61 - 80 of 340 Jobs

Process Validation Engineer

Tranzeal, Inc.

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

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

Cleaning Validation Engineer

Zachary Piper Solutions, LLC

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

Manufacturing Associate

Zachary Piper Solutions, LLC

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

Validation Area Specialist

Zachary Piper Solutions, LLC

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/

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

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

Facilities Suite & Elastomer Maintenance Mechanic

Shimento, Inc.

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

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

QC Technician II (Micro)

Zachary Piper Solutions, LLC

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.

GMP Process Engineer (Hybrid)

NetSource, Inc.

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

Document Control Associate

Aditi Consulting

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

Analytical Validation Engineer

Zachary Piper Solutions, LLC

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

Engineering - Bio Process Associate - 1st Shift , Devens MA

Futran Solutions

Massachusetts, USA

Contract

Job Description: Bio Process Associate 1st Shift--hours are 7AM - 3PM Monday - Friday. Onsite, Devens--Local candidates Only **Note there are 3 openings on this req** Description: The Bioprocess Associate uses current Good Manufacturing Practices (cGMPs) in the execution of commercial manufacturing processes for the manufacture of therapeutic proteins used in medicines that are revolutionizing the treatment of serious disease. Job Responsibilities: Operate production equipment within an assign

Quality Control Supervisor

Zachary Piper Solutions, LLC

Frederick, Maryland, USA

Full-time

Piper Companies is currently looking for an experienced Quality Control Supervisor in Frederick, MD in a hybrid role. Responsibilities for the Quality Control Supervisor include: Participate in and complete analytical testing in support of release and characterization of genetically-engineered cell therapy products, with a focus on cell-based, PCR, flow cytometry, and ELISA assays Maintain team responsible for laboratory inventory of materials and reagents Environmental monitoring Execute p

Scientific - Assistant Scientist

Futran Solutions

Seattle, Washington, USA

Full-time

Job Description: Job Title: Assistant Scientist Location: Seattle, WA*Onsite Schedule: M-F normal business hours Top Skills: Associate Degree in Biology, Chemical Engineering, Bioengineering or relevant scientific discipline with 0-2 years of industry bioprocess experience. Mammalian cell culture and cell banking experience Experience with cell therapy process development or manufacturing Job scope or job description: The Global Manufacturing Sciences team plays a key role in supporting activ

Commissioning Qualification Validation Engineer

Zachary Piper Solutions, LLC

Durham, North Carolina, USA

Full-time

Piper Companies is currently looking for an experienced Commissioning Qualification Validation Engineer (CQV) in Raritan, New Jersey (NJ) to work for an innovative and growing pharmaceutical manufacturer. Responsibilities for the Commissioning Qualification Validation Engineer (CQV) include: Commissioning: Lead commissioning activities for new laboratory equipment, systems, and facilities, ensuring they are installed and function as intended. Qualification: Develop, execute, and document qualif

Validation Engineer

Zachary Piper Solutions, LLC

Lynwood, California, USA

Full-time

Piper Companies is looking for a Pharmaceutical Validation Engineer to support commissioning and decommissioning activities for a major pharmaceutical company in the Los Angeles County area. Responsibilities for the Validation Engineer include: Experience in Pharmaceutical Laboratory Operations Proficiency with cleaning validation as this is a multi-product production space Must be familiar and have experience with laboratory and manufacturing instrument selection, installation (IQ/OQ) and qua

CSV CONSULTANT :: Remote

TESTINGXPERTS, INC. DBA DAMCOSOFT

New Jersey, USA

Third Party, Contract

Mandatory Skills CSV, Compliance and Assurance services, LIFE-SCIENCES (GXP FDA CSV IQ/OQ/PQ), Veeva, Argus, Defect Tracking Tools_JIRA Primary Skill- Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management Secondary Skill- JIRA Veeva Argus Agile and Waterfall methodology Jo Description: Strong experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems P

Line Controller - 2nd Shift

E. A. Sween Company

Eden Prairie, Minnesota, USA

Full-time

Who We Are Since 1955, we have been on a mission To Passionately Feed Millions Daily with High Quality Food People Enjoy! We are a third-generation family-owned and professionally managed organization with a commitment to strategic growth. We continue to be successful because of talented people, just like you, who choose to join our family and call E.A. Sween home. We pride ourselves on fostering a welcoming, respectful, and rewarding culture where employees are encouraged to bring their whole