1 - 20 of 297 Jobs

Manufacturing /Production Technician (Pharma/GMP)

Cube Hub, Inc.

Redwood City, California, USA

Contract

Job Title : Manufacturing Technician Location : Redwood City, CA, 94063 Duration : 12 months Contract-possible to extend Shift Details : 5:30am-2pm Pay rate- $23/h to $25/h Job Description: Typical Accountabilities Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role. Complete all required training on the Code of Conduct and supporting Policies and Standards on time. Report

Project Manager - Pharma/Biotech - GMP/Drug Development

AgreeYa Solutions

New Albany, Ohio, USA

Contract

Job Title: Project Manager Location: New Albany OH Fully onsite at New Albany, OH- standard business hours Ideal candidate: Engineer or other technical background (mechanical, industrial, chemical etc.). Experience leading technical projects from start to finish. Supporting process development. Biotech, med device, or pharmaceuticals or other GMP manufacturing experiences preferred. Min. 3 years of experiences preferred. Candidate should showcase they have executed projects took ownership full

QC Information Services Analyst (GMP, LIMS, IT Support) - LG

Cube Hub, Inc.

Maryland, USA

Contract

Description: Job title: Senior QCISO Analyst Location: Fredrick, MD - 100% onsite Working Hours- M-F 8am-4pm or 9am-5pm Typical day will include project work, password resets, user access requests, software troubling shooting, make restricted folders for users, writing SOPs, executing text scripts. Manager is looking for Software IT experience including software configuration and user management. As a QC Information Systems (QCIS) Specialist, you will act as an administrator of computerized sy

GMP, LIMS, Wet Lab and Pharma Manuf Analyst Cell and Gene Therapy

CSI (Consultant Specialists Inc.)

South San Francisco, California, USA

Contract

Very proactive, experience working with data systems that produce data, experience around manufacturing Understanding of the needs and operations of a Wet lab, including ELN and LIMS systems Experience implementing IT solutions that need GMP validation Experience working in an agile development team Familiarity with agile methods and tools like User Stories, Story Maps, and Personas Description: BA, Clinical Stage Cell Therapy Process & Analytical Development - Data and Analytics The Business

GMP Process Engineer (Hybrid)

NetSource, Inc.

Wilson, North Carolina, USA

Contract

Please note that this is a 8-month contract. Candidate will need to be in commutable distance to Wilson, NCRole will initially be remote until the Wilson, NC building opens then they will be required to be onsiteRequirements: - Must have a Bachelor's degree - At least 2 years of experience - Experience in Biologics, Manufacturing, or Engineering - Less focus on "large capital construction systems" - Must have Delta Vee system knowledge - Must have Upstream and/or Downstream experience Top 3 Ski

GXP/GMP Lab Validation Technician (ONSITE)

NetSource, Inc.

Malvern, Pennsylvania, USA

Contract

Please note that this is a 1-year contract position. Qualifications: - role will be ONSITE - Minimum of an Associates Degree is required - Must be detail oriented, a go-getter, be willing to follow-up on tasks and chase items down when needed - Must have at least 1-2 years of experience - Must have GXP experience - Have knowledge of instrument validation and maintenance processes - Will be responsible for scheduling vendors for repair services and maintenance - Will "maintain" instruments, will

Facilities Project Manager

DivIHN Integration Inc.

Round Lake, Illinois, USA

Contract

DivIHN (pronounced divine ) is a CMMI ML3-certified Technology and Talent solutions firm. Driven by a unique Purpose, Culture, and Value Delivery Model, we enable meaningful connections between talented professionals and forward-thinking organizations. Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent. Visit us at to learn more and view our open positions. Please apply o

QA Associate 1

Aditi Consulting

Winchester, Kentucky, USA

Contract

Payrate: $26.60- $27.60/hr.Shift: FRI, SAT, SUN (6:00 PM - 6:00 AM)Summary: The QA Associate is responsible for the Quality support functions associated with the manufacturing of solid oral dosage products for a given business unit. The essential responsibilities associated with this position are oversight of the manufacturing operations (as dictated by cGMP, CFR, and SOP) through document review/approval, real time monitoring/approval of manufacturing activities and testing/approval of in-proce

Validation (CQV) Engineer

Tech Rakers

Indianapolis, Indiana, USA

Contract

Title: Validation (CQV) Engineer Qualifications and Requirements Bachelor's degree in Engineering, Pharmaceutical Science, or related technical field4-8 years of experience in a CQV role within pharmaceutical, biotech, or medical device industriesWorking knowledge of GMP regulations, Computerised System Validation and GAMP5Hands-on experience with qualification protocols for pharmaceutical manufacturing equipment and utilitiesFamiliarity with automation systems used in pharmaceutical manufacturi

SAP Plant Maintenance (SAP PM)

IT Resonance Inc.

Remote

Contract, Third Party

SAP Plant Maintenance (SAP PM) 12 months Remote with travel to onsite (Chicago IL) Must have food & beverage manufacturing or consumer packaged goods industry experience Solid/Strong comm skills compliance with food industry standards (e.g., FDA, GMP, HACCP) Regards Stephen DJA stephen at itresonance dot com

Computer System Validation Specialist

SGS Consulting

Remote

Contract

Job Title: Computer System Validation (CSV) Specialist Duration: 08 Months + (Possible Extension) Location: Wilmington, DE 19803 (Remote) Schedule: M-F: 08 AM 05 PM Kindly Do not apply if you are not or Permanent Resident of USA. Qualifications: The official position title is Computer System Validation (CSV) specialist to support the Newark manufacturing facility with validation of new and existing computerized systems.This role will primarily support the Newark manufacturing facility but may r

Quality Analyst

Talent Software Services, Inc

Kansas City, Kansas, USA

Contract

Quality AnalystJob Summary: Talent Software Services is in search of a Quality Analyst for a contract position in Kansas City, KS. The opportunity will be six months with a strong chance for a long-term extension.Primary Responsibilities/Accountabilities: Requires proficiency in Quality Assurance Procedural work and expertise in Application work by combining hands-on experimentation with scientific principles and knowledge from science/engineering education to drive foundational technical unders

Manager 2 - Process Engineering

Motion Recruitment Partners, LLC

Horsham, Pennsylvania, USA

Full-time

Principal Process Engineer / Manufacturing Fortune 500 Medical, Biotechnical and Pharmaceutical company is looking to add a Principal Process Engineer to their team in Wilson, NC. This is an initial contract opportunity with perm potential. If you are looking to work for a company that is making a difference for the world you find it. Required Skills & Experience Candidate will need to be commutable distance to Wilson, NC. Role will initially be remote until the Wilson; NC building opens then t

SAP QM Architect

LGL Technologies

Pittsburgh, Pennsylvania, USA

Contract

Position: SAP QM Architect Location: Pittsburgh, PA, USA (Hybrid 2-3 days onsite/week) Client: West Pharma Duration: 9+ Months Must-Have Skills:Strong SAP QM experience with S/4 HANAHands-on SAP PP, with 3+ full lifecycle implementationsExperience working in Agile environments (User Stories, Sprint Teams)Familiarity with SOX, FDA GMP compliance, and change controlNice to Have:SAP EWM, MM, and PM exposureShop Floor / MES Interface knowledgeStrong knowledge of HANA, Agile/Scrum or ITIL certifi

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

Facilities/Utilities SME (Pharmaceutical)

Zachary Piper Solutions, LLC

Bloomington, Indiana, USA

Full-time

Piper Companies is currently seeking a Facilities/Utilities SME to support construction, startup, and handover of a new pharmaceutical manufacturing facility in Bloomington, Indiana. Responsibilities for the Facilities/Utilities SME Oversee clean and dirty utilities: WFI, clean/plant steam, boilers, chillers, condensate, and process gases Review utility designs, P&IDs, and support commissioning and qualification Manage facilities/utilities tradesmen and contractors onsite Ensure utility systems

QC Analyst

Zachary Piper Solutions, LLC

Elkridge, Maryland, USA

Full-time

Piper Life Sciences is seeking QC Analyst to join a rapidly growing biopharmaceutical company in the Elkridge, MD area. Responsibilities for the QC Analyst include : Complete duties related to EM monitoring, which include endotoxin, bioburden, TOC, etc . Use specialized instruments and equipment to monitor environmental parameters and ensure accurate measurements. Ensure that environmental regulations and standards are being met by conducting regular inspections and tests. Compile and analyze

Staffing - Mechanical Technician II

The Fountain Group

Newton, North Carolina, USA

Full-time, Contract

Immediate opening for a Mechanical Technician located in Newton, NC (Onsite). Details for the position are as follows: Job Description: Travel Requirements: Project locations will range from Newton NC and Hickory North Carolina. This position is in the Engineering Project and is focused on capacity additions and the associated line installations & debug from a mechanical perspective. Lead and/or participate on manufacturing engineering projects and support teams for the purposes of capacity ins

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

Manufacturing Associate

Zachary Piper Solutions, LLC

Elkridge, Maryland, USA

Full-time

Piper Health and Sciences is seeking a skilled and motivated Manufacturing Associate to join a biotechnology company in Elkridge, MD. The Manufacturing Associate will provide support to upstream, downstream, and fill finish operations. Responsibilities of the Manufacturing Associate: Execute manufacturing of drug product following GMP guidelines Maintain inventory of all GMP manufacturing processing rooms Prepare buffers and reagents, TFF, chromatography Monitor equipment and clean/saniti