GMP jobs

Wilson, North Carolina

•

3d ago

Please note that this is a Contract position and is On-Site. Job Description: - Will be onsite in Wilson, NC - May travel 1 time in a year Qualifications: Minimum of a Bachelor's or equivalent University Degree required in Chemical or Mechanical Engineering MS/MBA/Ph.D. PE Certificate preferred Experience and Skills: A minimum of three (3) years of process/plant engineering experience in GMP MFG large molecule biologics facilities. Experience in green or brown field GMP MFG facility start-up

Easy Apply

Contract

Depends on Experience

Sr. GMP Manufacturing Process/Plant Engineer (On-Site)

Wilson, North Carolina

•

3d ago

Please note that this is a Contract position and is On-Site. Job Description: Skills: A minimum of eight (8) years of process/plant engineering experience in GMP MFG large molecule biologics facilities. Experience in green or brown field GMP MFG facility start-up including process systems, automation, utilities, facilities and operations. Strong technical background in Process and Manufacturing engineering, strong analytical skills to synthesize business needs, manufacturing requirements, engine

Easy Apply

Contract

Depends on Experience

GMP Associate I Plant Manufacturing (Bottling)

Clinton, Pennsylvania

•

Today

Job Title: GMP Associate I Plant Manufacturing (Bottling) Clinton (Onsite) | Contract: 6 Months Shift: B Team | 2-2-3 Schedule | 6:30 AM 6:45 PM Job Description: Seeking a GMP Associate I to support bottling/manufacturing operations in a cleanroom environment. Responsibilities include operating production equipment, bottling/packaging, loading hoppers, completing GMP/GDP documentation, performing quality checks, and troubleshooting basic HMI issues. Requirements: High school diploma or equival

Easy Apply

Contract

Quality Engineer (GMP/Pharma Manufacturing)

Phillipsburg, New Jersey

•

3d ago

Role: GMP Quality Assurance Engineer / Quality Systems Engineer Location: Phillipsburg, NJ (Onsite M-F) Duration: 18 Months Contract-to-Hire Client: Avantor Interview Process: 15-min Teams + 2-hour onsite interview Job Description: The ideal candidate will have experience in pharmaceutical, biotech, or chemical manufacturing environments and strong knowledge of cGMP and ISO standards. Required Skills: 5+ years of Quality Engineering / Quality Assurance experience Experience in pharmaceutical,

Easy Apply

Contract

Technical Writer - GmP /Manufacturing procedures

Norwood, Massachusetts

•

10d ago

Technical Writer - GmP /Manufacturing procedures RANDSTAD / Moderna staffing SOW Contract Norwood, MA Day-to-day activities include but are not limited to the following: -Support the Facilities & Utilities and onsite quality and regulatory groups to define and address all issues of non-compliance. -Write, Revise, and Implement SOPs for utility and facility systems -Work with in house Moderna SMEs on protocol and trainings -Additional duties as needed and as directed

Easy Apply

Contract, Third Party

55 - 60

Associate Director of IT Operations (GMP IT/OT)

Troy, New York

•

Today

The Associate Director of IT Operations (GMP IT/OT) ensures the reliable operation, delivery, and management of IT/Operational Technology (IT/OT) infrastructure and services, with a focus on supporting a highly regulated GxP environment. This role provides strategic direction, operational management, and administrative oversight for the daily IT operational activities, including hardware, communications & WiFi infrastructure, and service delivery. The position also ensures integration and alignm

Full-time

USD 126,300.00 - 241,200.00 per year

Automating Quality Control (QC) testing

Independence Township, New Jersey

•

5d ago

We are seeking an experienced contractor to support the development, qualification, and implementation of automated QC methods for cell therapy assays. This hands-on role will focus on designing, programming, and optimizing automation scripts and workflows for platforms such as Hamilton and Tecan, ensuring seamless technical transfer and compliance within a GMP environment. The successful candidate will collaborate with QC, analytical development, and automation teams to drive continuous improve

Easy Apply

Contract, Third Party

50 - 60

Automation Manufacturing Engineer

Columbus, Ohio

•

12d ago

Job Summary: - Serve as an Automation Manufacturing Engineer supporting commercial manufacturing and packaging operations - Troubleshoot and resolve high-level automation and vision system issues on the production lines - Collaborate closely with the maintenance crew to support automated equipment - Work with Siemens, Allen Bradley, and B&R control systems - Ensure compliance with GMP (Good Manufacturing Practice) standards for both equipment and processes - Support pharmaceutical manufa

Easy Apply

Contract, Third Party

$60 - $62

GxP Systems Engineer

Norwood, Massachusetts

•

5d ago

Job Title: GxP Systems Engineer Location: Norwood & Marlborough, MA Job Function: Digital (GxP Digital Quality Systems) The Role Client is seeking a GxP Systems Engineer, who will be responsible for the design, deployment and management of our expanding portfolio of first-in-kind automation and digital enterprise instrumentation systems that support the Quality Control GMP laboratories and system integration with our connected Digital platforms. This role will be a member of the Digital Quality

Easy Apply

Contract

$65 - $70

Validation Engineer / CQV Engineer

Cincinnati, Ohio

•

2d ago

Job Summary: - Support validation and commissioning/qualification/validation (CQV) activities onsite for sterile manufacturing and fill/finish operations. - Execute hands-on OQ/PQ (Operational/Performance Qualification) protocols and equipment qualification in a GMP-regulated environment. - Prepare and manage GMP documentation, including protocol execution, discrepancy/deviation resolution, and qualification deliverables. - Work independently and efficiently in a fast-paced, project-driven

Easy Apply

Third Party, Contract

$50 - $60

DeltaV Automation

Muskegon, Michigan

•

2d ago

Role requires a senior level automation engineer comfortable operating independently while supporting others. No CSV authorship responsibility: CSV activities are supported indirectly through automation execution and issue resolution. DeltaV DCS automation experience in pharmaceutical / biopharma manufacturing Strong troubleshooting and problem solving skills in live manufacturing environments, including commissioning, issue triage, and rapid resolution under GMP constraints Deep understandi

Easy Apply

Contract

70 - 80

Engineering Technician B7 II

Evansville, Indiana

•

4d ago

Arthur Lawrence is looking for an Engineering Technician B7 II one of our clients in Evansville, IN. Please find the job description below and send us your updated resume if interested: Must-Have Skills: 5+ years of pharmaceutical industry experience Strong understanding of validation/qualification processes and regulatory compliance requirementsBachelor s degree in Science, Engineering, or a related discipline Nice to Have Skills: 5+ years of validation and qualification experience Familiarity

Easy Apply

Contract

$40+

Senior Automation Engineer

Muskegon, Michigan

•

2d ago

Amtex SystemsInc is an information technology and talent solutions company offering talent and BI consulting to the companies in US for over 25 years. Our solutions are designed to fill resource gaps, by providing the right candidates who deliver value to the organization. Our propensity to nurture and build strong relationships with our clients helps us better understand their business demands and gives us the ability to provide services that are on time and rise above the rest. Senior Automati

Easy Apply

Third Party, Contract

Depends on Experience

Validation Engineer/Technician with CSV / CQV Focus

Worcester, Massachusetts

•

2d ago

Arthur Lawrence is looking for a Validation Engineer/Technician with CSV / CQV Focus one of our clients in Worcester, MA. Please find the job description below and send us your updated resume if interested: Must-Have Skills: Experience in validation, calibration, or CQV within a pharmaceutical or regulated environment Strong knowledge of GMP and 21 CFR Part 11 compliance, including CSV (Computerized System Validation) Hands-on experience with equipment qualification (IQ/OQ/PQ), process validati

Easy Apply

Contract

$40+

Desktop Engineer/ Support

Cambridge, Massachusetts

•

Today

Location - Cambridge,MA / Danvers,MA - Candidate should be flexible to work at either location. Max vendor rate is /hr 5 days/week fully onsite Desktop Engineer Technician Skillset Required : Experience in supporting overall manufacturing / lab IT systems and IT devices. Familiarity with manufacturing, lab and Data Center IT equipment Includes but is not limited to scanners, printers (Zebra, etc..), tablets, PCs attached to specialized test equipment, PCs used on the manufacturing line, etc..

Easy Apply

Contract

Sanitation Technician

Carrollton, Texas

•

Today

Sazerac Company Overview: Our company is a leader in maintaining the highest standards of cleanliness and safety across our facilities and operations. We prioritize environmental sustainability, health, and hygiene to ensure a safe and healthy environment for our employees, customers, and community.As a Sanitation Technician, you will play a vital role in supporting our mission by ensuring that all work areas, equipment, and surfaces are clean, sanitized, and compliant with industry regulations.

Full-time

Senior DeltaV Automation Engineer - Only W2

Remote or Muskegon, Michigan

•

Today

Role: Senior DeltaV Automation Engineer Location: Muskegon, MI (Onsite) Job Type: Contract (W2) Years of Experience: 12 years required Skill Matrix: Name Required LS Yes Emerson Delta V Yes Role requires a senior level automation engineer comfortable operating independently while supporting others. No CSV authorship responsibility: CSV activities are supported indirectly through automation execution and issue resolution. DeltaV DCS automation experience in pharmaceutical / biopharma manufacturi

Easy Apply

Contract

Senior MES Computer System Validation (CSV) Consultant - Concord, NC (Onsite)

Concord, North Carolina

•

11d ago

Position Title: Senior Computer System Validation (CSV) Consultant Location: Concord, NC (Onsite) Duration: 12 Months Job Summary Experienced Senior Computer System Validation (CSV) Consultant to support validation and compliance activities for MES and other GMP-regulated systems within the pharmaceutical/life sciences environment. The ideal candidate should possess strong expertise in Computer System Validation (CSV), IT Governance, and Compliance, with hands-on experience validating manufactu

Easy Apply

Contract, Third Party

Depends on Experience

Production Operator (Manufacturing)

El Segundo, California

•

3d ago

Production Operator El Segundo, CA (Onsite) Contract - NO 3RD PARTY RESUMES ALLOWED OVERVIEW The Commercialization team within the Company is dedicated to creating food products that are leading the gold standard. They are looking for an outstanding individual to join the team located at the Pilot Plant in El Segundo, CA as a Production Operator. As a Production Operator, you will play a key supporting role in the production and packaging process of delicious products. You will handle and moni

Easy Apply

Contract

20 - 22

Senior Design Verification Lead

Lebanon, Indiana

•

11d ago

Hello , My name isCharles PowellandI am a staffing Specialist atVoto Consulting LLC. I am reaching out to you on an exciting job opportunity with one of our clients. Job Title : Senior Design Verification Lead Drug Substance Manufacturing (New Site Build) Duration : 2 Year Contract Location : Onsite in Lebanon, IN Interview : 2 Virtual Interviews ( relocation candidates are okay) Preferred Pharma and Site Expansion experience Update : Heavy P&ID experience, work on P&ID design reviews, revi

Easy Apply

Contract

75+

Filter Results

Job post features

Posted date

Work settings

Employment type

Distance

Employer type

Work authorization