61 - 80 of 563 Jobs

Sr DeltaV Automation Engineer

TeamSuccess LLC DBA HiEd Success

Muskegon, Michigan, USA

Contract

Sr DeltaV Automation Engineer Muskegon, MI - onsite Please note: We need someone who has developed automation code within DeltaV (Control Modules through to Equipment Modules, Phases and Recipes) and familiar with troubleshooting code errors, not just associates with a background in using DeltaV from on operator perspective. Job Summary: This is an onsite role to help with commissioning efforts of a DeltaV system and mentor other Junior and Intermediate Engineers. The client and the project tea

Virology Deviation Management Specialist

Zachary Piper Solutions, LLC

West Point, Pennsylvania, USA

Full-time

Piper Companies is looking for a Virology Deviation Management Specialist for a leading pharmaceutical manufacturer in West Point, PA. Responsibilities: Conduct microbiological testing within investigations to prove root causeRecommend corrective and preventive actions (CAPAs)Conduct deviation OOS investigations related to testing within pharmaceutical manufacturing Qualifications: 2+ years of experience within GMP/FDA regulated environmentFamiliarity with virology Strong background in pharm

CAD and Document Control Assistant (floor plans, large company)

CSI (Consultant Specialists Inc.)

South San Francisco, California, USA

Contract

W2 ONLY. NO C2C. No recent grads. This is NOT and entry level role. Must Have: 3 to 5 years of Architectural and Mechanical Drafting experience. Large Corporate experience. GMP Documentation is highly preferred. Responsibilities: Creation and editing of 2D/3D drawings using the latest release of AutoCAD. Support drafting work involving Architectural, Mechanical, Electrical, Plumbing and Process drawings. Proactively interact with CAD and Document Control staff, clients and contractors relating

CSV Engineer

Katalyst Healthcares and Lifesciences

Robbinsville Township, New Jersey, USA

Full-time

Responsibilities: Company Product. 503B compounding facility. The project the contractor will be working on CSV remediation of Lab Equipment Systems. They cutoff of connection to the network and automated systems and are looking to garner them all into one standalone system. Requirements: Waters EMPOWER Data Management Systems, GAMP 3-4 ISP Guidelines different GAMP Category, 3-5 years Isolators, Documentation skills, clear and concise protocol writing attention to detail. Someone that can

MES POMSnet LEAD--BOSTON,MA (ONSITE)

Altitude Technology Solutions Inc

Boston, Massachusetts, USA

Contract, Third Party

ROLE- MES POMSnet LEAD LOCATION- BOSTON,MA (ONSITE) NOTE: pharma or bioindustry should be present Role Description: 3-5 years of experience providing IT or application support for Manufacturing Execution Systems (MES) in a pharmaceutical, biotech, or life sciences environment.? Experience with POMSnet MES is highly preferred; Rockwell or other MES experience is also desirable.? Strong understanding of manufacturing processes, batch records, workflows, and data capture requirements in GMP enviro

CSV Engineer

Katalyst Healthcares and Lifesciences

Portsmouth, New Hampshire, USA

Full-time

Responsibilities: Hands on experience in Implementation & Validation of various computerized systems like MES (Syncade) & PLC (COTS). Strong knowledge of Software Development Lifecycle (SDLC), including 21CFR part 11/Annex 11, Data Integrity and computerized system validation requirements. Experience at working independently as well as in a team-oriented, collaborative environment is essential. Author and Execute CSV life cycle documentation. Requirements: CSV experience of 4+ years.

Disaster Recovery

CSI (Consultant Specialists Inc.)

Hillsboro, Oregon, USA

Contract

As IT OT Infrastructure & Services Engineer, you will be responsible for disaster recovery & business continuity documentation and testing services for the local Manufacturing Infrastructure and act as the key contact for the Global Teams delivering and operating the Global Infrastructure. In partnering the site your focus is always on Make Assess Release (MAR) in alignment with site priorities as well as demand originating from Projects. Responsibilities: Developing Disaster Recovery Plans: Col

System Construction Project Manager (ONSITE)

NetSource, Inc.

Wilson, North Carolina, USA

Contract

Please note that this is a 8-month contract. The primary location for this role is Wilson, NC. Design is taking place in Conshohocken, PA.The design phase requires a hybrid work location of remote and onsite in Wilson, as well as routine travel to Conshohocken.Once the design phase is completed, this role will support the construction and operational start-up of the site.For this, you will be required to be on site full-time in Wilson, NC.Travel info: 25% domestic between PA and Wilson, NCPositi

Biomanufacturing Material Handler

SGS Consulting

Durham, North Carolina, USA

Contract

Job Title: Material Handler II Duration: 06 Months+ (Contract to Hire) Location: Durham (RTP), NC 27709 Schedule: Monday - Friday 8am - 5pm_minimal overtime MUST HAVE A TRUE UNDERSTANDING OF WORKING IN A cGMP WAREHOUSE ** Cross training opportunity in Dispensary Biomanufacturing ** Job Description: In support of manufacturing, the material handler will receive raw materials, process manufacturing orders, weigh and dispense activities, and shipping of final drug substance.The role is focused on

Manufacturing Associate

ProKatchers LLC

King of Prussia, Pennsylvania, USA

Full-time

Job DescriptionJob Title : Downstream Associate Scientist / Manufacturing Associate Location : King of Prussia, PA 19406 Duration : 12 months (with possible extension to 18 months total) Job Description : Preparation of buffer solutions, chromatographic separation, filtration and concentration operation, etc.Completing daily manufacturing tasks per standard operating procedures and batch document instructions.Documenting all manufacturing activities clearly and accurately.Ensures all production

Sr. Regulatory Affairs Specialist - SaMD/SiMD

PRISMATIK DENTALCRAFT, INC.

Irvine, California, USA

Full-time

Job DescriptionPrismatik Dentalcraft is a division of Glidewell Dental. Essential Functions: Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies.Maintains company registrations and device listings in the US, Canada, and the EU.Analyzes and reports department metrics.Supports and maintains technical files, MDD certifications, and declarations of conformity in support of EU product registrations/CE mark.Informs coordinator of product recalls.Pe

Quality Engineer

Medicoil, Inc.

Lake Geneva, Wisconsin, USA

Full-time

Job DescriptionQuality Engineer Location: Lake Geneva, WI Company: Medicoil About the Role: Medicoil is seeking a Quality Engineer to enhance product quality and drive continuous improvement. You'll play a key role in maintaining our ISO 13485:2016 quality management system, leading root cause analysis, and collaborating across teams to optimize processes. What You ll Do: Support audits, internal assessments, and compliance with ISO 13485:2016.Develop and improve FMEAs, control plans, and suppli

Manufacturing Technician - cGMP

Intellectt Inc

Severn, Maryland, USA

Full-time

Job DescriptionRole: Manufacturing Technician cGMP Location: Harmans, MD Duration: 3+ months, potential to convert to full-time based on performance What You ll Do: Perform day-to-day manufacturing support activities in a cGMP-regulated environment.Prepare and filter media and buffer solutions using proper aseptic and cleanroom techniques.Operate production equipment such as pH/conductivity meters, pumps, tubing welders, and filter testers.Dispense, label, stage, and transfer raw materials and p

QA Associate-GMP

Zachary Piper Solutions, LLC

Lansing, Michigan, USA

Full-time

Piper Companies is looking for a QA Specialist to join a clinical pharmaceuticals company located in Lansing, MI. Responsibilities of the QA Specialist include: Complete communication with both internal and external vendors Create new SOPS and improve existing ones Deal with quality records through initiation, tracking, and closure (Ex: Deviations, Change Controls, CAPAs, Out of Specification records) Complete reviews of manufacturing batch records Qualifications for the QA Specialist include

Business Systems Analyst - FICO

Leeds Professional Resources

Boca Raton, Florida, USA

Full-time

Job DescriptionRESPONSIBILITES Function as a technical resource to facilitate the various stages of the data solutions life cycle including Investigation, Analysis, Design, Testing, Installation, Maintenance and Training.Function as subject matter expert of applications, including third-party applications, that interface with SAP such as Blackline, Vertex, Concur, and SAP Analytics Cloud (SAC).Function as subject matter expert of internal SAP FICO business processes.SAP S4HANA Finance experience

Manufacturing Associate II (Downstream)

Zachary Piper Solutions, LLC

Gaithersburg, Maryland, USA

Full-time

Piper Health and Sciences is seeking a skilled and motivated Manufacturing Associate II (Downstream) to join a biopharmaceutical company in the Gaithersburg, MD area. The Manufacturing Associate II is a crucial role in supporting the downstream manufacturing team. This position involves operating and maintaining downstream processing equipment, performing filtration and chromatography techniques and supporting production activities in a cleanroom environment. Responsibilities of the Manufactu

Chemical Process Engineer - Food Manufacturing

Jobot

Indianapolis, Indiana, USA

Full-time

This Jobot Job is hosted by: Kurt Holzmuller Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $80,000 - $110,000 per year A bit about us: We are a global leader in the consumer packaged goods space. We specialize in enhancing the taste of beverages like coffee, tea, and water through a range of low-calorie sweeteners, creamers, and flavor enhancers. As a process engineer on our team, you will be responsible for leading technical initiatives t

Sr Microbiology SME

Bytecubit Technologies

Halifax, Nova Scotia, Canada

Contract

Job Title: Sr Microbiology SMELocation: Nova Scotia, Canada (Hybrid Split between onsite Prince Edward Island and Nova Scotia and some remote work) (Must be ok with frequent travel to Prince Edward Island PEI)Duration: 3 monthsPay Rate: $50/hr-$70/hr (depending on experience)Job Description:Looking for a Microbiology SME to oversee 7 microbiologists onsite.Microbiologists are overseeing lab work and sampling will need to be done onsite.Looking for a candidate that has experience in leading a mic

Drug Manufacturing Technician

BEPC Inc. - Business Excellence Professional Consulting

Santa Rosa, California, USA

Full-time

Job DescriptionJob Title: Drug Manufacturing Technician Job ID: ABOJP00040899 Location: Santa Rosa, CA 95403 Type: W2 1-Year Contract Duration: 07/14/2025 to 12/22/2025 Category: Industrial Labor Type: Industrial Contingent Type: US Positions Open: 1 Pay Rate: $18/hr Work Hours: Monday Friday, 9:30 AM 6:30 PM Timesheet Type: Time In/Time Out Frequency: Weekly Hours per Week: 40 Job Description This is a non-exempt position. Any hours over 40 per week will be paid at time and a half. As a Drug Ma

HVAC SME (Pharmaceutical)

Zachary Piper Solutions, LLC

Bloomington, Indiana, USA

Full-time

Piper Companies is currently seeking an experienced HVAC SME to support the design, installation, and commissioning of HVAC systems for a new pharmaceutical manufacturing facility in Bloomington, Indiana. Responsibilities for the HVAC SME Provide technical oversight of HVAC and environmental systems supporting cleanrooms and GMP spaces Review HVAC designs, drawings, and control strategies (including BMS integration) Support installation, commissioning, and qualification activities Ensure complia