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TKC Holdings jobs in Raleigh, NC
- 60 jobsFood Service Worker / Utility Worker
TKC Holdings
TKC Holdings job in Raleigh, NC
Wage Rate $18.75/hour Are you looking for a career with premium benefits and the potential for growth? At Trinity Services Group, we have created something special, a better place to work and grow. Many employees start just expecting a paycheck but end up with a rewarding career. We provide exceptional training and a clear career path. We also offer a $250 bonus for completing our Rookie's Fast Track Program within the first 60 days! We now also offer DailyPay providing you immediate access to earned wages. Work Today, Get Paid Today! We are proud to be a military and veteran friendly employer. About This Position This position is working inside a jail/correctional facility at the Wake County Detention Center. The Food Service Worker accurately and efficiently prepares and serves a variety of food items in accordance with assigned work instructions and menus within a correctional setting. This position also utilizes a variety of food preparation utensils and machines in preparing food. Our ideal Food Service Worker excels at the following: * Passionate about food and service * Has a solid understanding of food handling regulations * Desire to always learn more * Ability to work as a team member, as well as independently * Ability to multi-task and adapt to changes quickly * Dependable and flexible Responsibilities * Prepare and assist team members in the preparation of quality foods according to the planned menu, recipes, and work instructions in a timely manner. * The duties of the Food Service Worker include, but are not limited to, cleaning as you go, maintaining a neat and food safe workstation, pulling trash, sweeping, mopping, and any other duties assigned within the facility. * Serve food during planned meal schedules and according to department policies and procedures. * Utilize kitchen utensils/equipment to cook, prepare and serve food according to recipes. Use proper utensils to serve menued portions and as appropriate to meet clients' nutritional needs. * Abide by all food safety regulations pertaining to sanitation, food handling and storage. * Maintain a clean work area/environment that includes cleaning of refrigerators/freezers, cooking equipment, and serving equipment. * Function in a fast-paced environment, perform routine kitchen tasks, while being organized and clean. * Keep up with garbage collection and keep kitchen floors clean from excess food/trash. * This role includes physical demands such as lifting, bending, pushing, kneeling, walking, and standing for extended periods of time. * Be able to stand and be on your feet for much of the scheduled shift. * Perform other related duties as assigned. What You'll Need * Required: * High School Diploma or Equivalent, and you must be at least 18 years of age * Preferred: * Prior institutional food service or restaurant experience is a plus Benefits Trinity Services Group (TSG) offers comprehensive benefits to all regular-full time employees: * Medical w/prescription coverage * Benefit Credit received when enrolled in a TKC medical plan, to help offset your benefit costs. Benefit Credit of $750 annually, will be divided evenly among your paychecks throughout the Plan Year. * Dental * Vision * Basic Life and Basic Accidental Death and Dismemberment Insurance * Voluntary benefits (i.e. short term, long term disability and many more) options may be selected to create the right package for you TSG also understands the importance of work life balance and planning for the future. To help with both of these, employees are eligible for: * Paid Time Off * Company Match for the 401(k) Retirement Savings Plan * We now also offer DailyPay providing you immediate access to earned wages. EEO Statement Equal Employment Employer as to all protected groups, including protected veterans and individuals with disabilities. We maintain a drug-free workplace. A copy of our Privacy Policy and CA Employee Privacy Notice can be found here: ****************************************** Responsibilities This position is working inside a jail/correctional facility at the Wake County Detention Center. The Food Service Worker accurately and efficiently prepares and serves a variety of food items in accordance with assigned work instructions and menus within a correctional setting. This position also utilizes a variety of food preparation utensils and machines in preparing food. Our ideal Food Service Worker excels at the following: - Passionate about food and service - Has a solid understanding of food handling regulations - Desire to always learn more - Ability to work as a team member, as well as independently - Ability to multi-task and adapt to changes quickly - Dependable and flexible Responsibilities - Prepare and assist team members in the preparation of quality foods according to the planned menu, recipes, and work instructions in a timely manner. - The duties of the Food Service Worker include, but are not limited to, cleaning as you go, maintaining a neat and food safe workstation, pulling trash, sweeping, mopping, and any other duties assigned within the facility. - Serve food during planned meal schedules and according to department policies and procedures. - Utilize kitchen utensils/equipment to cook, prepare and serve food according to recipes. Use proper utensils to serve menued portions and as appropriate to meet clients' nutritional needs. - Abide by all food safety regulations pertaining to sanitation, food handling and storage. - Maintain a clean work area/environment that includes cleaning of refrigerators/freezers, cooking equipment, and serving equipment. - Function in a fast-paced environment, perform routine kitchen tasks, while being organized and clean. - Keep up with garbage collection and keep kitchen floors clean from excess food/trash. - This role includes physical demands such as lifting, bending, pushing, kneeling, walking, and standing for extended periods of time. - Be able to stand and be on your feet for much of the scheduled shift. - Perform other related duties as assigned.$18.8 hourly Auto-Apply 48d agoSenior IT Technical Support Analyst
Artech Information System
Raleigh, NC job
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 Candidate will manage Corporate Security applications from an on-going support perspective as well as lifecycle and change management. Requirements • AMAG/CCURE/Salient/Passage Point experience strongly preferred; familiarity with physical access control and video management systems technology a must • Active Directory, HR Data integration, windows server experience • Experience with lifecycle management and upgrades • Ability to write and work with business partners to execute System and Unit Test Plans • Experience with Service Transitions from Projects to Production • Experience using ITIL for incident and problem management • Vendor management experience • Ability to multi-task as candidate will manage concurrent workstreams • Strong communication skills as project teams will primarily be virtual Qualifications Nice to have • Experience with GSK IT systems and processes • Experience with managing GSK GxP validated systems, including writing GxP documentation and managing the project through the documentation process • Experience with Lean Sigma Additional Information For more information, please contact Tinny Jindal ************$69k-92k yearly est. 60d+ agoManufacturing Technician
Artech Information System
Sanford, NC job
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 • The person filling this position operates all equipment in two assigned Manufacturing areas. He or she will also clean equipment and facilities, and provide documentation of all duties in accordance with Good Manufacturing Practices. Incumbent will perform all duties in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies and procedures. The incumbent will be required to attend quality-training programs and orientations on an annual or as needed basis. • This individual will be required to become familiar with domestic and international regulatory requirements associated with manufacturing and biological processes. Annual performance goals and objectives will be evaluated against specific quality performance requirements as defined by the Manufacturing Supervisor. • Mandatory commitment to report to management any potential or actual deviations from regulatory requirements. Ongoing input regarding quality process improvements. • Master documentation procedures by following detailed written and verbal instructions in order to complete assigned tasks (follow area SOP s). Demonstrate knowledge of procedures by performing tasks and duties and maintaining detailed records in a manner compliant with cGMPs. • Perform routine job duties, which may include vacuuming, mopping ceilings, walls and floors, emptying trashcans, etc. Prepare production glassware and other equipment by operating industrial washers, autoclaves and depyrogenation ovens. • Clean and sterilize process equipment (tanks, fermentors) as needed. Demonstrate and instruct proper gowning and aseptic processing procedures. Work with individuals as a team. • Work various shifts and some weekends. Operate and troubleshoot production equipment in assigned area and report unusual conditions or concerns about the process or equipment to area Supervisor. Train new employees on production processes. • Perform lab work, such as: performing sample dilutions, pH, and conductivity readings. The following combinations of education and work experience are considered acceptable: BA/BS Tech/Bus/Industry/Science with minimum 2 years direct regulated manufacturing pharma/biotech experience AAS Science related with minimum 4 years direct regulated manufacturing pharma/biotech experience HS or equivalent with minimum 8 years direct regulated manufacturing pharma/biotech experience Or progression from Bio-processing Technician Level I. that includes additional internal development curriculum List certificates (if any) required. • 1. Must complete training in assigned area and comply with applicable safety, OSHA, and environmental safety requirements. 2. Must complete training and comply with applicable cGMP requirements. State type and minimum number of years of prior experience required to perform job duties. • A minimum of four years pharmaceutical experience in biological manufacturing is preferred. List specific skills and minimum expertise (ie., typing speed (WPM), fully trained ability to learn, etc.) required to perform job duties. • 1. Moderate repetitive standing, ladder climbing, repetitive bending, pushing, and lifting (up to 40 lbs) required on a daily basis. • 2. Basic understanding of the metric system. • 3. Be able to rationalize by suggesting solutions to unusual conditions and/or process concerns. • 4. Must possess mechanical ability to assemble and operate equipment. • 5. Must pay attention to detail by following procedures and noting unusual conditions. • 6. Must have written and oral communication to read procedures, write accurate observations and follow directions Position Comments visible to MSP and Supplier: Skills Skills Skills:Category Name Required Experience No items to display. • Additional Skills: GMP experience required Pharma experience highly preferred Bioprocessing experience in a cGMP environment, knowledge of Clean and Steam in Place Systems, perform facility cleanings, collecting WFI and Clean Steam samples. Experience with autoclave and industrial washers . Qualifications A minimum of four years pharmaceutical experience in biological manufacturing is preferred. List specific skills and minimum expertise (ie., typing speed (WPM), fully trained ability to learn, etc.) required to perform job duties. • 1. Moderate repetitive standing, ladder climbing, repetitive bending, pushing, and lifting (up to 40 lbs) required on a daily basis. • 2. Basic understanding of the metric system. • 3. Be able to rationalize by suggesting solutions to unusual conditions and/or process concerns. • 4. Must possess mechanical ability to assemble and operate equipment. • 5. Must pay attention to detail by following procedures and noting unusual conditions. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter$30k-40k yearly est. 60d+ agoValidation Consultant
Artech Information System
Zebulon, NC job
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 Job Purpose and Key Responsibilities: (Why jobexists/what it must achieve) Ensure that the GSK Zebulon - Building Management System (BMS) Replacement Project commissioning / validation program smeet all regulatory and local requirements. Responsible for the development, planning, and implementation of commissioning, qualification and validation for the manufacturing, packaging, facilities, computer controls, and cleaning processes. Write, review and execute documentation to conduct all commissioning and / or validation activities to support equipment modification / upgrade projects and maintain existing validated states. Requires expertise in regulatory compliance,ability to determine requirements to validate and discern appropriate level of validation for the process. Responsible for driving all aspects of the Commissioning Life Cycle and / or Validation Life Cycle from design throug hoperation and improvement. Develop, update, and maintain the Project Validation Master Plans and Project Commissioning Mast Plans. Coordinate resources needed to complete commissioning and / or validation tests. Provide commissioning / validation support during the design, evaluati on, and procurement stages. Monitor commissioning /validation criteria and assure compliance. Collaborate with Engineering on the developmentof Installation and Operational Qualification documents. Write and execute process, packaging, computer,facility, and cleaning validation protocols and summary reports. Interface with Manufacturing, Packaging, Logistics, Engineering, and external vendors to facilitate and drive protocol execution. Author, review, revise, or approve Standard Operating Procedures (SOPs) as required. Maintain up to date knowledge of commissioning and validation requirements, practices, and procedures and instruct other members of the project team. Develop and implement improvement initiatives with filling/packaging/computer and facility/utility validation activities. Manage simultaneous projects.Participate on cross-functional teams, who address specific problems, facilitate discussion and research, enabling procedures to become more efficient, and to build and enhance inter departmental relationships. Specialized Knowledge: (breadth & depthacross disciplines or functions; expertise in field required) Bachelors degree in a technical or scientific discipline or related work experience. Minimum 3 years experience in Manufacturingvalidation and the Pharmaceutical or Healthcare Industry required Workingknowledge of cGMP regulations In depth knowledge of process, packaging,facility, and cleaning validation Good computer skills and Microsoft Word,Excel, and PowerPoint. Quality and detail oriented with documentation skills. Excellent written and oral communication skills.Ability to develop and facilitate validation training Flexibility to work extended hours to achieve results. Prior experience at the Zebulon site andpossession of current hard badge are preferred. Qualifications BA/BS + 5 years Pharmaceutical exp. MS + 3 years Pharmaceutical exp. 2 years Pharmaceutical QA exp. Knowledge of cGMP's/FDA and other Regulatoryrequirements, and Quality Systems Knowledge of Engineering Technology Advanced understanding and skills with MS Word,and Excel Work Experience Proven project management experience in leading,researching, developing, data analysis, and executing GMP / System Life Cycle /Validation documentation and reports for utilities system (VP, Commissioning,IQ, OQ, PQ) Hands on validation experience utilities system sand supporting automation processes including HVAC, Compressors, Water systems,Dust collectors, Building Management System(BMS) (Rockwell Automation, GEMS),Environmental Monitoring Systems (EMS) (Rockwell Automation, GEMS), Lab instrumentation, Temperature and humidity profiling, (facilities, chambers,process equipment) Ability to perform calibrations and generatecalibration reports Additional Information Thanks and Regards Tinny Jindal ******************************$93k-127k yearly est. Easy Apply 3h agoSecurity Coordinator
Artech Information System
Zebulon, NC job
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 Job Title: Security Coordinator Location: RTP, NC 27709 Duration: 10+ Months (Contract) Requirement: The role is responsible for the triage and input of reported incidents onto the incident management system. Qualifications/Minimum Required (Education/Experience/Competencies): Ability to handle confidential and sensitive issues Ability to present information clearly and logically Good organization and communication skills and the ability to deal with all levels of the organization Team player that can interact and establish relationships with other client Professionals Ability to multitask Ability to work independently with little or no supervision Technical Skills: • General IT Technical experience required • General understanding of IT Security concepts • Must have experience with Microsoft Office (Outlook, Sharepoint, Live Meeting, etc.) • Management of data and relationships within technical tool solutions Purpose/Key Responsibilities: Successful candidate will be responsible for the following activities: CSIR Coordination: • Responsibility for first level support of the CSIR Process • Respond to investigations of common incident types by following written standard operating procedures • Perform a variety of routine incident management tasks • Maintain all documentation associated with investigations • Follow agreed procedures for notification of CSIR investigations • Assist with providing feedback on the clarity of standard operating procedures and updating the procedures, where appropriate • Assist with design, creation and development of online CSIR documentation and content Qualifications Require security coordinator .General IT Technical experience required Additional Information Regards, Shubham ************ shubham.sATartechinfoDOTcom$31k-53k yearly est. 60d+ agoQuality Control Analyst II - Biochemistry, 4556313
Artech Information System
Holly Springs, NC job
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 Job Purpose Primary responsibilities for this position include performing tasks associated with release testing and reviewing laboratory data. The analyst will be responsible for ensuring that the Seqirus samples are collected, tested and reviewed according to quality requirements and results reported are valid, accurate and documented per applicable regulatory and corporate requirements. Major Accountabilities Performs testing and associated tasks without errors per applicable SOPs and protocols. Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written. Participates in lean lab operation, 6S laboratory layout, preventive action & continuous improvement programs. Participates in cross-training to support staff availability within QC department. Performs shift-work as necessary to support manufacturing operations. Skills: 3+ years of directly related laboratory experience or equivalent Knowledge of laboratory practices and instruments required Knowledge of GMP's, safety regulations and data integrity preferred Experience with DNA Threshold analysis Qualifications Education: Bachelor's degree in Scientific discipline or associate's degree and 3+ years of industry experience or equivalent. Additional Information For more information, please contact Akriti Gupta ************** Morristown, NJ 07960$63k-99k yearly est. 60d+ agoMedical Writer/Technical Writer
Artech Information System
Sanford, NC job
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 Summarize the primary purpose & key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (i.e. Global vs. Country/Region) It may be helpful to complete this section after you have finished the other sections of the document. Incumbent will assist in the creation, review and revision of documents (SOPs, forms, jobs aids, training material, etc.) and other manufacturing department documents. Incumbent will work with co-workers and supervisors to understand the objective of each document to ensure that all documents contain the required content. Incumbent will interpret information and organize it properly for accuracy, readability and format, while ensuring the proper grammar and spelling is used in all documents. Perform all duties in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies and procedures. POSITION RESPONSIBILITIES • In order of importance, list the primary responsibilities critical to the performance of the position. It is recommended not to list actual tasks but focus on essential responsibilities that highlight accountability and level of judgment required. • Edit and format incoming requests for new or revised documents (SOPs, forms, jobs aids, training material, etc.) and assist in tracking each revision through the approval workflow. • Provide assistance with development of new and revised documents including suggestions for suitable terminology, content, and format while ensuring that site policies comply with Corporate guidelines. • Participate in the bi-annual review of Standard Operating Procedures, forms and other related documents. Complete commitments as assigned to facilitate Corrective Actions/Preventative Actions. • Participate in the bi-annual review of Standard Operating Procedures, forms and other related documents. Complete commitments as assigned to facilitate Corrective Actions/Preventative Actions. • Assist in maintaining control of documentation to include accurate document history and change revision documentation. Qualifications EDUCATION AND EXPERIENCE • Indicate the formal education, certification or license required and/or preferred. Include the minimum number of years of relevant experience required for the position (where legally permissible). • Bachelor s degree in Science, Communications, or English, with at least 2 years related experience in technical writing, preferably in a pharmaceutical or related environment • AS in Communications or related field with minimum of 5 years related experience in technical writing, preferably in a Biopharmaceutical or other regulated environment. TECHNICAL SKILLS REQUIREMENTS • Indicate the technical skills required and/or preferred, as applicable. • Able to edit documents quickly and efficiently to incorporate required revisions • Develops and applies standardized document formats where applicable. • Able to learn and navigate document control and e-systems to facilitate document routing and approval • Able to effectively proofread documents prepared by self and others for content and others to ensure accuracy. • Able to write clearly and concisely with strong English background with excellent grammar, good writing skills and knowledge of sentence structure • Effective active listening skills. Able to translate verbal guidance into precise operating instructions • Adheres to and applies standard document formats while maintaining technical content of new and revised documents • Demonstrates an ability to adapt to shifting priorities, change, stress and to find appropriate balance between needs of the organization, others and self. Incorporates insights of other people into ongoing work. • Able to learn and understand pharmaceutical processes in order to design related SOPs. • Understanding of cGMP and Safety regulations • Strong organizational and communication skills • Team based collaborative problem solving • Strong understanding of cGMPs Additional Information Best Regards, Anuj Mehta ************$59k-84k yearly est. 60d+ agoQlik Sense Developer/Tech Lead
Artech Information System
Zebulon, NC job
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 Detailed responsibilities. • Experience in developing application using Qlik Sense enterprise and Desktop version. Enterprise Version is must • Ability to translate business requirements into technical requirements to build data model • Given a business requirement, identify the dimensions and measures • based on business requirements, identify KPIs, dimensions and measures • Propose the appropriate business solution for various types of users and devices • Experience in Application UI design and implementation • Design, create and validate data model in Qlik Sense and QlikView • Strong communication • Pharma commercial functional experience Additional Information Best Regards, Shobha Mishra ************$99k-140k yearly est. 60d+ agoCollections Specialist - L1
Artech Information System
Raleigh, NC job
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 Key Accountabilities/Responsibilities: Collection and accounts receivable management for AR trade customers Ensure the complete and timely collection of accounts receivable Analyze aged trial balance of accounts receivable Communicate with customers and negotiate repayment terms Respond to customer inquiries on a timely basis Reconciliation of accounts receivable Prepare special reports as required Prepare and recommend credit files Monthly reporting and journal entries JD Edwards and other system support for the Credit Department Credit department processes support and improvement Qualifications Knowledge/Skills Required Outstanding customer service Outstanding communication and negotiation skills Excellent analytical skills Ability manage time effectively and efficiently Ability to handle multiple assignments and high stress situations with professionalism Credit and accounts receivable experience preferred Excellent knowledge of Microsoft Windows, Word, Excel and JD Edwards College degree or equivalent experience is required and University degree is an asset Accounting knowledge (university course or equivalent) Additional Information For more information, Please contact Shobha Mishra ************ sent me your resume shobha.mishra ATartechinfo.com$28k-36k yearly est. 3h agoScientific Associate I
Artech Information System
Holly Springs, NC job
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 • Candidate will provide support on analytical projects of varying size and demonstrate awareness of broader project objectives. • The fundamental analytical techniques to support vaccines and other biological products should be understood and practiced in an education setting, along with basic understanding of method development, qualification and validation. • The successful applicant will be able to analyze information and standard practices using existing procedures to solve routine problems, and be accountable for self-development to enhance contribution. Major Accountabilities: • Analytical assay execution in support of vaccine process and product development programs, e.g. HPLC/UPLC, gel electrophoresis, ELISA etc. • Data collection and reporting with knowledge of GLP/GMP environments. • Perform tasks under limited supervision and able to execute experiments independently. • Able to work under tight deadlines. • Understand business drivers and be able to work under tight deadlines. • Reviews laboratory documentation • Partner with diverse team members from various functions, countries and members at various levels in the organization. • Solve complex problems using analytical thinking gained through formal education, experience and sound judgment. • Self-development to enhance contribution Skills: • Hands on experience on HPLC/UPLC, electrophoresis, immunoassay and other protein analysis methods are required for the position. • Ability to work under limited supervision and take scientific direction from scientists. • Excellent communication and presentation skills. Qualifications Education: BS degree in a scientific discipline. Internship or Academic experience preferred. Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960$59k-83k yearly est. 3h agoDatabase Administrator - Applications L3
Artech Information System
Raleigh, NC job
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 Database knowledge: Oracle and Teradata Level of knowledge/expertise: 5+ years of experience Query Language: Complex Oracle/Teradata SQL Level of knowledge/expertise: 8+ years of experience Reporting Tool Knowledge: Business Objects or Similar Level of Knowledge/expertise: 2+ years of experience Provides support for assigned databases responding to data and user problems. Monitors database error logs, etc, to ensure proper capacity and availability. Designs / Creates Oracle database Tables / Triggers / Indexes / Views / Packages in co-operation with application developers, addressing necessary performance / security issues. Supports activities of developers and users as they implement new processes and applications. Knowledge of system and object level security. Skilled in troubleshooting techniques primarily focused data analysis. Qualifications Database knowledge: Oracle and Teradata Level of knowledge/expertise: 5+ years of experience Additional Information For more information, Please Contact ************ Shobha Mishra$74k-104k yearly est. 60d+ agoLab Scientist
Artech Information System
Rocky Mount, NC job
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 • Responsible for general laboratory and operational support. • BS in Chemistry, MS preferred • At least 6 years analytical laboratory experience in a GMP regulated environment for BS or 4 years with MS or PhD. • Experience in parenteral drug product pharmaceutical manufacturing is plus. • S uccessful hands-on analytical testing experience in a GMP environment. • Must have mastered at least four (4) analytical technologies, i.e., GC, HPLC, LC/MS, ICP, AA, FTIR, UV-VIS, RAMAN SPECTROMETER, ION Chromatography, etc. ADDITIONAL SKILLS/PREFERENCES: • Demonstrate proficiency in computerized systems. • Comprehend mathematical concepts such as logarithms, algebra, conversions, fractions, decimals, and rounding. • Demonstrated ability to troubleshoot analytical methods and equipment. • Experience and use of LIMS, Empower, Trackwise, Nugenesis. • Demonstrated capability to perform technical review of laboratory testing results and to identify and investigate suspect results. • Strong organizational skills and ability to multi task across projects and activities. • Must have the ability to understand and follow written procedures. • Must be self-motivated and work with minimal direction. • Utilize good judgment in making decisions within limitations of recognized standard methods and procedures. • Must maintain GMP compliance within the assigned laboratory. • Complete all training, written exams, and laboratory certifications. • Must be able to temporarily work a flexible schedule to meet business needs. • Must maintain certification within the assigned area. • Must be able to train other analyst in use of analytical instruments. • Work effectively with other laboratory team members. • Communicate results of testing effectively, accurately and in a timely manner. • Must be able to work with appropriate Personal Protective Equipment (PPE) required for biological and/or chemical hazards. • Must be able to obtain and maintain multiple laboratory technique proficiencies (as dictated by laboratory and business needs). • Must be able to handle multiple duties and projects at the same time and be able to work in a fast-paced environment. • Must be viewed by peers, supervisors and managers as having strong technical and/or leadership skills. • Must be able to work any shift on a routine basis to provide training and coverage for other analysts as needed. • Ability to work with hazardous chemicals safely while performing assays. • Must physically be able to meet requirements of a laboratory environment. Qualifications BS in Chemistry, MS preferred At least 6 years analytical laboratory experience in a GMP regulated environment for BS or 4 years with MS or PhD. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter$50k-70k yearly est. 3h agoTitle: System Analyst - L3 US
Artech Information System
Raleigh, NC job
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 Corporate Security, Senior IT Technical Support Analyst Candidate will manage Corporate Security applications from an on-going support perspective as well as lifecycle and change management. Requirements • AMAG/CCURE/Salient/Passage Point experience strongly preferred; familiarity with physical access control and video management systems technology a must • Active Directory, HR Data integration, windows server experience • Experience with lifecycle management and upgrades • Ability to write and work with business partners to execute System and Unit Test Plans • Experience with Service Transitions from Projects to Production • Experience using ITIL for incident and problem management • Vendor management experience. • Ability to multi-task as candidate will manage concurrent workstream • Strong communication skills as project teams will primarily be virtual Nice to have • Experience with client IT systems and processes • Experience with managing client GxP validated systems, including writing GxP documentation and managing the project through the documentation process • Experience with Lean Sigma Qualifications • Experience with client IT systems and processes • Experience with managing client GxP validated systems, including writing GxP documentation and managing the project through the documentation process • Experience with Lean Sigma Additional Information For more information, please contact Shobha Mishra Shobha.MishraATartechinfo.com ************$65k-86k yearly est. 60d+ agoDesktop Support Level 1
Artech Information System
Cary, NC job
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 Primary Skills: • Should have experience into Desktop/ Desk side support/ Windows experience (Windows Based) • Should have experience in working in enterprise call centre environment. Provide hardware / software / network problem diagnosis / resolution via telephone/email/chat for customer's end users • Coordinate and manage relationships with vendors and support staff that provide hardware / software / network problem resolution. • Administer and provide User account provisioning. • 1-2 years help desk, customer service, and support experience with problem solving involving hardware, software, and networks. • Phone support experience necessary. • ITIL knowledge of V2 or V3. Especially on Service Desk, Incident, Problem, and Change Management • Technical helpdesk or technical call center experience is necessary. • Disciplined, systematic problem solving skills required. • Hands-on work experience with the following: • Windows Operating systems • Clients: Windows7, Windows Vista, Windows XP, Windows 2000 • Servers: Windows 2000, Windows 2003, Windows 2008, • Knowledge of Active Directory, Exchange 2003/2007 • ITSM ticketing tools such as Remedy, HP Service Centre, Peregrine Service Centre • User account creation for Active Directory, Exchange Mailboxes, Distribution lists • Remote desktop connectivity applications like SMS, Bombard, WebEx, Live Meeting, and Windows Native tools • MS Office Suite (XP, 2003, 2007): MS-Word, MS-Excel, MS-PowerPoint, MS-Outlook, MS Project, and MS Visio • Internet browsers (e.g. Explorer, Chrome, Firefox), • VPN and remote dial-in users • Support for laptop, desktops, and printers • Others: Adobe Acrobat and other common desktop applications like WinZip, etc. Qualifications Desktop support Level 1 Additional Information Client : HCL America; This is a Contract-to-Hire role.$60k-90k yearly est. 3h agoBench Scientist
Artech Information System
Sanford, NC job
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 • The incumbent will join the Manufacturing Science and Technology (MSAT) organization supporting biological therapeutics and vaccines. Within MSAT, the candidate will work in the Purification Group, which develops processes for isolation and purification of recombinant proteins, polysaccharides, bioconjugates, and other biologics. • Execution of lab or pilot-scale purifications using column chromatography, Tangential Flow Filtration (TFF), and/or Normal Flow Filtration (NFF), as needed. • Preparation of equipment, solutions, consumable materials, etc. as needed to support experiment execution. • Preparation of technical reports and presentations to communicate results to scientists and management, as required. Qualifications Able to execute experimental protocols, interpret data, and communicate results from experimental studies conducted at lab, pilot, or commercial scales. Additional Information Best Regards, Anuj Mehta ************$69k-100k yearly est. 60d+ agoManufacturing Technician
Artech Information System
Sanford, NC job
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 • The person filling this position operates all equipment in two assigned Manufacturing areas. • He or she will also clean equipment and facilities, and provide documentation of all duties in accordance with Good Manufacturing Practices. • Incumbent will perform all duties in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies and procedures. • The incumbent will be required to attend quality-training programs and orientations on an annual or as needed basis. • This individual will be required to become familiar with domestic and international regulatory requirements associated with manufacturing and biological processes. • Annual performance goals and objectives will be evaluated against specific quality performance requirements as defined by the Manufacturing Supervisor. • Mandatory commitment to report to management any potential or actual deviations from regulatory requirements. • Ongoing input regarding quality process improvements. • Master documentation procedures by following detailed written and verbal instructions in order to complete assigned tasks (follow area SOP s). • Demonstrate knowledge of procedures by performing tasks and duties and maintaining detailed records in a manner compliant with cGMPs. • Perform routine job duties, which may include vacuuming, mopping ceilings, walls and floors, emptying trashcans, etc. • Prepare production glassware and other equipment by operating industrial washers, autoclaves and depyrogenation ovens. • Clean and sterilize process equipment (tanks, fermentors) as needed. • Demonstrate and instruct proper gowning and aseptic processing procedures. • Work with individuals as a team. • Work various shifts and some weekends. • Operate and troubleshoot production equipment in assigned area and report unusual conditions or concerns about the process or equipment to area Supervisor. • Train new employees on production processes. • Perform lab work, such as: performing sample dilutions, pH, and conductivity readings. The following combinations of education and work experience are considered acceptable: • BA/BS Tech/Bus/Industry/Science with minimum 2 years direct regulated manufacturing pharma/biotech experience • AAS Science related with minimum 4 years direct regulated manufacturing pharma/biotech experience • HS or equivalent with minimum 8 years direct regulated manufacturing pharma/biotech experience • Or progression from Bio-processing Technician Level I. that includes additional internal development curriculum List certificates (if any) required. • Must complete training in assigned area and comply with applicable safety, OSHA, and environmental safety requirements. • Must complete training and comply with applicable cGMP requirements. Minimum number of years of prior experience required to perform job duties. A minimum of four years pharmaceutical experience in biological manufacturing is preferred. List specific skills and minimum expertise (ie., typing speed (WPM), fully trained ability to learn, etc.) required to perform job duties • Moderate repetitive standing, ladder climbing, repetitive bending, pushing, and lifting (up to 40 lbs) required on a daily basis. • Basic understanding of the metric system. • Be able to rationalize by suggesting solutions to unusual conditions and/or process concerns. • Must possess mechanical ability to assemble and operate equipment. • Must pay attention to detail by following procedures and noting unusual conditions. • Must have written and oral communication to read procedures, write accurate observations and follow directions Additional Skills: • GMP experience required • Pharma experience highly preferred • Bioprocessing experience in a cGMP environment, knowledge of Clean and Steam in Place Systems, perform facility cleanings, collecting WFI and Clean Steam samples. • Experience with autoclave and industrial washers Qualifications • BA/BS Tech/Bus/Industry/Science with minimum 2 years direct regulated manufacturing pharma/biotech experience • AAS Science related with minimum 4 years direct regulated manufacturing pharma/biotech experience • HS or equivalent with minimum 8 years direct regulated manufacturing pharma/biotech experience • Or progression from Bio-processing Technician Level I. that includes additional internal development curriculum Additional Information Akriti Gupta Associate Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter$30k-40k yearly est. 60d+ agoValidation Consultant
Artech Information System
Zebulon, NC job
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 Job Purpose and Key Responsibilities: (Why jobexists/what it must achieve) Ensure that the GSK Zebulon - Building Management System (BMS) Replacement Project commissioning / validation program smeet all regulatory and local requirements. Responsible for the development, planning, and implementation of commissioning, qualification and validation for the manufacturing, packaging, facilities, computer controls, and cleaning processes. Write, review and execute documentation to conduct all commissioning and / or validation activities to support equipment modification / upgrade projects and maintain existing validated states. Requires expertise in regulatory compliance,ability to determine requirements to validate and discern appropriate level of validation for the process. Responsible for driving all aspects of the Commissioning Life Cycle and / or Validation Life Cycle from design throug hoperation and improvement. Develop, update, and maintain the Project Validation Master Plans and Project Commissioning Mast Plans. Coordinate resources needed to complete commissioning and / or validation tests. Provide commissioning / validation support during the design, evaluation, and procurement stages. Monitor commissioning /validation criteria and assure compliance. Collaborate with Engineering on the developmentof Installation and Operational Qualification documents. Write and execute process, packaging, computer,facility, and cleaning validation protocols and summary reports. Interface with Manufacturing, Packaging, Logistics, Engineering, and external vendors to facilitate and drive protocol execution. Author, review, revise, or approve Standard Operating Procedures (SOPs) as required. Maintain up to date knowledge of commissioning and validation requirements, practices, and procedures and instruct other members of the project team. Develop and implement improvement initiatives with filling/packaging/computer and facility/utility validation activities. Manage simultaneous projects.Participate on cross-functional teams, who address specific problems, facilitate discussion and research, enabling procedures to become more efficient, and to build and enhance inter departmental relationships. Specialized Knowledge: (breadth & depthacross disciplines or functions; expertise in field required) Bachelors degree in a technical or scientific discipline or related work experience. Minimum 3 years experience in Manufacturingvalidation and the Pharmaceutical or Healthcare Industry required Workingknowledge of cGMP regulations In depth knowledge of process, packaging,facility, and cleaning validation Good computer skills and Microsoft Word,Excel, and PowerPoint. Quality and detail oriented with documentation skills. Excellent written and oral communication skills.Ability to develop and facilitate validation training Flexibility to work extended hours to achieve results. Prior experience at the Zebulon site andpossession of current hard badge are preferred. Qualifications BA/BS + 5 years Pharmaceutical exp. MS + 3 years Pharmaceutical exp. 2 years Pharmaceutical QA exp. Knowledge of cGMP's/FDA and other Regulatoryrequirements, and Quality Systems Knowledge of Engineering Technology Advanced understanding and skills with MS Word,and Excel Work Experience Proven project management experience in leading,researching, developing, data analysis, and executing GMP / System Life Cycle /Validation documentation and reports for utilities system (VP, Commissioning,IQ, OQ, PQ) Hands on validation experience utilities system sand supporting automation processes including HVAC, Compressors, Water systems,Dust collectors, Building Management System(BMS) (Rockwell Automation, GEMS),Environmental Monitoring Systems (EMS) (Rockwell Automation, GEMS), Lab instrumentation, Temperature and humidity profiling, (facilities, chambers,process equipment) Ability to perform calibrations and generatecalibration reports Additional Information Thanks and Regards Tinny Jindal ******************************$93k-127k yearly est. Easy Apply 60d+ agoSecurity Coordinator
Artech Information System
Zebulon, NC job
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 Job Title: Security Coordinator Location: RTP, NC 27709 Duration: 10+ Months (Contract) Requirement: The role is responsible for the triage and input of reported incidents onto the incident management system. Qualifications/Minimum Required (Education/Experience/Competencies): Ability to handle confidential and sensitive issues Ability to present information clearly and logically Good organization and communication skills and the ability to deal with all levels of the organization Team player that can interact and establish relationships with other client Professionals Ability to multitask Ability to work independently with little or no supervision Technical Skills: • General IT Technical experience required • General understanding of IT Security concepts • Must have experience with Microsoft Office (Outlook, Sharepoint, Live Meeting, etc.) • Management of data and relationships within technical tool solutions Purpose/Key Responsibilities: Successful candidate will be responsible for the following activities: CSIR Coordination: • Responsibility for first level support of the CSIR Process • Respond to investigations of common incident types by following written standard operating procedures • Perform a variety of routine incident management tasks • Maintain all documentation associated with investigations • Follow agreed procedures for notification of CSIR investigations • Assist with providing feedback on the clarity of standard operating procedures and updating the procedures, where appropriate • Assist with design, creation and development of online CSIR documentation and content Qualifications Require security coordinator . General IT Technical experience required Additional Information Regards, Shubham ************ shubham.sATartechinfoDOTcom$31k-53k yearly est. 3h agoMainframe
Artech Information System
Wilson, NC job
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 Position:Mainframe Job location : Wilson NC Highlighted skills must be there in the resume . Requirements: · Practical experience in Mainframe Storage · z/OS, DFSMS, DFHSM, DFDSS, ICF CATALOG · Rexx / ACS routines, Test and Activate SMS configuration · DFhsm, - maintenance / re-org/ Audit / Migrate / Backups · ICKDSF · z/OS HW · HDS Storage, VTS 7700 · Replication experience (Tivoli MM Global replication, EMC SRDF/A, HDS HUR) · z/OS SW · CA-1, Vantage, FDR, DFDSS · Support problem solving efforts and change implementation on z/OS environments · Basic knowledge of SMP/E · Basic knowledge of RACF · SAS reporting experience is a plus Additional Information For more information, Please contact Shubham ************$73k-95k yearly est. 3h agoCollections Specialist - L1
Artech Information System
Raleigh, NC job
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 Key Accountabilities/Responsibilities: Collection and accounts receivable management for AR trade customers Ensure the complete and timely collection of accounts receivable Analyze aged trial balance of accounts receivable Communicate with customers and negotiate repayment terms Respond to customer inquiries on a timely basis Reconciliation of accounts receivable Prepare special reports as required Prepare and recommend credit files Monthly reporting and journal entries JD Edwards and other system support for the Credit Department Credit department processes support and improvement Qualifications Knowledge/Skills Required Outstanding customer service Outstanding communication and negotiation skills Excellent analytical skills Ability manage time effectively and efficiently Ability to handle multiple assignments and high stress situations with professionalism Credit and accounts receivable experience preferred Excellent knowledge of Microsoft Windows, Word, Excel and JD Edwards College degree or equivalent experience is required and University degree is an asset Accounting knowledge (university course or equivalent) Additional Information For more information, Please contact Shobha Mishra ************ sent me your resume shobha.mishra ATartechinfo.com$28k-36k yearly est. 60d+ ago
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