1 - 20 of 372 Jobs

GMP/GDP Pharma Quality Engineer (ONSITE)(No C2C/H1B)

NetSource, Inc.

Ewing Township, New Jersey, USA

Contract

No C2C/H1B Please note that this is a 5+ months contract position. Work Location: Titusville, NJ Required: BA/BS Technical / Life Science Desirable: MA/MS/MBA Business / Technical /Life ScienceSupport Quality and Compliance Initiatives from Enterprise Quality and/or Global Business QualityEssential knowledge and skills Knowledge 5 years experience in the Pharmaceutical or related industry; Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP; Up-to-date knowledge of DEA reg

GMP/GDP Pharma Quality Engineer (ONSITE)(No C2C/H1B)

NetSource, Inc.

Ewing Township, New Jersey, USA

Contract

No C2C/H1B Please note that this is a 5+ months contract position. Work Location: Titusville, NJ Required: BA/BS Technical / Life Science Desirable: MA/MS/MBA Business / Technical /Life ScienceSupport Quality and Compliance Initiatives from Enterprise Quality and/or Global Business QualityEssential knowledge and skills Knowledge 5 years experience in the Pharmaceutical or related industry; Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP; Up-to-date knowledge of DEA reg

Project Manager - Gxp

Oraapps Inc

Remote

Contract

Job Title -Project Manager Gxp Location - Remote Contract Duration - 6+ Months Requirement: - 8+ years full lifecycle PM experience - Demonstrated PMLC/SDLC experience/success - Ability to quickly adapt to a maturing project environment - Ability to manage multiple concurrent priorities - MS Project and the ability to execute project plan is a must have MUST BE STRONG MS PROJECT - GXP & GMP Experience - Heavy experience required Plus: - GMP project experience, preferably as a PM - PMP certific

Technical Writer

Devfi

Santa Monica, California, USA

Contract

Role: Technical Writer Location: Santa Monica, CA Duration: 6 Months Responsibilities (include but are not limited to): Author and Finalize appropriate Module 3 documents and Response to Agency Questions in collaboration with Regulatory CMC and Technical Subject Matter Experts.Experience in analytical method development of vector and T cell, extended characterization of vector and T cell products, awareness of ICHs and global compendial requirements governing analytical development and character

Production Worker

Cynet Systems

Casa Grande, Arizona, USA

Contract

Job Description: Inspects, labels and packages raw and finished products. May be required to maintain records according to Good Candidateufacturing Practices. Maybe working in a clean-room environment. Moderate supervision is required. Tier Level 2.

Manufacturing Engineer (Sarasota, FL)

Connect Tech+Talent

Sarasota, Florida, USA

Contract

Role: Manufacturing Engineer Location: Gainesville, FL & Sarasota, FL Experience: 8 Years Durations: 6+ Months Skills: IQ-OQ-PQ Experience in medical parts manufacturing experience is the key, with process validation expertise around 8 to 10 yrs experience, and Medical Device experience is mandatory. Job Description: Protocol Review & Compliance: Study and assess Installation Qualification (IQ), Operational Qualification (OQ),and Performance Qualification (PQ) protocols and reports for regulato

Plant Technician

Apolis

Saint Joseph, Missouri, USA

Full-time, Contract

Job Title- Plant Technician Location St. Joseph, MO Duration- 12 Month+ Contract Pay Rate: $24/Hour On w2JOB SUMMARY: This position is responsible for assisting with organizing and performing pilot plant trials and associated support work under general supervision. This is a temporary contract position for the pilot plant operation.ESSENTIAL FUNCTIONS: 1. Perform pilot plant trials in a safe and efficient manner under supervision 2. Set-up, operate and clean food-processing equipment under supe

Mid Tooling and Validation Engineer

Bytecubit Technologies

Buffalo Grove, Illinois, USA

Contract

Job Title: Mid Tooling and Validation Engineer Location: Buffalo Grove, IL Duration: 3+ months Pay Rate: $40-55hr(Depending on experience) Job Description: Need to hire consultant for injection molding projects. This candidate will start on one project and move to another to help fill the gaps. May include some travel to support molding FOT/FAT activity. Must Have Skills/Experience: 3 years toolmaking 3 years tooling engineering Solidworks Nice to Have Skills/Experience: Mold Validation (IQ/OQ/P

Raw Materials Technical Specialist

Aditi Consulting

Remote or Cambridge, Massachusetts, USA

Contract

Payrate: $38.00 - $40.00/hr. Summary: The ideal candidate will have a strong background in documentation and regulatory specification development within a GMP-compliant environment. They should bring experience in project management and raw material specification, ideally from pharmaceutical, biotech, or similarly regulated industries (such as aerospace or chemical engineering). The role is fully remote and requires someone who can work independently with minimal supervision while contributing t

Maintenance Technician

Aditi Consulting

New Albany, Ohio, USA

Contract

Payrate: $25.00 - $30.00/hr. Summary: In this role you will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements, repairs, and modifications. You will evaluate and determine if process equipment maintenance, and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards in the Inspection and Packaging area. Responsibilities: Take part in the coordination of tech su

Manager-Strategic Sourcing and Supplier Management

NexInfo Solutions, Inc.

Foster City, California, USA

Contract, Third Party

About Nexinfo; NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors. They offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions. The company aims to help businesses across industries achieve their goals through industry best practices, lean process design, and advanced software solutions. Their ERP-related services address challenges

Quality Control Analyst

Aditi Consulting

Winchester, Kentucky, USA

Contract

Payrate: $27.00 - $27.76/hr.Summary: A QC Analyst is an entry level position for individuals who use their understanding of science to perform the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. Their work is hands on in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. This position performs the quality testing needed for raw material, in-process, finished goods, stabilit

General Labor

CONAGRA

Troy, Ohio, USA

Full-time

Job DescriptionShift: 3:00 PM-2:00 AM Hourly Rate: $19.85 an hour + $1.50 shift differential Position Summary: Responsible for sorting, in-feeding, and boxing Slim Jim product in the SJ packaging area. Position Responsibilities/Qualifications: Safety is the #1 responsibility.Follow all GMP's and USDA guidelines.Must be able to work overtime and weekends as neededProperly complete required paperwork on a daily basis per Quality guidelinesParticipate in the development, implementation and susta

Senior Associate

Aditi Consulting

Holly Springs, North Carolina, USA

Contract

Payrate: $22.00 - $25.00/hr. Responsibilities: Data verification Review of protocols plant floor support as needed Maintenance of team schedule/timelines/dashboards Top 3 Must Have Skill: Proficiency in knowledge of cGMP environment Attention to Detail Experience with process engineering technical reports/process validation protocols and documentation Education: Entry level is okay, but 1-2 years of industry experience would be helpful Pay Transparency: The typical base pay for this role acro

Product + Tech. Steward/Val + TT Lead | B5 | II

Arthur Lawrence

Indianapolis, Indiana, USA

Contract

Arthur Lawrence is looking to hire a Product + Tech. Steward/Val + TT Lead | B5 | II for one of our clients inIndianapolis, IN. Please find the job description below and send us your updated resume if interested: Must-Have Skills: Minimum 8+ years of experience in pharmaceutical manufacturing (Process Expert, QA/QC, or similar role) Strong understanding of pharmaceutical processes, GMP, and regulatory requirements Proficiency in English and the local site language Demonstrated experience with

Validation Engineer

Katalyst Healthcares and Lifesciences

Albany, New York, USA

Full-time

Responsibilities: Execute validation activities across the full equipment lifecycle (FAT, SAT, Commissioning, DQ, IQ, OQ, PQ). Apply GAMP 5 methodology in a GMP-regulated environment. Support Greenfield project initiatives and equipment startup. Handle deviations, change controls, and validation deliverables. Collaborate with cross-functional teams including QA, Engineering, and Manufacturing. Requirements: Prior experience with fill-finish equipment including syringe assembly, serializati

Machine & Equipment Technical Engineer / Senior Process Engineer

Stellent IT LLC

Bloomington, Indiana, USA

Third Party, Contract

Job Title:- Machine & Equipment Technical Engineer / Senior Process Engineer Job Location:- Bloomington, IN (Onsite) Long Term Contract Pharma Machine & Equipment Technical Engineer Responsibilities: Provide the technical expertise and tactical bandwidth for creative problem-solving based on industry best practices, to retrofit and optimize the SL3 machine/equipment for client product. Optimize the line's capabilities and prepare for new product technical transfer, with a focus on technical c

Industrial Maintenance Technician

Express Employment Professionals

Yuba City, California, USA

Full-time

Industrial Maintenance Technician Yuba-Sutter Area Express Employment Professionals is seeking an experienced Industrial Maintenance Technician for a well-established manufacturing facility in the Yuba-Sutter area. This is a long-term opportunity with a respected employer offering consistent hours and a team-oriented environment. Responsibilities: Perform routine and preventative maintenance on production equipment, conveyors, packaging lines, and facility systems.Diagnose and repair mechanica

Supplier Quality?Engineer (Software Suppliers)

Primary Talent Partners

Mounds View, Minnesota, USA

Contract

Primary Talent Partners has a new contract opening for a Software Supplier Quality Engineer with our medical device client in Mounds View, MN. This is a 12-month contract with a potential for extension.Pay: $40.00 - $50.00/hr; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Responsibilities may include the following and other duties may be assigned: Ensures that suppliers deliver quality parts, materials, and services. Qualifies suppliers according

Crimping Technician

Advantage Technical

Irvine, California, USA

Full-time

Join forces with Advantage Technical and we can connect you with a leader in innovative medical devices. Our client's mission is to simplify life with revolutionary products and make a positive impact on the lives of people. We are seeking a dedicated Crimping Technician to join their diverse team that makes a difference every day! Pay: $23.10/hr. Schedule: 4:00pm - 12:30am Key Responsibilities: Set up, operate, and maintain equipment with minimal supervision, including basic repairs and prevent