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Process Development Engineer (Life Sciences/Biotechnology/Medical Devices)

Dawar Consulting

Santa Clara, California, USA

Contract

Our client, a world leader in diagnostics and life sciences, is looking for a "Process Development Engineer based out of Santa Clara, CA. Job Duration: Long Term Contract (Possibility Of Further Extension & Conversion) Pay Rate: $65-$70/hr on W2 Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K As a member of the Manufacturing Sciences and Technology (MSAT) team, the Process Development Engineer provides critical technical and operational support to consumable and cartridge manuf

Assistant Director Regulatory Affairs

Zachary Piper Solutions, LLC

Eden Prairie, Minnesota, USA

Full-time

Piper Companies is looking for an Assistant Director of Regulatory Affairs to join a biotechnology company focusing on products to address life threatening conditions. This is a full-time position and onsite in Eden Prairie, MN (relocation assistance available). Essential Duties of the Assistant Director of Regulatory Affairs: Main point person responsible for writing INDs. 50-60% of time will be writing related. Writing sections of IND with support of cross functional teams. Opportunity to gai

Facilities Associate

Zachary Piper Solutions, LLC

Manchester, New Hampshire, USA

Full-time

Piper Health & Sciences isseeking a skilled and dedicated Facilities Associate (Laboratory Operations) to join a dynamic and innovative biotechnology organization in the Manchester, NH area. The Facilities Associate will be responsible for maintaining the infrastructure and ensuring the smooth operation of our biotechnology facility. Essential Duties of the Facilities Associate: Perform routine maintenance and repairs on HVAC systems to ensure optimal functioning and climate control.Handle elec

Urgent Opening- QA Validation Engineer - Cypress, CA

SunRay Enterprise Inc

Cypress, California, USA

Contract

Hello Professional, Hope you are doing well. This is Dharm from Sunray Corporation I found your resume suitable for one of the prime position with one of our client. Please find below the job description and let me know if you would be comfortable with Role : QA Validation EngineerLocation : Cypress, CADuration : 9+ Months Role OverviewExperience in Pharmaceutical Manufacturing, Biotechnology, and Medical device companies Performed Computer System Validation of cloud/server-based systemsInvol

Instructional Designer

Aditi Consulting

Remote or Thousand Oaks, California, USA

Contract

Payrate: $45.30 - $49.13/hr. Summary: As an individual contributor, this Instructional Designer position will have minimal supervision that will collaborate with subject matter experts to design, develop and implement instructional materials. This role will be responsible for creating engaging content that meets learning objectives using authoring tools and for delivery in corporate learning management system (LMS). Key Responsibilities: Collaborate with subject matter experts to develop simplif

Manufacturing Tech II

Zachary Piper Solutions, LLC

Elkridge, Maryland, USA

Full-time

Piper Health and Sciences is seeking a skilled and motivated Manufacturing Technician II to join a biotechnology company specializing in immunotherapy products in the Elkridge, MD area. This role has Monday - Friday, 8AM-5PM working hours (NO weekends/overnights!). Responsibilities of the Manufacturing Technician II: Execute manufacturing of drug product following GMP guidelines Maintain inventory of all GMP manufacturing processing rooms Prepare buffers and reagents Monitor equipment and c

Manufacturing Associate II (Downstream)

Zachary Piper Solutions, LLC

Gaithersburg, Maryland, USA

Full-time

Piper Health and Sciences is seeking a skilled and motivated Manufacturing Associate II (Downstream) to join a biopharmaceutical company in the Gaithersburg, MD area. The Manufacturing Associate II is a crucial role in supporting the downstream manufacturing team. This position involves operating and maintaining downstream processing equipment, performing filtration and chromatography techniques and supporting production activities in a cleanroom environment. Responsibilities of the Manufactu

QA Specialist

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Health and Sciences is actively seeking a QA Specialist to work for a large global pharmaceutical company focusing on their consumer product line. This a remote / work from home position. Responsibilities for Quality Assurance (QA) Specialist: Oversee quality assurance activities including label review and batch record review for global product line Responsible for reviewing and approving deviations, investigations, bill of materials, and change controls Ensure timely close out of all inv

Validation Engineer

Katalyst Healthcares and Lifesciences

Burlington, Massachusetts, USA

Full-time

Roles & Responsibilities: Bachelor's degree in engineering or a related technical discipline required. Minimum 5years of experience in procurement, sourcing, and supplier management. Proven success in sourcing within electromechanical components or complex assemblies. Medical device, pharmaceutical, or biotechnology industry experience strongly preferred. Strong negotiation skills with a track record of achieving cost and delivery targets. Familiarity with procurement software (e.g., SAP C

Cell Culture Media Scientist

Zachary Piper Solutions, LLC

Minneapolis, Minnesota, USA

Full-time

Piper Companies is seeking a Cell Culture Media Scientist to join a top biotechnology company in Minneapolis, MN. Responsibilities of the Cell Culture Media Scientist: Develop and optimize scientific methods related to cell culture media for advanced biological research. Independently lead technical projects, contributing specialized expertise to fill key knowledge gaps. Design and conduct experiments to support research and development initiatives. Collaborate with cross-functional teams t

Senior Software Automation Engineer

Motion Recruitment Partners, LLC

Arlington, Virginia, USA

Full-time

A full-time opportunity is now available for a Senior Software Automation Engineer in Rockville, MD with a hybrid work schedule. This role focuses on advanced automation technology including robotics software design using C# and .NET to support new product development and enhance manufacturing capabilities. This is a great opportunity to join a company making a real impact in global health and research through advanced molecular measurement technologies. They're looking for an experienced engine

Quality Project Manager

Zachary Piper Solutions, LLC

Holly Springs, North Carolina, USA

Full-time

Piper Companies is seeking a Quality Project Manager to join a growing leader in the pharmaceutical/biotechnology space for an onsite position in Holly Springs, North Carolina (NC). The Quality Project Manager will act as the key liaison between the CQV Team and PMO, using data-driven forecasting and reporting to optimize personnel capacity, improve resource planning, and ensure seamless execution of Project Quality deliverables. Responsibilities of the Quality Project Manager include: Serve a

CQV Engineer

Katalyst Healthcares and Lifesciences

Pennington, New Jersey, USA

Full-time

Responsibilities: Prepare commissioning, qualification, and validation documents for equipment, utilities, and systems. Verify that systems and equipment operate according to design specifications and regulatory requirements. Prepare and maintain comprehensive validation documentation, including test protocols, reports, and standard operating procedures. Work closely with engineering, quality assurance, and production teams to resolve issues related to CQV. Implement corrective actions and impro

Bio Process Associate - 2nd Shift

TSR Consulting Services, Inc.

Harvard, Massachusetts, USA

Contract

Our client, a leading pharmaceutical company, is hiring a Bio Process Associate, on a contract basis. Job ID: 82449 Work Location: Devens, MA - 100% on site Shift: 5p- 5a Summary: Work in a cGMP laboratory and/or manufacturing environment following techniques which require one to maintain a high attention to detail. Properly use Personal Protective Equipment (PPE), gowning for restricted areas, aseptic processing, handling chemicals, and work in a general office environment. Contingent Workers

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

Clinical Solutions Analyst

Zachary Piper Solutions, LLC

Remote

Full-time

Piper Companies is seeking a Clinical Solutions Analyst who understands software and computerized systems in the clinical trial process. The Clinical Solutions Analyst will be remote , supporting a Raleigh, NC headquarters. Requirements for the Clinical Solutions Analyst include: - Collaborate with relevant business users (clinical project managers, clinical research associates, data managers, etc) to understand solution requirements, develop and document business processes, and provide ongoing

Validation Engineer

Katalyst Healthcares and Lifesciences

Richmond, Virginia, USA

Full-time

Responsibilities: Develop and implement comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly. Lead the validation of various systems, including SEA Vision Yudoo and AVI systems, ensuring compliance with industry standards and regulatory requirements. Prepare, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Validation Summary Reports (VSR). Collaborate with cross-functi

Validation Engineer

Katalyst Healthcares and Lifesciences

Richmond, Virginia, USA

Full-time

Responsibilities: Develop and implement comprehensive validation plans for packaging lines, labelers, case packers, and low-speed pen assembly. Lead the validation of various systems, including SEA Vision Yudoo and AVI systems, ensuring compliance with industry standards and regulatory requirements. Prepare, execute, and document Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Validation Summary Reports (VSR). Collaborate with cross-functional

Engineering - Bio Process Associate - 3rd Shift , Devens MA - Immediate position

Futran Solutions

Massachusetts, USA

Contract

Job Description: Bio Process Associate 3rd shift role--so shift diff included on Rate Onsite in Devens--Local Candidates Only Operates control systems and processes in Biotechnology Pilot Plants as assigned. Prepares process buffers and reagents. Cleans equipment and maintain area in clean and orderly fashion. Recognizes and reports safety, maintenance and operational variances to area management. Communicates status of operations to area management in a timely manner. Follows detailed SOP

Identity and Access Management (IAM) Engineer / Okta / Irving, TX / Hybrid

Motion Recruitment Partners, LLC

Irving, Texas, USA

Full-time

Our client, which is a leader in the biotechnology space, is looking for an Identity and Access Management Engineer to join their team. This is a rapidly growing company and is needing another individual who can help with their IAM initiative (mainly helping with their automation and scaling). This team is expanding due to their need for additional technical security overall. Ideally, they are looking for someone who is skilled with Okta (primarily) but also has good knowledge on Entra. This rol