Quality control analyst jobs in Athens, GA - 36 jobs

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 Performs analysis of product quality inspection of parts, raw materials, and/or packaging components using calibrated measurement equipment to verify product meets specifications. Completes documentation relating to material inspection and enters data into database/software systems; such as MES, SAP or LIMS. Communicates defect information to supervisor and quality assurance for corrective actions. Assists with 5S cleaning procedures. Ensures the inspections of material are accomplished per SOP and quality standards, while meeting the production plan. Actively participates in natural work groups to identify process problems and contribute solutions. Participates in day-to-day business activities, safety, quality, and training needs. ISO/FDA/GMP compliance. Skills: Qualifications Education: Additional Information For more information, Please contact Sneha ************ ***********************************

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: Quality Job Sub Function: Quality Control Job Category: Professional All Job Posting Locations: Athens, Georgia, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine We are searching for the best talent for an Analyst 1, Lab Quality Control to be in Athens, GA. Benefits you will enjoy starting your first day: Competitive pay based on experience, night shift differential, plus an annual performance bonus. Full medical, dental and vision coverage, competitive 401k, HSA/FSA, and company paid Pension plan. 120 hours paid vacation, plus 40 hours paid sick leave and an additional 40 hours paid personal leave. Tuition Reimbursement for eligible degree programs. Purpose: The Associate Analyst is responsible for testing and analyzing raw materials, in-process samples, and products such as chemicals and Active Pharmaceutical Ingredients (API) to determine stability, purity, chemical content, and other characteristics. They follow standardized test-methods, procedures, and work instructions, document test results, and communicate status of test results. What you will be responsible for: Set up, operate, and clean laboratory equipment used to support production of intermediate, raw material, and finished products for API, medical device raw material components, and other products as directed; complete all associated support activities in the laboratory. Assure that QC laboratories run in a safe, clean, and environmentally sound manner. Review peer laboratory data to ensure accuracy and completeness. Demonstrate and develop experience on HPLC, UPLC, Karl Fischer, UV analysis, NIR, and other analytical techniques and train other laboratory personnel on these techniques. Develop skills to troubleshoot and perform minor maintenance, calibration, and repair of laboratory instrumentation. Provide input on investigations (OOS, OOT, invalid assays, and other lab-related non-conformances including investigations of audit observations) as needed. Support the implementation of relevant CAPAs and monitor effectiveness of CAPAs. Carry out duties in compliance with all state and federal regulations and guidelines including FDA, ISO, EPA, OSHA, and DEA, and adheres to all company and site policies and procedures. Qualifications / Requirements: Required: Requires ability and flexibility to work weekends and overtime (on a scheduled or emergency basis) to support shift operations. High school diploma or two-year technical degree in a science or laboratory related field with four (4) years of Experience in a Quality Control (GMP regulated) Laboratory OR Bachelor's or Master's degree in Chemistry or related science degree. Preferred: Experience applying mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlational techniques, sampling theory, and/or factor analysis. Experience identifying and defining problems, collecting data, establishing facts, and making scientific-based conclusions. Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals and medical device. Experience in Lab Operations and/or Quality processes/systems in a GMP Lab setting, Experience working with Lab Systems or processes such as eLIMs, TrackWise, Non-conformances, and/or Change Control. Familiarity with a variety of laboratory equipment, such as: GC, HPLC, UPLC, and/or Karl Fisher. Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting role! Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (********************************) or contact AskGS to be directed to your accommodation resource. #LI-Onsite Required Skills: Preferred Skills: Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: Quality Job Sub Function: Quality Control Job Category: Professional All Job Posting Locations: Athens, Georgia, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine We are searching for the best talent for an Analyst 1, Lab Quality Control to be in Athens, GA. Benefits you will enjoy starting your first day: Competitive pay based on experience, night shift differential, plus an annual performance bonus. Full medical, dental and vision coverage, competitive 401k, HSA/FSA, and company paid Pension plan. 120 hours paid vacation, plus 40 hours paid sick leave and an additional 40 hours paid personal leave. Tuition Reimbursement for eligible degree programs. Purpose: The Associate Analyst is responsible for testing and analyzing raw materials, in-process samples, and products such as chemicals and Active Pharmaceutical Ingredients (API) to determine stability, purity, chemical content, and other characteristics. They follow standardized test-methods, procedures, and work instructions, document test results, and communicate status of test results. What you will be responsible for: Set up, operate, and clean laboratory equipment used to support production of intermediate, raw material, and finished products for API, medical device raw material components, and other products as directed; complete all associated support activities in the laboratory. Assure that QC laboratories run in a safe, clean, and environmentally sound manner. Review peer laboratory data to ensure accuracy and completeness. Demonstrate and develop experience on HPLC, UPLC, Karl Fischer, UV analysis, NIR, and other analytical techniques and train other laboratory personnel on these techniques. Develop skills to troubleshoot and perform minor maintenance, calibration, and repair of laboratory instrumentation. Provide input on investigations (OOS, OOT, invalid assays, and other lab-related non-conformances including investigations of audit observations) as needed. Support the implementation of relevant CAPAs and monitor effectiveness of CAPAs. Carry out duties in compliance with all state and federal regulations and guidelines including FDA, ISO, EPA, OSHA, and DEA, and adheres to all company and site policies and procedures. Qualifications / Requirements: Required: Requires ability and flexibility to work weekends and overtime (on a scheduled or emergency basis) to support shift operations. High school diploma or two-year technical degree in a science or laboratory related field with four (4) years of Experience in a Quality Control (GMP regulated) Laboratory OR Bachelor's or Master's degree in Chemistry or related science degree. Preferred: Experience applying mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlational techniques, sampling theory, and/or factor analysis. Experience identifying and defining problems, collecting data, establishing facts, and making scientific-based conclusions. Knowledgeable of FDA/EMEA regulatory requirements applicable to pharmaceuticals and medical device. Experience in Lab Operations and/or Quality processes/systems in a GMP Lab setting, Experience working with Lab Systems or processes such as eLIMs, TrackWise, Non-conformances, and/or Change Control. Familiarity with a variety of laboratory equipment, such as: GC, HPLC, UPLC, and/or Karl Fisher. Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting role! Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (********************************) or contact AskGS to be directed to your accommodation resource. #LI-Onsite Required Skills: Preferred Skills: Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy

Information Classification Title Associate Controller FLSA Exempt FTE 1.00 Minimum Qualifications Bachelor's degree in a related field or equivalent plus 12 years of professional experience to include 5 years of supervisory experience Preferred Qualifications Preferred qualifications include experience working in higher education and MBA. Position Summary Serves the University of Georgia as Associate Controller and is responsible for the operations of accounting, payroll, and commitment accounting departments. The Associate Controller works with the directors to: * Maintain excellent service to the campus community and external customers * Sustain processing accuracy, fiscal integrity, and security of data * Coordinate the implementation of system improvements and integrations * Determine solutions for improved business transaction processing * Distribute business service information to the campus community * Prepare management and financial reports * Maintain administrative policies and procedures * Ensure compliance with various federal, state, Board of Regents and University policies and directives This individual will report to the Controller in the Finance Division and will assist the Controller with special projects, assignments, and financial analysis. Knowledge, Skills, Abilities and/or Competencies * Knowledge and experience with generally acceptable accounting principles and Governmental Accounting Standards. * Knowledge of payroll accounting concepts and IRS regulations * Knowledge of financial systems and the ability to extract and analyze financial data. * Excellent oral and written communication skills. Physical Demands * Normal Business Office * Sitting at a computer for long periods of time Is driving a responsibility of this position? No Is this a Position of Trust? Yes Does this position have operation, access, or control of financial resources? Yes Does this position require a P-Card? No Is having a P-Card an essential function of this position? No Does this position have direct interaction or care of children under the age of 18 or direct patient care? No Does this position have Security Access (e.g., public safety, IT security, personnel records, patient records, or access to chemicals and medications) Yes Credit and P-Card policy Be advised a credit check will be required for all positions with financial responsibilities. For additional information about the credit check criteria, visit the UGA Credit Background Check website. Background Investigation Policy Offers of employment are contingent upon completion of a background investigation including, a criminal background check demonstrating your eligibility for employment with the University of Georgia; confirmation of the credentials and employment history reflected in your application materials (including reference checks) as they relate to the job-based requirements of the position applied for; and, if applicable, a satisfactory credit check. You may also be subject to a pre-employment drug test for positions with high-risk responsibilities, if applicable. Please visit the UGA Background Check website. Duties/Responsibilities Duties/Responsibilities Departmental Leadership and Oversight * Oversee the overall operation and supervision of the Accounting Department in compliance with UGA policies and procedures. * Direct financial reporting, monthly and year-end closing activities, performance assessments, and updates to departmental policies and procedures. * Supervise the Directors and operations of the Payroll and Commitment Management departments to ensure consistency and compliance with university standards. Percentage of time 50 Duties/Responsibilities Collaboration, Communication, and Strategic Support * Represent the Accounting and Payroll Department on UGA and USG committees and institutional work groups. * Collaborate with administrative offices such as Human Resources, Budgets, and Faculty Affairs, as well as USG Shared Services Center and OneUSG Connect support staff. * Lead departmental efforts with EITS and other campus units to strengthen sensitive data protection measures. * Communicate policy and procedural updates to university departments and ensure strong customer service to internal and external stakeholders. * Assist the Controller with problem-solving, analysis, interpretation, data acquisition, and reporting tasks. Percentage of time 30 Duties/Responsibilities Policy Administration, Compliance, and Guidance * Administer and interpret applicable federal and state laws, Board of Regents policies, and accounting standards (GASB and FASB) relevant to university accounting and financial reporting. * Provide guidance to managers and directors on complex policy, procedural, and regulatory issues, including audit and accounting concerns, software/equipment needs, and training initiatives. * Resolve and respond to departmental questions by interpreting federal, state, BOR, and UGA policies, balancing compliance with the intent and spirit of the regulation Percentage of time 20 Contact Information Recruitment Contact Contact Details For questions concerning this position or recruitment progression, please refer to the Recruitment Contact listed below. Recruitment Contact Name Allison Davis Recruitment Contact Email *************** Recruitment Contact Phone ************ Posting Specific Questions Required fields are indicated with an asterisk (*). Applicant Documents Required Documents * Resume/CV * Cover Letter Optional Documents Persons needing accommodations or assistance with the accessibility of materials related to this search are encouraged to contact University HR (*************). The University of Georgia is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, genetic information, national origin, race, religion, sex, or veteran status or other protected status.

The SR Associate, Quality Control Data will manage the following functions in the Quality Control Department. This includes LIMS, Sample Life Cycle Management and Quality Control test documentation life cycle management in compliance with procedures and regulatory requirements. The incumbent will be responsible as an approved USDA sampler and providing Quality Assurance and Production support as needed.As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. **Duties & Responsibilities** + Sample Life Cycle Management including responsible for daily sample submission receipt (including the maintenance of the logbook, LIMS, coolers, and freezers), preparation of retention samples and maintenance of retention samples and retention database. + Regulatory Compliance including responsible for preparation and shipment of USDA samples using APHIS Form 2020. + Documentation Life Cycle Management including responsible for managing Quality Control test documentation of active ingredient and final product (filing and generating associated test reports). + Data Integrity including responsible for Quality Control test record issuance and reconciliation. + Information Support including functioning as a Quality Control liaison with Planning, Quality Assurance and Production to provide necessary information regarding samples and test dates to allow proper management of formulation and packaging activities and management of safety stocks and back-order prevention. + Product Release including assisting in the preparation of accurate and timely submissions to USDA for product release using the APHIS Form 2008 and international documentation as needed to release product according to applicable procedures. + As assigned, assists in Conditional Releases, Early Expiration, Spanish/Brazil/ROW assignments and document creation/revision as needed according to applicable procedures. + Accountable to all related USDA, international, and GMP Biologics requirements at the Athens site for maintaining product registrations in >90 countries. + Ensures quality samples and data in Quality Control through: Management of samples, Distribution, and reconciliation of test documentation, Filing of test documentation, Generation of test reports as well as Planning and Production support for testing information. **Requirements** + Associates degree + 2 years of relevant industry experience required; Bachelor's degree in a scientific discipline, preferred. + Functional knowledge of computer systems such as laboratory information management systems (LIMS) is required. + Functional knowledge of product manufacturing activities is recommended. + Previous experience in a Manufacturing environment in Quality Assurance, Quality Control, or Production preferred. + Solid verbal and written communication skills, including document review and editing skills. + Detail oriented. + Strong time management skills. + Strong organizational skills with ability to multi-task and prioritize. + Experience in root cause analysis tools. + Ability to understand and comply with Quality Assurance and regulatory requirements (9CFR, Outlines of Production, Change Control, Deviation, CAPA, OOX, etc.). + Computer skills in Microsoft Office applications and the ability to learn new applications quickly and easily. **Desired Skills, Experience and Abilities** All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.

Performs operations necessary for quality testing. Performs generally supervised, routine tasks, following SOPs, which may include: environmental monitoring testing, water testing, simple routine testing of in-process and final products in accordance with GMP. Collect environmental monitoring samples (both viable and non-viable air and surface) in manufacturing aseptic processing areas Environmental monitoring plate reads Conduct contaminant identification. Assist with protocol testing as needed Prepping and maintenance of supplies and environmental monitoring equipment. Utilize standard operating procedures to conduct environmental monitoring activities. Use data management systems to enter and track results. Demonstrate a visible & tangible commitment to HSE. In addition to the above, other assigned duties & projects deemed appropriate within the position scope. Able to operate assigned lab equipment. May order supplies needed in the labs. May assist in preparation of media, washing of glassware and operation of autoclave. Contacts are primarily with immediate supervisor and other experienced operators.

Benefits: 401(k) 401(k) matching Bonus based on performance Competitive salary Paid time off We are seeking a highly skilled Manufacturing Operational Consultant to join our dynamic team. This role offers the opportunity to work with diverse manufacturing facilities, streamline processes, and drive continuous improvement. Critical Thinking: Strong analytical and problem-solving skills, with the ability to draw meaningful hypothesis/conclusions from complex data sets and circumstances due to the biological nature of the product. Ultimately...be Inquisitive! Project management experience, including the ability to lead cross-functional teams and drive successful implementations. Operational Analysis: Conduct comprehensive assessments of manufacturing processes and operations to identify inefficiencies and areas for improvement. Analyze production data, performance metrics, and key performance indicators to evaluate current operational effectiveness. Strategic Planning: Collaborate with cross-functional teams to develop and implement strategic plans for process optimization and operational excellence. Provide recommendations for technology integration, workflow improvements, and resource utilization. Process Improvement: Design and implement innovative solutions to enhance production efficiency, reduce waste, and improve overall quality. Develop and implement lean manufacturing principles and continuous improvement initiatives. Training and Development: Provide training and mentorship to manufacturing teams on best practices, new processes, and tools. Work closely with team members to instill a culture of continuous improvement and operational excellence. Change Management: Guide and support organizational change initiatives to ensure smooth transitions and minimize disruptions. Foster a culture of adaptability and collaboration within the manufacturing environment. Client Collaboration: Engage with clients to understand their specific manufacturing challenges and objectives. Develop customized solutions that align with client goals and industry best practices. Bachelor's degree in Engineering, Operations Management, or a related field. Master's degree preferred. Proven experience in manufacturing operations and process improvement, with a minimum of [X] years in a consulting role. In-depth knowledge of lean manufacturing principles, Six Sigma, and other operational excellence methodologies. Strong analytical and problem-solving skills, with the ability to interpret complex data and draw meaningful conclusions. Excellent communication and interpersonal skills, with the ability to collaborate effectively at all organizational levels. Project management experience, including the ability to lead cross-functional teams and drive successful implementations. Compensation: $95,000.00 - $125,000.00 per year Experience the Difference with Express in Alpharetta, GA Our Express Employment Professionals Office in Alpharetta, Georgia is a locally owned and operated full-service staffing agency that offers staffing opportunities throughout the Forsyth County area. Along with that, we also work to provide workforce solutions to the top local Employers in the community. We strive to exceed expectations by pairing the staffing services we offer to companies in our community with talented Job Seekers who are the lookout for quality employment. We recruit our candidates in our community when we can, which has proven excellent turnout, consistent attendance records and high conversions from temporary to full-time employment offered to our Associates. Express Associates have a wide assortment of job opportunities in Alpharetta, Norcross, Cumming, Duluth, Sugar Creek, Buford, Johns Creek, and Suwanee, Georgia. Our team at Express Alpharetta is committed to recruiting, screening and placing only the most skilled candidates in our area. Combining our international headquarters with our local recruitment efforts, it's easy to see the value of our competitive advantage! We are proud to be the premier employment agency in Alpharetta that helps local businesses meet their staffing needs and goals.

Title: Quality Control Technician III Pay Rate: $21.00 23.50/hr on W2 Duration: 12 Months Work schedule: 9 am 5 pm, no shift work Normal 9 am 5 pm, no shift work Performs operations necessary for quality testing. Performs generally supervised, routine tasks, following SOPs, which may include: environmental monitoring testing, water testing, simple routine testing of in-process and final products in accordance with GMP. Collect environmental monitoring samples (both viable and non-viable air and surface) in manufacturing aseptic processing areas Environmental monitoring plate reads Conduct contaminant identification. Assist with protocol testing as needed Prepping and maintenance of supplies and environmental monitoring equipment. Utilize standard operating procedures to conduct environmental monitoring activities. Use data management systems to enter and track results. Demonstrate a visible & tangible commitment to HSE. In addition to the above, other assigned duties & projects deemed appropriate within the position scope. Able to operate assigned lab equipment. May order supplies needed in the labs. May assist in preparation of media, washing of glassware and operation of autoclave. Contacts are primarily with immediate supervisor and other experienced operators. Experience: 1 to 2 years Skills: Experience with enumeration of bacterial colonies on agar plates Experience with gram stain techniques Experience with aseptic techniques, clean room operations, or microbial control. Ability to meet standards for aseptic gowning qualification Demonstrated interpersonal skills including flexibility, collaboration and ability to work in a team environment. Computer literate with knowledge of Microsoft business office applications Experience with LIMS systems Education Bachelor s Degree with a degree focused in Microbiology is preferred. Associate's degree or pursuing a relevant degree with applicable microbiological experience considered

TempToFT Testing Solder Paste batches in the lab. Will also be handling packing slips, BOL and sometimes dealing with shipping companies. Must have Microsoft Office experience, Excel, Word. Looking for someone that will be punctual in attendance and deadlines. Must be a team player. 1965 Evergreen Blvd. , Suite 400, Duluth, GA 30096, United States of America

The Quality Control Technician will be responsible for all aspects of the quality programs and functions. These include maintaining all HACCP, food safety records, plant audits, mock recall programs and training the plant on these issues and procedures. Performs testing to validate the microbiological quality of current and new ingredients, suppliers, and packages. Provides test data to assure the production of high quality products. Tests current and new concentrate ingredients in process and finished concentrates, and beverages products in development and finished products. The QC Technician will also work with the R&D Team on new product launches. ESSENTIAL DUTIES AND RESPONSIBILITIES: Knowledge of all cleaning agents and applications, external, internal, cleaners, and sanitizers. Properly document and follow all procedures set forth in the frequency guide and standards. Ability to properly fill out batch reports, calculate variations in batch sizes, proper attributes, standards, and other data required on batch report documented per formula. Ability to properly measure and follow proper mixing procedures. Ability to evaluate and troubleshoot batch and make corrections. Ability to perform all testing, evaluations, and documentation of results while following procedures. Ability to troubleshoot and take corrective action on the line. Ability to properly prepare batch tanks for batching, tank rinsing, tank sanitation, odor, and tasting. Full knowledge and capabilities to perform internal pest control program, location of stations, checking and cleaning of stations, and proper documentation on hand of pest control program. Assist supervisors in resolving Quality Control issues, tracking quality trends, recommending and implementing plans to improve quality and production efficiency. Responsible for compliance with Federal and State legislation by establishing and enforcing quality standards; testing materials and product. Ability to collect, analyze and summarize process quality information and trends. Computer literacy required with proficiency in Microsoft Office products including Excel and Word. Typically faces situations that have a variety of interpretations and require careful evaluation. LANGUAGE SKILLS: Ability to read, analyze, and interpret common information, reports and other documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or company representatives. Ability to effectively present information to management. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk, stand for long periods of time, sit and talk or hear. The employee frequently is required to use hands and fingers, to handle, or feel, sit for long periods of time, stand frequently, bend, squat, reach and turn to access files and office equipment. Must be able to lift up to 50 pounds. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Field positions will be exposed to various unfamiliar conditions where Personal Protective Equipment (PPE) must be worn and which may include, but are not limited to manufacturing and warehouse plants, and other locations as directed by supervisor. The noise level in the work environment is usually moderate, but increases significantly in warehouse and manufacturing plants. MINIMUM QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. High School Diploma or GED preferred or equivalent experience. 2-3 years hands-on work experience in the carbonated soft drink industry preferred. Experience in quality control testing procedures and internal and external sanitation of beverage equipment with a clear understanding of all aspects of blending, product attributes recordkeeping, yields, etc. Strong computer skills, including Microsoft business applications and various reporting software. Exceptional interpersonal and verbal communication skills Understands and can follow all OSHA required training. Must be 18 years or older Favorable background and drug exam. Ability and willingness to work a flexible Full Time schedule that may include weekends and holidays. Must be able to provide own transportation to various locations in organizational service areas, as required by duties. Shasta Beverages, Inc. provides equal employment opportunities to all applicants for employment without regard to race, color, religion, sex, national origin, age, disability, gender, genetics, gender identity, disabled veterans or sexual orientation.

Are you an analytical, detail-oriented individual who thrives in a hands-on, innovative environment? Omega Bio-tek, a leader in nucleic acid purification technologies, is looking for a Research & Development Lab Technician to join our team! The R&D Lab Technician will support R&D Department functions by collecting samples, performing testing, documenting and communicating results, and operating and maintaining laboratory equipment. This is your opportunity to play a crucial role in developing cutting-edge solutions while enjoying a dynamic work environment where your contributions are valued. If you're passionate about scientific research and love the idea of working in a flexible, fun, and collaborative lab environment, we invite you to apply! What you will do: Assist in magnetic bead-based development by applying basic chemistry knowledge, particularly in chemical synthesis methods Play a key role in laboratory functions such as DNA extraction, RNA extraction, PCR, qPCR, capillary sequencing and Next Generation Sequencing Generate clear and concise technical reports Execute experimental strategy developed by manager and senior laboratory personnel Work with senior laboratory personnel to review progress and present results Maintain laboratory, cleaning, maintenance, and safety per SOPs Revise and update SOPs, as needed Follow established company SOP and ISO 9001 Guidelines What you will need: BS or MS degree in a life science area, chemistry background preferred 2+ years previous synthetic chemistry or molecular biology laboratory or equivalent experience Experience or knowledge of workflows with DNA & RNA extraction Able to obtain half face respirator certification upon hire Ability to lift 30 lbs What you will bring: Solid communication, organizational, and time-management skills Must demonstrate excellent organizational skills and ability to manage large amounts of technical data and documentation Proficiency with standard computer software Strong attention to detail What we offer: Medical, dental, and vision insurance 100% employer paid short-term and long-term disability & life insurance Generous PTO package Paid day off to celebrate your birthday! Quarterly and yearly bonus incentives Up to 4% match for 401k and Roth Pet insurance Employee Assistance Program Employee Discount Program And much more! What else you need to know: Location: Norcross, GA Hours: Monday - Friday, Flexible start time to be determined with your manager, between 7 AM-9 AM About Omega Bio-tek OUR HISTORY Since its founding in 1998, Omega Bio-tek has been at the forefront of nucleic acid purification by offering products for clinical and basic research, biotechnology, and agricultural applications. DNA and RNA extraction is the first step for so many downstream analyses, and efficient and clean nucleic isolation is crucial. Our goal is to offer high-quality products to help you improve your workflows. For the best option for all of your extraction needs, we offer multiple nucleic acid extraction chemistries including magnetic beads, silica membranes, and salting out. These three different methods are available in a wide range of different kits and configurations for a total of over 900 products. Omega Bio-tek's headquarters are located in Norcross, Georgia, about 25 miles outside of downtown Atlanta. We are proud to be Great Place to Work Certified. We own and operate a 38,000 ft2 facility. We offer products for manual and automated processing and we support our customers by having Hamilton Microlab STAR™, Beckman Coulter Biomek FX, and Thermo KingFisher instruments in-house. If you're ready to make a meaningful impact apply to the Research & Development Lab Technician position at Omega Bio-tek today!

Our Story: Dover Food Retail (DFR) is a leading manufacturer of Display Cases, Specialty Products, Refrigeration Systems, Power Systems and Comprehensive Services; and l eading our industry by Innovating What's Next in glass doors and intelligent merchandising technologies that keep food safe under brands such as HillPhoenix and Anthony. DFR is part of the Climate and Sustainability Technologies segment of the Dover Corporation (NYSE: DOV). Dover is a diversified global manufacturer with annual revenues in excess of $7 billion. DFR is built on creativity and customer-centric innovation delivered by people invigorated by a strong sense of responsibility to help our customers win in their marketplaces. The relationships we build with our customers are as important to our success as the products we manufacture. This collaborative environment delivers FRESH THINKING, reassuring our customers that they choose the best when they choose to work with the people of Dover Food Retail. Job Title: Customer Quality/Warranty Intern Location: Conyers, GA What we're looking for: We are looking for an Engineering Intern to join our Customer Quality and Warranty Management team. This role will assist Customer Quality in the collection, investigation, root cause and solutions of customer/field issues. The role will partner with Warranty team on analysis and investigation of warranty claims to drive improvements in product design and manufacturing process. What you'll be responsible for in this role: You will be working with teams to understand customer feedback and using engineering principles, problem solving techniques, and teaming/communication skills to develop and implement timely solutions. In collaboration with Service teams, collect and analyze data for customer complaints/issues and warranty Understand customer symptoms and develop problem statements using structured problem solving techniques. Obtain failed units and conduct failure analysis to understand Root Cause of Symptom Collaborate with Engineering, Manufacturing, Product Mgt, Quality, Supplier Quality to understand customer and product requirements, design intent and manufacturing processes to develop root cause of failure. Partner with responsible party to drive timely resolution of solutions In collaboration with Service teams, create service bulletins to rapidly share knowledge. Partner with Quality Analytics team to create data models which provide early detection to potential product quality concerns What are the basic qualifications? Enrollment in 4-year Engineering degree program Minimum 3.0 GPA on a 4.0 scale What are the preferred qualifications? Rising Junior to rising Senior Level progressing towards a bachelor's degree in Engineering: Mechanical, Electrical, or Industrial Analytical and conceptual thinking, using logic and reason, creative and strategic thinking Effective statistical analysis skills Effective research and communication skills Effective with written and oral communications Problem solving - being able to solve complex problems effectively and efficiently To be a great fit for the role: Strong Business Acumen and Sound Judgement Builds and Manages Collaborative Relationships Results Driven How We Define Our Values and Why You Should Join Our Team: The backbone behind our collection of outstanding businesses is a team of dedicated employees who protect and enhance our valued reputation for quality and delivering what we promise. It's our values that define Dover to all of our key audiences: our shareholders, customers, prospective employees and especially to ourselves. These values must be expressed in our work and embody our actions, as they form the basis by which we do our jobs, make decisions, and measure our performance. It's our unwavering commitment to maintaining our values that defines who we are as a Company. Collaborative Entrepreneurial Spirit Winning Through Customers Respects and Values People Expectations for Results High Ethical Standards, Openness, and Trust The statements herein are intended to describe the general nature and level of work being performed by employees and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company. Dover Food Retail is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other factors prohibited by law.

BHJ USA, LLC. is a leading supplier of fresh/frozen meat blends to both the wet and dry pet food industries. This position is responsible for performing a variety of tasks in the quality control of the processing of raw materials for the pet food, pharmaceutical and feed industries. Supports QA staff by maintaining logs and record books; troubleshooting and resolving problems; helping with special projects, and data entry by performing the following tasks:• Records observations and measurements and reports results• Calibrates thermometers and other critical instruments used to verify customer specifications and standards.• Reports deviations in data to Quality Manager and pursues corrective actions for resolution.• Produces and distributes Certificates of Analysis (COA's) and finished material holds or releases to required personnel• Monitors cooler and freezer for cleanliness and temperature specifications to protect integrity of raw material.• Conducts live analytical test in all commodities to ensure required customer specifications are in range.• Formulates recipes that adhere with customer specific analytics and weights while utilizing inventory availability minimizing product loss increasing profit margins.• Prepares supplier incident reports by compiling data relative to product or transport/supplier services outside of compliance.• Oversees production supervisors on all tanker/trailer seal identification procedures to ensure they are conducted correctly and documentation is accurate before releasing finished product to carrier.• Observes temperatures on all inbound/outbound loads accepting/releasing or rejecting according to specifications.• Inspects raw product to ensure that it conforms to established quality control guidelines such as kill dates and signs of decomposition.• Verifies all production paperwork such as LOT# association adherence to recipe and weight for tracking purposes.• Inspects the condition of the machine/equipment and tools to ensure no adverse conditions exists that may cause contamination. If found out of compliance a work order is issued to identify area in question.• Adheres to all safety guidelines and wearing of all required safety gear (PPE)• Adheres to attendance guidelines of the company.Will be frequently exposed to cool and wet conditions. Must be able to lift up to 30 pounds on a frequent basis and be able to work around raw beef, chicken or other similar raw materials and odors. We support a drug free workplace and conduct pre-employment drug screening. Must be authorized to work in the U.S. We participate in E-Verify. EEO Employer.

What We Do FOX Factory designs, engineers, manufactures and markets performance-defining products and systems for customers worldwide. Our premium brand, performance-defining products and systems are used primarily on bicycles, side-by-side vehicles, on-road vehicles with and without off-road capabilities, off-road vehicles and trucks, all-terrain vehicles, snowmobiles, specialty vehicles and applications, motorcycles, and commercial trucks. Some of our products are specifically designed for and marketed to a variety of leading cycling and powered vehicle original equipment manufacturers ("OEMs"), while others are distributed to consumers through a global dealer and distribution network. Fox Factory Holding Corp. is the holding company of FOX Factory, Inc. and is publicly traded (FOXF) on Nasdaq. Why you should join us Not only do we provide competitive wages, you will also have access to great benefits and employee discounts. But more importantly, it's a fun environment where we truly enjoy working as a team and bringing great products to our customers! If this sounds like something you would love to do, and a place you want to be a part of, get in touch with us by submitting your application. We look forward to hearing from you! Position Summary: Inspects finished products, products being processed, incoming materials, parts and assemblies, etc. for conformance to company standards. Position Responsibilities: * Checks randomly selected samples and verifies accuracy of equipment or process. * Reports conditions requiring immediate repair. * Uses advanced inspection methods to develop and conduct quality programs. * Works under general supervision. * Keeps records and makes reports indicating results of inspections. * Uses experience and judgment for planning and accomplishing goals. * May inspect work areas to detect unsafe conditions. * May obtain samples to conduct studies in laboratory analysis and determines measures to be taken to remedy deviations from standards. * Conduct Product and Process audits and LPA (Layered process audits). Specific Knowledge, Skills or Abilities Required: * Strong and accurate data entry skills * Intermediate skills in using Microsoft tools (Outlook, Word, Excel) * Excellent organization skills * Excellent problem-solving skills. * Self-motivated - able to work with minimal supervision * Use of powered hand tools * Operating a Forklift * Testing of raw materials and/or finished products, which may or may not include industry standard test methods (e.g. ANSI/ASME measuring standards) Position Qualifications: Education: HS graduate or equivalent Experience: 1+ years of experience in quality and/or inventory Previous experience with Geometric Dimensioning and Tolerancing (GD&T) Previous experience with Oracle, SAP or other database management systems Work Environment and Physical Requirements: Activity Constantly - 6+ hours : Stand, Walk, Twist/Turn, Stoop/Bend Frequently - 3 to 6 hrs. : Lift to 50 lbs. * Manufacturing Environment * Working in hot and cold climates * Personal Protective Equipment - Ear protection is readily available in high level noise areas * Working around machinery with moving parts * Working around moving objects or vehicles, * Potential for slippery and uneven walking surfaces including use of ladders * Working in close proximity to others * Exposure to offensive odors * Vision abilities required to validate and enter data on computer as well as calibrated measurement tools * Exposures to and working with hazardous waste Disclaimer: This list does not represent all physical demands. Descriptions are representative of those that must be met by employee to successfully perform the essential functions of the job. Reasonable accommodation may be provided to enable individuals with disabilities to perform the jobs' essential functions. Note: FOX provides equal employment opportunities for all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, gender identity, sexual orientation, marital status, religion, age, physical disability (including HIV and AIDS), mental disability, results of genetic testing, or service in the military, or any other characteristic protected by the laws or regulations of any jurisdiction in which we operate. We base all employment decisions -including recruitment, selection, training, compensation, benefits, discipline, promotions, transfers, layoffs, terminations and social/recreational programs - on merit and the principles of equal employment opportunity. Fox offers an excellent compensation package and wide-ranging opportunities for professional development. Medical, Dental, Vision, Health Spending and Dependent Care Savings Accounts, Disability and Life Insurance benefit programs are available, as is a 401k plan with employer matching. Eligibility for all benefit programs is defined by the applicable plan document or employee handbook.

Job Description BHJ USA, LLC. is a leading supplier of fresh/frozen meat blends to both the wet and dry pet food industries. This position is responsible for performing a variety of tasks in the quality control of the processing of raw materials for the pet food, pharmaceutical and feed industries. Supports QA staff by maintaining logs and record books; troubleshooting and resolving problems; helping with special projects, and data entry by performing the following tasks: • Records observations and measurements and reports results • Calibrates thermometers and other critical instruments used to verify customer specifications and standards. • Reports deviations in data to Quality Manager and pursues corrective actions for resolution. • Produces and distributes Certificates of Analysis (COA's) and finished material holds or releases to required personnel • Monitors cooler and freezer for cleanliness and temperature specifications to protect integrity of raw material. • Conducts live analytical test in all commodities to ensure required customer specifications are in range. • Formulates recipes that adhere with customer specific analytics and weights while utilizing inventory availability minimizing product loss increasing profit margins. • Prepares supplier incident reports by compiling data relative to product or transport/supplier services outside of compliance. • Oversees production supervisors on all tanker/trailer seal identification procedures to ensure they are conducted correctly and documentation is accurate before releasing finished product to carrier. • Observes temperatures on all inbound/outbound loads accepting/releasing or rejecting according to specifications. • Inspects raw product to ensure that it conforms to established quality control guidelines such as kill dates and signs of decomposition. • Verifies all production paperwork such as LOT# association adherence to recipe and weight for tracking purposes. • Inspects the condition of the machine/equipment and tools to ensure no adverse conditions exists that may cause contamination. If found out of compliance a work order is issued to identify area in question. • Adheres to all safety guidelines and wearing of all required safety gear (PPE) • Adheres to attendance guidelines of the company. Will be frequently exposed to cool and wet conditions. Must be able to lift up to 30 pounds on a frequent basis and be able to work around raw beef, chicken or other similar raw materials and odors. We support a drug free workplace and conduct pre-employment drug screening. Must be authorized to work in the U.S. We participate in E-Verify. EEO Employer.

Catalyst Nutraceuticals has been one of the fastest growing manufacturers in sports nutrition and other dietary supplements. We have built our business around quality, service, and the ability provide the absolute best product for our customers. We currently manufacture flavored powders and capsules but it is our flavors and ability to work with our customers that has helped set us apart in a competitive industry. We are looking for a Quality Control Inspector to join our team and be a contributing part of our tremendous growth! Essential duties & responsibilities- Responsibilities include but are not limited to * QC inspections and testing. Routine quality check of samples and production lines * Production documentation preparation and Document control * Root cause analysis and corrective actions. Monitors and follows up on corrective actions to ensure successful implementation and notify responsible personnel when corrective actions are delinquent * Maintain paper and electronic records * Maintain organized and efficient work flow and demonstrate high degree of accuracy * Provide technical support to Operations and Management * Able to prioritize and complete on-going tasks assigned by QC Manager * Work collaboratively and safely in production and lab environment * Lab organization Qualification: * Science background. Food science, Nutrition science, Pharmacy or manufacturing background is a BIG PLUS * Basic knowledge about sample collection, lab sampling, Good Manufacturing Practices (GMP, cGMP), Standard Operating Procedures (SOP), good documentation, attention to details * Demonstrated proficiency in writing and composition skills required * Basic computer job skills including logging on to systems, ability to communicate by email, enter database information, create presentations, download forms, and preserve/backup important data. Intermediate to advanced skill in Microsoft Word and Excel required * Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals * Required: Excellent attendance and reliability Requirements * Must be able to perform repetitive movements of bending, twisting, pumping, lifting, and pushing including picking up 25 kg (55 pounds) constantly throughout the day. * Must be able to tolerate standing for long periods of time. * Must be able to tolerate heat and or cold variations * Must be able to tolerate sitting for possibly extended periods of time and using a computer and magnifying glass to view small print * Must be attentive and alert to cautions of forklift and other personnel walking in the Quarantine Cage area.

IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst - Day Shift position at its facility in Stone Mountain, GA. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field (required) - Strong attention to detail - Proficiency with data entry and computer applications - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position and is eligible for standard benefits after a brief waiting period. The schedule for this position is on a rotating shift basis, with hours from 7:00AM to 7:00PM: the first week is Wednesday-Thursday; the second week is Monday, Tuesday, Friday, Saturday, and Sunday. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from

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 Performs analysis of product quality inspection of parts, raw materials, and/or packaging components using calibrated measurement equipment to verify product meets specifications. Completes documentation relating to material inspection and enters data into database/software systems; such as MES, SAP or LIMS. Communicates defect information to supervisor and quality assurance for corrective actions. Assists with 5S cleaning procedures. Ensures the inspections of material are accomplished per SOP and quality standards, while meeting the production plan. Actively participates in natural work groups to identify process problems and contribute solutions. Participates in day-to-day business activities, safety, quality, and training needs. ISO/FDA/GMP compliance. Skills: Qualifications Education: Additional Information For more information, Please contact Sneha ************ ***********************************

Catalyst Nutraceuticals has been one of the fastest growing manufacturers in sports nutrition and other dietary supplements. We have built our business around quality, service, and the ability provide the absolute best product for our customers. We currently manufacture flavored powders and capsules but it is our flavors and ability to work with our customers that has helped set us apart in a competitive industry. We are looking for a 2nd Shift Quality Control Inspector to join our team and be a contributing part of our tremendous growth! Essential duties & responsibilities- Responsibilities include but are not limited to * QC inspections and testing. Routine quality check of samples and production lines * Production documentation preparation and Document control * Root cause analysis and corrective actions. Monitors and follows up on corrective actions to ensure successful implementation and notify responsible personnel when corrective actions are delinquent * Maintain paper and electronic records * Maintain organized and efficient work flow and demonstrate high degree of accuracy * Provide technical support to Operations and Management * Able to prioritize and complete on-going tasks assigned by QC Manager * Work collaboratively and safely in production and lab environment * Lab organization Qualification: * Science background. Food science, Nutrition science, Pharmacy or manufacturing background is a BIG PLUS * Basic knowledge about sample collection, lab sampling, Good Manufacturing Practices (GMP, cGMP), Standard Operating Procedures (SOP), good documentation, attention to details * Demonstrated proficiency in writing and composition skills required * Basic computer job skills including logging on to systems, ability to communicate by email, enter database information, create presentations, download forms, and preserve/backup important data. Intermediate to advanced skill in Microsoft Word and Excel required * Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals * Required: Excellent attendance and reliability * Must be able to perform repetitive movements of bending, twisting, pumping, lifting, and pushing including picking up 25 kg (55 pounds) constantly throughout the day. * Must be able to tolerate standing for long periods of time. * Must be able to tolerate heat and or cold variations * Must be able to tolerate sitting for possibly extended periods of time and using a computer and magnifying glass to view small print * Must be attentive and alert to cautions of forklift and other personnel walking in the Quarantine Cage area.