(USA-PR-Cayey) Quality Inspector / Manufacturing

Job DescriptionConducts all system inspections relating o the manufacturing of products including formulation, filling, sealing, labeling, and packaging operations. Follows QSR, ISO, safety and environmental regulations. RequirementsCandidates must be available to work any shift including 12 hours shift.High school graduate. Able to read and write English. Two years experience in manufacturing environments. Q.C. or P.C. experience highly desirable. Computer literate including MS Word, MS Excel and IBM Lotus Notes. Why Kelly®?At Kelly Services®, we work with the best. Our clients include 95 of the Fortune 100™ companies, and more than 70,000 hiring managers rely on Kelly annually to access the best talent to drive their business forward. If you only make one career connection today, connect with Kelly. About Kelly Services® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $ 5.3 billion. Visit kellyservices.com and connect with us on Facebook, LinkedIn and Twitter. Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.]] Category: Manufacturing/ Production/ Operations
Jobs

(USA-PR-Juncos) Associate Quality Control |PR

Associate Quality Control Under general supervision, responsible for one or more of the following activities in Quality Control including analytical testing, characterization, method development, and sample and data management. Perform routine laboratory procedures. May perform aseptic aliquot ting, sampling and analysis for compendia and non-compendia methods. May perform non-routine lab procedures under close supervision. Perform or review one or more of the following: sample testing, standards preparation and testing procedures, compendia and non-compendia test methods, environmental monitoring, reagents and solutions preparation, sample management and equipment maintenance. Prepare complete, accurate, concise laboratory documentation. Data entry, review, analysis and communication of results. Perform general lab housekeeping. Maintain/operate specialized equipment. Participate in the document revision process. Comply with safety guidelines, cGMPs and other applicable regulatory requirements. May participate in lab investigations/ audits. Maintain training proficiency. May approve lab results. Requirement Bachelors degree in Science. At least 1 year of experience in laboratory or quality control Available to work any shift (24/7) Why Kelly®? With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 11,000 scientific professionals last year. You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today. About Kelly Services® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $ 5.3 billion. Visit kellyservices.com and connect with us on Facebook, LinkedIn and Twitter. Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.]] Category: Biotech/Clinical/R&D/Science
Jobs

(USA-FL-Largo) Quality Control (QC) Inspector

Quality Control (QC) Inspector Pharma Exp Contract to Perm We have six (6) openings. (3 on 1st Shift & 3 on 2nd Shift) 1st Shift somewhere between 630am – 830 am, working to 130pm – 430pm (need to determine exact start times) 2nd Shift somewhere between 330pm – 430pm, working to 1100pm – 100am (need to determine exact start times) RESPONSIBILITIES Perform on-line inspection activities including appropriate documentation as required. These activities include pre- and post-line clearances, inspection of staged components for correctness, in-process sample evaluation, finished goods inspection, verification of line clearances at appropriate times. Prepare QA documentation for upcoming lots. Verify release and correct staging for materials prior to weighing for the compounding department. Release compounding bulk to packaging. Perform initial review of compounding and packaging batch records. Perform review of purified water use log. Ensure that corrections are made, and mentor the guidance of corrections found within packaging batch records, and compounding batch records. Assist in verification of product, raw material, and component expiration dates. Initiate the collections of finished goods sampling for special/additional testing. Obtain, prepare, and store all retain samples. Maintain the retain areas in a neat and orderly manner. Obtain, prepare, and ensure accuracy of stability samples as directed by the Quality Control Department. Obtain, prepare, and submit specified laboratory samples during packaging for chemical and microbiological testing as required. Perform Raw Material Sampling and submit samples to Laboratory for testing. Inspection of Labeling materials, and recommend disposition of said labels. Monitor the compounding of controlled drugs and other compounding activities as required by procedure(s). Perform annual retain sample review and assist with retain destruction. Assist in taking inventory of materials, as required. Follow all SOP’s (Standard Operating Procedures) pertinent to quality assurance inspection. Attend training sessions in order to maintain and increase skills and knowledge of current good manufacturing practices (cGMPs) and safety awareness. Perform other duties as assigned by the Quality Assurance Supervisor. EDUCATION AND EXPERIENCE An Associate Degree is required. Detail oriented, and proficient in mathematics. Two years’ experience in pharmaceutical industry preferably in quality assurance functions and a working knowledge of cGMP’s. PHYSICAL REQUIREMENTS Prolonged periods of sitting or standing or constant walking. The ability to lift up to 25 pounds. The ability to climb ladders or stairs while carrying up to 25 pounds. ACCOUNTABILITY Reports directly to the Quality Assurance Supervisor. You can also email me directly to antc056@kellyservices.com Why Kelly®? With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 11,000 scientific professionals last year. You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today. About Kelly Services® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $ 5.3 billion. Visit kellyservices.com and connect with us on Facebook, LinkedIn and Twitter. Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.]] Category: Biotech/Clinical/R&D/Science
Jobs

(USA-NC-Cary) Raw Material Quality Engineer

Raw Material Quality Engineer – NC, WI or IA We currently have a great and rewarding opportunity for a Raw Material Quality Engineer to support a leading, global manufacturer company of silicone release liners at either their NC, WI or IA locations. The Raw Material Quality Engineer will be responsible for driving quality improvement across the supplier base for this company. Position Overview & Responsibilities: Lead Raw Material quality efforts Raw Material specifications Manage Raw Material CoA’s Lead Raw Material QIT (Quality Improvement Team) efforts and manage action items in coordination with sourcing Manage vendor ratings Work closely with sourcing and manufacturing facilities Perform data analysis using statistical software In support of Raw Material specification limits SPC (Statistical Process Control) and SQC (Statistical Quality Control) Identify improvement opportunities Ensure compliance with Quality Management System (based on ISO 9001) Support sourcing with LegalHarvest Verification tracking as needed Supplier quality improvement audits Supplier qualification audits Position Qualifications: BS degree in engineering, math, or science 3 – 7 years of experience in data analysis 3 – 7 years of experience in quality systems, with ISO certifications’ experience preferred Computer skills: Advanced MS Excel and PowerPoint preferred Database (MS Access) experience preferred Statistical software essential, Minitab preferred Why Kelly®? Kelly puts you in charge of your career, with access to cutting edge projects and technologies in industry leading organizations. Top companies throughout the world have trusted Kelly as a premier source of engineering talent and services since 1965. And engineering job seekers know Kelly as a firm with an unmatched reputation for quality, integrity and professionalism. Whether you seek the variety and flexibility of working on short term project engagements, or prefer contract-to-hire or direct hire placement with our clients, apply with Kelly to explore opportunities that suit your specific professional interests. About Kelly Services® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $ 5.3 billion. Visit kellyservices.com and connect with us on Facebook, LinkedIn and Twitter. Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.]] Category: Engineering
Jobs

(USA-GA-Cartersville) Quality Assurance Manager

Quality Assurance Manager FUNCTIONAL RESPONSIBILITY Understands, communicates, and shares Company vision throughout division/organization and provide cross-functional perspective, direction, and support Provides leadership and personal support; coaches, guides, nurtures and develops the right people; leads by example Drives Company focus, manages culture, encourages strong work ethic, and fosters an environment of trust and respect Develops group and individual performance plans in alignment with Company goals and objectives; communicates clearly defined individual and group objectives; maintains level of productivity in unit Trains employees to do their job; sets standards for work performance Monitors performance and provides feedback to direct reports through formal and informal performance feedback; regularly communicates with staff to achieve mutual understanding and desired results Recognizes and addresses performance strengths and limitations of subordinates Manages employee attendance to ensure compliance with Company standards; approve/monitor overtime Communicates and supports Company policies and decisions in a positive manner Develops staffing needs, selects new employees, makes recommendations in job evaluation and compensation, recommends termination actions Conducts team meetings with department employees; includes monthly safety topic, ISO, DOE and other applicable training Handles employee issues, concerns, and complaints in an objective and confidential manner Provides employees with a safe, comfortable, and rewarding work environment Prepares and monitors department budget ESSENTIAL DUTIES Plans and executes all phases of quality control within the bottling operations adhering to quality, productivity, held inventory, capacity, customer, compliance and budgetary standards Ensures team is in place, trained and performing at optimal levels in order to deliver daily bottling production requirements/standards and other essential deliverables Creates and manages scheduling of technicians to ensure efficient quality control performance and coverage Executes continuous improvement collaboration and champions initiatives that improve overall quality control, bottling processes, equipment performance, production capacity, package quality and related measures Enforces Safety, ISO, HACCP, cGMP, DOE and other applicable business critical standards NON-ESSENTIAL DUTIES Manages inventory controls of all QC Laboratories Ensures all administrative tasks are accurately completed in a timely manner Creates and sustains a high standard of housekeeping in the quality control areas utilizing the 5S Tool *Other duties may be assigned MINIMUM REQUIREMENTS Education and Experience Bachelor’s Degree in business, food science or related field. 7 to 10 years’ experience in bottling or consumer goods manufacturing. Requires in-depth experience in a high paced Lean production environment 5 to 7 years direct leadership and management in food/beverage manufacturing Knowledge, Skills, and Abilities Project management experience. Computer literacy in a SAP, statistical analysis software and Microsoft environment (Word, Excel, PowerPoint, Visio, OneNote, Outlook). Bottling equipment knowledge preferred. Understands packaging, analytical and microbiological lab equipment and processes Experience with computerized data management systems You can also apply directly to me antc056@kellyservices.com Why Kelly®? With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevant projects. Our connections can lead you to innovative scientific pursuits you’ll be proud to help advance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 11,000 scientific professionals last year. You pursued a career in science to fuel your quest for knowledge and your desire to make the world a better place. Let Kelly fuel your career—connect with us today. About Kelly Services® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2016 was $ 5.3 billion. Visit kellyservices.com and connect with us on Facebook, LinkedIn and Twitter. Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.]] Category: Food Services/Hospitality
Jobs