GMP Jobs in Baltimore, MD

Refine Results
1 - 10 of 10 Jobs

QC Analyst (Micro)

Zachary Piper Solutions, LLC

Baltimore, Maryland, USA

Full-time

Piper Life Sciences is seeking a QC Analyst for a well-known biotech organization in the Baltimore, MD area. The QC Analyst will be supporting microbiology, environmental monitoring (EM) and utility testing programs for a GMP facility. Responsibilities for the QC Analyst: Create and maintain materials and reagents needed to execute experiments Perform environmental monitoring and utility testing of the GMP facility Conduct routine testing including bioburden, endotoxin testing & TOC testing Ass

Laboratory Technician

Zachary Piper Solutions, LLC

Baltimore, Maryland, USA

Full-time

Piper Health & Sciences is actively recruiting for several entry-level Laboratory Technician roles to gain hands-on experience with ELISA testing, cell cultures, and other immunoassays. This is an ideal role for recent science graduates who are looking to get their first job in the industry with an incredible biotechnology research organization in the Baltimore, MD area! Responsibilities for the Laboratory Technician include: Quality Control (QC) testing to support the organization's products Pe

Training Specialist - LMS Administrator

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Health and Sciences is actively seeking a Training Specialist and LMS Administrator to join a large global medical device company. This position is work from home / remote and candidate must sit in the east or central time zone. Responsibilities for Training Specialist - LMS Administrator: Oversee implementation, migration and maintenance of Training and Quality Management Systems Review and approve content development for training modules related to quality assurance, manufacturing, and

Senior ERP Business Analyst Finance

Prosum

Remote

Full-time

6 months w/extension or posible conversion to full time. No sponsorship given. ONLY accepting candidates close to Bothell which is in Settle, WA. Innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As a member of the Global IT team, the Senior ERP Business Analyst Finance plays a critical role in delivering successful solutions by partnering with business and technology groups to elicit requirements and manage the design and implementation o

Senior Staff Product Security Engineer - DRE (REMOTE)

Stryker

Remote or Fort Lauderdale, Florida, USA

Full-time

Why engineering at Stryker? At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a

Manufacturing IT Pharma 4.0 Sr. Systems Analyst

Sumeru

Remote

Contract, Third Party

Manufacturing IT Pharma 4.0 Sr. Systems Analyst Job Location:- Remote MES and Pharma background is mandatory and Pharma background with any of the project is fine The role of the Manufacturing IT Sr. Systems Analyst is to Captures business requirements and to document custom configuration needs. Reviews, analyzes, and modifies systems to system based on business needs for the PSG Manufacturing Pharma 4.0 IT program for new and existing sites. Strong organizational and multitasking skills wil

Computer System Validaiton Consultant

Kellton

Remote

Contract

Computer System Validaiton Consultant Hazelwood, MO (100% Remote) 12 months with possible extension or conversion Max PR- $54/hr on W2 Job Summary: As a Computer Systems Validation Consultant, you will play a critical role in interpreting and enforcing relevant GxP regulations and standards, ensuring consistent application across global GxP IT systems. Your responsibilities will include managing periodic reviews, providing oversight for non-GxP changes, authoring/reviewing technical documents, a