validation process specialist

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices...

Process Validation SpecialistLocation: Torrance, CA | Employment Type: Full-TimeSupport compliant, reliable manufacturing for clinical and commercial products.At PolyPeptide, we partner with pharmaceutical and biotech companies to support the development and manufacturing of peptide based therapies. We are looking for a Process Validation Specialist to...

Mentor Technical Group (MTG) provides technical support and solutions for the FDA-regulated life sciences industry. With offices in Caguas, Puerto Rico, and Boston, United States, we serve clients in six global markets, including the United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.Responsibilities:Support process...

**Title: Process Validation** **Length of Assignment: 12 Months** **Pay Rate:$50/hr-$54/hr on W2** **Location: Greenville, NC** **Work Schedule: 8am-5pm EST** **Responsibilities:** **Consultants day to day responsibilities:** Review existing validation plans, process documentation, risk assessments, batch records, SOPs, and prior qualification...

HonorVet Technologies (SDVOSB) provides specialized and scalable staffing solutions to pharmaceutical companies, medical device companies, biotech organizations, CROs, research laboratories, and life sciences organizations across the United States. With strong delivery capabilities and rapid turnaround times, we support contract, direct hire, project-based,...

Job Description: We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology transfer, and qualification activities for pre-filled syringe (PFS) manufacturing lines. The ideal candidate will have strong experience...

Job description: Our client is seeking a Senior Process Validation Engineer to support a large medical device manufacturer in re-establishing and standardizing global service center operations to ensure audit readiness and regulatory compliance. This individual will lead validation and documentation efforts across multiple service locations, ensuring...

Job Description: We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology transfer, and qualification activities for pre-filled syringe (PFS) manufacturing lines. The ideal candidate will have strong...

ELIQUENT Life Sciences is the leading global consulting firm providing solutions to life science companies researching, developing, and manufacturing innovative products to serve patients and respond to public health challenges around the world. ELIQUENT is committed to serving clients’ needs with extensive expertise, unwavering integrity, and strategic...

Direct Contingent Worker Posting Title Direct Contingent Worker Division *** Country USA Work Location Houston, TX Functional Area Technical Operations Job Type Full Time Employment Type Contract Job Description • Development of New Injection Molding Processes...

Job Description: We are seeking an experienced Process Validation Engineer to support new pharmaceutical manufacturing projects within a sterile GMP environment. This role will focus on process validation, technology transfer, and qualification activities for pre-filled syringe (PFS) manufacturing lines. The ideal candidate will have strong...

Company DescriptionA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every...

Company DescriptionUS Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website www.ustechsolutions.com.We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation...

Job Description: We are seeking a Process Validation Engineer to support validation and qualification activities in a GMP-regulated manufacturing environment. The ideal candidate will have experience with process validation, equipment qualification, CSV, temperature mapping, and regulatory compliance. Responsibilities: Execute process validation...

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. Perform Walk Downs of As-Built P&IDs and Redlining P&IDs as...

Roles & Responsibilities: Bachelor's degree in Engineering, Science, or related field. Experience with equipment qualification, validation, or regulatory compliance. Familiarity with Kneat digital platform or similar document management systems. Strong understanding of CSV (Computer Systems Validation) principles. Knowledge...

**Validation Process Engineer** **Position Summary:** - **Work Schedule:** M-F 8am-4:30pm - 100% on-site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation...

**Position Summary:** - Work Schedule: M-F 8am-4:30pm - 100% on-site Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to...

**Job Title: Process Validation - Pharma** **Location: Greenville, NC** **Duration: 12 Months** **Rate: $50 - $54/hr W2** **Experience: 5+ Years** **Position Overview:** We are seeking experienced Process Validation Consultants to support process validation and PPQ activities within a regulated pharmaceutical manufacturing environment. The ideal...

DescriptionDescription: Process Engineer reports to the Manager of Technical Services and plans, executes and functionally directs Process/Cleaning Validation/Study assignments and projects, which require sound pharmaceutical/engineering skills and independent judgment. Works as a team member, educates internal partners on the projects, monitors and...