1 - 20 of 344 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

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

IBM Maximo EAM Specialist

Transcend IT Solutions

Remote

Contract, Third Party

Position Title: IBM Maximo EAM Specialist Location: 100% Remote (East Coast is preferred,Duration: 6+ Months Job Details:MUST HAVE PAST THERMO FISHER EXPERIENCE! Maximo Experience is not the only key skill sets for the positions. Experience in Pharma/ Bio Tech is a MUST Maximo Life Science Industry Solution ExpertiseFDA regulatory experiencePharma validation, change managed, calibration data sheets for life sciencesSignature reference using FDA guidelinesGMP experienceTFS key application experie

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

Direct Client - Quality Assurance Specialist (food or beverage manufacturing QA)

ChaTeck Incorporated

Seattle, Washington, USA

Third Party, Contract

Role: Direct Client - Quality Assurance Associate (food or beverage manufacturing QA) Location: Seattle, WA (Hybrid Tuesday, Thursday, the third day is flexible based) Duration: 12+ Months Job description "Implementing and auditing the manufacturing quality strategy, food safety, process and program quality and regulatory compliance to ensure the continuous supply of safe, wholesome and premium quality products to customers Tops Skills Needed Top Candidate Skills & How Applied Years of Ex

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

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

Senior Electrical Engineer

Aditi Consulting

New Albany, Ohio, USA

Contract

Payrate: $50.00 - $54.00/hr. Summary: The Engineer position reports to the Manager of Engineering under the Engineering & Maintenance team at the facility. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations in the manufacturing facility. The site of the new advanced product assembly and packaging plant, this role will apply advanced and diverse engineering principles to the design a

Belt Operator

Agropur

Jerome, Idaho, USA

Full-time

Job DescriptionJob Description Job Type:Regular Invest in you, Join Agropur. We dairy you! What Agropur invests in YOU: Starting wage of $21.33Two pay increases within the first year up to $1.00$1.50 Shift Differential + Double Time on SundaysThursday -Saturday every other Sunday 5AM to 5PMCompetitive and comprehensive compensation and benefits package focusing on your physical, financial, and emotional health to include the following perks as well as the standard benefit offerings: Medical,

Process Engineer

Katalyst Healthcares and Lifesciences

Remote or New York, USA

Full-time

Responsibilities: Senior Process Engineer responsible for tech transfers within the manufacturing team. Support GMP-related activities. Experience in tech transfer and project management. Strong technical skills, including report writing and problem-solving. Excellent communication skills, with the ability to clearly relay technical information. Cell Therapy (CAR-T) experience (preferred). Willingness to travel (approximately 25%). t least 5 years of relevant experience.

C&Q Engineer

Sunrise Systems, Inc.

Wilson, North Carolina, USA

Contract

Job Title: C&Q Engineer Job ID: 25-09377 Location: Wilson, NC 27893 Duration: 17 Months On W2 Contract Job Purpose The C&Q Engineer is responsible for the execution of the defined C&Q scope of the following areas Black Utilities and HVAC. These are Client-side roles and key responsibilities are meeting the agreed objectives regarding time, schedule and functionality according to EHS, URS and GMP requirements. The C&Q Engineer SME is responsible for planning and executing commissioning activit

Lead/Sr Computer System Validation Engineer

Katalyst Healthcares and Lifesciences

Muskegon, Michigan, USA

Full-time

Responsibilities: The CSV Lead manages quality control checks on engineering project work. The CSV Lead will have 10 plus years of experience of automation systems computer systems validation in a GMP environment. The CSV Lead will be responsible to assist Client in designing the validation strategy for the overall project and to coordinate production of the required CSV protocols. The CSV Lead will provide leadership to the CSV team members in reviewing CSV protocols for the various streams

Licensed Boiler & Utilities Engineer

Jobot

Lauderdale, Minnesota, USA

Full-time

High-pressure role, high rewards - Chief B or 1st Class B needed! This Jobot Job is hosted by: Kal Mayer Are you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume. Salary: $35 - $50 per hour A bit about us: We're a high-performance production facility operating in the heart of St. Paul, MN. With a strong commitment to quality and safety, our team works around the clock to ensure reliable operations and exceptional results. Our workplace culture emphasizes col

C&Q Engineer

Katalyst Healthcares and Lifesciences

Wilson, North Carolina, USA

Full-time

Job description: The C&Q Engineer is responsible for the execution of the defined C&Q scope of the following areas - Black Utilities and HVAC. These are Client-side roles and key responsibilities are meeting the agreed objectives regarding time, schedule and functionality according to EHS, URS and GMP requirements. The C&Q Engineer SME is responsible for planning and executing commissioning activities related to all equipment groups within their area. Reporting to the Client C&Q Manager. Plannin

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

Reliability Engineer

Thermo Fisher Scientific

Rochester, New York, USA

Full-time

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Location/Division Specific Information This position is within Laboratory Plast