- 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 (Manassas, VA)
- ** Document Control Specialist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... help create engaging new products consumers will love. The ** Document Control Specialist** is responsible for creation...(Standard Operating Procedures and Test Methods) + Knowledge of GMP and Quality systems + Previous experience in Excel… more
- Kelly Services (Manassas, VA)
- Job Opportunity: Associate Document Control Location: Manassas VA Duration: Temp to Hire- Onsite Payrate: $32.00 Shift: Monday - Friday 7:30am - 3:30pm **Job ... System using technical writing best practices, ensuring proper formatting, numbering, and document control . * Issue batch records to Production and Packaging… more
- ManpowerGroup (Manassas, VA)
- **Our client, a leader in pharmaceutical manufacturing, is seeking an Associate Document Control Specialist to join their team.** As an Associate Document ... will align successfully in the organization. **Job Title:** Associate Document Control **Location:** Manassas, VA (On-site) **Pay...SQF, HACCP, and Food Quality Plans + Knowledge of GMP and Quality Systems **What's in it for me?**… more
- Adecco US, Inc. (Manassas, VA)
- …documents, deviations, and change controls. + Conduct internal audits and document non-conformances. + Participate in New Product Introductions (NPIs) and Change ... Control processes. + Track and help implement corrective and...Strong analytical, documentation, and organizational skills. + Familiarity with GMP , HACCP, SQF, and Quality Systems required. + Ability… 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
- 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
- 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
- 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 (Poolesville, MD)
- …the **Laboratory Animal Technician I** role, you will maintain, monitor, and document the health, well-being, and physical environment of animals on-site. You will ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more
- Charles River Laboratories (Bethesda, MD)
- …visits would also be a responsibility of this position. + Identify, document , and/or report environmental or cagewash abnormalities. + Use of computer programs ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more
- Charles River Laboratories (Bethesda, MD)
- …site in Bethesda, MD. As the **Technical Trainer** you will develop, deliver, document , and report technical skills training programs involving both small and large ... by delivering operational and cost efficiencies through the strategic insourcing of GMP , GLP and non-GLP research services from discovery through safety assessment.… more
- Charles River Laboratories (Rockville, MD)
- …data to large scale manufacturing. This responsibility includes scale up, document authorship, process data tracking, deviation investigation, and data analysis to ... This position interacts with Process Development, Manufacturing, Facilities, Quality Control , Quality Assurance, and Supply Chain to ensure project success.… more