Dawar Consulting

Hiring Alert!!! Post:Scientist I/II/Sr Location: Pleasanton, CA Position ID# 1369... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a Scientist II. Duties: The Scientist I/II/Sr Scientist will be a member of the Assay Development team in Pleasanton for the development of RUO and CE-IVD/IVD products for use on next-generation sequencing (NGS) systems. The successful candidate will help develop and implement R&D strategies for related NGS applications including nucleic acid extraction, library preparation, sequencing, and data analysis. This position is ideal for individuals interested in learning assay/product development, involving design control. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1369 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post: Customer Support Representative Location: Las Vegas, NV Position ID# 1366... Apply Now: https://bit.ly/2IKaUHu Job Description: Resource will be supporting the Service Coordination Center as a CSR. This position has responsibility for part ordering, case creation and dispatching of field personnel. Handles customer service inquiries and problems via telephone. May respond to email inquiries. Customer service is the primary function. Calls are predominantly routine, but may require deviation from standard screens, scripts, and procedures. Uses computerized system for tracking, information gathering, and or troubleshooting. Requires general knowledge of the organization, products, and or services. May assess needs and suggest alternative products or services. Requires ability to navigate a computerized data entry system or other relevant applications. Interfaces with external and internal customers on routine issues and inquiries. Knows and applies the fundamental concepts and tasks of specific area. Responds to customer inquiries (internal and external). May research information in order to follow up with inquiries. Work is generally routine in nature but may involve some non-routine issues. Some evaluation, originality or ingenuity is required. Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1366 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post: Sr. Quality System Analyst Training Location: Pleasanton, CA Position ID# 1365... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a Sr. Quality System Analyst Training. Skills: Must be able to manage and meet multiple project deliverables and deadlines. Ability to work independently and have proven time management skills. Excellent English, spelling, and grammar skills. Able to adapt to a fast-paced, changing environment. Must be able to work well with all levels of associates, from entry level to management. Must be well organized, thorough and detail oriented. Education: Must possess a combination of education and experience as follows: Minimum Associate's degree in Biological Sciences, Chemistry, or medical field 2+ years or relevant experience in the medical, diagnostics, or pharmaceutical industry with a focus on training processes &/or systems. Proficient with Microsoft Office (Word, Excel, PowerPoint and Visio) Knowledge of electronic Learning Management System (LMS) a plus (i.e., SAP LSO, Cornerstone, MediaLab, Oracle, Plateau Systems, etc.). Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1365 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Technical Product Support Specialist I Location: Indianapolis, IN Position ID# 1364... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a " Technical Product Support Specialist I" Duties: Provides technical support to customers, answering basic questions on function and usage of products via the Technical Support Center. May also provide technical assistance to sales, marketing and other departments. Analyzes basic problems with nonfunctioning electro/mechanical equipment, software applications or reagents to identify problem area(s) and recommend corrective action. Serves as the primary support liaison between Client and the customer. Recommends solutions to customer’s application questions. Maintains database of problems so that recurring problems can be analyzed and reported. Knows and applies the fundamental concepts, practices and procedures of the particular field of specialization. Significant on-the-job training or formalized education in specific area. Requires some evaluation, originality or ingenuity. Work is varied and may be somewhat difficult in nature but usually involves limited responsibility. Contributes independently or with a team towards a program or department goal or service. Interfaces with internal customers and departments. Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1364 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post: Healthcare Provider Customer Sales Associate Location: Indianapolis, IN Position ID# 1363... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a Healthcare Provider Customer Sales Associate. **Working hours are Mon-Fri 9am-6pm. Duties: Responsible for meeting and exceeding sales objectives of core bG and portfolio products in mid-tier Health Care Provider across the US, primarily by telephone, email, and other digital platforms. Must develop customer prospects and create and maintain relationships with decision makers. Contacts existing and potential new customers. Additionally, position requires the ability to create the value proposition in presentations to customers. Position suitable for entry level sales account manager. Has working knowledge of company products and services. Aptitude to do moderate analysis of territory metrics. Normally receives general instructions on routine work, detailed instructions on new projects, products or assignments. Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions. Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a Healthcare Provider Customer Sales Associate. **Working hours are Mon-Fri 9am-6pm. Duties: Responsible for meeting and exceeding sales objectives of core bG and portfolio products in mid-tier Health Care Provider across the US, primarily by telephone, email, and other digital platforms. Must develop customer prospects and create and maintain relationships with decision makers. Contacts existing and potential new customers. Additionally, position requires the ability to create the value proposition in presentations to customers. Position suitable for entry level sales account manager. Has working knowledge of company products and services. Aptitude to do moderate analysis of territory metrics. Normally receives general instructions on routine work, detailed instructions on new projects, products or assignments. Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1363 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Quality Specialist III Location: Santa Clara, CA Position ID# 1362... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a " Quality Specialist III". Duties: Responsible for supporting development and implementation of Quality Management System (QMS) and supporting infrastructure/tools in compliance with FDA Quality System Regulation (QSR) regulations, International Standards Organization (ISO) regulations, and client's corporate requirements. Actively participate in quality integration efforts for the Santa Clara site by supporting the planning, implementation and monitoring of integration milestones. Partner with stakeholders to define and implement integration actions. Responsible for supporting QMS harmonization effort at the Santa Clara site. Write and revise Quality Systems procedures, perform gap assessments and assist in driving compliance. Understanding of laboratory procedures and GLP requirements is a plus. Responsible for supporting QMS documentation using Electronic Document Management System (EDMS). Support coordination of document and record retention program for the site in alignment with the client's corporate requirements. Partner in defining procedures related to documentation storage and retrieval. Support management and maintenance of training program for the site. Experience in Change management, Supplier qualification, Inspection and CAPA management is an added advantage. Exposure to internal, external, laboratory, supplier auditing programs as appropriate. A proven ability to work creatively and analytically in a problem-solving and process-oriented environment. Expected to operate independently, holding him/herself accountable to proactively fulfill tasks and achieve results within assigned timelines. A proven ability to work in a collaborative, team-based environment dependent upon effective teamwork to achieve goals and company objectives. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1362 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Technical Writer Location: Branchburg, NJ... Position ID# 1359 Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a "Technical Writer" Duties: This position is responsible for validation activities in a cGMP /CBER regulated medical device manufacturing environment. As a member of the Design Transfer and Technical Support Team, this position will participate in Process Validation activities including preparation of validation documents such as protocols, final reports and plans. This candidate will be responsible for preparing, reviewing and/or approving validation documents to support new product launches and any changes to existing validated processes for regulated on-market products. These validations may include the manufacturing and filling processes for bulk reagents (large and small scale) and for production intermediates such as Oligonucleotides, Control Stocks and Enzymes. Duties include the preparation of validation plans, protocols and reports, analysis of data, and developing validation strategies in accordance with industry guidelines and SOPs. This position must be able to lead validation deliverables / projects, manage multiple competing timelines and priorities and work in a cross-functional team. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1359 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Senior EBS Developer Location: Remote Position ID# 1357... Apply Now: https://bit.ly/2IKaUHu Our client, the leading third-party provider of enterprise software support services, is looking for Senior EBS Developer Remote Description: 8+ years of extensive design and development experience with Oracle EBS Payroll product development or enhancement building. Understanding of other Oracle HRMS products is required. A track record of successful roles in several Enterprise Application projects (including full development and full QA lifecycle processes) Knowledge of localizations: architecture, implementation and key functionality. Experience creating and reviewing detailed technical documentation and unit test plans. Familiarity with administrative tools i.e. Oracle AOL/FND. Worked remotely in a virtual environment. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1357 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Regulatory Specialist II Location: San Jose, CA Position ID# 1356... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a " Regulatory Specialist II" Duties: Primarily assist in activities associated with transition from IVDD to IVDR regulatory approval of on-market in vitro diagnostic medical devices in global markets. Secondarily, assist in submission activities for a variety of device regulatory approvals including the CE mark, US premarket approvals (PMAs), US premarket notifications (510(k)s), post-approval reports, export certificates, establishment registrations and listings, etc. Acquire and maintain current knowledge of applicable regulatory requirements and scientific/technical issues in the geographic and discipline as relevant to assigned projects. May interface with regulatory authorities on regulatory and technical matters, as directed. May provide regulatory support on project teams. May assist in the creation of Operating Procedures and policy guidelines. May assist in review of labeling changes, as well as advertising and promotional materials. May assist as the internal regulatory consultant for on-market product issues. May assist in review of proposed device changes. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1356 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Clinical Trial Assistant Location: Tucson, AZ Position ID# 1355... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a " Clinical Trial Assistant". Duties: Trial Master Files / Site Trial files: Work with study teams to identify TMF requirements and developing, maintaining, and archiving trial documentation in accordance with related SOPs working under minimal oversight. Clinical Trial Materials / Binders / Labels: Work with study teams to identify specifications and develop study related materials to those specifications working under minimal oversight. Receiving: Receives, inspects and inventories Clinical Trial Supplies insuring appropriate quality, quantities and storage conditions of materials / supplies, completing relevant documentation as necessary, and communications with Clinical Teams. Picking / Packing / Shipping: Follows moderate to complex instructions from Clinical Team to fill shipping requests of Clinical Trial Supplies and/or Samples insuring accuracy of items and quantities, appropriate packing materials and shipping conditions (e.g., frozen, refrigerated and ambient), as well as shipping instructions to insure compliance with all DOT, IATA, and local and federal regulations. Establish good working relationships across all Life Cycles and Facilities groups to effectively deliver work objectives. Accurately and effectively communicate needs, issues, and project status with manager, Clinical Teams, Warehouse and Shipping staff. Performs additional duties as requested by manager or designee. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1355 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:IT Desktop Support Location: Milpitas, CA Position ID# 1353... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a Marketing Cloud Consultant. Duties: Client is seeking an experienced Salesforce Marketing Cloud Consultant to become part of the Global Marketing team to drive maximum value and success with our affiliate country organizations. The Marketing Consultant will work with affiliate Marketing Managers in developing and implementing a cohesive approach to levering Salesforce Marketing Cloud technology to achieve business goals. A successful Marketing Consultant leverages deep understanding of email marketing in combination with Salesforce Marketing Cloud application knowledge. In this role you will work collaboratively with other Marketing staff and directly with affiliates to help them evolve and optimize their marketing strategies and tactics. This consultative position is primarily focused on one-to-one email communications. Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1353 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:IT Desktop Support Location: Milpitas, CA Position ID# 1352... Apply Now: https://bit.ly/2IKaUHu Our Semiconductor client is a world leader in design and manufacturing of advanced optical inspection and metrology tools, is looking for an "IT Desktop Support". Skills And Education: Technical/trade school certificate in Computer Science, Information Technology, or related field; or equivalent combination of education and work-related experience required Typically requires 2 plus years job related experience Preferred Bachelor's degree Vendor certifications (Microsoft, Cisco, ITI, HP, others) Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1352 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post:Ethics & Compliance Contract Attorney Location: Indianapolis, IN Position ID# 1351... Apply Now: https://bit.ly/2IKaUHu Our client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a Ethics & Compliance Contract Attorney. Duties: The Legal Counsel will work as part of the Ethics and Compliance team within Client’s Corporate Law department. The successful candidate will counsel the various business units on the Anti-kickback laws, the Sunshine Act and other laws. The Legal Counsel’s responsibilities will include, but not be limited to: Ensuring compliance with Client’s Business Code of Conduct and the Compliance Monitoring Program. Work as a liaison between clients and business unit attorneys to ensure effective mitigation of risks associated with fraud and abuse and HIPPA areas of law. Develop, initiate, maintain and revise policies and procedures for the general operation of the Compliance Program. Assist in maintaining and monitoring an effective program to ensure compliance with policies, laws, and regulations. Collaborates with other departments and manages compliance investigations. Identifies potential areas of compliance vulnerabilities and risks; develops/implements corrective action plans Work with Ethics and Compliance team to develop and implement an effective compliance communication and training plan for the client. Work with global business area and affiliate attorneys as necessary to assist clients in achieving business goals Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1351 Apply Now: https://bit.ly/2IKaUHu

Hiring Alert!!! Post: Security Engineer Location: Las Vegas, NV Position ID# 1350... Apply Now: https://bit.ly/2IKaUHu CISSP CISM. ISO 27001 NIST, SIEMs, next gen anti-virus software, DLP, intrusion detection, firewalls, content filtering Interested candidates, please click on the link below and to apply..... Candidates can also send their resume at: [email protected]. Position ID# 1350 Apply Now: https://bit.ly/2IKaUHu