Job Seekers

61-80 of 89 results
Sort By


Accountability Objective: Responsible for the completion of assigned US Regulatory Submission and Compliance activities the company and its designated suppliers; coordinate assigned US and OUS regulatory reporting, such as MDRs, Vigilance Reports, Clinical Progress Reports, and Post-Approval Reports; provide support for: US and OUS regulatory submissions of new and existing products marketed by the company; assure compliance with US and OUS international regulatory requirements for Class III....


NO RELOCATION ASSISTANCE Summary: Fast growing division of a global medical device leader is for a Regulatory Affairs lead for new product introduction and support existing products. Requirements:Bachelors degree3-8 years experience with 510(k), CE-Marking and other Regulatory market approval submissions for Class II and III medical devicesGlobal regulatory submission experience highly preferredExperience working new products from initial development through commercializationExperience....


DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....

- Los Angeles, CA

Grow your career while working and being trained in the exciting field of Oncology Clinical Research. This opportunity is for a large growing clinical trial site in W. Los Angeles. Requirements:*Experienced Oncology Nurse (RN required, OCN is a plus) *CA License*Must be able to follow the protocol and see that it is followed*Good communication skills and work well with patients and doctors *Full-time Mon-Fri *Must be commutable to W. Los Angeles Responsibilities may include: - Screening....


Top Tier Progressive Bio Pharmaceutical company with offices in Seattle and San Francisco is expanding They are looking to hire a Director of Regulatory Advertising and Promo Description Company rates #1 in Northwest! They are a clinical-stage company developing novel cellular immunotherapies based on two distinct and complementary platforms – Chimeric Antigen Receptors (CARs) and T Cell Receptors (TCRs) technologies. Our goal is to revolutionize medicine by re-engaging the body’s immune....


Unique Opportunity!This position intersects Coatings / Formulations / Process Engineering / New Application Development / Manufacturing.Looking for a SME Principal Engineer in Oral Solid Dose, preferably an Organic Chemist that has moved from the bench to a coatings manufacturing environment but still involved in formulations, troubleshooting. Company offers cutting edge technology, a leadership role, an opportunity to interface with executive management and provide manufacturing solutions to....


Vice President, Regulatory Affairs San Francisco Bay Area Our client is seeking a Vice President, Regulatory Affairs who will be responsible for regulatory strategy, oversight, and guidance drug development program. The successful candidate will bring strong leadership abilities to oversee the Regulatory Affairs team, a successful history of effectively leading IND and NDA filings through approval, and interacting effectively with the FDA and other foreign regulatory bodies. This position....

- San Francisco, CA

Our client in the San Francisco Bay area, has a new opportunity for Medical Director with expertise in Oncology NGS. This is a full-time, onsite position, with the opportunity to make an impact, company is seeking a driver to lead change. Medical Director, Oncology NGS San Francisco Bay AreaServes as company’s internal and external oncology / medical expert collaborating with several departments / business units including marketing, market access, salesRespond to questions from physicians and....


Minimum Requirements: B.S. or M.S. degree in Organic Chemistry10+ years of experience with lubricant additives used in greases and machining oils.Must have experience developing, formulating and testing lubricant additives and specialty lubricants.Plus would be supervision experience.Job Description: Our client is a family oriented, specialty chemical producer with multiple product lines. This person will be working with the lube oil additives division. These lube oils are used for....

- Any US State

Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....


Traditional SHE leader's role dealing with a Chemical manufacturing facility. MUST HAVE PSM BACKGROUND AND EXPERIENCE. Will not even look at anyone without it. Lead the plant’s safety, health, environmental and security programs, as well as the operation of the Utilities function. Take the lead on all compliance with all safety and environmental regulations and policies. Lead effort in compliance with environmental regulations, permits and reporting requirements. Responsible for the operation....

- Any US State

Wanted: An Equine Nutritionist passionate about helping horse owners feed their animals well who can work with proprietary cutting-edge nutrition technology to create consistent quality products and has commercial experience working for a feed company or feed supplier. This person will help lead the direction for future equine products through research and development while supporting sales reps and feed dealers. This position can be home-based for candidates living east of the Mississippi who


Lead the development and execution of all engineering and construction projects associated with midstream natural gas production, compression, and transmission for energy clients throughout the Marcellus and Utica Shale plays. As the principal Mechanical Lead and Subject Matter Expert (SME) for all midstream and upstream operations, you will support new business development in securing EPC work with a variety energy companies throughout the western PA, eastern OH, and WV. The Mechanical Lead....


Lead the development and execution of all engineering and construction projects associated with midstream natural gas production, compression, and transmission for energy clients throughout the Marcellus and Utica Shale plays. As the principal Mechanical Lead and Subject Matter Expert (SME) for all midstream and upstream operations, you will support new business development in securing EPC work with a variety energy companies throughout the western PA, eastern OH, and WV. The Mechanical Lead....

- Boston, MA

Highly successful technology company seeks a skilled Applied Scientist to join their specialized Search engineering team. This team helps build and power the engine that responds to tens of billions of queries per day, searching through terabytes of data in milliseconds. This team designs, builds, and deploys high performance, fault-tolerant distributed search systems used by millions of people every day.The search team is also responsible for building a platform that will enhance the customer

- Boston, MA

NO VISA's Our client is a rapidly growing company that is on a mission to reinvent the way scientific research is done. They are a SaaS company that bridges software, hardware, and innovation. You will be responsible for architecting, managing and scaling the entire IOT platform that is built on Rancher/Docker and AWS. The RoleTake ownership for health, scalability and availability of our cloud services and IOT platform.Automate the deployment pipeline between our pre-production to production....


Quality Supervisor - Food or Beverage Product Manufacturing - Day Shift - $65-75,000 plus 10% bonus target We are seeking a Quality Supervisor for a multi-site food product manufacturer. Opportunities for future career advancement abound with this prominent national manufacturer. This is a 50 person plant, 24x7 operation, day shift role. Supervises one lab tech currently. Relocation Assistance is provided! Big company Benefits! General Purpose of the Quality Supervisor position Ensure all....


Reporting to the Executive Director of Early Development this physician will serve inside the medical sciences group as a leader in Hematology/Oncology early development. This Oncologist will lead early phase clinical development of oncology compounds from first-in-man studies through proof of concept. They will define, design, and execute early phase clinical and translational projects as the initial strategy for drug development. This physician should be trained in Oncology and have....

- Anywhere in, SD

Established animal nutrition group is having exceptional success in the Dakotas and is looking to add a Swine Consultant to their team. Client base is in SD, ND and MN. This person will enjoy a significant consulting role with swine producers by helping producers improve in the areas of nutrition, animal health, environmental and genetics. Expertise in some of these areas is required. Candidates can live anywhere in South Dakota and office from their home. One key focus of this role is new....


Senior Regulatory Affairs Specialist (Medical Device) Newark, DE (Relocation Assistance Provided) Competitive Base Salary, Bonus 10%, 6 401K Match, Full Benefits, 4 weeks PTO We have a newly created opening for a Senior Regulatory Affairs Specialist position with a longstanding client; multi-billion global medical instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized, complex medical products that....

61-80 of 89 results
Unless noted above, applicants MUST be authorized to work in the US without Visa Sponsorship. US citizens and Green Card holders ONLY. We do not provide relocation assistance for those living outside the continental US. Please only click apply if you meet the specific requirements of the job listing, you are able to work in the location listed, and are comfortable with the salary range indicated above. Thanks for your interest. We look forward to working with you.