- Novo Nordisk Inc. (Boulder, CO)
- …are driving change. Are you ready to make a difference? The Position The Specialist , API Manufacturing works in Novo Nordisk's Boulder, Colorado Pilot Plant and ... the supply of API and meeting production goals, the Specialist , API Manufacturing actively supports continuous improvement...root cause investigation analysis Support the technology transfer of manufacturing processes into Phase I/ II cGMP … more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- The QA Specialist II - Engineering/Validation is responsible for cGMP compliance ensuring all FDA regulations, internal procedures/specifications, and other ... Requirements Must possess strong knowledge of sterile drug product manufacturing .Must be detail-oriented with exceptional planning and organizational skills.Must be… more
- Novo Nordisk Inc. (Durham, NC)
- …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... shop floor. Relationships Manager, Quality Assurance. Essential Functions Ensures site compliance with Regulations, ISO standards, corporate & local SOPs Reviews &… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This ... Reviews and assesses deviations; includes tracking, follow-up and reporting/trending Reviews manufacturing and support records to certify compliance with… more
- Novo Nordisk Inc. (Durham, NC)
- …of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable ... of all deliverables. Relationships Manager. Essential Functions Ensure accuracy & compliance of validation & equipment records Responsible for validation of QC… more
- Catalent Pharma Solutions (Greenville, NC)
- The ** Manufacturing Equipment Specialist /Mechanic II ** assists commercial operations staff in the maintenance and operation of manufacturing equipment. ... a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer,...and Catalent employee. **The role:** + Equivalent experience as Manufacturing Equipment Specialist I + Demonstrates the… more
- Mallinckrodt Pharmaceuticals (Hobart, NY)
- Job Title Operations Compliance Specialist II - Second Shift Requisition JR000012567 Operations Compliance Specialist II - Second Shift (Open) ... followed and evaluates the organization's products, materials, and facilities for compliance . Determines if current methods and techniques result in meeting… more
- Takeda Pharmaceuticals (Lexington, MA)
- …is true to the best of my knowledge. **Job Description** **Job Title** : Quality Compliance Specialist II **Location** : Lexington, MA **About the role:** ... risk-based audit execution, issue escalation, procurement strategy and regulatory compliance . This is a hybrid position that reports to...a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the… more
- BAE Systems (Greenlawn, NY)
- …at a BAE Systems facility 100% of the time. The role of the Ops Specialist II is to help oversee and manage the programs/projects within Operations ... whole and the balance of the company. The Ops Specialist II aids in preparing project execution...Management. + Utilizing departmental standards, generate Operational plans (ie Manufacturing , Sales) and schedules and utilize them to provide… more
- Gilead Sciences, Inc. (Foster City, CA)
- …the Global Quality Systems and Compliance organization, the Quality Systems Specialist II - Document Management will be responsible for partnering with ... impact. Join Gilead and help create possible, together. **Job Description** **Quality Systems Specialist II - Document Management** Gilead Sciences, Inc. is a… more
- Catalent Pharma Solutions (Greendale, IN)
- **Quality Assurance Specialist II ** **Position Summary** Welcome to Greendale, Indiana! Greendale is one of two gummy technology development and manufacturing ... complex ingredients to help create engaging new products consumers will love. The Quality Specialist II is responsible for auditing the products and processes at… more
- WuXi AppTec (Philadelphia, PA)
- …vision insurance + and much more The **Technical Operations Specialist II ** is responsible for generating and/or review manufacturing related technical ... of scientific and process data per good document practices + Follows compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs)… more
- Gilead Sciences, Inc. (Foster City, CA)
- …to the Global Quality Systems and Compliance organization, the Quality Systems Specialist II - GxP Training will be responsible for partnering with Business ... impact. Join Gilead and help create possible, together. **Job Description** **Quality Systems Specialist II ** **- GxP Training** Gilead Sciences, Inc. is a… more
- J&J Family of Companies (Athens, GA)
- Quality Specialist II - 2406184055W **Description** Janssen Pharmaceuticals, Inc a member of Johnson & Johnson's Family of Companies, is recruiting for a Quality ... Specialist II to be located at Athens,...for humanity. Learn more at https://www.jnj.com/. This role ensures compliance with regulatory requirements and internal company procedures. Ensures… more
- Jacobs (Boise, ID)
- …regulatory requirements, both in the US and internationally. Jacobs is seeking a Pretreatment Specialist II to join our team. As a Pretreatment Specialist ... representation concerning IPP permits and staff or to achieve regulatory compliance with pretreatment permits. Additionally, a Pretreatment Specialist develops… more
- Novo Nordisk (Boulder, CO)
- …are driving change. Are you ready to make a difference? The Position The Specialist , API Manufacturing works in Novo Nordisk's Boulder, Colorado Pilot Plant and ... the supply of API and meeting production goals, the Specialist , API Manufacturing actively supports continuous improvement...cause investigation analysis + Support the technology transfer of manufacturing processes into Phase I/ II cGMP … more
- The University of Texas at Arlington (Arlington, TX)
- **Software Systems Specialist II ** **Bookmark this Posting** **|** **Print Preview** **|** **Apply for this Job** **Please see Special Instructions for more ... Position Information **Posting Number** S05089P **Position Title** Software Systems Specialist II **Department** TMAC **Location** Arlington **Job Family**… more
- Abbott (Austin, TX)
- …working mothers, female executives, and scientists. **The Opportunity** This **Regulatory Affairs Specialist II ** position will work on-site out of our Austin, ... Abbott Diabetes Care Division. This role supports change control for manufacturing /operations activities as well as provides regulatory direction on cross functional… more
- WuXi AppTec (Philadelphia, PA)
- **Overview** Pharmaceutical Manufacturing : The EHS Specialist II will be responsible for supporting EHS compliance and risk management within the PHL ... Campus. The EHS specialist will monitor and improve processes to prevent and...programs. * Developing and supporting implementation of site-specific EH&S compliance programs based on federal, state and local regulations,… more
- ManpowerGroup (Des Plaines, IL)
- …with a leading **Medical Device Co** in the **Des Plaines IL area** for a **QA Specialist II ** role to assist their team. This is an Onsite role. **Industry: ... Medical Device Co** **Title:** **QA Specialist II ** **Location: ONSITE - Des Plaines...labeling and the associated RMS change requests while ensuring compliance with company policies and procedures. Able to navigate… more
Related Job Searches:
Compliance,
Compliance Manufacturing,
Compliance Specialist,
Compliance Specialist II,
Compliance Specialist Manufacturing,
II,
Manufacturing,
Manufacturing Specialist II,
Specialist,
Specialist II