- ManpowerGroup (Rockville, MD)
- Our client, a leader in the pharmaceutical industry, is seeking a Pharma Document Control Associate to join their team. The ideal candidate will have strong ... will align successfully in the organization. **Job Title:** Pharma Document Control Associate **Location:** Rockville, MD **Pay...per respective SOP. + Archive and maintain GLP and GMP documents with an accurate inventory, both on and… more
- Catalent Pharma Solutions (Harmans, MD)
- …are met and leading continuous improvement initiatives. The Document Control function supports both the GMP and development operations. Catalent, ... support Phase I/II/III/commercial operations. + Manages document control processes and systems for GMP activities...document control processes and systems for GMP activities in compliance with internal procedures and policies,… more
- Adecco US, Inc. (Sterling, VA)
- … Control Technician include but are not limited to:** + Conduct and document food quality control inspections + Monitor employee hygiene and Good ... Adecco is assisting a local client recruiting for **Quality Control Technician** opportunities in **Sterling, VA** . This is...Manufacturing Practices ( GMP ) + Collect samples for testing and assist with… more
- Adecco US, Inc. (Sterling, VA)
- Adecco is assisting a local client recruiting for **Quality Control Technician** opportunities in **Sterling, VA** . This is an excellent opportunity to join a ... in the door with a company known for premium food production. If **Quality Control Technician** sounds like something you would be interested in, and you meet the… more
- Charles River Laboratories (Rockville, MD)
- …including investigation/deviation management, CAPA tracking, Effectiveness Verification, change control , internal and external audits. This position will facilitate ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. **Key Responsibilities and Duties:** *… more
- Charles River Laboratories (Rockville, MD)
- …investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as ... industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. Key Responsibilities and Duties: Establishes… more
- Charles River Laboratories (Rockville, MD)
- …investigation/deviation management, CAPA tracking, Effectiveness Verification, and change control . This position will facilitate the compiling, trending (as ... and industry standards, quality improvements, and efficiency for phase appropriate GMP manufacture of biological products. This includes but is not limited… more
- Gilead Sciences, Inc. (Frederick, MD)
- … control , deviations, corrective and preventative actions (CAPA), training, and document control . The Director will provide technical expertise and strategic ... change control , deviation management, CAPA, training, and document control . + Serves as the primary...regulatory submissions and on-site inspections related to quality systems. ** GMP Compliance and Quality Control :** + Ensure… more
- Catalent Pharma Solutions (Harmans, MD)
- …recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders ... critical computer systems and laboratory documentation to support the commercial GMP manufacturing of biological drug substance and drug product. Responsibilities… more
- Catalent Pharma Solutions (Harmans, MD)
- …: + Serve as the QA-CSV liaison with the Engineering, Quality Control , IT and Validation organizations to support SaaS enterprise computer systems validation ... and LES modules, Electronic Laboratory Notebook (ELN), OpenText Documentum Electronic Document Management System (EDMS), MODA Software, JDE Edwards etc. + Design… more
- Catalent Pharma Solutions (Harmans, MD)
- …Quality Systems to implement equipment, facility, and automation change control , document revisions, and conduct equipment/system/instrumentation failure ... recognized tradition of quality and service. Catalent provides process development and GMP manufacturing services for Phase I/II clinical trials to industry leaders… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing (QCM) product documentation reviews, and test design for ... + Conducts thorough review and evaluation of QCM [i.e., quality control and manufacturing] documents and other data received from pharmaceutical, ingredient… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …related to current Good Manufacturing Practice (cGMP) site audits, quality control and manufacturing (QCM) product documentation reviews, and test design. In ... Manufacturing Practice (cGMP) facilities engaged in the manufacturer and/or quality control of dietary supplements and/or pharmaceuticals. * Knowledge of and… more
- Charles River Laboratories (Rockville, MD)
- …Records (BPRs) and associated supporting documentation including logbooks, Quality Control (QC) testing reports, environmental monitoring reports, etc. * Support ... to drive completion * Create, review and approve documents in electronic document management systems * Serve as QOps representative for client project teams… more
- TAI (Frederick, MD)
- …maintenance program. + Identify and recommend initiatives for continuous improvement. + Document and review GMP maintenance activities in SAP. + Assisting ... What You'll Be Doing:** + Painting, drywall, cleaning, pest control , light plumbing work, light door repairs and adjustments,...cGMP regulations, FDA, USP and ISPE guidelines + Champion GMP compliance and maintenance best practices to support a… more
- Gilead Sciences, Inc. (Frederick, MD)
- …and administration of computer systems and lab instruments in a regulated GMP environment. + Provide maintenance and support requests to address IT operational ... IT teams to deliver innovative, scalable, and compliant IT solutions. + Document user and functional requirements. + Support IT architecture by working closely… more
- Charles River Laboratories (Hanover, MD)
- …meet specifications, standards, cost-efficient, with adequate supply for testing. + Document inventory properly and communicate any issues with upper management ... + Manage, log, assign lot numbers (as applicable) and appropriately document all Receipt (incoming) and Shipment (outgoing) of materials, documents, testing… more
- Charles River Laboratories (Poolesville, MD)
- …Maryland. As the **Technical Trainer I** , you will develop, deliver, document , and report technical skills training programs involving both small and large ... regulations. Additional responsibilities include: + Direct, schedule, perform and document all relevant Task-specific technical, husbandry and administrative training… more
- Charles River Laboratories (Bethesda, MD)
- …As the Animal Care Technician II, you will maintain, monitor, and document the health, breeding colony production, technical support, and physical environment within ... all related records, logs, forms, cage cards -Applying quality assurance/quality control standards to ensure Statement of Work expectations are fulfilled **Job… more
- EMCOR Group (Baltimore, MD)
- …FTP sites and virtual plan rooms. + Familiarity with project management/ document control software. + Familiarity with construction/financial software packages. ... with efficiency and accuracy estimates within the industry methods (eg fixed-price, GMP , IPD, unit price, T&M, cost-plus, incentive contracts). Prepare scope letters… more