- Merck & Co. (Rahway, NJ)
- …analysis and corrective action processes.Stay updated on emerging regulations and industry trends affecting device quality and regulatory affairs.Strategic ... Job DescriptionThe Executive Director, Device Quality & Regulatory will play a pivotal leadership...a pivotal leadership role within the organization, overseeing the quality assurance and regulatory CMC for complex medical devices,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …preferred Experience Qualifications4+ years of professional experience within the pharmaceutical industry working within Quality Assurance is required.Must have ... R&D PV QA organizational strategy. This position will proactively collaborate with other Global quality colleagues to drive the global QA vision and act as the US QA… more
- Eisai, Inc (Los Angeles, CA)
- …an account (not limited to CEO, CFO, CMO, Case Management, Dir. of Quality , Industry Relations, Technology Dir, etc.).Evaluate unique needs of the assigned ... local and national, health care issues/strategies, customer issues/trends, pathway and quality trends and best practices to establish credibility beyond product and… more
- Aequor (Swiftwater, MN)
- …Affairs/ Quality Assurance or an appropriate combination of other relevant industry experience eg, Quality and/or Manufacturing Requires knowledge and ... but not essential Knowledge of global regulations/guidelines, key Health Authority/ Industry Guidance and trends are helpfulQualifications Education / Experience… more
- Merck & Co. (Rahway, NJ)
- …facilities to ensure that functional testing methods meet regulatory requirements, industry standards, and internal Quality Management System (QMS) ... within the pharmaceutical, medical device, or combination product (preferred) industry .Demonstrated leadership experience in leading and managing teams, preferably… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …and Adobe Acrobat.Education RequirementsBachelor's Degree and three (3) to five (5) years in the Pharmaceutical Industry , preferably in a Quality Systems Role. ... master documentation. This position will additionally serve as a final Quality Reviewer/Approver for internal documentation. The Documentation Control Supervisor is… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of digital spaces, Marketing and Regulatory/Legal aspects to drive compliance with legal, quality and industry standards for customer engagement and data use. ... cross-functional relationships; checking to ensure compliance to Legal, Regulatory and industry standards; reviewing and analyzing experience data and KPIs (key… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …best practices, Marketing and Regulatory/Legal aspects to ensure compliance with legal, quality and industry standards for customer engagement and data use. ... strong cross-functional relationships; ensuring compliance to Legal, Regulatory and industry standards; establishing KPIs (key performance indicators) to measure and… more
- Aequor (Thousand Oaks, CA)
- …working knowledge of Microsoft Word 3&plus years' experience preferably in R&D/pharmaceutical industry , with knowledge of quality and compliance. Other duties as ... of regulated or process documents with the ability to deliver high quality documentation including technical writing. The primary responsibilities may include, but… more
- Merck & Co. (Durham, NC)
- Job DescriptionResponsibilities: Responsible for the quality aspects of good manufacturing practices (GMP) computerized systems and the supporting infrastructure ... company policies, procedures, and regulatory expectations. Be involved in all quality -related activities for computerized systems which are required by the company… more
- Aequor (West Greenwich, RI)
- …8-5 PM What is the working environment for this role? Role supports quality management systems, office based, EW will be supporting recall regulatory reporting 50% ... who is comfortable working remotely and able to work independently, understanding quality management systems (QMS systems), looking for a candidate who has… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Position Summary:The Quality Execution Counsel is a managing member of the Quality Department to oversee and manage the prompt and effective execution of ... quality activities. This position supports the Quality ...continuous improvement are the key objectives. This challenging, career-altering unique-in-the- industry position offers a non-traditional legal career path that… more
- Tris Pharma (Monmouth Junction, NJ)
- …Junction, New Jersey, Tris has an immediate opening for a Manager, Quality Management Systems (QMS). Summary:The Manager, Quality Management Systems (QMS) ... supports, oversees and manages the Quality Assurance (QA) Investigations and Product Quality ...and/or cGMP compliance experience in the pharmaceutical or biotechnology industry in positions of increasing technical responsibility (minimum 3… more
- Aequor (Houston, TX)
- …will be responsible for maintaining the integrity and efficiency of our Quality Management System, ensuring compliance with industry standards, and facilitating ... Job title - Quality Assurance Analyst I Location - Houston, TX...degree or experience in medical devices or a regulated industry . Qualifications:- Bachelor's degree in a related field or… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Quality Execution CoordinatorPosition Summary:The Quality Execution Coordinator is an integral member of the Quality Department who oversees and manages the ... prompt and effective execution of quality activities. This position supports the Quality ...continuous improvement are the key objectives. This challenging and unique-in-the- industry position builds on an experienced paralegal or legal… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Performs walk-through audits of NNUSBPI Manufacturing facilities Releases product based on Quality Assurance record review and approval by Manager, Quality ... certify compliance with specifications and procedures Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, walk… more
- Aequor (Thousand Oaks, CA)
- …; quality assurance or manufacturing experience in the pharmaceutical industry Must have experience with GMP processes and documentation. Without that ... the duration of the contract. 5 years of QA experience in the biotech industry , with a focus on GMP compliance Hands-on experience in manufacturing, packaging, and… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything ... records. Will be a QA presence on the manufacturing floor. Relationships Quality Assurance. Essential Functions Reviews all manufacturing and support records to… more
- Aequor (Thousand Oaks, CA)
- Fully remoteResponsibilities: Coordinate Global Incoming Quality Process Operations to support Global Process Owner lead. Interface with IQA Network, various sites ... Complete and approve multisite procedures, deviation, change control and other quality records to support RM Network. Candidate must have strong leadership… more
- Aequor (Chattanooga, TN)
- …degree supplemented with relevant experience. Experience in pharmaceutical/biopharmaceutical industry . Experience with relevant quality standards, including ... commissioning, qualification and validation. Well-develop. Well-developed communication skills, both verbal and written. Based on level, should have demonstrated experience managing teams consisting of internal staff, supervising engineering and construction… more
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