- Merck & Co. (Rahway, NJ)
- Job DescriptionOur company's Device Product & Process Development (DPPD) Team designs, develops, and commercializes novel biologic/drug/vaccine - device enabled ... their intended site of action.- The DPPD Team manages the development of the device constituent of our company's pipeline of combination products across a variety of… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management efforts ... development, commercialization, and lifecycle management. This individual will oversee device risk management activities to ensure the delivery of high-quality… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionReporting to the Director of Medical Device and Combination Product Quality Assurance, the Associate Director Quality Engineering & Quality Assurance ... is responsible for independent compliance support of Medical Devices including the device constituent part of Combination Products. This position will interact with… more
- AT&T (Reynoldsburg, OH)
- …AT&T internet (and fiber where available) and AT&T phoneA company paid device and service plan, giving you first-hand expertise with our latest technology.Weekly ... Hours:40Time Type:RegularLocation:Reynoldsburg, OhioIt is the policy of AT&T to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed,… more
- Merck & Co. (Rahway, NJ)
- …(PSCS) deliverable which is the development of robust compositions, processes and device / packaging that enable patient centric products for patients. The successful ... concepts, tools, and requirements for all dosage forms (liquid, lyo, drug- device combinations)Review and approval of data and technical documentsAbility to recruit,… more
- Aequor (NV)
- …following platforms Chromatography, Bioassay, PCR, Microbiology, Immunoassay, CE, Gel, Device , Viral, and General (compendia). Biopharmaceutical leader founded on ... with the following method platforms is highly preferred: Chromatography, Bioassay, Device , PCR, Microbiology, Immunoassay, CE/Gel, Viral, and General. Protocol and… more
- HireLifeScience (Piscataway, NJ)
- …for finding Life Science jobs in the Pharmaceutical, Biotechnology and Medical Device industries. Our parent company, Aequor Technologies, LLC. is a Global ... national clients in the life science industries, pharma, biotech and medical device -Identify, qualify, call on and establish long-term business relationships with… more
- Merck & Co. (Rahway, NJ)
- …and support for Clinical Supply Chain Strategy, Quality Planning, Medical Device /Combination Products and New Technologies, Global SAP Process Stewardship for our ... Supplies, Global Quality, Global Regulatory Affairs, Global Clinical Trial Operations, Device Development and our Research & Development Division's IT team as… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …and experience with the following is preferred: Instrumentation & Control Device operation and troubleshooting Programmable Logic Controllers Supervisory Control & ... EMEA Regulatory requirements Experience at a medium to large scale medical device , pharmaceutical or biotechnology process firm in an automation role AutoCAD… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …regulatory requirements. This position has experience working within the medical device and/or pharmaceutical industry across complex disease areas, and experience ... of clinical data management medical coding experience in a medical device , pharmaceutical company, or similar environment (eg, CRO) requiredOncology, immunology, or… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …administration preferred Knowledge, Skills, and Abilities: Instrumentation & Control Device operation and troubleshooting PPCL Programing experience is preferred ... 10 plus years of experience at a medium to large scale medical device , Pharmaceutical or biotechnology process firm in an automation role is desired Demonstrated… more
- Lundbeck (Little Rock, AR)
- …college or university 2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must demonstrate the ... intellectual capacity to score highly on disease and product training exams, including being certified on product knowledge annually Self-starter, with a strong work ethic and outstanding communication skills Must be computer literate with proficiency in… more
- Aequor (Framingham, MA)
- …packaging, labeling, and assembly of Seprafilm Adhesion Barrier, a Class III Medical Device . Signs and dates batch records for activities performed and verifies the ... work of other production staff members. Work is assigned and reviewed by the Production Manager and/or more Senior Team Leaders. Instructions will be in the form of written batch records and must be able to understand and comprehend verbal instructions from… more
- Merck & Co. (Rahway, NJ)
- …Experience and Skills: Experience in the pharmaceutical, biotechnology, chemical, medical device , or closely related industry.- Experience in one or more functional ... areas such as quality assurance, laboratory, manufacturing, production, equipment/facilities management, regulatory. Good Manufacturing Practice (GMP) or related small molecule API regulation knowledge and expertise. Strong leadership, collaboration, teamwork,… more
- Novo Nordisk Inc. (Durham, NC)
- …cGMP related experience required, preferably in the pharmaceutical or medical device industry General knowledge of Batch Review Processes (BRP), validation processes ... and Quality Management Systems (QMS) preferred General knowledge of quality oversight & on floor production support preferred Good written & verbal communication skills required Basic computer skills in MS Office, PowerPoint, Word, Excel, etc. required… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization ... (CRO). CRA experience preferred- Time spent directly in a medical environment (eg as a Study Site Coordinator) is also considered relevant preferred Travel Ability to travel up to 5% In-house office position that may require occasional travel.Daiichi Sankyo,… more
- Aequor (Thousand Oaks, CA)
- …a local number Phone conference ID: 329 280 597# Join on a video conferencing device Tenant key: Video ID: 113 337 657 0 More info For organizers: Meeting options ... | Reset dial-in PIN In this vital role you will partner closely with managers, Employment Law, and other internal key stakeholders to align with the Values, Leadership Attributes and Policies. Staff Relations is responsible for a wide range of employee… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and promotion, anti-kickback, antitrust, privacy, pharmaceutical or medical device product liability) preferred though not required Strong problem-solving ... skills - demonstrates and exercises creativity and initiative Strong written and verbal communications skills - able to effectively collaborate and communicate with other client groups within the company We commit to an inclusive recruitment process and… more
- Merck & Co. (Rahway, NJ)
- …to commercialization. Our development teams ensure robust composition, primary packaging/ device , and process selection through deep fundamental understanding and ... characterization such that the process is scalable without compromising stability, safety, efficacy, and delivery. During development, we leverage smart experimental design, cutting edge analytical tools, and predictive approaches to inform molecule,… more
- Merck & Co. (Rahway, NJ)
- …development programs.-Additional experience in drug substance manufacturing and medical device and/or combination products would be preferred.- Key Responsibilities: ... Activities that this position would be responsible for include:Leading overall quality relationships with contract manufacturing organizations,Negotiation of site and global Technical and Quality Agreements,Participating in contractor GMP audits as a Subject… more
