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Maintenance Mechanic/ GMP Asset Mechanic

Sunrise Systems, Inc.

Tampa, Florida, USA

Contract

Job Title: Maintenance Mechanic/ GMP Asset Mechanic Location: 4910 Savarese Circle, Tampa, FL 33634 Duration: 12 Months (Possible Extension or Conversion) Position Type: Hourly contract Position (W2 only) Description: The GMP Asset Mechanic is responsible to ensure that GMP production assets are evaluated prior to purchase, qualified and documented as needed, maintained and commissioned prior to use, and properly decommissioned and stored for future use. This individual reviews: equipment and

Production Operator

Advantage Technical

Acton, Massachusetts, USA

Full-time

Are you looking for an opportunity to be part of something groundbreaking? This is your chance to join a company making major investments in U.S. manufacturing, expanding globally, and driving innovation in the medical device industry. As a Production Operator in Boston, MA, you'll be crucial in delivering life-changing technology while working in a cutting-edge facility. Schedule: 2nd Shift Pay: $24.30 per hour What You'll Bring: High school diploma or GED required. At least 2 years of experi

Senior Validation Engineer

Zachary Piper Solutions, LLC

Copiague, New York, USA

Full-time

Piper Companies is seeking a Senior Validation Engineer to join a leading pharmaceutical manufacturing company located in Long Island, NY. The Senior Validation Engineer will ensure compliance by developing and executing testing protocols for equipment, processes, and utilities in a pharmaceutical cGMP environment. Responsibilities of the Senior Validation Engineer include: Manage end to end, hands on, validation for products, processes, equipment and packaging Supports all qualification tasks

Calibration Coordinator

bioMerieux

Hazelwood, Missouri, USA

Full-time

Position Summary & Responsibilities: Work within and maintain the site calibration program. Liaison with Calibration vendors to provide calibration and maintenance technical activities as well as coordinating calibration scheduling between bioMerieux departments serviced by the Calibration Department and vendors. Work within and maintain the Calibration Program.Review calibration documentation and labeling.Maintain and update calibration records and database to ensure accurate documentation; d

Upstream Manufacturing Associate

Zachary Piper Solutions, LLC

Washington, District of Columbia, USA

Full-time

Upstream Manufacturing Associate - Clinical Production Piper Health and Sciences is seeking an Upstream Manufacturing Associate to support clinical production in a cGMP biopharmaceutical environment. This role offers hands-on experience in bioprocessing and cell culture, helping advance therapies into clinical trials. Ideal for candidates looking to grow in biotech manufacturing . Responsibilities for Upstream Manufacturing Associate Include: Operate upstream biomanufacturing equipment: biorea

Pharmaceutical Manufacturing Technician C shift

Merck Group

Verona, Wisconsin, USA

Full-time

Work Location: Verona, Wisconsin Shift: Yes Department: LS-SC-POWMA6 Verona Manufacturing 6 Hiring Manager: Cory Noltemeyer This information is for internals only. Please do not share outside of the organization. Your Role Employee is responsible to adhere to the GMP requirements defined within 21 CFR parts 210 &211, 820, ICH Q7, Safety standards set under ISO 14001 & 45001. This position primarily involves the safe and efficient manufacturing of active pharmaceutical ingredients (API's) acco

Engineering - Bio Process Associate - 3rd Shift , Devens MA - Immediate position

Futran Solutions

Massachusetts, USA

Contract

Job Description: Bio Process Associate 3rd shift role--so shift diff included on Rate Onsite in Devens--Local Candidates Only Operates control systems and processes in Biotechnology Pilot Plants as assigned. Prepares process buffers and reagents. Cleans equipment and maintain area in clean and orderly fashion. Recognizes and reports safety, maintenance and operational variances to area management. Communicates status of operations to area management in a timely manner. Follows detailed SOP

Internal Quality Auditor

Judge Group, Inc.

Lewisville, Texas, USA

Full-time

Location: Lewisville, TX Description: Our client is currently seeking a Engineering Consultant Top 5 Qualifications Investigations, Root Cause Analysis, or Corrective Actions - Critical Experience in Computer System Validation - Critical Annual Product Review - Would be Nice Experience with Validation, Process, Cleaning, or Equipment Validation - Would be Nice Experience with Stability Programs - Would be Nice Preferred Certifications: Certified Quality Auditor Certified Quality Engineer

Quality Control Analyst I

Sunrise Systems, Inc.

Cincinnati, Ohio, USA

Contract

Job Title: Quality Control Analyst I Location: Cincinnati, OH Duration: 06 months on W2 contract (Temp to perm based on openings and performance). Shift Schedule: Monday - Friday 8:00am - 5:00pm Bill and Pay Rate is based on skill set Core essential skill sets candidates must have to be considered for the role:BS or higher in science related discipline, chemistry is preferredLab experienceRecent College graduates welcome Job Description:Perform routine and non-routine chemical testing of comm

I&C Technician

Apex Systems

Philadelphia, Pennsylvania, USA

Full-time

Job#: 2077232 Job Description: Instrumentation & Controls (I&C) Technician / SME! We're looking for a skilled and detail-oriented I&C Technician / Subject Matter Expert to support the installation, verification, and operation of instrumentation and control systems. This role works closely with Automation, Facilities, Metrology, construction, and commissioning teams to ensure compliance with design specifications, industry standards, and regulatory requirements. Key Responsibilities: Perform lo

Facilities Maintenance Technician (boilers, HVAC, electrical systems)

Cube Hub, Inc.

Santa Monica, California, USA

Contract

Job Title : Facilities Maintenance Technician Location : Tarzana, CA, 91356 must be able to go to the Santa Monica site for training etc. a few times per year. Duration : 12 months Contract-possible to extend Shift Details : For the first 4-6 weeks, Mon-Fri, 5:00am to 1:00 pm, then the schedule will change to Tuesday to Sat, or Sun to Thursday Job Description: Schedule: For the first 4-6 weeks, Mon-Fri, 5:00am to 1:00 pm, then the schedule will change to Tuesday to Sat, or Sun to Thursday D

QA Clinical Supplies Specialist

Zachary Piper Solutions, LLC

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a QA Clinical Supplies Specialist to join a major pharmaceutical manufacturing company located in Lansdale, PA. This is a Hybrid role. The QA Clinical Supplies Specialist will ensure the quality, compliance and integrity of clinical trial supplies. Responsibilities of the QA Clinical Supplies Specialist include: Ensure clinical supply materials meet company policies and regulatory standards. Lead projects aimed at improving process performance, including yiel

Quality Control Chemist I

Sunrise Systems, Inc.

Johns Creek, Georgia, USA

Contract

Job title: Quality Control Chemist I Job ID: 25-08182 Location: Johns Creek, GA (Onsite) Duration: 24 months Contract on W2 Schedule: Two-week rotating schedule 12-hour shifts. Week 1: Monday, Thursday and Friday. Week 2: Tuesday, Wednesday, Saturday and Sunday. POSITION PURPOSE: Conduct Quality Control testing of materials and production samples as required to support contact lens production, performing assigned tasks according to approved SOP's, methods, and procedures with adherence to cG

Specialist Quality Management

INSPYR Solutions

Lewisville, Texas, USA

Contract

Title: Quality Systems Analyst Rate: $40-45/hour Location: Lewisville, TX Duration: 18+ month contract Work Requirements: , or Authorized to Work in the USQuality Systems Analyst Serves as an internal auditor and a member of the Quality Systems team. Serves as technical/subject matter specialist for compliance related issues and works to resolve these issues and improve quality. Assists in the day- to-day operations of Quality Systems processes, such as Document Control Management, Change Contr

Quality Control Analyst @ Fort Washington, PA 19034

Infobahn Softworld Inc.

Fort Washington, Pennsylvania, USA

Contract, Third Party

Title: Quality Control Analyst Location: 7050 Camp Hill Road, Fort Washington, PA 19034 Duration: 12 Months Contract Job Description: Needs to work 3rd shifts 9:30PM to 8:00AM The QA Specialist is responsible for providing daily Quality Assurance support to the manufacturing site to ensure internal and regulatory cGMP and CFR requirements are met. Quality Assurance support areas include but are not limited to Batch Record Review, Product Release, Standard Operating Procedures, Investigations,

QA Validation Specialist II

Stellent IT LLC

Waltham, Massachusetts, USA

Contract, Third Party

Job Title:-QA Validation Specialist II Job Location:- Waltham MA (Hybrid) Long Term Contract Client is looking for a contractor as a Specialist II to join their growing QA Validation group. This is expected to be a 6 month contract position. The role is expected to be onsite in Waltham, MA 3-4 days per week. Here's What You'll Do: Provide QA oversight of CQV activities for the cGMP manufacturing facility and quality control laboratories. Provide QA oversight for periodic review and requalifica

Supply Chain Business Analyst- SAP ERP

Sunrise Systems, Inc.

Lawrence Township, New Jersey, USA

Contract

Job Title: Supply Chain Business Analyst- SAP ERP Job ID: 25-08321 Location: Summit, NJ, 07901 Duration: 12 Months of Contract Minimum 50% onsite required (candidate need to be flexible to come more than 50% if needed) Work Schedule: Mon-Fri (normal business hours) Bachelor's degree required Must Haves:Supply Chain Planning, Master Data, SAP ERPGreen Field SAP implementation and Master Data experienceEnd to End Business planning Process KnowledgeSummary: The Cell Therapy External Manufacturing

Facilities Sr. Specialist

Avantor

Massachusetts, USA

Full-time

The Opportunity: Under limited supervision, plan, organize, and design the most efficient and cost-effective layout of organization facilities and buildings including architectural and structural components. Estimate material and labor costs for repairs, replacements, and improvements. Serve as liaison with outside contractors and vendors of equipment and supplies. May be involved in office move coordination.Avantor is looking for a dedicated Sr. Facilities & Maintenance Technician to join our

Technical Operations Specialist I

WuXi AppTec

Philadelphia, Pennsylvania, USA

Full-time

Job DescriptionAdvanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need. Working at Advanced Therapies means being part of a dynamic, fas

Senior Engineer - Engineering Technical Authority

Amgen Inc

Remote or Thousand Oaks, California, USA

Full-time

Career Category Engineering Job Description Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients ea