Other Jobs refers to employment opportunities that don't fall within the commonly known categories, showcasing the diversity of the workforce and the variety of skills individuals offer. These roles often require unique skill sets or qualifications, catering to niche markets or specialized tasks. They can range from unconventional roles in creative industries to specific positions in technology or science fields. The defining feature of Other Jobs is their departure from traditional job titles, offering flexibility, creativity, and sometimes the chance for individuals to turn unconventional talents into professional endeavors.
Other Jobs is a broader category encompassing a variety of employment positions that do not necessarily fit into standard job classifications. This can include temporary gigs, rare professions, or emerging roles that are still defining their place in the job market. The primary characteristic of Other Jobs is their diversity, offering opportunities that might be unique, unconventional, or highly specialized. Another feature of such jobs is their flexibility, which often attracts individuals seeking non-traditional work schedules or the freedom to pursue multiple interests simultaneously.
Other Jobs is a category that encompasses a diverse range of employment opportunities outside traditional or mainstream careers. This category can include freelance work, gig economy roles, alternative industry positions, or even unconventional vocations that don't fit neatly into established job classifications. The key characteristics of other jobs are their non-standard nature, flexibility in terms of hours and commitment, and often, an entrepreneurial or creative spirit. They are ideal for individuals seeking less conventional career paths and those who wish to tailor their work-life to personal preferences or circumstances.
Other Jobs is a broad category encompassing the myriad of professions that don't neatly fit into traditional job classifications. They can range from gig economy roles to positions requiring highly specialized skills not commonly recognized in standard industry sectors. The key characteristic of Other Jobs is their diversity, with opportunities that can be tailored to unique talents, flexible schedules, and often innovative or unorthodox work environments. This category can serve as a flexible and creative employment avenue for those with niche skills or those seeking non-traditional career paths.
on 12 hour shifts and 36 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Travel Allied - CT Tech About Advantis Medical Advantis Medical Staffing is ranked #1 by travel clinicians because of our relentless focus on matching our travel clinicians with their next dream assignment.
We accomplish this by making significant investments in technology and have married it with an exceptional human experience from our recruiter and support teams. You’re going places. We can help. Benefits Weekly pay Holiday Pay Guaranteed Hours 401k retirement plan Referral bonus Employee assistance programs Medical benefits Dental benefits Vision benefits For more details: jobs-search. org/technology_newton-c434659/job_i1971383275
serve. We offer medical, dental and vision coverage, life insurance, retirement plan, employee assistance programs, company discounts, perks and more for most full-time executive protection jobs! The Armed Security Response Team (SRT) Agent is responsible for safeguarding the client in Cambridge, MA.
Individuals must be able to perform in a dynamic environment and possess the physical, operational and tactical capabilities to address wide-ranging security related tasks. This position is a full-time opportunity working 3 or 4 12-hour shifts a week. Must be able to work days, nights, weekends and holidays as well as overtime as needed. Responsibilities: Provide covert and overt protection
to the client and properties, while maintaining a low-profile. Provide real-time information about the surrounding area of the work site. Safeguard the work site, personnel and maintain highly sensitive information.
Work within a cross-functional team Must have strong interpersonal skills and the ability to tactfully negotiate conflict and remain flexible Must possess ability to interact with all levels of corporate management, liaison internally and externally with various departments and personnel. Must be able to brief, defend, persuade and instruct others on security requirements and policies. Must have strong oral communication and representational skills and have the ability to
write in a clear and precise manner. Requirements: Minimum of 4 years' experience in extensive military, law enforcement, or corporate security experience, preferably in a military special operations branch or protective operations.
Must possess a high school diploma or equivalent Valid driver's license and a clean driving record Ability to acquire state security and firearm credentials Demonstrate a high level of proficiency with handguns. Current First Aid, CPR, AED certification required. Previous medical training is highly desirable. Licensing requirements are subject to state and/or local laws and regulations and may be required prior to employment Benefits: $42 per hour Allied Universal Executive Protection and Intelligence Services offers industry leading benefits, which are available to all full-time employees : Medical/Dental/Vision coverage Free employee life insurance Paid employee training and development 401K Employee assistance programs Paid holidays and flexible PTO (Paid Time Off) Career advancement opportunities Great company culture and work/life balance No phone calls.
Please allow 7-10 business days for applicant feedback. Allied Universal Executive Protection and Intelligence Services is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, interaction, interactionual orientation, gender identity and expression, marital or civil partnership status, pregnancy, age, disability, veteran status or any other protected factor under federal, state or local law.
CA PPO# 17384; CA PI# 28245; Office: 11677 Central Avenue, Suite C, Chino, CA 91710 Allied Universal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, interaction, interactionual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law.
For more information: If you have any questions regarding Equal Employment Opportunity, Affirmative Action, Diversity and Inclusion, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: /offices.
Other Jobs is a category that encompasses a diverse range of employment opportunities outside traditional or mainstream careers. This category can include freelance work, gig economy roles, alternative industry positions, or even unconventional vocations that don't fit neatly into established job classifications. The key characteristics of other jobs are their non-standard nature, flexibility in terms of hours and commitment, and often, an entrepreneurial or creative spirit. They are ideal for individuals seeking less conventional career paths and those who wish to tailor their work-life to personal preferences or circumstances.
of Parks, the Gardener: Performs a variety of manual work involved in planting, caring for, and maintaining gardens, shrubs, lawns, flowers, trees, and other plants. Seeds lawns and gardens, including pruning of trees and shrubs. Plants and transplants flowers.
Performs weeding, watering and fertilizing. Cares for lawns and ornamental gardens. Determines care needed by plants, trees, flowers, shrubs, and lawns; with assistance of the appropriate supervisors. Performs related manual tasks such as cutting grass, clearing snow, raking, digging, edging and pruning. Uses equipment, tools, and vehicles necessary to gardening work and snow clearing Performs other duties as required from time-to-time
including snow and other inclement weather or emergency duties. MINIMUM REQUIREMENTS: Possession of a current and valid Commercial Driver's License Class B plus a current and valid Hoisting License class 2B (backhoes and loaders) as issued by the Department of Public Safety.
Department of Transportation medical certifications may be required of applicants pursuant to the Teamsters Local 25 collective bargaining agreement. A minimum of 1 year demonstrated work experience in planting, caring and maintaining gardens, PHYSICAL DEMANDS: Lifting between 25-100 pounds, repetitive proper bending, squatting, stretching, pushing, climbing, dragging, and pulling. OTHER INFORMATION: Exposure to all
weather conditions. Work in a moderate to high noise level environment caused by sound of machinery or powered equipment being used.
Occasional odor may occur during the course of work. Required to adhere to all safety rules and regulations as well as dress code policies. Perform other related duties as assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. REQUIRED DOCUMENTS: Please upload the below documents to complete your application. Resume PDN-9a3ccad7-dd8a-4bf2-b109-85f2da7e5b70For more details: jobs-search. org/marketing_cambridge-c434666/gardener-special-meoiia-cambridge_i1959026041
small molecule, RNA, oligonucleotide, and novel chemical modalities (i. e. liquid nanoparticles, next-generation peptides, etc. ). The role has end-to-end CMC product responsibilities from pre-clinical to commercial life cycle process development activities, process platform strategies, and regulatory CMC management/filings across the pharma modality portfolio.
This role is ultimately accountable for delivering GMP-ready processes to manufacturing, phase-appropriate process optimization (i. e. COGS optimization), and regulatory CMC filing/approvability across all global healthcare agencies. In addition to process and analytical development, the position oversees multi-disciplinary international
teams supporting Quality oversight, CMO/CRO execution and strategy, regulatory filings, and manufacturing technology transfer. The leader guides, coaches, and develops team members to lead, collaborate, and engage in a matrix set of responsibilities with Biogen; this includes direct line reports as well as the facilitation of dotted line responsibilities of staff, and considerable partnership/alignment with Asset Development Program Management (ADPM) group.
This role sits on the PO&T leadership team, is the primary decision maker as a member of the PO&T Governance Committee (GC) for this modality, and has extensive interface and influence with critical stakeholders including Discovery
& Research, Translational Sciences, and Clinical Development, external partners/collaborators representing PO&T on partner joint steering committees and various industry influencing forums.
This role is located in Cambridge, MA. Qualifications Who You Are You are able to balance deep technical expertise with strategic product planning and insights. You demonstrate exceptional leadership abilities including organizational awareness, business acumen, political astuteness, influencing/negotiations, decision-making ability, conflict resolution, and demonstrated ability to influence and inspire teams. You have proven successful in managing complex development portfolios and project plans and developing internal talent as well as demonstrated success in alliance and partner management.
Required Skills MS, Ph D preferred in medical-related field Minimum of 15+ years of relevant experience in the medical industry, including product development and/or commercialization experience Must have demonstrated experience in leading/engaging others in a direct and highly matrixed and fast growing and global healthcare organization, and broad technical knowledge across multiple modalities Additional Information Why Biogen? Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team.
We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired.
Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to interaction, gender identity or expression, interactionual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States. PDN-9a692b6f-bab4-4c98-9990-c2857439c343For more details: jobs-search.
org/manufacturing_cambridge-c434666/head-of-product-development-regcmc-pharma-cambridge_i1959027024
Supervisor performs a variety of manual labor tasks in the care of trees; assists Tree Climbers by handling ropes and guiding tree limbs to the ground; does not climb trees; assists in tree surgery by cleaning, preparing sterilizing, and trimming areas of trees and aids in cutting and clearing foliage away from overhead utility facilities; assists in searching out and spraying for insect control; prunes trees and shrubs; cuts down trees and shrubs, chops and saws limbs; cleans up after work is completed and keeps tools clean, sharp, and in operational condition.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. MINIMUM REQUIREMENTS:
At least one year of experience in related field Must possess a current Hoisting Engineer License Class 1-B Must possess a current and valid Commercial Driver's License Classification B Must present a valid Department of Transportation medical certificate.
Must possess a satisfactory driving record o Candidates must also provide, upon interview, a copy of their unattested driving record, obtainable at the RMV and dated within the previous six months Candidates may need to register with the FMCSA Commercial Driver's License Drug and Alcohol Clearinghouse clearinghouse. fmcsa. dot. gov/register All candidates will participate in an on-road driving backssment as part of the interview process.
Internal applicants must have a permanent civil service status.
PREFERRED: Arborist certification strongly preferred. PHYSICAL DEMANDS: All labor positions, skilled, semi-skilled, and unskilled in the Cambridge Department of Public Works require a combination of: Lifting between 25-100 pounds, proper bending, squatting, stretching, pushing, climbing, dragging, and pulling. OTHER INFORMATION: Exposure to all weather conditions. Work in a moderate to high noise level environment caused by sound of machinery or powered equipment being used. Occasional odor may occur during the course of work. Required to adhere to all safety rules and regulations as well as dress code policies.
Perform other related duties as assigned. Additional hourly compensations for the attainment of the Arborist certification. ADDITIONAL BENEFITS: Competitive Health, Dental and Vision benefits Vacation and sick leave eligible Sick Incentive Pay eligible3 Personal Days14 Paid Holidays REQUIRED DOCUMENTS: Please upload the following document to complete your application. Resume #P1PDN-99206bac-a81a-5c098a266411For more details: jobs-search. org/marketing_cambridge-c434666/forestry-worker-special-meoiia-cambridge_i1959024679
one or more key GSK products. The role will be responsible for leading and defining comparability studies and suitable analytical characterization strategies to support post-approval changes. The ASTL has ownership and accountability for the Analytical Product Strategy end to end taking accountability from the R&D Analytical Leader at PPQ Process Performance and Qualification stage.
Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today. Key Responsibilities: To provide technical analytical leadership for programs, projects and activities related to the specific product/s under the ASTL accountability to ensure business priorities
and targets are met eg. NPI, product transfers, change management, regulatory submissions. Lead and define comparability studies and suitable analytical characterization strategies to support post-approval changes for the accountable product/s.
To partner with teams across the business in a matrix-fashion in order to meet asset analytical needs, and to identify and mitigate analytical risks i. e. with R&D Analytical, PSC Analytical (site and central), Technical (site and central), Regulatory To ensure that the analytical method knowledge is embedded in the onward Technical Transfer to other GSK sites and to external sites To compile and recommend acceptance criteria for release and stability
tests to feed into the comparability strategies around TT/process change/scale change/material change.
To provide analytical input and expertise into comparability protocols and summary reports for regulatory changes/documents. To take non-routine physical properties data and recommendations from Materials Science, and build into comparability backssment reports, if applicable To drive PAT and new technologies for analytical testing linked to the Product Control Strategy (PCS)Own and accountable for the Analytical Product Strategy (APS). Maintenance and update of the APS through the post-approval product lifecycle eg. recommending specification strategy, recommending novel analytical technologies based on product needs.
Ensure that analytical methods developed by R&D are robust with respect to product lifecycle, focussing on the highest risk / most complex methods To ensure that the analytical method knowledge is embedded in the onward Technical Transfer to other GSK sites and to external sites Support analytical and comparability aspects for the regulatory submission of accountable product. Eg. support authoring regulatory files and RTQs responses relevant to analytical and area of expertise. Provide leadership and expertise for all analytical aspects of root cause analysis investigations (RCA) related to the accountable product.
Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Ph. D. 10+ years', OR MS 12+ years', OR BS 15+ years' experience in biomedical/medical analytical Experience with large molecule and vaccines Preferred Qualifications: If you have the following characteristics, it would be a plus: Comprehensive knowledge of external regulatory requirements (MHRA, FDA), and internal/external quality and safety requirements. Experienced in technology transfer, with an understanding of the product development process Knowledge of current and emerging Regulatory Strategies (Quality by Design, GMP for 21st century, ICH Q7, Q8, Q9, Q10) and Product Lifecycle Management.
Project management and prioritization skills gained within a complex matrix. Track record of improving products, processes and trouble-shooting, execution of technical activities including experimentation and analytical methods validation activitieinteractioncellent problem solver and ability to think and work creatively. Demonstrated experience leading technical aspects of root cause analysis investigations Demonstrated experience in the medical industry in leading the Technical aspects of Product Lifecycle Management related to large molecule products and/or vaccines (polysaccharide vaccines is an asset).
Demonstrated knowledge of Quality by Design and risk management approaches Strong technical acumen and communication skills with the ability to articulate complex, technical details to stakeholders and enable cross functional collaboration across sites, supply chain, R&D and CMO/CRO. Why GSK? GSK is a global biopharma company with a special purpose -to unite science, technology and talent to get ahead of disease together -so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns -as an organization where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be.
A place where they can be themselves -feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. #LI-GSKPlease visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why Us? GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organization where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030. Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.
We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at -xyz X (US Toll Free) or xyz X (outside US). GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, interaction, pregnancy, marital status, interactionual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site. PDN-9acbcc48-582f-45c8-94da-3f69ca8f89ee For more details: jobs-search.
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We take pride in our city's diversity and strive to create a workplace that is reflective of the community we serve. The city is also deeply committed to creating an environment in which all our employees are treated equitably and feel included. We seek to hire, develop, and advance individuals who value antiracism, diversity, equity, and inclusion (ADEI), and are committed to embedding ADEI best practices and tenets in all aspects of our work.
About The Department of Human Service Programs: The Department of Human Service Programs (DHSP) creates and coordinates services that enhance the quality of life for Cambridge residents. Driven by the needs of residents, DHSP's extensive services
and programs touch almost every sector in the city: from newborns to senior citizens, from school-aged children to homeless families, from non-profit organizations to local employers.
ABOUT THE ROLE: Reporting to the C-CAN Program Manager, the Specialist will serve a key function within the Cambridge Coordinated Access Network (Cambridge CAN or C-CAN), the community's multi-agency system that connects people experiencing a housing crisis to resources and referrals to housing placements. The C-CAN program is the city's Coordinated Entry System, a HUD required process that allows users to make consistent decisions from available information to efficiently and effectively connect people
to interventions that will rapidly end their homelessness. The coordinated Access Specialist will directly administer backssments to clients at intake and serve on a team of dedicated C-CAN staff working to organize and coordinate backssments, referrals, and communications among partners.
ESSENTIAL DUTIES AND RESPONSIBILITIES: The Coordinated Access Specialist will work on a team of one other Specialist and the C-CAN Program Manager. Many of the duties and the responsibilities will be shared within the team and redistributed as needed to ensure successful function of the Coordinated Access Network. This Specialist role will be focused on the external outreach and marketing of the program in addition to supporting typical processing and functions of C-CAN.
The Coordinated Access Specialist's specific duties include, but are not limited, to the following: Administer the Cambridge CAN suite of intake, screening, backssment, and referral tools to new clients presenting at the Cambridge Multi-Service Center; enter backssed clients' information into Cambridge's Homeless Management System (HMIS)Respond to phone inquiries and walk-ins, referring clients to appropriate services and backssment points as needed. Maintain strong knowledge of relevant homeless-specific and mainstream resources for referral to support a wide range of client needs.
Support data collection, entry and integrity efforts across the Continuum of Care (Co C), the group of municipal and nonprofit partners working collaboratively to address homelessness in the community. Participate in outreach efforts to community members who are experiencing homelessness. Maintain Cambridge CAN's HMIS Data and contribute to Co C-wide strategic/planning efforts. Provide internal technical assistance to Coordinated Access partner agencies on intake, backssment, and prioritization. Participate in meetings between C-CAN partner agency staff, including a weekly case conference and operational or program evaluation check-ins.
Serve as liaison between C-CAN and relevant provider and community partners, including responding promptly to inquiries by phone and email. Actively work to improve the level of system access for the full diversity of people who are homeless and at risk of homelessness in Cambridge, as well as to promote a low-barrier Housing First orientation that values equity. Develop and carry out outreach strategies to promote Coordinated Access within the Co C and the wider community, as appropriate.
Improve marketing efforts digitally and in print to increase community awareness and education around C-CAN program and related resources. Plan events, attend community meetings and support community efforts to further outreach efforts. Actively participate in the Department's Race and Equity Initiative. Other duties as assigned. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. MINIMUM REQUIREMENTSBachelor's Degree required or equivalent combination of education, training and experience. Minimum of five years in human/homeless services.
Strong organizational and administrative skills. Excellent oral and written communications skills. Crisis intervention skills, including the ability to assist clients in challenging situations and to support staff in their ability to provide assistance. Proficiency in personal computer skills such as Microsoft Office Suite; experience with HMIS or other database systems. Experience coordinating a multi-partner initiative or project. Ability to exercise mature judgment in complex situations. The City of Cambridge's workforce, like the community it serves, is diverse.
Applicants must have the ability to work and interact effectively with individuals and groups with a variety of identities, cultures, backgrounds, and ideologies. PREFERRED QUALIFICATIONS: Experience in services to people experiencing homelessness strongly preferred, as well as work in a diverse setting. Knowledge of Cambridge and surrounding communities helpful. SUMMARY OF BENEFITS : H ealth, dental and vision insurance. vacation, personal and sick days. sick incentive pay eligibility. management bonus of $2700/year. City employee commuter benefits (T-Pass reimbursement, Bluebikes membership, EZRide Shuttle membership).
PHYSICAL REQUIREMENTS, WORKING CONDITIONS, AND ACCOMMODATIONS: Ability to access, input and retrieve information from a computer. Ability to answer phones and maintain multiple files. Ability to lift a minimum of at least 10 lbs. Ability to travel to meetings within the city. Be comfortable to w ork primarily in a standard office environment with moderate noise level, telephones, personal computers, printers, and other office equipment. This position may be eligible for hybrid work under the City's Telework Policy depending on operational needs. Reasonable accommodations will be made to enable qualified individuals with disabilities to perform essential job functions.
REQUIRED DOCUMENTS: Please upload the below documents to complete your application: Resume Cover Letter #P1PDN-99be0ea2-cfba-4fa3-9cca-c89a2d344219For more details: jobs-search. org/marketing_cambridge-c434666/coordinated-access-specialist-cambridge_i1959025242
partners, community specialists and skilled nursing facilities. Our vision is to transform care to improve lives. Atrius Health provides high-quality, patient-centered, coordinated, cost effective care to every patient we serve. By establishing a solid foundation of shared decision making, understanding and trust with each of its patients, Atrius Health enhances their health and enriches their lives.
Atrius Health is part of Optum, a health services company focused on building the leading value-based care system in the country. If you would like to know a bit more about this opportunity, or are considering applying, then please read the following job information. SUMMARYThe LGBTQ Care
Facilitator, as a member of a LGBTQ Adult primary healthcare team, facilitates the process of care for Atrius's LGBTQ Adult Primary Care patients, coordinates an accessible plan of care and backss for clinical triggers.
They will serve as a liaison among the primary care team, specialist physicians, behavioral health team members, care management social workers, and the patient and/or patient's family. This role is scoped for 1 year, with the potential for renewal. The Care Facilitator is a critical team member in creating an exceptional patient experience. Vital to this role is forming longitudinal relationships with LGBTQ patients, regularly backssing their clinical or social needs,
and coordinating with primary care, case management, and social work teams to refer patients to community support services, aligned with their LGBTQ identity and values.
As part of forming longitudinal relationships, the facilitator is expected to maintain an understanding of the patient's identity, pronouns, preferred language and cultural beliefs and values which impact care, patient experience or recommended treatment plan. The person in this role will also provide data management of the LGBTQ patient population, and conduct patient outreach for follow-ups, referrals, and specialized care needs. The Care Facilitator populates standardized clinical and social information in the administrative areas of the care plan in the patient's medical record, and collects data, and generates reports.
Ensures clinicians are informed of assigned patients' status and may present performance metrics to larger group of clinicians. Attends required specialty meetings and participates in care improvement activities as needed to improve quality performance. These activities include, but are not limited to, a monthly patient advisory council workshop and ongoing training for the care team and front office staff. EDUCATION/LICENSES/CERTIFICATIONSHigh School diploma or equivalency certificate (e.
g. GED, Hi SET, TASC Test) from an accredited institution or governmental unit required. College degree in health care administration or psychology strongly preferred. A bachelor's degree in related field (typically in healthcare administration, psychology or healthcare related field) can at times be substituted for work experience. EXPERIENCEExperience typically acquired through three years of experience in a clinical setting. Previous training or experience work in population health management preferred. MR experience and/or aptitude to master the EMR based on other technology experience required.
Experience working with the LGBTQ community in a facilitator or coordinator capacity and/or exposure to the local LGBTQ ecosystem is preferred. SKILLSProficiency in data management, including the ability to extract data and develop spreadsheets, required. Knowledge and understanding of medical terminology required. Proficiency in Microsoft Office, especially Excel is required. Strong interpersonal and communication skills needed with the ability to interact effectively with patients and medical professionals. Ability to demonstrate a high level of cultural competence and sensitivity to patient needs and concerns.
Ability to engage patients in problem solving. Sound judgment with the ability to work and make decisions in a fast-paced environment. Computer skills that include proficiency with electronic medical records (EMR), Microsoft Office - especially Word and Excel are required. Knowledge and understanding of medical terminology. Excellent telephone skills, strong customer service and ability to build relationships with patients are required. Atrius Health is committed to a policy of non-discrimination and equal employment opportunity. All patients, employees, applicants, and other constituents of Atrius Health will be treated with respect and dignity regardless of race, national origin, gender, age, religion, disability, veteran status, marital/domestic partner status, parental status, interactionual orientation and gender identity and/or expression, or other dimensions of diversity.
BENEFITS INCLUDE: Up to 8% company retirement contribution Generous Paid Time Off 10 paid holidays Paid professional development Generous health and welfare benefit package Atrius Health is an equal opportunity/affirmative action employer and does not discriminate in recruiting, hiring, training, promoting or any other employment practices on the basis of race, color, religion, interaction, marital status, age, interactionual orientation, gender identity, national origin, military service or application for military service, veteran or disability status.
Applicants have rights under Federal Employment Laws: Family and Medical Leave Act (FMLA); Equal Employment Opportunity (EEO); and Employee Polygraph Protection Act (EPPA). VEVRAA Federal Contractor Request Priority Protected Veteran & Disabled Referrals for all of our locations within the state PDN-9a8d4eb8-7e88-4b27-b0f7-97cd04cab336For more details: jobs-search.
org/technology_newton-c434659/lgbtq-care-facilitator-newton_i1959027105
perform duties as outlined by the Head Fire Mechanic and the Technical Services Deputy Chief. Duties include but are not limited to: Diagnose, repair and maintain a variety of fire apparatus, equipment and vehicles. Perform preventative maintenance duties as needed.
Diagnose, and repair air brake, electrical and hydraulic systems. Diagnose, and repair a variety of diesel and gas engines, transmissions. Diagnose, and repair fire pumps and related systems. Diagnose, and repair aerial devices and related systems. Design and fabricate specialized equipment; perform welding, weld and fabricate parts as necessary. Respond to emergency calls as needed to assist department personnel or transport
vehicles and equipment as required. Operate and maintain a variety of hand and power tools and diagnostic equipment. Operate computer based diagnostic software.
Maintain records of maintenance. Perform other duties as assigned. MINIMUM REQUIREMENTS: Two (2) years of automotive mechanic experience, preferably in diesel fire equipment and apparatus. EVT (Emergency Vehicle Technician) certification to comply with NFPA 1071 standard. EPA 609 A/C certification. Familiarity with specialized emergency vehicles systems and multiplex electrical systems. PREFERENCES: Pierce Mfg. experience preferred. Ford experience preferred. Familiarity with on-board apparatus computer systems. Familiarity with
Cummins Insite, Ford IDS, and Detroit Diesel Diagnostik Link software.
Valid Mass driver's license required. (Practical tests may be required)PHYSICAL DEMANDS/WORK ENVIRONMENT: Lift heavy objects up to 75 lbs. Climbing and working at elevated heights. Use a variety of hand and power tools. Work in confined areas. Work out-of-doors in inclement weather. Exposure to heat, cold, dampness, dust, pollen, odors, fumes, etc. Exposure to hazards of electrical shock, falls, noise, equipment operation, etc. Exposure to chemicals, petroleum products, cleaning agents, fumes, etc. May require working extended hours. REQUIRED DOCUMENTS: Please upload the below documents to complete your application: Resume #P2 PDN-9acb9dff7f-9e59-fc33d9cb3b37For more details: jobs-search.
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in Biogen's GMTO function. In this role, you will manage overall manufacturing responsibilities across the portfolio, technical transfer of processes and methods (both Biogen internal assets and strategic partner programs run in Biogen) into internal factories and external CDMO plants, including (in differing proportions of shared accountability with Development, depending on modality) early clinical programs, late-stage/PPQ, and commercial programs going to new sites.
Deploys GMS technical TT leads, technical product leads, process SMEs, Process Sciences labs/scientists, Materials Sciences lab/scientists, and data analytics scientists to ensure new campaign success; materials and consumables
suitability for use; supplier technical readiness; tools for campaign, batch, and materials visibility; process troubleshooting and correction; and development and implementation of lifecycle process improvements for commercial assets.
You will also ensure that new processes, materials, control technologies, and monitoring approaches and tools are manufacturing-ready in a phase-appropriate/stage-gated manner. MAIN RESPONSIBILITIES With broad accountability in driving the shared goals of GMTO and PO&T, this leader sits on the Senior Leadership Team (SLT) for GMTO and provides insight and recommendations to guide and set the strategy for the overall GMTO organization and interacts with/presents
to the PO&T SLT as needed. In this role, you must also maintain a degree of visibility to tactical considerations and issues that relate to or impact clinical and commercial processes, as well as the transfer of processes into internal factories and external plants.
You will partner collaboratively with peers and leaders in the other PO&T line functions to ensure that GMTO is ready to both receive and execute new processes/products, and to ensure that new technologies for process and plant are robust, implementable, and sustainable in a manufacturing environment. You will serve on joint steering committees for major strategic partners. As a leader of GMS, the role is highly impactful to GMTO operations and to the success of PO&T's assets: this team's work ensures successful timelines for starting and completing clinical and PPQ campaigns in high run-rate plants and CDMOs; technical support during clinical and commercial campaigns; timely investigation and correction of manufacturing process issues; and contribution to and review of key sections of regulatory filings for new assets.
Ensures that late-stage processes are ready for process validation, and owns and drives the process validation master plan, protocols, and reports. The Materials Science team ensures vendor technical readiness for raw material and consumables supply to Biogen and provide raw materials analytical characterization and monitoring to look for " unknowns" before materials are committed to GMP batches.
The site teams provide expert process support as needed for Operations, both internally and externally. Also, they provide technical management of strategic partner relationships, including tech transfer and batch/campaign/issue visibility for partners. Directs direct reports (GMS Leadership Team) to ensure success in meeting PO&T's strategic goals and Asset Team timelines and milestones.
Sets strategy and goals of GMS to align with GMTO and PO&T and responds agilely to new asset acquisition and partner opportunities as they arise. Ensures that GMS site and global line functions are working in a matrixed framework to drive the needs of internal asset timelines, strategic partner program timelines, and GMTO. Partners with leadership in Global Engineering, Manufacturing, ADPM, Quality, and Regulatory Affairs to ensure that cross-functional teams are working smoothly to deliver and maintain processes and controls that are timely, phase-appropriately ready for manufacturing, and compliant, to meet clinical and commercial Supply Chain needs.
Understands and responds to business priorities and translates into tactical objectives and work direction for the site MS teams. Includes the direct and matrixed GMS team listed above. Ensures that production schedules and Asset Program deliverables are not compromised due to tech transfer/process transfer issues, partnering with the other GMS line functions as required. Manages budget (~$22MM OPEX, ~$2.5MM CAPEX yearly), staffing, and performance management duties for GMS. Mentors direct and indirect reports on development planning and possibilities for their careers, both within GMS and across Biogen.
Ensures compliance of investigative activities across modalities within the GMS team with c Gx P regulations and maintains a high degree of regulatory compliance with FDA, EMA, and other agency guidelines and regulations to ensure solid data packages and data-integral reports for filings. Responsible for relevant CMC sections of clinical and commercial product regulatory filings. Provides technical SME support during site regulatory inspections, both from directly reporting staff at the inspection site and from the matrixed GMS line functions.
Responsible for overall process validation process monitoring and CPV to ensure process robustness and to identify process improvements inclusive and exclusive of LCM opportunities. Improvement plans to drive year over year soft and hard savings across the organization. Qualifications The ideal candidate will be an established leader in this space and will have led and motivated teams. Professional Qualifications A minimum of 15 years' experience in a biomedical/medical manufacturing environment with at least 8-10 years of senior management experience.
Education: Degree in Biochemistry, Chemistry, Chemical or Bioprocess Engineering, Biology, or closely allied discipline; Ph. D. in relevant fields is preferred. Deep technical and scientific competencies across multiple modalities. Demonstrated success in managing, motivating, and continually strengthening a large, complex, and multi-disciplinary organization. High complexity of challenges and decision-making requirements - management of a multi-line team that covers all phases of GMP operations, internally and externally, across all modalities in which Biogen works.
Demonstrated capabilities in transforming and modernizing a sizable operation by appropriately leveraging standards and technology and innovative end-to-end thinking. Ability to build, convincingly communicate and execute strategic and operational plans for a global function. Strong ability to prioritize and deploy resources across the organization rapidly to respond to changes in schedule, shifts in modality needs, and operational surprises, and at the same build business models for major areas of accountability for GMS so that the delivering team can apply standard work as much as possible for efficient use of resources.
Exceptional interpersonal skills including the ability to influence behaviors and negotiate and resolve challenges with poise, tact, and diplomacy. Exceptional leadership skills, with the ability to communicate vision, set direction, as well as inspire, motivate, and mentor a cross-functional team. Ability to travel as needed both domestically and internationally Must be able to work on campus 2-3 days a week Personal Characteristics A proven ability to operate effectively in a rapidly changing environment where analytical skills and agility are equally as important; a strategic thinker who is operationally focused who can manage diverse agendas and personalities Self-aware, self-motivated, self-confident individual who is comfortable operating with minimal direction and thrives in a dynamic environment as a leader influencing change and transformation Credible and savvy business person who is well networked across the industry and will be perceived as a trusted consultant and functional expert to senior management.
Must be an influential advisor; bold and courageous while having the antennae to understand cultural and political nuance Knowledgeable in leading-edge security business practices, trends, and information; aware of strategies and tactics being applied in the marketplace that are innovative Able to engender trust and respect quickly as a manager of people, with a priority on staff development.
A capability builder at both the organizational level as well as the individual level An individual of unquestioned personal and business integrity who will be viewed as trustworthy both within the company, as well as with external relations A mission-driven individual with high energy and high levels of perseverance; works towards both individual and team goals Additional Information All your information will be kept confidential according to EEO guidelines.
Why Biogen? Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients' lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve.
We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to interaction, gender identity or expression, interactionual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law.
Biogen is an E-Verify Employer in the United States. PDN-9aab8b8c-2ad6-44c0-9c5f-781fc74d2ab3For more details: jobs-search. org/manufacturing_cambridge-c434666/head-of-global-manufacturing-sciences-cambridge_i1959027829
