10 process validation opportunities in West Chester updated today
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Org Marketing Statement Porter, a division of Parker Hannifin Corporation, is a global leader in analytical, dental, industrial and medical instrumentation. Since 1968, the company has specialized in the development, manufacture and sale of precision instruments that measure and control low flow gas
Responsibilities: Write and execute commissioning, qualification, & validation protocols for facilities, utilities, and process equipment. Oversee and review design and construction work related to cGMP manufacturing facility. Review submittals, IOM, control sequences, and start up procedures. Perfo
At Bloom Energy, our vision for a world powered by clean, reliable, and affordable energy is more than just a dream—we’re making it reality. For over two decades, we’ve been at the forefront of the global energy transition, pioneering solutions that empower critical industries to thrive in a rapidly
A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand d
A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand d
Job DetailsJob Location: Main Corporate Office - Malvern, PA 19355Position Type: Full TimePosition Summary The Senior Director, CMC Lead is responsible for developing and executing the Chemistry, Manufacturing & Controls (CMC) strategy across Ocugen’s gene therapy pipeline, with primary responsibili
Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, m
Description Under guidance from the Manufacturing Engineer Manager, the Manufacturing Engineer will improve the capability, productivity, and efficiency of all manufacturing processes. The Manufacturing Engineer will review all finishing processes to optimize efficiency, yields, and productivity. Th
OCUGEN OPCO INCJob DetailsJob Location: Main Corporate Office - Malvern, PA 19355Position Type: Full TimePosition Summary We are seeking an experienced CMC leader to drive BLA-stage readiness for AAV gene therapy programs. This role serves as the strategic technical interface between laboratory development, GMP ma
JOB TITLE: Quality Systems Specialist DEPARTMENT: Quality REPORTS TO: CTO SUMMARY: The Quality Systems Specialist is a technical role responsible for executing critical inspection processes and maintaining the integrity of the Quality Management System (QMS). Unlike generalist quality roles, this po
Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled per
*Role: Validation SME – Design Controls Remediation** 9 months Remote *(Can extend upto 24 Months)** *Role Summary** The Validation SME will serve as the subject matter expert for design validation, performing gap assessment and remediation to confirm that the medical device meets user needs and int
CAI*Are You Ready?** CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled
VALSPECValspec-a global provider of system validation and lifecycle services-provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital
Yochana10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP ap
Job Title: CSV/ Manufacturing Systems Engineer - II (Associate) Location: West Point, PA 19486 Duration: 6 Months Pay rate: $44-49/hr on W2 Summary: We are seeking a detail-oriented professional with experience in computer system validation and GMP-regulated environments to support periodic reviews
Computer System Validation, Computed system assurance, GAMP, GxP risk assessments, Change Management 10+ years' Experience in Validating systems and Experienced in CSV activities in GxP related applications like SAP Systems, Product Serialization systems, MES systems Perform review for GxP systems t
Validation Specialist (Life Sciences) Develop and maintain SOPs, user manuals, validation protocols, and regulatory submission documents. Translate complex scientific and technical concepts into clear, concise documentation. Collaborate with SMEs to gather and verify technical information. Ensure do
Insight GlobalJob Description Our biopharmaceutical client is seeking an Equipment Validation Scientist to support automation systems and laboratory equipment within regulated clinical and non‑clinical bioanalytic and vaccine modernization labs in West Point, PA. This role sits within the Discovery, Preclinical &
$40,000 – $63,000/year
Estimation confidence: Low
Estimate based on market data for West Chester. Actual salaries may vary depending on experience, company, and area.
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