- Merck & Co. (Durham, NC)
- …in Durham, NC. This state-of-the-art facility established in 2004, manufactures our Company lifesaving vaccines in bulk and finished forms.- Due to the importance ... of this facility in our Company Vaccine Manufacturing network, the facility has seen rapid...related to the vaccine process Lead technical studies and author documentation associated with site commercialization efforts Participate in… more
- Merck & Co. (Rahway, NJ)
- …equipment integrated processes such as ultrasonic welding and vision inspection systems. Author technical content of assembly process FMEAs to capture patient and ... (FAT) and report project progress, risks, and mitigations to the team. Author protocols, reports, create drawings and specifications to ensure proper documentation… more
- Merck & Co. (San Francisco, CA)
- …art tools. With MIDD as an essential component of decision-making at our Company , this position offers an opportunity for the Associate Director to drive pipeline ... and/or lead QP2 efforts on drug/vaccine development programs, and author or co- author strategic documents. - Associate...Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can… more
- Insmed Incorporated (San Diego, CA)
- Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most ... into innovative solutions for patients. That's why we've been named the No. 1 company to work for in the biopharma industry in Science's Top Employers survey for… more
- Merck & Co. (Rahway, NJ)
- …of clinical research activities involving new or marketed Oncology medicines. Our company Oncology medicines span all phases of clinical development (pre-clinical to ... who will be willing and able to assist in the evaluation of our company drugsAttending appropriate scientific meetings to maintain his or her competency and to… more
- Merck & Co. (Rahway, NJ)
- …center, primarily for sterile operations under the remit of Our Company 's Research Labs Pharmaceutical Sciences (Pharm Sci), Pharmaceutical Operations Engineering ... and are suitable for both GMP and developmental use.- Author , review and approve GMP procedures and documentation, with...Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can… more
- Merck & Co. (Rahway, NJ)
- …(AR&D) External Capabilities, Validation, and Compliance (ECVC) department of our company 's Research Laboratories Division is seeking applicants for a Metrology and ... quality audits and maintain laboratory state of permanent inspection readiness Author or contribute to Standard Operating Procedures (SOP) draftingOriginate and own… more
- Merck & Co. (Rahway, NJ)
- …make a significant impact in the world of biopharmaceuticals purification? At-Our Company , we are at the forefront of innovation in the-Manufacturing Division, ... on cross-functional teams to foster collaboration and innovation.Document Excellence: Author regulatory and technical documentation, ensuring all processes align… more
- Merck & Co. (Rahway, NJ)
- …on opportunities to improve building flexibility, efficiency, compliance, and safety. Author lessons learnt and summary reports to capture knowledge gained.Mentor ... Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can...EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented,… more
- Merck & Co. (Rahway, NJ)
- …on opportunities to improve building flexibility, efficiency, compliance, and safety. - Author lessons learnt and summary reports to capture knowledge gained. - ... Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can...EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented,… more
- Twist BioScience (South San Francisco, CA)
- …reflects regulatory requirements and product specifications.What You'll Be Doing Initiate, author , and maintain Safety Data Sheets (SDS) for all Twist products, ... Operations within a biotechnology, life sciences, or chemical manufacturing company or another Regulated Industry. Expertise in developing technical documentation,… more
- Formation Bio (New York, NY)
- About Formation BioFormation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug ... ultimately helping to bring new medicines to patients. The company is backed by investors across pharma and tech,...comply with global regulatory expectations (eg, FDA, EMA, ICH); author and review regulatory submissions including INDs, BLAs, and… more
- Acadia Pharmaceuticals Inc. (Princeton, NJ)
- …in development and on market. This will include management of internal global Company Core Data Sheet (CCDS) process, labeling SOP, initial draft label development, ... process, and managing post-approval labeling updates. Primary Responsibilities Guide, develop and author draft labeling text (eg USPI, PPI, Med Guide, EU SmPC,… more
- Arcosa Lightweight (Memphis, TN)
- …subsidiary, is searching for a Sales Operations Manager to support the company 's strategy of enhancing the continued growth and development of sales operations. ... support of the sales team. We are a proud subsidiary of the infrastructure company , Arcosa, Inc. We commit to and pride ourselves on providing reliable structures,… more
- Bertelsmann (New York, NY)
- …maximization of sales and for accurate forecasting. Attending regional trade shows, author signings/pre-pub events and other industry and account related events in ... eligible for annual profit award or bonus, subject to Company results. Please apply by July 14th using our...sexual orientation, gender identity, disability, or protected veteran status. Company : Penguin Random House LLC Country: United States of… more
- Northrop Grumman (Linthicum Heights, MD)
- …key decisions regarding Equipment Automation deployment and configuration Define requirements, author code, test and deploy custom solutions to factory automation ... network configurations on network devices (Modbus/TCP, AMQP, MQTT, etc.) Author technical documentation that outlines equipment integration and factory automation… more
- Bristol-Myers Squibb Company (Devens, MA)
- …review boards, regulatory inspections (internal and external audits). Own and author responses to regulatory requests. Review and approve laboratory investigations. ... and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically… more
- Shake Shack (Chesterfield, MO)
- …Spending Accounts* Supplemental Life Insurance and Short-Term Disability* 401(k) plan with Company Match* Paid Time Off/ Sick Time* Employer Assistance Program (EAP) ... created by Danny Meyer, Founder and CEO of Union Square Hospitality Group and best-selling author of Setting the Table. Shack Fans lined up daily, making the cart a… more
- Michael Page (Quincy, MA)
- …of contracts (fee payment, rental equipment, income/expenses, etc.) to protect company 's interest and simultaneously maintain good relationship with client and ... progress, problems and scheduling. Assist in preparation of bid day information. Author and issue meeting minutes promptly. Schedule and assist in progress meetings… more
- Universal Engineering Sciences (Cincinnati, OH)
- …with UES's goals. Responsibilities Travel to various job sites in a company provided vehicle Mentor and grow Environmental team members' environmental testing and ... and other necessary field work Perform tests, sampling of environmental materials, and author reports including, but not limited to Wetlands Delineation, Phase I and… more
