GMP jobs in Florida

QC/GMP Bloodborne Manufacturing (ONSITE)

Pompano Beach, Florida

•

Today

Please note that this is a 1-year contract position. Qualifications: A Bachelor's degree in Medical Technology, Biology, Chemistry or a related field of study and a minimum of 1-3 years experience with QC, GMP, and analytical procedures is required.Experience with analytical instrumentation such as AutoVue and ProVue is preferred. Familiarity with the guidelines and regulations of FDA, OSHA, ISO and cGMP is preferred.Manual dexterity to handle instruments, complete repetitive motions, and stand

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Contract

Depends on Experience

Project Manager - Gxp

Remote

•

Today

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

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Contract

Depends on Experience

Manufacturing Engineer (Sarasota, FL)

Sarasota, Florida

•

Yesterday

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

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Contract

Depends on Experience

Raw Materials Technical Specialist

Remote or Hybrid in Cambridge, Massachusetts

•

4d ago

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

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Contract

$38 - $40 hr

Manufacturing Engineer Medical Devices (CNC Machining Focus)

Gainesville, Florida

•

Today

Title: Manufacturing Engineer Medical Devices (CNC Machining Focus) Location: Gainesville, FL (On-site) Duration: Long Term Contract Position Summary: We are looking for an experienced Manufacturing Engineer with a strong background in CNC machining for precision medical device components. The candidate will be responsible for developing, optimizing, and validating CNC machining processes to meet stringent quality and regulatory requirements. Key Responsibilities: Develop, program, and optimize

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Contract

Depends on Experience

Manufacturing Engineer Medical Devices (Compression Molding Focus)

Gainesville, Florida

•

Today

Title: Manufacturing Engineer Medical Devices (Compression Molding Focus) Location: Gainesville, FL (On-site) Duration: Long Term Contract Position Summary: Our client is seeking a Manufacturing Engineer with expertise in compression molding processes for the production of high-quality medical device components. The ideal candidate will drive process development, optimization, and validation activities to ensure compliance with medical industry standards. Key Responsibilities: Develop and optimi

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Contract

Depends on Experience

Manufacturing Engineer Medical Devices (IQ/OQ/PQ Focus)

Gainesville, Florida

•

Today

Title: Manufacturing Engineer Medical Devices (IQ/OQ/PQ Focus) Location: Gainesville, FL (On-site) Duration: Long Term Contract Position Summary: Our client is seeking a highly skilled Manufacturing Engineer with a strong background in the medical device industry and extensive experience in IQ/OQ/PQ validation activities. The successful candidate will ensure that manufacturing processes meet regulatory requirements, improve efficiency, and maintain the highest quality standards. Key Responsibili

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Contract

Depends on Experience

Senior Commissioning, Qualification & Validation (CQV) Engineer

Remote or Athens, Georgia

•

Today

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn m

Full-time

Field Service Engineer II (LCMS) (REMOTE - NYC, NJ, PA)

Remote or New York, New York

•

Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description When you join us at Thermo Fisher Scientific, you'll be part of an inquisitive team that shares your passion for exploration and discovery. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to

Full-time

USD 34.61 - 51.92 per hour

Staff Software Engineer, Manufacturing Engineering

Remote or Atlanta, Georgia

•

Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description About Us: At Thermo Fisher Scientific, our mission is to enable our customers to make the world healthier, cleaner, and safer. We are revolutionizing the manufacturing industry with brand new technology and innovative solutio

Full-time

Manufacturing Engineer

Gainesville, Florida

•

Today

Position: Manufacturing Engineer Location: Gainesville, FL (Onsite) Job Type: Contract/FTE Required Qualification & Skills: Bachelor s or master s degree in mechanical engineering, Biomedical Engineering, or related field.5+ years of experience in medical device manufacturing, with hands-on experience in CNC Machining and DCM.Strong understanding of FDA, ISO 13485, and GMP requirements.Proficiency in statistical analysis tools (e.g., Minitab, JMP).Experience with QMS systems and documentation pr

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Full-time

Depends on Experience

Sr Automation Engineer III

Remote or Foster City, California

•

Today

At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead's team plays a critical ro

Full-time

USD 182,070.00 - 235,620.00 per year

Mechanical Engineer II

Remote or Lawrence, Massachusetts

•

Today

PURPOSE AND SCOPE: The Mechanical Engineer II will play a key role in improving our Home HD products and our patients' lives. This individual will apply sound engineering principles in the support of our current product portfolio and will be involved in different parts of a product's life, including but not limited to the feasibility evaluation for new features and products to improve the quality, performance, and cost of dialysis therapy. You will be part of a team with responsibility for suppo

Full-time

Senior Electrical Engineer

Remote or Cincinnati, Ohio

•

Today

Full-time

Senior Director IT Quality Assurance & Compliance

Remote or Sleepy Hollow, New York

•

Today

As a Senior Director of IT, Quality Assurance and Compliance, you will lead a team of those managing 20 to 30 members The focus is to provide leadership, coaching, and technical support to the IT QA & Compliance Management Team. This role is an on-site position 4 days/week at our Sleepy Hollow, NY or Warren, NJ office. There will be occasional travel to other sites in the Rensselaer, NY area. If eligible, we can offer relocation benefits. We are unable to offer a fully remote option. A typical

Full-time

USD 212,900.00 - 354,800.00 per year

Process Engineer

Remote or New York

•

Today

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.

Full-time

Sr. Manager FSQ Center of Plate (COP) (Hybrid: Onsite and Remote Work)

Remote or Rosemont, Illinois

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Today

This position has been segmented as Hybrid meaning there is a combination of three onsite days per week and the rest remote. Responsibilities:FSQA lead and subject matter expert of assigned product categories for the Company's Product Data Management and Specification System and be a primary driver of continuous improvement to the system.Supports the management of the private label customer feedback systemManages investigations regarding product safety and quality.Collaborates with suppliers to

Full-time

Validation Engineer

Sarasota, Florida

•

Today

Job Description: Protocol Review & Compliance: Study and assess Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols and reports for regulatory and procedural compliance. Process Audits & Documentation: Conduct thorough audits of manufacturing processes to identify documentation gaps. Update Quality Management System (QMS) documents to reflect findings and ensure alignment with current standards. Process Optimization: Design and execute De

Full-time

Bioinformatics Software Architect

Remote or Indiana

•

Today

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job Description Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies

Full-time

Biomedical Engineer

Remote or West Chester, Pennsylvania

•

Today

Full-time

USD 61,000.00 - 98,000.00 per year

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GMP jobs in Florida, USA