- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Method Development & Testing is responsible for leading a Center of Excellence (CoE) focused on developing and validating ... GMP testing nodes in support of clinical and PPQ supplies. Additionally, the Associate Director leads, manages, and develops a team responsible for providing routine… more
- Merck & Co. (Rahway, NJ)
- …drug products.Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and ... packaging, compatibility characterization for processing and administration, and supporting regulatory filings.Build deep fundamental knowledge around the drug product… more
- Merck & Co. (Rahway, NJ)
- …are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise in Liquid ... validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials.… more
- Novo Nordisk Inc. (Durham, NC)
- …including 14 paid holidays Health Insurance, Dental Insurance, Vision Insurance - effective day one Guaranteed 8 % 401K contribution plus individual company match ... processes for our operations areas to meet business and regulatory requirements in bulk processing. Additional responsibilities includes but...on process improvement. This position will also train on days working Monday - Thursday, 6:00 am - 430pm… more
- Merck & Co. (South San Francisco, CA)
- …approaches in drug safetyStay abreast with new AI approaches and regulatory landscape in the field of predictive toxicologyQualifications:Education:Ph.D. (with 4+ ... years) or Master's (with 8 + years) in computer science, computational biology, cheminformatics or...be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the… more
- CHRISTUS Health (Tenneryville, TX)
- …or Certifications BLS required. RN License in state of employment or compact. Work Schedule: 5 Days - 8 Hours Work Type: Full Time EEO is the law - click ... feedback and assistance concerning customer satisfaction, staff development, and associate performance and satisfaction. The Supervisor is responsible for the… more
- LSI Solutions (Victor, NY)
- …state-of-the-art devices. After all, our ultimate customer is the patient. POSITION TITLE: Regulatory Associate I, II SALARY RANGE: $85,000 - $104,000 POSITION ... HOURS: 8 :00AM - 5:00PM POSITION LOCATION: Onsite at LSI Solutions...Victor, NY POSITION AT-A-GLANCE: Primary responsibilities of the clinically-focused Regulatory Associate will be collecting and collating… more
- LSI Solutions (Victor, NY)
- …with state-of-the-art devices. After all, our customer is ultimately the patient. JOB TITLE: Regulatory Specialist (Labeling) - Days 8 :00AM to 5:00PM SALARY ... III, and Senior: Base Level from the prerequisite role ( Regulatory Associate ) Essential Functions: + Understand and...Specialist: + Bachelor or Master's degree in a technical, regulatory , or life sciences discipline with 8 +… more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Director, Associate General Counsel, Global Regulatory Compliance Date: Oct 17, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: ... the world take one of our medicines every single day . An amazing number, but we're always looking for...make a difference with. **The opportunity** The Sr. Director, Associate General Counsel, Global Regulatory Compliance role… more
- Randstad US (Newbury Park, CA)
- regulatory affairs senior associate . + newbury...of experience OR High school diploma / GED and 8 years of experience skills: GCP (Good Clinical Practice), ... work hours: 9 to 5 education: High School responsibilities: + Maintain Regulatory document management and tracking systems + Support Activities for Clinical Trial… more
