129 jobs found for takeda internship regulatory operations in stoneham, massachusetts

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: 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

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

Randstad in partnership with one of the largest pharmaceutical companies in the worldis seeking a Specialist/Senior Specialist to support Quality On The Floor (OTF) oversight of manufacturing activities and Facilities at Moderna Inc. This position will be based in our cGMP Manufacturing site in Burlington, MA and will directly support the growing Personalized Medicine Program. salary: $30 - $38 per hourshift: Firstwork hours: 8 AM - 4 PMeducation

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

Randstad in partnership with one of the largest pharmaceutical companies in the world is seeking a Sr. Research Associate for mRNA Manufacturing of Personalized Cancer Vaccines based at their GMP Manufacturing site in Norwood, MA. The individual in this role will be primarily responsible for review of data generated by our Analytical Technical Operations team supporting our in-process testing, STAT, priority, release, and stability workflows. salary: 

Randstad in partnership with one of the largest pharmaceutical companies in the world is seeking a Research Associate for mRNA Manufacturing of Personalized Cancer Vaccines based at their GMP Manufacturing site in Norwood, MA. In this role, you will be an essential member of our testing team, using your laboratory experience to conduct and analyze a variety of key assays. This six-month contract position offers the opportunity to leverage your scientific

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 world's 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 t

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: 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. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, ou

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

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

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

Randstad in partnership with one of the largest pharmaceutical companies in the world is seeking a cGMP Associate for mRNA Manufacturing of Personalized Cancer Vaccines based at their GMP Manufacturing site in Norwood, MA. They are hiring multiple shifts. Day and Overnights. These are 12 hour rotating shifts. (pitman schedule) The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based personalized cancer vacci

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. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longti

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

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

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

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

job summary: Exciting new opportunity for an experienced Compliance Specialist who will work closely within the Manufacturing Compliance group to achieve department goals. The Compliance Specialist is also responsible for owning and driving manufacturing compliance improvement through deviation resolution, applied root cause analysis and the application of CAPA to elevate safety, quality, cost, on-time delivery, and right first-time performance. The Compl

job summary: The QC Microbiology associate is responsible for the performance of the cGMP routine/non-routine QC sampling and testing within the function of the QC Microbiology Laboratory supporting our Vaccine manufacturing site. This is a first shift position. location: Cambridge, Massachusetts job type: Contract salary: $45.00 - 47.69 per hour work hours: 9 to 5 education: Bachelors responsibilities: Perform routine environmental mon

job summary: As the world's 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

Randstad in partnership with one of the largest pharmaceutical companies in the world is seeking a cGMP Associate for mRNA Manufacturing of Personalized Cancer Vaccines based at their GMP Manufacturing site in Norwood, MA. They are hiring multiple shifts. Day and Overnights. These are 12 hour rotating shifts. (pitman schedule) The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based personalized cancer vacci

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

Are you an experienced records specialist seeking employment with one or more years of experience? We have a position open for you! This position is in a large law firm seeking a records specialist. Apply today and I will reach out to you as soon as possible! The desired start date is May 28, 2024. Join our team!salary: $19 - $19 per hourshift: Firstwork hours: 8:30 AM - 5 PMeducation: High SchoolResponsibilitiesProvide maintenance of data, recor

working in a printing facility putting together training binders for a large client. Requirements: must be able to read, write and speak English must have great attention to detail team player 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 abilitie

· Maintains Quality Management System (QMS) programs and initiatives. · Provides critical information for audits and reviews/analyzes data and documentation. · Maintains all required documentation to meet the required security compliance standards and to meet audit control standards, Standard Operating Procedures (SOP), Forms, spreadsheets, data analytics. · Performs and documents required monthly user reviews for associate's access, both data and physical