65 jobs found for writer in hudson, massachusetts

Randstad in partnership with the leading audio business on the planet, has an immediate opening for a content writer. This position will require internal interviews and investigating. The Internal Communications Content Writer plays a key role in creating and executing internal communications that engage, inspire and empower employees around the world. In support of the global Internal Communications team, we are looking for a multi-talented professiona

PROVIDING EXCELLENT SERVICE TO THE INDUSTRIAL AUTOMOTIVE INDUSTRY. COME JOIN US! We are representing a reputable commercial automotive service center committed to providing top-quality maintenance and repair services to their valued customers. With a focus on exceptional customer service and technical expertise, they strive to exceed expectations with every visit. As they continue to grow, they are seeking a skilled and customer-focused Service Advisor/Wr

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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

job summary: The primary purpose of the Clinical Scientist's position is to assist/support the Clinical Research Director (CRD) in the medical/scientific contribution for the clinical studies on activities pertaining to the Study Medical Manager responsibilities e.g.: managing or contributing to the operational activities from clinical trial set-up to clinical study report in compliance with quality and regulatory processes. The clinical scientist will be

job summary: A R&D Technician is needed for a biomedical/biotechnology engineering firm and multinational manufacturer of medical devices in the Marlborough, MA area. This position involves assisting R&D engineers and scientists in designing, analyzing, and testing pilot and production equipment for medical device development, ensuring compliance with quality standards and driving innovation in process optimization. location: Marlborough, Massachusetts

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve thei

We are pioneers in harnessing the power of mRNA technology to develop groundbreaking therapies and vaccines that have the potential to transform lives. Our state-of-the-art manufacturing facility is dedicated to producing high-quality mRNA-based products that address unmet medical needs globally. As a Manufacturing Associate, you will play a pivotal role in our mission by contributing to the production process of cutting-edge mRNA therapeutics and vaccine

job summary: Your Responsibilities: As a core member of multiple new product development teams, the Regulatory Affairs Specialist will provide timely and valued regulatory guidance (written and / or verbal) by owning the following tasks: 1. Advise internal stakeholders (marketing, manufacturing, R&D, etc.) regarding current/pending guidance, regulations, Agency/industry initiatives, etc. to ensure regulatory strategy is in alignment with company objective

Join one of the largest, fastest growing pharmaceutical companies in the US that is patient focused in their pursuit of life changing treatments! Our client is currently hiring Global Pharmaceutical Publications Consultant to join their team in Boston. As a Global Pharmaceutical Publications Consultant you will be responsible for leading the company-sponsored publication programs. The assigned publications will have global reach, may involve complexity

Do you want to join a company that is committed to creating an inclusive and diverse environment for our team members across the globe? Who is passionate about being an active contributor to the communities where we live, and work, as well as to global communities through our charity and learning initiatives? We need you! salary: $30 - $32 per hourshift: Firstwork hours: 6 AM - 4 PMeducation: BachelorsResponsibilitiesWhat you will be doing: F

We are pioneers in harnessing the power of mRNA technology to develop groundbreaking therapies and vaccines that have the potential to transform lives. Our state-of-the-art manufacturing facility is dedicated to producing high-quality mRNA-based products that address unmet medical needs globally. As a Manufacturing Associate, you will play a pivotal role in our mission by contributing to the production process of cutting-edge mRNA therapeutics and vaccine

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 knowled

We are pioneers in harnessing the power of mRNA technology to develop groundbreaking therapies and vaccines that have the potential to transform lives. Our state-of-the-art manufacturing facility is dedicated to producing high-quality mRNA-based products that address unmet medical needs globally. As a Biotech Manufacturing Associate, you will play a pivotal role in our mission by contributing to the production process of cutting-edge mRNA therapeutics and

job summary: A Packaging Lab Technician is needed for a biomedical/biotechnology engineering firm and multinational manufacturer of medical devices in the Marlborough, MA area. This job conducts analytical testing to ensure compliance with cGMP regulations, prioritizing patient safety and product quality, while also providing support for process validations and adhering to quality system standards. location: Marlborough, Massachusetts job type: Contra

job summary: Essential Functions: MDM System Maintenance: Lead in the maintenance and administration of MDM systems in collaboration with internal resources. Project Support: Support large-scale end-to-end MDM project implementation. Quality Management: Conduct data quality functions including audit/assessment, entity resolution, data profiling, and exception management configuration in MDM. echnical Planning & Requirements Gathering: Lead technic

If you need more incentive to apply for this role, in addition to on the job training and the potential for a permanent position with advancement opportunities, we also offer: Medical benefits (available after first paycheck is deposited) Vision, dental and 401K Discounts on major cell phone provider plans, including T-Mobile and AT&T, ranging from 15% to 18% (no waiting period) And more!! Call, email or apply online today and interview within 24 h

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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

Lift and carry boxes weighing up to 50 lbs. without assistance for prolonged periods, Load, operate and move hand carts, pallet jacks, Operate hand held scanner, Load and shrink wrap pallets at ground level, or on carts, Load boxes onto pallets and load pallets onto trucks manually and with material handling aids Requirements: Walk, stand, kneel, squat, stoop and bend for extended periods of time Read and write English Background check and drug test Steel

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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that

Randstad is working with a law firm in the Woburn area to fill a position supporting 2-3 attorneys and providing general administrative and legal support. This person will be responsible for managing legal binders and all case information, drafting and issuing subpoenas, and overall ensuring that cases are managed. Experience in the legal field, 2-3+ years, along with knowledge and proven ability to perform the above tasks are required. This is a great opp

job summary: management framework. You will also be responsible for managing investigations sourced from various sources, such as threat intelligence. Your role is pivotal in making critical decisions, refining IR processes, and communicating with stakeholders at all levels, including the C-Suite. Leveraging your extensive expertise, you will drive initiatives that bolster our cybersecurity defenses and foster a culture of continuous improvement an

The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to i

The individual in this role will be part of a cohesive team responsible for supporting cGMP mRNA drug products produced at this facility. He/she will provide quality oversight and expertise to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will have experience in quality oversight or manufacturing experience in early stage clinical products. They will be able to i

Are you looking to join a company that can provide great stability and an amazing work culture? Do you want to further the reach of healthcare in your community and beyond? If you said yes, then We Want You! Play a critical role in ensuring the success of our endeavors. . Join us today and become a part of a future for all. WE NEED YOU!Salary: $21 - $23 per hourWork hours: 8 AM - 5 PMEducation: High SchoolResponsibilitiesHere's your daily respons

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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

Position: Quality Inspector Location: Billerica MA Job Type: Full-time (6 Month contract, ability to be extended) Shifts: 1st: 6AM-3PM ($24/HR) 2nd: 2PM-11PM ($25.50/HR) 3rd: 10PM-7AM ($27/HR) 4th: 6AM-6PM ($25.50/HR) 5th: 6PM-6AM ($27/HR) Overview: We are seeking a meticulous and detail-oriented Quality Inspector to join our team. The primary responsibility of the Quality Inspector will be to ensure compliance with quality stand

packing finished product and prepare for shipment processing shipments for domestic and international customers multi-task FedEx/UPS/DHL on-line enter in all required data into the computer Requirements: prior shipping experience lift up to 50lbs great attention to detail self motivated willing to submit to background check CHECK OUT WHAT'S IN IT FOR YOU? Randstad benefits: Medical, Dental, Sick leave, Life Insurance, Disability Insurance, 401K (after 6

small parts - medical device assembly, complete and maintain accurate written records, device history, data sheets and lot control, LEAN manufacturing principles Requirements: small hand tool experience soldering irons, dial calipers, pressure gages etc. willingness to be cross trained in department must have excellent dexterity, fine motor skills and eyesight prior experience working under microscope and/or magnifying light basic math skills willing to s

Shipping/receiving, loading/unloading, pulling orders setting up product on delivery trays & staging for delivery Requirements: lift up to 50lbs ability to work in a freezer for short periods of time to pick product great attention to detail team player who can work independently read English steel toe shoes CHECK OUT WHAT'S IN IT FOR YOU? Randstad benefits: - Medical, Dental, Sick leave, Life Insurance, Disability Insurance, 401K (after 6 months 2