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Deviation Management Specialist

Zachary Piper Solutions, LLC

•

Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a Deviation Management Specialist to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities for the Deviation Management Specialist Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. Write quality incident and deviation reports, ensuring thoro
Posted 2 days ago | Updated 5 hours ago

Maintenance Technician - 1st Shift

ABR Employment Services

•

Ripon, Wisconsin, USA

Full-time

ABR Employment Services is recruiting for a 1st Shift Maintenance Technician for a client company in Ripon, WI. About the Role: Join a stable and growing food manufacturing company as a Maintenance Technician on 1st shift. In this role, you'll handle preventative maintenance, troubleshooting, and repairs on production and facility equipment. Your work will help ensure smooth operations, food safety, and equipment reliability. We're looking for someone mechanically inclined with experience in a
Posted 19 days ago | Updated 1 hour ago

Validation Engineer

Zachary Piper Solutions, LLC

•

Lynwood, California, USA

Full-time

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Lynwood, California. Responsibilities for the Validation Engineer Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.Coordinate validation efforts across shifts, pr
Posted 2 days ago | Updated 5 hours ago

CMMS Data Specialist

Cushman & Wakefield

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Boston, Massachusetts, USA

Full-time

Job Title CMMS Data Specialist Job Description Summary The role involves managing asset-related data within the Computerized Maintenance Management System (CMMS) to support operational readiness at all Vertex sites, including labs and facilities. Key responsibilities include submitting electronic change requests for asset maintenance, calibration, and spare parts, as well as tracking the progress and activation of CMMS attributes. The position requires ensuring accurate asset information input,
Posted 20 days ago | Updated 7 hours ago

Process Validation Engineer

Tranzeal, Inc.

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Tucson, Arizona, USA

Contract

Role: Process Validation EngineerLocation: Tucson, AZ Description:We are seeking a highly motivated and detail-oriented Process Validation Engineer with 1-3 years of experience to join our team. The Process Validation Engineer will be responsible for developing and executing process validation and/or process verification protocols and reports to ensure that manufacturing processes are compliant with regulatory requirements and company standards. This role involves collaborating with cross-functi
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Posted 8 days ago

Virology Deviation Management Consultant

Zachary Piper Solutions, LLC

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Lansdale, Pennsylvania, USA

Full-time

Piper Companies is seeking a Deviation Management Consultant to fill an opportunity with a reputable Pharmaceutical company in Lansdale, PA. Responsibilities: Investigate deviations by assessing product impact, identifying root causes, and implementing corrective/preventative actions. Author and update GMP documentation, including SOPs, batch records, validation documents, and change controls. Write quality incident and deviation reports, ensuring thorough analysis and compliance. Collabor
Posted 9 days ago | Updated 5 hours ago

Virology Deviation Management Specialist

Zachary Piper Solutions, LLC

•

West Point, Pennsylvania, USA

Full-time

Piper Companies is looking for a Virology Deviation Management Specialist for a leading pharmaceutical manufacturer in West Point, PA. Responsibilities: Conduct deviation management supporting a Virology quality control team Conduct technical writing of deviation investigation results and initiate CAPAs Fully support all aspects of assigned projects and run the business activities, including but not limited to: participate in decision making, leading laboratory investigations, issue ident
Posted 9 days ago | Updated 5 hours ago

Cleaning Validation Engineer

Zachary Piper Solutions, LLC

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Holly Springs, North Carolina, USA

Full-time

Piper Companies is seeking a Cleaning Validation Engineer to join a growing leader in the pharmaceutical/biotechnology space for an onsite position in Holly Springs, North Carolina (NC) . The Cleaning Validation Engineer will play a critical role in the development, implementation, and maintenance of cleaning validation processes for our new manufacturing facility. This position requires a thorough understanding of cleaning validation principles, regulatory requirements, and industry best prac
Posted 5 days ago | Updated 5 hours ago

Validation Area Specialist

Zachary Piper Solutions, LLC

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Clayton, North Carolina, USA

Full-time

Piper Companies is seeking a Validation Area Specialist to join a growing leader in the pharmaceutical/biotechnology space for an onsite position in Clayton, North Carolina (NC). The Validation Area Specialist will ensure quality and compliance in biotech processes by conducting validations, managing documentation, and leading technical investigations while collaborating across departments. Responsibilities of the Validation Area Specialist include: Execute and review validation processes (IQ/
Posted 5 days ago | Updated 5 hours ago

Manufacturing Associate

Zachary Piper Solutions, LLC

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Durham, North Carolina, USA

Full-time

Piper Companies is seeking a Manufacturing Associate for an onsite contract position in Durham, North Carolina (NC). The Manufacturing Associate will be responsible for overseeing the creation and management of batch records to ensure the efficient operation of equipment and processes as well as supporting regular manufacturing operations and scaling of cGMP manufacturing. Responsibilities of the Manufacturing Associate include: Full GMP training program with classroom and hands-on shadowing w
Posted 5 days ago | Updated 5 hours ago

Cleaning Validation Engineer

Zachary Piper Solutions, LLC

•

Holly Springs, North Carolina, USA

Full-time

Piper Companies is looking for a Cleaning Validation Engineer that will play a critical role in the development, implementation, and maintenance of cleaning validation processes for a brand new manufacturing facility. This position requires a thorough understanding of cleaning validation principles, regulatory requirements, and industry best practices. The successful candidate will ensure that all cleaning procedures are validated and compliant with GMP standards. Responsibilities of the Cleani
Posted 5 days ago | Updated 5 hours ago

Senior CQV Engineer

Zachary Piper Solutions, LLC

•

Raleigh, North Carolina, USA

Full-time

Piper Companies is actively seeking a Senior CQV (Commissioning, Qualification, and Validation) Engineer to join our team. The ideal candidate will have 7-10 years of CQV experience with large-scale process equipment, including upstream, downstream, and CIP (Clean-In-Place) systems. This role is critical to ensuring the successful commissioning and validation of our biopharmaceutical manufacturing processes. This is a Monday - Friday, traditional hours role located in the greater Raleigh, NC are
Posted 5 days ago | Updated 5 hours ago

Facilities Suite & Elastomer Maintenance Mechanic

Shimento, Inc.

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Portsmouth, New Hampshire, USA

Contract

Title: Facilities Suite & Elastomer Maintenance Mechanic II - Location: 101 International Drive Portsmouth NH USA 03801 Long Term Onsite Position Description: Performs advanced maintenance and troubleshooting on direct and indirect manufacturing equipment and elastomer systems, with minimal supervision, in compliance with GMP, SOPs, and safety protocols.Executes preventive maintenance for Suite & Elastomer systems and supports complex repairs to maintain optimal equipment performance.Documents
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Posted 5 days ago | Updated 1 hour ago

Validation Engineer

Zachary Piper Solutions, LLC

•

Copiague, New York, USA

Full-time

Piper Companies is currently seeking an experienced Validation Engineer tosupport a highly reputable Pharmaceutical company in Copiague, NY. Responsibilities for the Validation Engineer Oversee validation activities, including risk analysis, packaging, cleaning, and equipment qualification for new and updated processes.Develop, review, and execute validation protocols, reports, and documentation while ensuring compliance with GMP standards.Coordinate validation efforts across shifts, providing
Posted 2 days ago | Updated 5 hours ago

QC Technician II (Micro)

Zachary Piper Solutions, LLC

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Columbia, Maryland, USA

Full-time

Piper Health & Sciences is seeking a QC Technician II to support the quality control microbiology department of a growing biotechnology company in the Columbia, MD area. This role is first shift, Monday - Friday working schedule. Responsibilities for the QC Technician II include: Perform routine and in-process environmental monitoring (EM) sampling in a cleanroom environment. Conduct and monitor environmental parameters including viable sampling, personnel sampling, temperatures, humidity, etc.
Posted 5 days ago | Updated 5 hours ago

GMP Process Engineer (Hybrid)

NetSource, Inc.

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Wilson, North Carolina, USA

Contract

Please note that this is a 8-month contract. Candidate will need to be in commutable distance to Wilson, NCRole will initially be remote until the Wilson, NC building opens then they will be required to be onsiteRequirements: - Must have a Bachelor's degree - At least 2 years of experience - Experience in Biologics, Manufacturing, or Engineering - Less focus on "large capital construction systems" - Must have Delta Vee system knowledge - Must have Upstream and/or Downstream experience Top 3 Ski
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Posted 23 days ago | Updated moments ago

Document Control Associate

Aditi Consulting

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Manassas, Virginia, USA

Contract

Payrate: $30.00 - $32.00/hr. Summary: The creation and maintenance of the Quality System documentation. Communicate any deviations to management. Assist the Quality Assurance team with special projects as required. Comply with SQF, Food Safety Plan (HACCP), Food Quality Plan (FQP) standards. Job Duties: Create, revise, and maintain all documentation related to the Quality System using technical writing best practices, ensuring proper formatting, numbering, and document control. Issue batch recor
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Posted 7 days ago | Updated 1 day ago

Manufacturing Tech 1, Service - Night Shift (B)

bioMerieux

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Durham, North Carolina, USA

Full-time

Benefits at bioMerieux: Low-cost medical, dental, and vision benefits starting day one. 11 paid holidays 160 hours of paid time off Annual bonus 9.5% 401k company contribution with no vesting period Tuition reimbursement up to $10,000 per calendar year Onsite cafeteria with daily food stipend Position Summary & Responsibilities: Normal working hours: 7:00pm - 7:30am working a 2-2-3 rotation schedule. The anticipated hiring range for this role is $19.25 - 20.00/hr with shift differential and an
Posted 5 days ago | Updated 5 hours ago

Analytical Validation Engineer

Zachary Piper Solutions, LLC

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Hopewell Township, New Jersey, USA

Full-time

Piper Companies is looking for an Analytical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Titusville, NJ area. Responsibilities for the Analytical Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Must be familiar and have experience with laboratory instrument selection, installation (IQ/OQ) and qualification (PQ) Experience supporting laboratory investigations from beginning to end, includ
Posted 5 days ago | Updated 5 hours ago

Manufacturing Engineer-Medical Device

Trelleborg Group

•

Paso Robles, California, USA

Full-time

Join Our Team at Trelleborg Medical Solutions! Imagine working for one of the world's leading contract medical device manufacturers, nestled just 30 miles from California's stunning Central Coast. At Trelleborg Medical Solutions, we are not just a premier manufacturer of life-saving medical components; we are a forward-thinking company committed to excellence and innovation. Our journey in lean manufacturing has been ongoing for years, and we are on the path to becoming a showcase of excellence
Posted 8 days ago | Updated 6 hours ago