Program Manager, Regulatory Affairs - Canton, MA

Job summary: Join a company where you will have an opportunity to grow professionally and personally and give strength to others by Empowering Healing. We offer a strong benefits package opportunities for growth and the chance to contribute to our mission: · to provide an integr ...

This is a Regulatory Affairs & Compliance Lead role at Sensitech, where you will be the regulatory subject-matter expert for their comprehensive product portfolio. · Develop and implement regulatory strategies for new and modified products to enable entry into target markets. · ...

Sensitech Inc., a Carrier company under the Climate Solutions Transportation (CST) segment, is a global leader in supply chain visibility solutions. Sensitech helps ensure the quality and integrity of temperature-sensitive products across the pharmaceutical, food, and industrial ...

As the Regulatory Affairs & Compliance Lead at Sensitech, you will be the regulatory subject-matter expert for our comprehensive product portfolio. · The Regulatory Affairs & Compliance Lead collaborates cross-functionally with Product Development, Quality, Manufacturing, Marketi ...

We are seeking a Regulatory Affairs & Compliance Lead to join our team at Sensitech Inc., a global leader in supply chain visibility solutions. As the regulatory subject-matter expert for our comprehensive product portfolio, you will collaborate cross-functionally with Product De ...

As a Regulatory Affairs Specialist at Mass General Brigham, you will be responsible for ensuring compliance with regulatory requirements and maintaining an updated library of FDA regulations and guidance documents. · AUTHORS AND REVIEWS OF STANDARD OPERATING PROCEDURES,T techNICA ...

As a pivotal member of the Corbus Product Development Team(s) (PDT) supports Corbus' drug development by leading the preparation and/or oversight of regulatory submissions and inputting into the regulatory strategy as the US regulatory lead for Corbus' programs. · This role will ...

Competitive Power Ventures, Inc. ("CPV"), with headquarters in Silver Spring, MD, and an office in Braintree, MA is a leading clean energy company built around the belief that progressive companies can be powerful leaders in creating a better world. · CPV is looking for a Manager ...

As a pivotal member of the Corbus Product Development Team(s) (PDT) supports Corbus' drug development by leading the preparation and/or oversight of regulatory submissions and inputting into the regulatory strategy as the US regulatory lead for Corbus' programs. · This role will ...

· Company Description · Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collaber ...

The Regulatory Affairs Specialist is responsible for coordinating customer complaints within the organization's Quality Management System (QMS). This role ensures accurate recording and processing of complaints in compliance with internal procedures, ISO 13485, and applicable reg ...

The Regulatory Affairs Associate role at SharkNinja involves managing customer complaints within the organization's Quality Management System (QMS). This includes reviewing submissions for completeness, logging complaints accurately in the QMS, and ensuring timely progression thr ...

The Regulatory Affairs Specialist is responsible for coordinating customer complaints and ensuring compliance with internal procedures and regulatory requirements. · Monitor designated sources for new complaints. · Accurately log complaints in the QMS. · ...

· Company Description · Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collaber ...

We are looking for a talented and detail-oriented Regulatory Affairs Specialist with 2-3 years of experience in regulatory affairs, · specifically with expertise in regulatory codes, particularly USDA codes.Ensure compliance with regulatory standards and codes governing the food ...

This job involves preparing regulatory submissions while ensuring compliance with current regulations. The specialist will maintain meticulous regulatory documentation. · Proficiency in Regulatory Documentation. · Strong understanding of Regulatory Compliance. · ...

About Us · We are a fast‑growing biopharmaceutical organization advancing a pipeline of innovative therapies aimed at transforming patient lives. As our programs progress, we are expanding our Regulatory Affairs team with a strategic, detail‑oriented leader who thrives in dynamic ...

In this role you be part of a Regulatory Affairs Team to develop and deploy innovative and compliant regulatory strategies across business and markets to achieve the highest standards for patient safety and product efficacy. · ...

Werfen · Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment ...

· Company Description · Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, ...