Page 2 - 113 jobs found for human resources in mansfield, massachusetts

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

The Strategic Sourcing Manager is responsible for identifying opportunities and implementing sourcing strategies in order to optimize cost, quality, and efficiency. The ideal candidate will have at least 7 years’ experience as strategic sourcing manager on indirect categories. Postion is 100% Work From Home. MUST work the EST time zone. No exceptions. Qualifications and Skills: Degree qualified (BA Degree in Supply Chain, Business Managemen

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 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 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

We are currently seeking a detail-oriented and proactive Office Assistant to join a well-established jewelry manufacturer. As an integral member of the administrative team, you will play a key role in ensuring the smooth operation of our office and supporting various departments with administrative tasks. Ideal candidates will have excellent customer service skills, be open to supporting a small office and be proficient in MS office & Excel. Apply directly

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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treat

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

Randstad has partnered with a Law Firm in Boston to assist with filling their open Legal Assistant opportunity. The role will provide administrative support to the team with document filing and preparation, reception duties, updating confidential information, and maintaining calendars. If you have at least a year of administrative experience within a law firm then this could be a great opportunity for you! This is a temporary position estimated to last ap

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

Randstad, the world’s leading partner for talent, is investing in an Account Manager for our Randstad Digital specialty. As an Account Manager, you will be responsible for driving new business through direct client engagement, territory planning, and selling our services. We prioritize building lasting relationships with clients and candidates, aiming to deeply understand their needs for mutual success. What you get to do: Analyze market trends, lever

Randstad is working with a stable and well-established firm in Downtown Boston to fill a pivotal role supporting attorneys. This person will need to maintain a high level of tact, discretion, and professionalism, acting on behalf of attorneys and the firm. Candidates with legal/litigation experience preferred, but applicable professional services experience and competency will be considered. This is an onsite position requiring availability of working offi

job summary: Our client is a well-known private Ivy League research University and Education Leader and they are looking for a Makerspace Manager to join their growing team on a 3-4 month contract. The Makerspace Manager will be responsible for assisting faculty and the Makerspace Director in the design, development, and implementation of innovative making activities and workshops. You will also help create and define processes, procedures, safety guideli

Responsible for ensuring facilities have accurate and up-to-date licensing information on record with government agencies and internal databases. This includes preparing and filing notifications to regulatory agencies all while meeting high quality standards and internal and external deadlines. This person will support process improvements and creating and implementing Standards of Operations. In addition, they will be responsible to monitor and respond

Reporting to the Associate Director of Quality Control, Moderna is seeking a Quality Control Raw Materials Associate I based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned. This position will be 1 st shift working Monday through Friday.salary: $32 - $38 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorsRes

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 a premier academic healthcare system, committed to delivering exceptional care, advancing medical research, and educating the next generation of healthcare professionals. With world-renowned hospitals and a network of leading physicians, researchers, and staff, we are dedicated to improving the health and well-being of individuals and communities across Massachusetts and beyond.salary: $21 - $26 per hourshift: Firstwork hours: 8 AM - 5 PMe

We have an exciting new opportunity with our client in Quincy, MA who is looking for an experienced Building Maintenance/Operations worker! The ideal candidate would have experience with building maintence, daily operations, and maintaining code and compliance. The hours for this position are 7AM - 3PM Monday-Friday. Candidate must be flexible in willing to remain on call in case of an emergency. The salary range for this position is between $55k-63

job summary: Location:Durham North Carolina Skills: - SQL - Agile Delivery environments - Data analysis and presentation skills The Team The Health Care Technology Group (HCG) supports the recordkeeping and administration of Health Benefits (Medical, Dental and Vision plans) as well as the Health Savings and Reimbursement Account plans on behalf of Fidelity's corporate clients, their employees and retirees. The Technology associates on the HCG Platfo

Randstad has partnered up with a company who is seeking a visionary leader to spearhead their financial planning and analysis efforts as Director. Join our client's team at the forefront of innovation, where your strategic insights will drive informed decision-making and propel our company towards unparalleled growth and success. If you're ready to shape the future of finance, we invite you to lead with us and apply now!salary: $190,000 - $210,00

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

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: Produce pharmaceutical components and products by following current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) within a cleanroom environment. Responsibilities include, but not limited to operation and performance on equipment used in the manufacturing unit processes. Perform the weighing of manufacturing ingredients and the manufacturing of the intermediate formulations. Tasks include documentation, data entry

job summary: We are looking for a seasoned Construction Project Manager to join a great team. This is a direct hire opportunity located in the NYC area. This person will oversee the planning, permitting, design, and construction of residential and commercial projects across various scales. This role involves managing projects from inception to completion, ensuring compliance with zoning codes and ordinances, and representing the owner in community and reg

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

Hey! Are you interested in advancing your career with one of the oldest and largest Financial Institutions in the United States? Our client is a Fortune 500 Financial, Medicak and Healthcare Services Company and they are hiring a Data Analyst! Please review the above job description and let us know your interest!salary: $37.96 - $37.97 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorsResponsibilities Analytical rigor – capabi

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

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