbial and manufacturing data to identify trends, process discrepancies, and opportunities for continuous improvements.• Lead or provide technical support for root cause investigations associated with sterility assurance programs. • Participate and/or provide technical sterility assurance support during internal and external audits. • Create, execute, review, and/or approve technical documents and change controls related to sterility assurance programs. • Work within cross-functional teams to implement TS/MS objective and deliver on business and quality objectives. Basic Qualifications: • Bachelor's or master's degree in microbiology, Biology, Biochemistry, Biochemical Engineering, Chemical Engineering, or other related scientific discipline. • Demonstrated understanding and relevant experience of scientific principles required for manufacturing parenteral drug products within operations, microbiology, environmental monitoring, sterility assurance, validation, technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. • (Senior) 2+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). • (Principal) 5+ years in pharmaceutical manufacturing (Microbiology, TSMS, Sterility Assurance, or related dept). Additional Skills/Preferences: • Possess strong interpersonal skills to work cross-functionally within a team. • Possess strong self-management and organizational skills. • Possess strong oral and written communication skills for communicating to colleagues, management, and other departments. • Experience with data analysis and trending. • Ability to wear appropriate PPE and other safety related equipment or considerations in manufacturing warehouse, or laboratory areas. • Ability to gown into facility dedicated cleanroom attire, as required to perform job responsibilities. Additional Information: • Role is Monday through Friday based and will be phased from a project support role to a routine support role as the development facility and processes progress. Must be flexible in providing support to accommodate other inputs (production schedules, shutdowns, etc.). Occasional extended hours and / or off-hour work may be required. • Tasks may require repetitive motion and standing or walking for long periods of time. • Travel may be required during the project phase for training and implementation of sterility assurance programs. This is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the . For GMP purposes, the job description should be updated for significant changes. As always, you should consult with your supervisor regarding your actual job responsibilities and any related duties that may be required for the position.

Senior Formulation Technician Duration: 12 Months Job Type: Contract Work Type: Onsite Shift: Monday to Friday from 06:00 AM to 02:30 PM Pay Range: $20 to $26 per hour Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary Work in a team-based manufacturing laboratory environment responsible for synthesizing, testing, and qualifying ion exchange media used in chromatography consumables, while maintaining high quality, safety, and compliance standards. Responsibilities Perform testing and qualification of resin products using specialized instruments to meet customer and production demands. Accurately record, analyze, and report test results; maintain complete and compliant documentation. Execute complex production work orders in accordance with established SOPs and procedures. Analyze data, derive conclusions, and prepare technical reports based on findings. Collaborate with cross-functional teams to support production and quality objectives. Adhere to ISO 9001 guidelines, GMP, and corporate quality policies. Comply with EH&S safety requirements and participate in safety improvement initiatives. Identify process improvement opportunities and propose corrective or preventive actions. Maintain a clean, organized, and inspection-ready laboratory environment. Required Skills Hands-on experience in a chemistry or biotechnology laboratory. Bachelor's degree in Chemistry, Biotechnology, or a related life sciences field. Experience in a manufacturing or regulated production environment. Familiarity with chromatography techniques and chromatography-related software. Exposure to Lean Manufacturing, PPI, or Continuous Improvement tools. Willingness and ability to learn new processes, tools, and technologies. Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Ability to read, understand, and follow written SOPs and verbal instructions in English. Strong mathematical skills, including basic arithmetic with whole numbers, fractions, and decimals. Proficiency in Microsoft Word, Excel, Outlook, and basic data handling. Strong documentation, organizational, and problem-solving skills. Effective verbal and written communication skills. Familiarity with common hand tools (e.g., wrenches, torque drivers, tweezers). Ability to work independently with minimal supervision while meeting deadlines and production targets. Strong punctuality, attendance, and ownership mindset. Understanding of production schedules and task prioritization. Compliance with GMP, QSRs, ISO, and IVD regulatory requirements. TekWissen Group is an equal opportunity employer supporting workforce diversity.

Senior Formulation Technician Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shift: First Shift - 06:00 AM to 02:30 PM Pay Rate: $20 to $22 per hour Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary: The Media Process Technician I works as part of a team to manufacture dehydrated and liquid cell culture media. The technician follows batch record instructions, weighs raw materials ranging from micrograms to kilograms, calibrates equipment, operates milling equipment, performs sterile filtration, and completes media manufacturing tasks. Responsibilities also include performing standard product testing (osmolality, pH, turbidity) and working closely with cross-functional groups such as R&D, procurement, quality, process technology, marketing, as well as internal/external customers and vendors. Responsibilities Stage and compound raw materials within specified weight tolerances (micrograms to kilograms). Perform milling, blending, aseptic liquid filling, and process control monitoring. Follow GMP and departmental procedures to manufacture dehydrated and liquid culture media according to production schedules. Complete all required documentation neatly, accurately, and in compliance with GMP. Perform cleaning, inspection, calibration, and assist in equipment maintenance; maintain logs and records. Troubleshoot equipment issues. Handle raw materials following GMP and Safety requirements. Use laboratory and production equipment (pipettors, balances, osmometer, turbidimeter, pH meters). Work safely to maintain an injury-free and incident-free workplace. Carry out assigned responsibilities under supervision. Promote a positive team environment through effective communication and engagement. Work overtime when required. Perform other duties as assigned to support business goals. Required Skills & Qualifications BS in Chemistry or related field (or equivalent combination of education, training, and experience). Minimum 6 months of experience in a high-paced chemistry lab or manufacturing environment. Ability to read, write, and follow testing and inspection procedures. Ability to maintain neat, accurate, complete records and logs. Mechanical aptitude; ability to disassemble and reassemble equipment. Good communication skills; able to work independently or as part of a team. Flexibility to work varying schedules, including overtime. Strong attention to detail and ability to focus on tasks continuously. Basic experience weighing multiple components. Basic computer skills, including MS Excel, Word, and PowerPoint. Ability to lift or move approximately 40 lbs. Desired Skills (Preferred but Not Required) Statistical analysis experience using Excel or Minitab. Experience handling multiple components and performing precise weighing. Familiarity with GMP environments, sterile filtration, and laboratory instrumentation. TekWissen Group is an equal opportunity employer supporting workforce diversity.

Pride Health is hiring a Quality Control Technician to support our client's medical facility based in Elmhurst, Illinois. This is a 13-week contract job opportunity and a great way to start working with a top-tier healthcare organization! Job Summary: The Sterile Processing Quality Control Technician ensures the highest standards of instrument cleanliness, assembly accuracy, and quality assurance in sterile processing operations. This role combines hands-on technical processing responsibilities with detailed inspection and documentation tasks critical to patient safety and process reliability. This position focuses on quality assurance beyond standard sterile processing technician duties, ensuring compliance with all regulatory and internal standards while maintaining an unwavering commitment to safety and process excellence. Job Responsibilities: -Follow all ANSI/AAMI standards, manufacturer Instructions for Use (IFUs), SOPs, and company Work Instructions. -Decontaminate used surgical instruments and equipment using proper PPE and protocols. -Disassemble, clean, and reassemble complex surgical instruments as required. -Accurately assemble and package instrument trays and sets per guidelines. -Operate washers, sterilizers, and other processing equipment safely and effectively. -Inspect instruments for cleanliness, functionality, and damage prior to packaging. -Document missing or damaged instruments per SOPs. Required Skills & Experience: -Hands-on experience in sterile processing, demonstrating proficiency in decontamination, assembly, and sterilization procedures. -Strong attention to detail. -Ability to work effectively under pressure in a fast-paced, team-oriented environment. -General knowledge of surgical instruments and processing protocols. -Knowledge of sterilization techniques, including steam sterilization and infection control practices. -Familiarity with ANSI/AAMI standards and manufacturer Instructions for Use (IFUs). Additional Information: Location: Elmhurst, Illinois Schedule: 2nd Shift- 3 pm-11:30 pm & 3rd Shift- 11:00 pm-7:30am Pay Range: $24/Hr. - $28/Hr. Start: 12/15/2025 *Offered pay rate will be based on education, experience, and healthcare credentials. Interested? Apply now! About Pride Health As a certified minority-owned business, Pride Global and its affiliates - including Russell Tobin, Pride Health, and Pride Now - are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics. Pride Global offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance, and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance, and employee discounts with preferred vendors.

Location: Rochester MA (100% On-site), 1st shift only 6:30A-3:30P M-F, salary range $72K-$82K, full-time role: health insurance with an HRA, dental, vision, LTD, and a 401(k) retirement plan with an employer match. 3 weeks PTO, 1 week sick. Generous relocation package offered. Qualified candidates are encouraged to apply. Large precast concrete supplier in Massachusetts and New Hampshire, providing high-quality products for over 70 years. Their extensive product range includes septic tanks, manholes, drainage structures, bulkheads, curbing, residential steps, and retaining wall systems, all crafted to precise specifications. They cater to engineers, contractors, and homeowners, emphasizing superior performance and exceptional customer service. The Quality Control Technician (“QC Technician”) will work within the production plant and is ultimately responsible for product testing. The QC Tech will assist in the execution of quality control processes, procedures and protocol associated with the production of pre and post concrete pours. Responsibility Responsible for ACI concrete field tests Responsible for quality control inspections in manufacturing plant Inspect forms before pouring (Pre-Pour). Inspect product after removed from forms (Post-Pour) Notifies Production Supervisor if deficiencies are found. Perform and/or schedule repairs on products as needed. Housekeeping - maintain a clean work area. Including cleanliness within breakroom, restroom, and general facility areas. Expected to maintain knowledge of precast plant techniques and procedures. May assist with precast production operation as needed. Characteristics Always committed to safety. Maintain a safe work area. Follow safe work practices as outlined in the Safety Program. Always committed to quality. Follow and implement quality control measures. Excellent attendance. Reliable means of transportation to and from work. Ability to learn, organize and prioritize work and handle multiple tasks. Outstanding attitude, honesty, and ethic at all times. Expected to use sound judgment, diplomacy, and discretion. Work independently or cooperatively with others. Self-drive in carrying out the functions of the job. Requirements: ACI Concrete Field-Testing Grade 1 Certified (preferred) NPCA PQS Training Must be at least 18 years of age per federal guidelines. Good communication skills, both verbal and written to all levels of staff Ability to remain focused in busy environment. Computers and tablets skills in order to perform tasks. Ability to read blueprints and sketches.

A Product Development Scientist role involves a wide range of activities, including developing and optimizing new product formulations and processes, conducting laboratory testing and evaluations. Key responsibilities include batching several iterations, ensuring technical accuracy in product development through stability studies, and documentation. Working with the team, time management, attention to detail, strong analytical skills, strong communication, following the timeline. Consumer Products - Skin Health BA Degree 2 to 4 years' experience Will need to go between Summit and Skillman office, 830-5 Skills required: documentation work organizing samples, delivering samples batching exp 2 years of formulation exp Skillman for batching - 5 days a week - majority of the role is in Skillman paperwork done in summit (1 day in summit) 4 days Skillman and 1 day summit (depend on the workload and paperwork) Timings : 8:30-5- Flexible basic lab instruments intern exp will also work making 2 batches a day and 8 batches a week About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Recruiter Details: Name: I.Prudvi kumar Email: ******************************* Internal Id: 25-50776

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Vaccine Immuno therapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. The candidate will have solid training and knowledge in virus/protein purification. The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Position Comments visible to MSP and Supplier: Additional Skills: Protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qualifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Qualifications BSs or MSc in biological sciences or biochemical/chemical engineering Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Vaccine Immunotherapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. • A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. • The candidate will have solid training and knowledge in virus/protein purification. • The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. • Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. • Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. • The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. • The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Additional Skills: protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qulaifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Additional Information Best Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Vaccine Immunotherapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. • A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. • The candidate will have solid training and knowledge in virus/protein purification. • The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. • Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. • Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. • The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. • The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Additional Skills: protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qulaifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Additional Information Best Regards, Anuj Mehta ************

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Vaccine Immuno therapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. The candidate will have solid training and knowledge in virus/protein purification. The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Position Comments visible to MSP and Supplier: Additional Skills: Protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qualifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Qualifications BSs or MSc in biological sciences or biochemical/chemical engineering Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

A manufacturing company in Norwalk, CT is looking for a Quality Control Operator. The ideal candidate will have a keen eye for detail, strong analytical skills, and a commitment to continuous improvement. Primary responsibilities will involve monitoring the production process, conducting routine inspections, and performing tests on materials and finished products. You will work closely with production teams to identify and rectify any quality issues, ensuring compliance with industry regulations and internal standards. The Quality Control Operator will also be responsible for maintaining accurate records of inspections and tests, providing feedback to team members, and assisting in the development of quality control procedures. Responsibilities Conduct routine inspections of products during various manufacturing stages. Perform tests on raw materials and finished products to ensure compliance with quality standards. Document inspection results and communicate findings to relevant team members. Identify and report any quality issues or deviations from established standards. Collaborate with production teams to implement corrective actions and improve processes. Assist in the development and maintenance of quality control procedures and protocols. Participate in internal audits and assist with external audits as needed. Requirements High school diploma or equivalent; additional certifications in quality control preferred. Proven experience in a quality control role, preferably in a manufacturing environment. Strong attention to detail and excellent analytical skills. Ability to interpret technical documents, blueprints, and quality standards. Strong communication skills, both written and verbal, with the ability to work effectively in a team. Pay is $22/hr Hours are Monday - Friday 7:50am - 4:20pm. Must be able to pass background check.

Employment Type: Intern Division: Field Operations Department: Quality Salary Range: $23 - $28/hour The Quality Intern supports the Quality department in implementing and monitoring quality management processes across multiple projects in various phases of construction. This role offers broad exposure to construction operations while working closely with Quality Program Managers to uphold and enhance project standards. Responsibilities / Essential Functions * Participate in the quality program by attending meetings, performing inspections, and verifying materials. * Assist with coordination and content development for Quality pre-operational meetings. * Provide technical support on project sites, including interpreting contract drawings and submittals. * Develop an understanding of project schedules and critical path activities. * Collaborate with Quality Program Managers on initiatives such as drain assembly analysis, finish floor build-up analysis, and water intrusion control planning. * Perform other tasks as assigned by the team. Key Skills * Excellent written and verbal communication skills. * Strong initiative and problem-solving abilities. * High attention to detail. * Effective time management with the ability to handle multiple responsibilities and meet deadlines. * Ability to work in a team environment with a primary focus on collaboration. Required Experience * Pursuing a Bachelor's Degree in Construction Management, Engineering, or a related field (preferred). * Demonstrated interest in construction management and the construction industry.

Job Description: The Temporary Microbiology LaboratoryTechnician is responsible for performing general microbiological laboratoryduties as outlined below: Prepare microbiological media including QC sterilitychecks and media growth promotion testing Prepare specimens and materials, including cleaning theworkspace Perform microbiological testing of water in accordancewith standard procedures, using aseptic technique. Maintain accurate, up-to-date and concise laboratoryrecords General housekeeping/upkeep/cleaning of laboratory Monitor, clean, and perform calibration checks forlaboratory equipment and machinery Dish washing of laboratory glassware Autoclave waste Stock laboratory supplies and maintain laboratoryinventory Back up for Lab Analyst with respect to generalmicrobiological duties Work in a team environment under minimal supervision Participate in laboratory investigations Additional responsibilities as needed Skills/Experience/Education Bachelor\'s degree or equivalent in Microbiology/Biologyor working towards said degree, with Microbiology related coursework Minimum of 6-12 months experience in a Microbiologylaboratory, preferred Knowledge of GMP and aseptic techniques preferred Strong interpersonal skills Works well in a team environment Ability to work with minimal supervision Strong multi-tasking skills Precise, accurate and detail oriented

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Job Title: Method Development Chemist Location: Minneapolis, MN Duration: 3+ months (Possibility of extension) local candidate needed - Minneapolis, MN. REQUIRED: Top 3 must haves: Chromatography experience analytical lavatory experience Seasoned HPLC chemist. Job Roles & Responsibilities 3 months contract position performing method development on GPC methodology. Perform and document laboratory work. Review and approve test records. Participate in the validation of the new GPC test method Basic Qualifications and Experience EDUCATION - Minimum BS in Chemistry or related scientific degrees EXPERIENCE - Minimum 1 year in a regulated industry environment with a Bachelor's Degree in Chemistry. Minimum 3 years of hands on experience operating HPLC Performing chemistry and/or material properties testing in a high throughput laboratory Documenting work accurately and completely Ability to use common software including MS Word, MS Excel, Powerpoint Self-motivated, able to plan/execute work tasks independently Critical thinking skills Safely handle chemical and hazardous materials Preferred Skills and Experience Prior experience and knowledge of materials properties and GPC testing Experience working with laboratory data management system Experience working with Empower chromatography software Additional Information · We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job. Thanks & Regards, Seema Chawhan Clinical Recruiter Integrated Resources, Inc. IT Life Sciences Allied Healthcare CRO Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I DIRECT # - 732-844-8724 Email id - seema @irionline.com| www.irionline.com LinkedIn: https://in.linkedin.com/in/seemachawhan Gold Seal JCAHO Certified ™ for Health Care Staffing “INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row

We are seeking a microbiological laboratory technician to join our team-oriented environment of food professionals. This individual will be responsible for various laboratory duties, including sample processing, media preparation, collection, data entry, and more. Responsibilities: •Process incoming samples •Accurately record detailed data •Perform Quality Assurance (QA) checks of the lab •Perform facility and field sampling of product & water •Use of lab equipment (e.g. scales, autoclaves) •Clean glassware, laboratory areas, and utensils •Media preparation •Perform pipetting and serial dilutions •Retrieve samples from various locations, as needed •All other duties assigned by management •Laboratory skills, including aseptic technique a plus, but not required •Ability to multi-task & adapt to a changing fast-paced environment required •Computer literacy and experience with Microsoft Office •Excellent verbal and written skills •Clean DMV record •Flexible schedule with availability to work weekends, evenings, and overtime •Strong math skills •Ability to lift 35 lbs. •Self-motivated, with excellent work ethic •Bilingual (Spanish) a plus •Science background a plus •Professional skills a plus Starting Hourly rate at $17-$19/hr.