- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- …aspects of upstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of upstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- IQVIA (Durham, NC)
- **Job Description** IQVIA Pharma Review provides outsourced medical copy review and approval services and advisory services to the pharmaceutical industry. As a ... be expected to be part of the relevant content review teams. In this role and as part of...client's strategy and expectations + Effectively collaborate with Commercial, Regulatory , and Legal business partners to provide strategic input… more
- Merck (Wilson, NC)
- …Manufacturing Operations, Drug Delivery Systems and Devices within our Manufacturing Division ( Associate Director). This role serves as a Virtual Plant Manager - ... for all dealings between our Company and the External Partner, the Associate Director External Manufacturing Operations is accountable for establishing a strong… more
- Catalent Pharma Solutions (Morrisville, NC)
- **Lab Associate , Product Development** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... Pharma Solutions is Morrisville, NC is hiring a Lab Associate for the Product Development Group. The Lab ...and data systems + Follow all safety, quality, and regulatory guidelines to ensure a compliant and efficient work… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The QA Associate Manager (Operations DSM Upstream) leads and supervises a team of QA professionals responsible for providing day-to-day ... adequate resources for shop floor QA activities (eg, BPR review , event triage), QA support activities (eg, DR/CAPA ...self and team to ensure compliance with cGMPs and regulatory requirements. + Provides training, coaching, and mentorship to… more
- Wolters Kluwer (Raleigh, NC)
- …to help save lives, improve the way we do business, build better judicial and regulatory systems. We help them get it right. **Who We Are: Wolters Kluwer: The world ... remote schedule, and amazing benefits. **What You'll be Doing:** As an Associate Director (Sales Channel/Affiliates), you will provide leadership and guidance to… more
- Lincoln Financial (Greensboro, NC)
- …this opportunity. **Requisition #:** 74869 **The Role at a Glance** As a Senior Associate Actuary in Life Valuation department of the Life Chief Actuary team, you ... strategies. *Maintain knowledge on current and emerging developments/trends including regulatory changes for life valuation, assess the impact, and...in a career at Lincoln, we encourage you to review our current openings and apply on our website.… more
- Otsuka America Pharmaceutical Inc. (Raleigh, NC)
- **Position Summary:** The Associate Director of Global Medical Affairs Omnichannel will be responsible for developing and leading the omnichannel strategy for Global ... + Ensure all omnichannel activities adhere to internal medical, legal, and regulatory standards. + Collaborate with Compliance and Legal to maintain robust … more
- Robert Half Legal (Greensboro, NC)
- …This role addresses matters related to contracts, intellectual property, regulatory compliance, risk management, and operational strategy while ensuring alignment ... laws and regulations (Source: SG25 US Legal.docx). + Draft, negotiate, and review critical contractual documents, such as vendor agreements, IT service contracts,… more
- Truist (Charlotte, NC)
- …America) **Please review the following job description:** The ALM Senior Associate will be responsible for consolidation and reporting of the firm's balance ... and analysis requests. + Subject matter expert on accounting and regulatory reporting requirements and reporting processes for assigned area of responsibility.… more