- Merck & Co. (Rahway, NJ)
- …sustained launch in alignment with the company's business goals, and quality and regulatory compliance .-Essential Duties and Responsibilities:Program Leadership ... Job DescriptionJob Summary: -The Director of Device Technology Transfer is a key...team members, fostering a collaborative and innovative team environment.Regulatory Compliance and Quality Assurance:Ensure that all activities… more
- Merck & Co. (Rahway, NJ)
- … mindset.Essential Knowledge, Duties & Responsibilities for the Director Include:Biopharmaceutics expertise supporting delivery of small molecule, peptides ... Job DescriptionOur company is a global health care leader with a diversified portfolio...and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop… more
- Merck & Co. (Rahway, NJ)
- …accelerate process and product development and manufacturing and ensure safety and quality of our products. The successful candidate will be accountable for ... cross-functional development teams to enable pipeline decisions. -The Executive Director , Biologics Analytical Research and Development (B-AR&D) is responsible for… more
- Merck & Co. (Rahway, NJ)
- …drive revenue and productivity, thereby advancing our company's contribution to global medical innovation.Enterprise IT (EIT) is an essential component of the ... EIT SAP Platform Team is responsible for our company's SAP Global Template asset, delivering enterprise-level capabilities through harmonized business processes and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description:Powerhouse Chief EngineerUnder the direction of the Associate Director of Engineering, The Chief Engineer is responsible for the ... staff of 24-hourly employees and is accountable for production, quality , environmental and safety considerations of the Power Plant.Responsible for:Directing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description Senior Consolidation Accountant: The Global Controller's organization at our Company ensures the financial integrity of the ... This integrity is reflected in the soundness of our balance sheet, the quality of the financial information provided to investors and regulatory bodies, and the… more
- Merck & Co. (Rahway, NJ)
- …project management responsibility. The Specialist -Engineering position will report to the Associate Director , Engineering and will be a member of the EF Team at the ... and innovation. They will work closely with the development engineers & chemists, compliance representatives, safety partners and other team members to ensure the … more
- Merck & Co. (Rahway, NJ)
- …needs for Finance by leveraging data analytics and understanding implications on global healthcare systems. Audit assignments are unique to each individual's skill ... payors, and regulatory and reputational risks while working intimately with our global business operations.-In addition, individuals will use data analytics to gain… more
- Merck & Co. (Rahway, NJ)
- …team at the FLEx Center in Rahway is looking for an Associate Director - Process Engineer to lead clinical supply manufacturing, scientific rigor of processes, ... will:Lead and strategically plan on-the-floor batch manufacturing to ensure safety and quality of clinical supplies to augment and accelerate our products.Author and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …labeling milestones. Collaborates with Global Labeling Operations and Compliance Leads to produce high quality labeling documentation.Establishes Processes ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...development or approval for either the US or EU.Ensure Compliance with Core Data Sheets/Label Changes: Manages updates to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …timely remediation.SOP Authorship and Review Maintain a close working relationship with Quality Assurance and participate in the Company Global SOP Committee. ... Director , Development SOP Management Join a Legacy of...Quality Management systems preferredExperience with requirements related to global health authority inspections, participation in inspection activities and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …deliver on GLP/GCLP commitments that are pivotal to early phase submissions.Collaborate with Global QMS to build a phase appropriate quality system that supports ... with expertise in: oncology, biologics or vaccines.Must have proven expertise within Quality Assurance Research to support Global Research QA including… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of labeling milestones. Collaborate with Global Labeling Operations and Compliance leads to product high quality labeling documentation.Establishes Process ... mentors and may manage assigned staff, partnering with the Global Labeling Operations & Compliance group and...milestones. Collaborates with Global Labeling Operations and Compliance Leads to produce high quality labeling… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... research areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to project teams, and supports change implementation. Coordinates with regional/ global RACMC, Quality Assurance, Pharmaceutical Technology, and other ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …execution, closely with the Business and other cross functional teams (eg Legal, Compliance , IT, etc.) for both US and Global engagements. Partners closely ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... related to study, project and submission. Manage CRO to ensure high quality compound and multi-compound level deliverables. Lead the development of global… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director of Quality Project Management and Strategyas part of the ... Quality team based in Raritan, NJ. Role OverviewThe Associate Director of Quality Project Management and Strategy role is an exempt level position with… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... of Daiichi Sankyo (DS) in the US, EU, Japan, and other global sites. These business functions include: Clinical Operations, Clinical Development, Biostatistics and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... clinical matters; Represents Clinical Development in Project Teams, possibly as Global Clinical Lead. ResponsibilitiesStudy Strategy: Clinical study leader (CSL) or… more
