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Now hiring for the following roles:

• Barista (Hiring on the spot)
• Shift Manager (Hiring on the spot)
• Store Manager (Preliminary interview)

Opportunities at these locations:

• Back Bay
• Beacon Hill
• Cambridge
• Downtown Crossing/ Financial District
• East Boston
• Seaport District
• Somerville

Bring copies of your resume and be prepared to be interviewed on the spot! Plan to check-in by 12:45 PM.

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Job Description Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Manager, Clinical Data Solutions in our Cambridge office.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Manager working on the Clinical Data Solutions team, you will be empowered to support the Takeda portfolio and participate in oversight activities, and a typical day will include:

POSITION OBJECTIVES:

Responsible for timely and high quality data management deliverables supporting the Takeda portfolio. Confirms asset and study level strategies and services are being implemented at the study level, including the application of standards. Conducts oversight of data management activities performed by Strategic Partners and/or other CROs and other 3rd party vendors to meet Takeda’s obligations described in ICH-GCP and Takeda’s business objectives. Activities include from protocol synopsis through database release and submission Contributes to the management of vendor partnerships to verify contractual assumptions in the study SOWs including the verification of monthly invoices. Acts as a first point of contact for CRO partners seeking sponsor input on study level problem solving and decision making. Serves as an expert for clinical data management best practices and acts as an ambassador on CDISC standards. POSITION ACCOUNTABILITIES:

Participates in study level vendor oversight activities. May represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and Takeda for all data related deliverables, especially in support of key decision points and regulatory submissions. Serves as a first point of contact for CROs partners when collaboration is needed to ensure established milestones and deliverables are met with the highest degree of quality. Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. Acts as a process expert for operational and oversight models. Maintains SOPs, process maps and templates and timelines to support functions operational and oversight models. May prepare metrics to support the function’s KPIs. Tracks study deliverables and evaluates study metrics to mitigate risk for major data management deliverables and milestones. Confirms archival and inspection readiness of all Data Management Trial Master File (TMF) documents Verifies external Data Management SOWs and timelines to ensure accuracy of invoices, investigates variances and supports forecasting. Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. Other duties as assigned EDUCATION, EXPERIENCE AND SKILLS:

BS/BA required preferably in a health-related, life science area and with a minimum of 6 years data management and/or drug development experience. Proven track record of strong project management skills and experience managing data management activities for large drug development programs Experience with all phases of development and at least 2 therapeutic areas. Ability to handle multiple development programs simultaneously. NDA/CTD Experience. Strong knowledge of electronic data capture and data warehouse technologies as applied to clinical trials. Strong working knowledge of (e)CRF design and data management functions/activities as applied to standards library development and maintenance. Good understanding of CDISC standards, and experience implementing standards. Strong knowledge of clinical study reporting requirements including SAS programming. Advanced knowledge of office software (Microsoft Office). Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes. Advanced knowledge of FDA and ICH regulations and industry standards and quality control principles. Experience in medical coding in the pharmaceutical/biotechnology industry including knowledge of coding tools. Good working knowledge of general statistical programming processes and practices. Advanced knowledge of medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processes. Demonstrated strong matrix leadership and communication skills Able to influence without authority Excellent teamwork, organizational, interpersonal, conflict resolution and problem-solving skills Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo Pragmatic and support change Is comfortable with ambiguity PHYSICAL DEMANDS:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Ability to sit and stand for long periods of time. Carrying, handling and reaching for objects. Manual dexterity to operate office equipment i.e. computers, phones, etc. TRAVEL REQUIREMENTS:

Requires approximately 5-20 % travel, including overnight and international travel to other Takeda sites, strategic partners, and therapeutic area required travel. WHAT TAKEDA CAN OFFER YOU:

401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs

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Job Description Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Manager, Clinical Data Solutions in our Cambridge office.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Manager working on the Clinical Data Solutions team, you will be empowered to support the Takeda portfolio and participate in oversight activities, and a typical day will include:

POSITION OBJECTIVES:

Responsible for timely and high quality data management deliverables supporting the Takeda portfolio. Confirms asset and study level strategies and services are being implemented at the study level, including the application of standards. Conducts oversight of data management activities performed by Strategic Partners and/or other CROs and other 3rd party vendors to meet Takeda’s obligations described in ICH-GCP and Takeda’s business objectives. Activities include from protocol synopsis through database release and submission Contributes to the management of vendor partnerships to verify contractual assumptions in the study SOWs including the verification of monthly invoices. Acts as a first point of contact for CRO partners seeking sponsor input on study level problem solving and decision making. Serves as an expert for clinical data management best practices and acts as an ambassador on CDISC standards. POSITION ACCOUNTABILITIES:

Participates in study level vendor oversight activities. May represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and Takeda for all data related deliverables, especially in support of key decision points and regulatory submissions. Serves as a first point of contact for CROs partners when collaboration is needed to ensure established milestones and deliverables are met with the highest degree of quality. Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. Acts as a process expert for operational and oversight models. Maintains SOPs, process maps and templates and timelines to support functions operational and oversight models. May prepare metrics to support the function’s KPIs. Tracks study deliverables and evaluates study metrics to mitigate risk for major data management deliverables and milestones. Confirms archival and inspection readiness of all Data Management Trial Master File (TMF) documents Verifies external Data Management SOWs and timelines to ensure accuracy of invoices, investigates variances and supports forecasting. Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. Other duties as assigned EDUCATION, EXPERIENCE AND SKILLS:

BS/BA required preferably in a health-related, life science area and with a minimum of 6 years data management and/or drug development experience. Proven track record of strong project management skills and experience managing data management activities for large drug development programs Experience with all phases of development and at least 2 therapeutic areas. Ability to handle multiple development programs simultaneously. NDA/CTD Experience. Strong knowledge of electronic data capture and data warehouse technologies as applied to clinical trials. Strong working knowledge of (e)CRF design and data management functions/activities as applied to standards library development and maintenance. Good understanding of CDISC standards, and experience implementing standards. Strong knowledge of clinical study reporting requirements including SAS programming. Advanced knowledge of office software (Microsoft Office). Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes. Advanced knowledge of FDA and ICH regulations and industry standards and quality control principles. Experience in medical coding in the pharmaceutical/biotechnology industry including knowledge of coding tools. Good working knowledge of general statistical programming processes and practices. Advanced knowledge of medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processes. Demonstrated strong matrix leadership and communication skills Able to influence without authority Excellent teamwork, organizational, interpersonal, conflict resolution and problem-solving skills Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo Pragmatic and support change Is comfortable with ambiguity PHYSICAL DEMANDS:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Ability to sit and stand for long periods of time. Carrying, handling and reaching for objects. Manual dexterity to operate office equipment i.e. computers, phones, etc. TRAVEL REQUIREMENTS:

Requires approximately 5-20 % travel, including overnight and international travel to other Takeda sites, strategic partners, and therapeutic area required travel. WHAT TAKEDA CAN OFFER YOU:

401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days Community Outreach Programs

email resume Williams9447@att.net Service company looking for HVAC Technician.

Familiar with upfront pricing EPA certified Sheet metal license a plus Familiar with hot water boilers High efficiency equipment Problem solver On call required-rotation Oil license a plus 2+ years of service experience

email resume Williams9447@att.net Company is looking for full time experienced security system technicians and installers based out of our Canton MA office.

Essential Duties and Requirements: • Applicants should have at least 3 years’ experience installing, terminating and working with access control, CCTV, programming, and alarm systems. • Licensed journeymen or Massachusetts Class D Systems Technicians are preferred, but not required. • Applicants will be working in both new construction environments and client offices. • Drill holes for wiring in wall studs, joists, ceilings, floors, and other areas as required. Examine systems to locate problems such as loose connections or broken insulation. • Feed cables through access holes, roof spaces, and cavity walls to reach fixture outlets, then position and terminate cables, wires and strapping. • Inspect installation sites and study work orders, building plans, and installation manuals in order to determine materials requirements and installation procedures have been met. • Install, maintain, or repair security systems, alarm devices, and related equipment, following blueprints of electrical layouts and building plans. • Mount and fasten control panels, door and window contacts, sensors, and video cameras, and attach low voltage wiring to connect components. • Mount raceways and conduits and fasten wires - As required by code. • Test and repair circuits and sensors, following wiring and system specifications. • Test backup batteries, keypad programming, sirens, and all security features in order to ensure proper functioning, and to diagnose malfunctions. • Keep informed of new products and developments. Request orders for replacement parts. • Performs a variety of marginal duties not listed, to be determined and assigned as needed. • Identifies, troubleshoots and resolves hardware, software, and basic network related problems encountered by end-users of the network. Has a basic understanding of IPV4 and how to assign a computer an IP address. • Computer networking skills preferred • Neat and professional appearance • Strong work ethic • Ability to work as part of a team • Good communication skills • Must have reliable transportation as travel is required • Must be able to pass a background check • Must comply with random drug screenings

email resume Williams9447@att.net Electrical Engineer

Opportunity for a degreed engineer (BSEE) to join a prestigious consultant engineering department in Boston. This individual will work on project teams in a collaborative environment producing engineering solutions for large scale and complex building projects. They will be responsible for power distribution, lighting, fire alarm and protections systems, emergency and standby power supply in accordance to all applicable codes and standards. Experience with software tools such as Revit, SKM, AGI 32 and AMPCALC 4 is preferred. Should have strong analytical ability and good verbal and written communication skills. Projects are in commercial, mission critical, healthcare, science and technology, government and specialty building market sectors. Successful candidates will have seven (7) years experience in MEP consulting or related fields. EIT or PE is preferred.

Competitive salaries and full benefits.

Manager, Clinical Data Solutions Takeda Pharmaceuticals - Cambridge, Massachusetts

Job Description Are you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Manager, Clinical Data Solutions in our Cambridge office.

Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As a Manager working on the Clinical Data Solutions team, you will be empowered to support the Takeda portfolio and participate in oversight activities, and a typical day will include:

POSITION OBJECTIVES:

Responsible for timely and high quality data management deliverables supporting the Takeda portfolio. Confirms asset and study level strategies and services are being implemented at the study level, including the application of standards. Conducts oversight of data management activities performed by Strategic Partners and/or other CROs and other 3rd party vendors to meet Takeda’s obligations described in ICH-GCP and Takeda’s business objectives. Activities include from protocol synopsis through database release and submission Contributes to the management of vendor partnerships to verify contractual assumptions in the study SOWs including the verification of monthly invoices. Acts as a first point of contact for CRO partners seeking sponsor input on study level problem solving and decision making. Serves as an expert for clinical data management best practices and acts as an ambassador on CDISC standards. POSITION ACCOUNTABILITIES:

Participates in study level vendor oversight activities. May represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and Takeda for all data related deliverables, especially in support of key decision points and regulatory submissions. Serves as a first point of contact for CROs partners when collaboration is needed to ensure established milestones and deliverables are met with the highest degree of quality. Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. Acts as a process expert for operational and oversight models. Maintains SOPs, process maps and templates and timelines to support functions operational and oversight models. May prepare metrics to support the function’s KPIs. Tracks study deliverables and evaluates study metrics to mitigate risk for major data management deliverables and milestones. Confirms archival and inspection readiness of all Data Management Trial Master File (TMF) documents Verifies external Data Management SOWs and timelines to ensure accuracy of invoices, investigates variances and supports forecasting. Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. Other duties as assigned EDUCATION, EXPERIENCE AND SKILLS:

BS/BA required preferably in a health-related, life science area and with a minimum of 6 years data management and/or drug development experience. Proven track record of strong project management skills and experience managing data management activities for large drug development programs Experience with all phases of development and at least 2 therapeutic areas. Ability to handle multiple development programs simultaneously. NDA/CTD Experience. Strong knowledge of electronic data capture and data warehouse technologies as applied to clinical trials. Strong working knowledge of (e)CRF design and data management functions/activities as applied to standards library development and maintenance. Good understanding of CDISC standards, and experience implementing standards. Strong knowledge of clinical study reporting requirements including SAS programming. Advanced knowledge of office software (Microsoft Office). Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes. Advanced knowledge of FDA and ICH regulations and industry standards and quality control principles. Experience in medical coding in the pharmaceutical/biotechnology industry including knowledge of coding tools. Good working knowledge of general statistical programming processes and practices. Advanced knowledge of medical terminology, medical coding, laboratory reference ranges, clinical diagnostic procedures, anatomy/physiology and nature of disease processes. Demonstrated strong matrix leadership and communication skills Able to influence without authority Excellent teamwork, organizational, interpersonal, conflict resolution and problem-solving skills Entrepreneurial and innovative; takes measured risks; thinks outside the box; challenge the status quo Pragmatic and support change Is comfortable with ambiguity PHYSICAL DEMANDS:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Ability to sit and stand for long periods of time. Carrying, handling and reaching for objects. Manual dexterity to operate office equipment i.e. computers, phones, etc. TRAVEL REQUIREMENTS:

Requires approximately 5-20 % travel, including overnight and international travel to other Takeda sites, strategic partners, and therapeutic area required travel. WHAT TAKEDA CAN OFFER YOU:

401(k) with company match and Annual Retirement Contribution Plan Tuition reimbursement Company match of charitable contributions Health & Wellness programs including onsite flu shots and health screenings Generous time off for vacation and the option to purchase additional vacation days

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