radiology technician salaries in boston, massachusetts

job summary: Seeking a Quality Technician on 1st Shift for a high growth materials manufacturing company in the Woburn, MA area. The Quality Tech would be responsible for: End-to-End Inspection: Managed full-cycle inspection processes (Receiving, In-Process, and Final) following established reliability procedures. Technical Analysis: Interpreted complex manuals and charts to make high-stakes acceptance/rejection decisions based on blueprint tolerances. Benefits offered: Comprehensive coverage for medical, prescription drugs, dental, vision, voluntary optional life, accident insurance, hospital indemnity insurance and critical illness insurance with competitive premium cost. 401(k) Plan with company matching contributions at 100% of the first 5% of pay.Company provided defined-contribution retirement plan with annual contribution equal to 3% of pay.Career development and tuition reimbursement.Other benefits including paid parental leave, short and long-term disability programs, adoption assistance, a Care.com membership and financial planning assistance are provided at no cost to you.Supplemental benefit programs including identity protection, legal protection, and pet wellness are available at competitive rates.Paid Time Off and Company-Paid Holidays.   location: WOBURN, Massachusetts job type: Permanent salary: $52,000 - 56,680 per year work hours: 8am to 4pm education: High School   responsibilities: End-to-End Inspection: Managed full-cycle inspection processes (Receiving, In-Process, and Final) following established reliability procedures.Technical Analysis: Interpreted complex manuals and charts to make high-stakes acceptance/rejection decisions based on blueprint tolerances.Strategic Support: Facilitated customer testing, reporting, and PPAP documentation to ensure seamless product delivery.Internal Auditing: Partnered with the Quality Manager to conduct internal audits, ensuring 100% compliance with military and engineering standards.Tool Accuracy: Maintained precision instrumentation through regular gage calibration and equipment requests.   qualifications: Experience level: ExperiencedMinimum 3 years of experienceEducation: High School (required)  skills: QualityProductionManufacturingPlasticsMaterialsTestingSafety Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Now Hiring: Kit Packaging Technician I – Be Part of Something Bigger! Location: North Billerica, MA Industry: Pharmaceuticals | Shift: 1st shift (6AM-4:30PM) M-Th w/overtime on Friday.      Type: Full-time Pay: $24.00 - $26.00 Are you detail-obsessed, reliable, and ready to make a real impact in the pharmaceutical world? Join a team that's packaging life-saving medications for global distribution! We're looking for a Kit Packaging Technician I who’s energized by precision, thrives in a team environment, and isn’t afraid to roll up their sleeves.  What You’ll Do: Inspect pharmaceutical vials with a sharp eye for detail Label and package medications—by hand or with the help of machines Follow SOPs, manufacturing batch records, and cGMP standards Keep production areas safe, clean, and efficient Jump into improvement initiatives and help keep things running smooth Communicate with your team and contribute to shared success   ✅ What You Bring: High School Diploma (Associate's Degree or manufacturing experience is a plus!) 0–3 years in manufacturing or packaging (pharma preferred but not required) Solid attention to detail and willingness to learn Ability to follow procedures and complete documentation accurately A team-player attitude and solid communication skills Willingness to work overtime when needed MUST HAVE EXPERIENCE WITH GMP/cGMP, ALCOA, and Batch Processing.    Why You'll Love It Here: ✨ Be part of a mission-driven team making a difference worldwide Gain hands-on experience in the pharmaceutical industry Opportunity to grow in a cGMP-regulated, high-performing environment A culture built on safety, collaboration, and continuous improvement  Sound like a fit? Apply today and start packing a better future! INTERESTED? APPLY NOW!  salary: $24 - $26 per hourshift: Firstwork hours: 6 AM - 4:30 PMeducation: High SchoolResponsibilities MUST have 1 year exp  GMP, GDP, ALCOA and worked with batch records. Responsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations  performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials.   Must follow SOP’s and the ability to follow manufacturing batch records. Understands and complies with cGMP work environment standards and support a solid safety culture. Ability to work in a fast paced work environment while maintaining attention to detail. Ability to work in a team oriented work environment. Willing to work overtime when required. Essential Functions Demonstrate the ability to conduct visual inspection per established qualification criteria. Demonstrates practical knowledge of subjects such as area clearances, product accountability, label control, product segregation and control, operator/check by and other basic skills required to work in a pharmaceutical environment. Understands and follows SOP’s. Fills out standardized forms correctly.  Instructs other team members on basic procedures.  Demonstrates fundamental writing skills, such as proper spelling, appropriate grammar and punctuation. Communicates effectively with team members and other internal groups.   Demonstrates the ability to listen. THIS IS A FIRST SHIFT POSITION - 6:00AM - 4:30PM, Mon-Thurs with OT on FridayThe essential functions of this role include:working up to 5 hrs of overtime per weekSkillsInspectionGMP (1 year of experience is required)clean roomQuality AssurancepackagingPharmaceuticalALCOA (1 year of experience is required)BATCH PROCESSING (27 years of experience is required)QualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $143.33 - 196.66 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Principal responsibilities include: - Supports the Global Safety Lead (GSL) for assigned oncology pharmaceutical / biological / drug-device combined products. - Responsible for safety surveillance, signal detection and risk management activities. - Supports cross-functional assessment of benefit-risk profile and communication of safety information for assigned compounds and products. - Provides pharmacovigilance functional area expertise and support to project teams for assigned developmental and/or marketed products. - Represent pharmacovigilance, both regionally and globally, as an authoritative and knowledgeable member of Global Program Teams (GPTs) and sub-teams, commensurate with position's seniority/experience. - Coordinates all aspects of signal detection and safety surveillance and review activities, in collaboration with the GSL, for assigned product(s). ACCOUNTABILITIES: - Analyze and interpret safety data from various sources including non-clinical, clinical, post-marketing and scientific literature. - Facilitate ongoing safety surveillance for assigned products, assisting with or leading data collection and assessment for the GPSE Safety Team (GST) and Safety Management Team (SMT). - Coordinate and perform signal identification, evaluation and management activities for assigned products, ensuring communication of all safety information that may impact the benefit-risk profile of assigned products to senior management. - Assist with or lead authoring of safety evaluations, defining scope and methodology and providing background information for aggregate safety reports, conducting preliminary safety analyses, and preparing ad hoc reports including Health Hazard Evaluations, Signal Evaluation Reports, and Health Authority responses. - Partner with cross-functional colleagues of the SMT and contribute to safety-related deliverables associated with new drug applications, benefit-risk assessments and activities related to risk minimization including RMPs. - Liaise with colleagues in relevant functional areas within and outside of PSPV to gather and provide input for appropriate sections of critical documents (e.g., protocols and amendments, ICFs, IBs, core data sheets, IMPDs, CSRs, INDs, NDAs, BLAs, and CTAs). - Liaise with other relevant functional areas both within and outside of global PV to best ensure the most efficient and timely attainment of compliant and patient focused safety data. - Represent PSPV in cross-functional teams or committees and external environments at a global and regional level as required, with the advanced communication skills this requires. - Assist with or lead the preparation and presentation of identified and potential patient safety risks and SMT recommendations on safety issues to cross-functional decision-making bodies such as the company Safety Board. Where acting as the GSL can expect to lead presentations to Safety Board, with the detailed preparatory work this implies and, where ad hoc issues arise, manage the short timelines that can ensue. - Build and maintain in-depth knowledge and understanding of designated products/studies, and close knowledge of protocols to effectively respond to safety issues. - Ensure up-to-date representation of safety information in Company Core Data Sheet (including Reference Safety Information) and Investigator Brochure, as well as other labeling documents. - Demonstrate outstanding knowledge of local and global health authority requirements. - Support PSPV in the maintenance of a highly effective global safety organization in full compliance to worldwide regulations. - Train and mentor newly hired peers and incumbent PV Scientists. - Maintain professional knowledge and accreditation by active participation in continuing medical education activities, and foster a community of continual learning.   qualifications: Bachelor of Science or Health Care Professional degree (e.g., RN, BSN, NP, PA, RPh) or equivalent qualification; advanced degree in scientific or medical field preferred.Minimum 10 years of relevant biotech/pharmaceutical experience.Excellent working understanding of safety database configuration and adverse event coding to direct advanced searches.In-depth knowledge of clinical trial methodology, pharmacovigilance regulations, safety data analysis and benefit-risk assessment, and understanding of drug development. #LI-LH1   skills: Pharmacovigilance, Drug Safety, Individual Case Safety Report (ICSR), Risk Management Plan (RMP), Safety Data Analysis, Informed Consent Form (ICF), Investigational Medicinal Product Dossier (IMPD) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.