PharmEng Technology Jobs in United States

We are seeking a skilled CQV Engineer to support commissioning and qualification activities for downstream process equipment within a large-scale biopharmaceutical manufacturing facility. · ...

We seek a motivated Project Manager to support capital projects within the pharmaceutical industry. · ...

+We are seeking a Sr. Process Automation Engineer for a contract-to-hire position located in Houston. · Provide 24x7 automation support to manufacturing by troubleshooting equipment systems and processes. · Mentor and train junior team members including technicians analysts engin ...

+Job summary · Capital Projects Engineer (12-Month Assignment Onsite) · +ResponsibilitiesServe as the engineering lead for assigned capital projects, managing the design process in collaboration with architectural/engineering (AE) firms and equipment vendors. · Oversee the develo ...

We are seeking a Technical Writer with experience in engineering documentation for a pharmaceutical manufacturing environment, with a strong focus on utilities and facility systems. · ...

Transformative Projects in Biopharmaceutical Manufacturing · Lead impactful capital projects enhancing manufacturing facilities development, expansion, and optimization. · Collaborate with cross-functional teams to manage CAPEX initiatives under cGMP regulations. · Key Responsibi ...

This role is responsible for providing high-level technical support to Fill/Finish operations, ensuring process reliability, equipment uptime, · and compliance with GMP standards.Provide real-time technical support for Fill/Finish production. · Lead and support the resolution of ...

Capital Projects Engineer · This role offers significant exposure to site-level capital project planning and execution with direct responsibility for key elements of design validation implementation in a regulated GMP environment.We are seeking an experienced engineer who will co ...

+About The Job Quality Assurance Specialist · Washington, DC · Contract · Job Description · To reduce 80% of on-site quality documentation and streamline processes to enhance efficiency and compliance. · + · + ...

About this role · Support preparation, analysis and optimization of manufacturing data and document flow. · Develop visualizations using existing foundations or external sources. · Collaborate with stakeholders to assess SeeQ software requirements. · Data Engineering Deliverables ...

We are seeking a detail-oriented and experienced Validation Engineer to support pharmaceutical manufacturing validation projects. The role focuses on the execution, review, and documentation of Installation and Operational Qualification (IOQ), Performance Qualification (PQ), and ...

As Senior Process Engineer lead cross-functional team develop GMP-compliant integrated process equipment pharmaceutical manufacturing. · ...

We are seeking a skilled EMPQ specialist to support CQV (Commissioning, Qualification and Validation) efforts focused on Environmental Monitoring Performance Qualification in a regulated pharmaceutical manufacturing environment. · ...

+ We are seeking a skilled CQV Turnover and Set to Work (STW) I&C Technician to prepare Direct Impact Systems for Commissioning and Qualification (C&Q) post-Mechanical Completion. · +Collaborate with STW teams to execute protocols for safe system energization and C&Q readiness. · ...

We are seeking a Technical Writer with experience in engineering documentation for a pharmaceutical manufacturing environment. · Experience: 3+ years as a Technical Writer in a pharmaceutical, biotech, or regulated manufacturing setting. · Familiarity with GMP, FDA 21 CFR Part 11 ...

We are looking for a Junior Design Process Engineer with 1- 3 years of experience in the Pharma industry. · This role offers true engineering creativity with exposure to a wide range of exciting, · complex projects in a collaborative and technical environment. · ...

We are seeking a LIMS Support Specialist to provide hands-on support to the Quality Control (QC) department. This role involves LIMS configuration, master data governance, and project support activities aligned with GMP and regulatory requirements. · Customize and configure the L ...

We are looking for a Senior Design Process Engineer to lead high-impact projects across the bio-pharmaceutical, personal care, and food sectors. · 8+ years in GMP process engineering ideally with skidded systems · ,Experience in process equipment and piping system design · ,Comm ...

The Analytical Validation Specialist III will assist in validation activities. · ...

We are seeking a skilled CQV Engineer to support commissioning and qualification activities for downstream process equipment within a large-scale biopharmaceutical manufacturing facility. This role involves hands-on work in a startup environment and collaboration with cross-funct ...