gmp Jobs

1 - 20 of 278 Jobs

Senior Scientist - Microbiology - GMPJob Title - Senior Scientist - Microbiology - GMP

Thermo Fisher ScientificCompany Name - Thermo Fisher Scientific

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Middleton, Wisconsin, USA

Full-time

Job Description Job Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ count

GMP Business AnalystJob Title - GMP Business Analyst

Softworld, Inc.Company Name - Softworld, Inc.

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Billerica, Massachusetts, USA

Contract

Job Title: GMP Business Analyst Job Location: Billerica MA 01821 Remote Onsite Requirements: SAP Plant Maintenance At least 5 years of experience working with SAP in a BA / Functional Experience supporting or working with Quality, Regulatory, and manufacturing organizations, preferably in the medical device, or any other regulatory controlled industry. Job Description: Global Equipment Management Quality Engineering requires a dedicated resource to work with the Business Lead to finalize dev

Supply Chain Specialist (GMP warehouse, 3PL, ERP, clinical, pharmaceutical ) - Santa Monica, CaliforniaJob Title - Supply Chain Specialist (GMP warehouse, 3PL, ERP, clinical, pharmaceutical ) - Santa Monica, California

Cube Hub, Inc.Company Name - Cube Hub, Inc.

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California, USA

Contract, Third Party

Supply Chain Specialist (GMP warehouse, 3PL, ERP, clinical, pharmaceutical ) Location: Santa Monica, California This is onsite from Day 1 Job Duration: 12 months Description: client is seeking a highly motivated individual with warehouse and related supply chain experience in the biotechnology/pharmaceutical industry. The Specialist will support client goal in commercializing innovative T cell therapy for cancer treatments. This role requires operational support to the Associate Director of S

Associate Validation Analyst II (GMP Labs)- Middleton, WI HybridJob Title - Associate Validation Analyst II (GMP Labs)- Middleton, WI Hybrid

Thermo Fisher ScientificCompany Name - Thermo Fisher Scientific

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Middleton, Wisconsin, USA

Full-time

Job Description At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing

GMP/ cGMP Filtration Manufacturing Operator (ONSITE)Job Title - GMP/ cGMP Filtration Manufacturing Operator (ONSITE)

NetSource, Inc.Company Name - NetSource, Inc.

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Raritan, New Jersey, USA

Contract

Please note that this is a 1 year contract position. Must be able to work Monday Friday, 6am to 2:30pm. Must be able to work overtime as required. Qualifications: A high school diploma or equivalent is Required. Prior Experience in a manufacturing environment is Preferred. Ability to prioritize multiple tasks and meet timelines. Knowledge of aseptic technique. Mathematical and mechanical aptitude. Ability to work in a fast-paced environment. Attention to detail, document tasks accurately and nea

Technical Writer V with FDA and GMP - HYBRIDJob Title - Technical Writer V with FDA and GMP - HYBRID

DivIHN Integration Inc.Company Name - DivIHN Integration Inc.

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Durham, North Carolina, 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

NetSuite Admin- GMPJob Title - NetSuite Admin- GMP

Anveta IncCompany Name - Anveta Inc

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Remote

Contract, Third Party

Our client which is a Pharmaceutical Firm is urgently looking to hire Senior Net Suite Admin ". (GMP Experience) Senior Net Suite Admin (GMP Experience) Location - Cranbury, NJ Long Term Project. 100 % Remote is fine (No PST Candidates). This will become RTH role after 6 12 months. Pharmaceutical Experience and GMP experience is required. Candidate need to fill the attached Self-Assessment GMP. Job Description The Sr. Net Suite Admin leads the administration, design, implementation, and support

GMP QAJob Title - GMP QA

Multivision Inc-ILCompany Name - Multivision Inc-IL

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Remote

Contract, Third Party

This is Non IT requirement - need resource from Manufacturing Sector QA External Manager Consultant with CDMO & Audit experience Position Location: Total remote position but would need site travel for Audits. Their current CDMO facilities are based out of Texas, New Jersey, Florida and Germany. Position Duration: To start with duration is from May 2024 for 12 months and subject to extension Interview process: Only 2 stage interview process with client and asap placement Reporting to: Will be rep

QC AssociateJob Title - QC Associate

SynkriomCompany Name - Synkriom

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Devens, Massachusetts, USA

Contract

Job Title: QC Associate Location: Devens, MA Duration: 6+ Months Contract Education and Experience Required: *BS with minimum of 1 year of experience in a GMP QC lab is required (or equivalent experience in a related biopharmaceutical GLP or GMP lab environment). *Strong technical lab skills using pipettes, analytical balances, pH meter, etc. is a must. Thanks & Regards Minhaj Uddin | Sr. US IT Recruiter | Synkriom | Contact:

Google Analytics Integration EngineerJob Title - Google Analytics Integration Engineer

InfoVision, Inc.Company Name - InfoVision, Inc.

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Ashburn, Virginia, USA

Third Party, Contract

Role: Google Analytics Integration Engineer Location: Ashburn, VA (2 days/week go to office ) Duration: 12+ Months Required skills: Google Analytics integration engineer with strong knowledge on following areas 1) GA4 2)Google search console 3) DV360 4) SA360 5) Google ADS 5) Campaign manager Integrate above GMP services to Google BQ Identify the effectiveness of the campaigns Link the anonymous prospects to internal prospect store If you are interested, please send me your updated resume alon

Quality Assurance TechnicianJob Title - Quality Assurance Technician

Opusing LLCCompany Name - Opusing LLC

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Tempe, Arizona, USA

Contract

Title: Quality Assurance Technician Location: Tempe, AZ Duration: 12 Months Contract Position Summary: This position is Technician for Field Assurance (FA) that will be responsible for maintaining the day-to-day activities in the Field Assurance (Complaint Handling) Lab. The associate will be responsible for contributing to the completion of complaint returned sample analysis in a timely manner. Familiarity with equipment, microscopes, biosafety laboratory practices, good laboratory practices i

Project ManagerJob Title - Project Manager

AgreeYa SolutionsCompany Name - AgreeYa Solutions

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New Albany, Ohio, USA

Contract

Job Title: Project Manager Senior Location: New Albany OH Ideal candidate: supporting process development. needs to have a biotech, med device, pharmaceuticals wants them to bring 5 years of experience.Experience with GMP environmentCandidate should showcase they have executed projects took ownership full lifecycle. Ideally smart sheets, MS Project, or other PM tools.This role serves as project manager for Final Drug Product New Process Introductions (NPI) into New Alabny OH.

Documentation SpecialistJob Title - Documentation Specialist

Talent GroupCompany Name - Talent Group

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Marlborough, Massachusetts, USA

Contract

Bachelor s degree OR a high school education and a minimum of 3 years experience in a GMP controlled environment.Coordinate the control of Quality Management System (QMS) and GMP critical documentation.Manage document reviews and approvals efficiently.Maintain accurate records of document status, change controls, reviews, and approvals.Ensure documents comply with established templates and standards.Verify accurate and traceable document cross-references.Organize and maintain the electronic docu

Senior ScientistJob Title - Senior Scientist

Cynet SystemsCompany Name - Cynet Systems

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Saint Paul, Minnesota, USA

Contract, Third Party

We are looking for Senior Scientist for our client in Saint Paul, MN Job Title: Senior Scientist Job Location: Saint Paul, MN Job Type: Contract Job Description: Responsibilities: The Contingent Scientist I will work within a team focused on the chemical characterization of medical devices in a highly regulated environment.The position will report to a chemistry supervisor or manager.The position is a hands-on and laboratory focused, entailing all aspects of chemical characterization from s

Verification Lead EngineerJob Title - Verification Lead Engineer

Talent GroupCompany Name - Talent Group

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Marlborough, Massachusetts, USA

Contract

Job Description: The Automation Verification Lead Engineer is responsible for requirement s analysis, test analysis, automated test procedure, test execution and maintenance of automation frameworks. You will work with the Product Care (sustaining engineering) cross-functional teams and lead testers to verify and validate software and automation hardware based on system/component user requirements and functional specifications.Responsibilities: Responsible for verification strategy, infrastruc

Calibration TechnicianJob Title - Calibration Technician

Diversity NexusCompany Name - Diversity Nexus

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Warren, New Jersey, USA

Contract

Job Title: Calibration Technician Job Location: Warren(need local candidates only) Job Duration: 12 months Employment Type: w2 hourly Advanced level (5+Yrs.)- experienceJob Description: 100% onsiteJob Responsibilities: To support manufacturing and laboratory operations calibration program in a timely manner and take preventive measures to assure proper functioning of operational equipment ensuring compliance with Company standards and regulatory requirements. This position must comply with all

Nestle Tollhouse Production OperatorJob Title - Nestle Tollhouse Production Operator

Nestle USACompany Name - Nestle USA

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Burlington, Wisconsin, USA

Full-time

Foods people love. Brands people trust. And a career that nourishes your future like no other. If you're driven by the passion to do something meaningful that changes lives, Nestl is the place for you. Nestl USA is one of seven operating companies that make up Nestl's presence in the United States. We're in 97% of American homes, and as the leading food and beverage company, our goals are to continue to deliver quality food and beverage products, strengthen our local communities, and reduce our

Manufacturing EngineerJob Title - Manufacturing Engineer

Kasmo Inc.Company Name - Kasmo Inc.

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Philadelphia, Pennsylvania, USA

Contract

Responsibilities: Provide quality engineering support for new and existing medical devices, ensuring adherence to all applicable quality system regulations.Conduct non-conformance investigations, including root cause analysis, documentation, and approval of material dispositions. Take prompt corrective actions to address quality concerns.Validate manufacturing processes, including equipment qualification and test method validations.Collaborate with manufacturing engineering to implement process

Technical WriterJob Title - Technical Writer

Collabera LLCCompany Name - Collabera LLC

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New Albany, Ohio, USA

Contract

About the Role We are seeking a candidate with an educational background in Science and/or Engineering to join our team in a technical documentation role within the GMP pharma and/or biotechnology industry The ideal candidate will have experience working with KNEAT CDOCs and be proficient in editing documentation while adhering to corporate policies and templates. Responsibilities: Develop, review, and update technical content such as SOPs, WIs, risk assessments, protocols, and reports for the

Construction Manager (Owner's Rep)Job Title - Construction Manager (Owner's Rep)

Oxford Global ResourcesCompany Name - Oxford Global Resources

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Raleigh, North Carolina, USA

Contract

Title: Construction Manager (Owner s Rep) Food&Bev Client Location: Raleigh NC (onsite, Locals only as there are no expenses nor PD offered) Length of Contract: 6 months (May-Oct) Pay Rate: $45-65/hr w2. Background/History: 10 yrs Experience, Brownfield, GMP, cGMP, Owner s Rep, Construction Management, New Equipment, Equipment Upgrades, layout changes, Process