Aseptic Manufacturing Specialist

**Job Description**We are seeking an experienced Aseptic Process Engineer/Lead to support the planning, execution, and completion of key aseptic related projects at Qrc Group, LLC.**Key Responsibilities**Support the development and implementation of aseptic manufacturing processes.Work collaboratively with cross-functional teams to achieve project...

As a Regulatory Consultant at Qrc Group Llc, you will play a crucial role in ensuring the company's compliance with FDA regulations and guidelines. Your expertise in aseptic manufacturing and FDA product submissions will be invaluable to our team.Your key responsibilities will include providing expert regulatory advice for aseptic manufacturing processes,...

**Job Overview**The Qrc Group, LLC is seeking an Aseptic Process Engineer/Lead to join our team. This role will be responsible for supporting the planning, execution, and completion of key aseptic related projects.**Responsibilities**Support the design and implementation of aseptic manufacturing processes.Collaborate with cross-functional teams to deliver...

We are seeking a highly skilled Regulatory Consultant to provide expert guidance and support in navigating the regulatory landscape, specifically in aseptic production environments.The ideal candidate will have strong understanding of FDA regulations and aseptic processing guidelines.Provide expert regulatory advice for aseptic manufacturing processes,...

**About the Role**Qrc Group, LLC is seeking an Aseptic Process Engineer/Lead to join our team. This role will be responsible for supporting the planning, execution, and completion of key aseptic related projects.**Responsibilities and Requirements**Support the design and implementation of aseptic manufacturing processes.Collaborate with cross-functional...

We are looking for a highly motivated and experienced Regulatory Consultant to join our team at Qrc Group Llc. As a Regulatory Consultant, you will be responsible for providing expert guidance and support in navigating the regulatory landscape, specifically in aseptic production environments.Your expertise in FDA regulations and aseptic processing guidelines...

Job OverviewThe Qrc Group, Llc is seeking a highly skilled Regulatory Consultant to join our team. As a key member of our regulatory affairs department, you will provide expert guidance and support in navigating the complex regulatory landscape.About the RoleIn this critical role, you will be responsible for providing expert regulatory advice for aseptic...

Key ResponsibilitiesLead and manage complex projects related to the development, validation, and commercialization of aseptic pharmaceutical or medical device products.Coordinate and oversee all stages of project execution from design, development, and validation through to FDA submission.Develop project timelines, resource allocation plans, and budgets,...

At Qrc Group Llc, we are seeking a highly experienced Pharmaceutical Engineering Expert to lead our efforts in aseptic processing and system development. The successful candidate will have a strong background in aseptic processing, FDA product submissions, and validation activities.Key responsibilities include:Developing, implementing, and improving aseptic...

We are looking for a Regulated Pharmaceutical Process Lead to join our team at Qrc Group Llc. As a key member of our organization, you will be responsible for leading efforts in designing, implementing, and improving aseptic processes and systems within a regulated pharmaceutical environment.The successful candidate will have a strong background in aseptic...

Join Our TeamWe are a collaborative and innovative organization dedicated to delivering high-quality solutions to our clients. As a Regulatory Consultant with Qrc Group, Llc, you will have the opportunity to work with a talented team of experts who are passionate about regulatory affairs.Your Key ResponsibilitiesProvide expert regulatory advice for aseptic...

Job DescriptionWe are seeking a highly skilled Regulatory Validation Specialist to join our team at Qrc Group Llc.The successful candidate will be responsible for leading projects focused on technology transfer, process optimization, and scale-up activities to support manufacturing operations.Oversee activities related to process validation, troubleshooting,...

Company Overview">At Qrc Group Llc, we are a leading provider of software and medical device equipment validation services. Our team is comprised of experienced professionals who specialize in ensuring the highest standards of quality and compliance.">Job Description">We are seeking a skilled CSV specialist to join our team as a data validation specialist....

About UsQrc Group Llc is a dynamic organization committed to delivering high-quality solutions. We are seeking a talented Pharmaceutical Project Management Specialist to join our team. As a specialist, you will be responsible for overseeing projects focused on the implementation of digital and AI solutions that drive process performance and enhance...

Are you passionate about ensuring the accuracy and reliability of medical devices? Do you have a strong background in computer system validation? We are looking for a skilled Csv Specialist to join our team at Qrc Group, Llc.Job Summary:This role involves performing validation activities on software and manufacturing equipment in the medical device industry....

We are seeking a skilled Health, Safety, and Environmental Specialist to join our team. As a key member of our operations team, you will be responsible for ensuring compliance with all relevant health, safety, and environmental regulations and company policies.About the RoleIn this role, you will work closely with our production team to identify and mitigate...

We are seeking an experienced Csv Specialist to join our team at Qrc Group, Llc. In this role, you will be responsible for performing validation activities on software and manufacturing equipment in the medical device industry.Responsibilities:Validating software and medical devices equipmentDeveloping and implementing validation protocolsEnsuring compliance...

At Qrc Group, Llc, we are seeking a highly skilled Csv Specialist to join our team. This role is responsible for performing validation activities on software and manufacturing equipment in the medical device industry.Key Responsibilities:Validating software and medical devices equipmentEnsuring compliance with industry standards and regulationsDeveloping and...

Join Our Team as an Accounts Receivable Specialist!At Fulcro Talent Acquisition, we're looking for a highly skilled Accounts Receivable Specialist to join our team!Company OverviewOur client is a leading owner of shopping centers throughout the island and the United States, urban complexes, manufacturing operations, and food distributors.Job DescriptionThe...

Quality Control Technician Job DescriptionAerotek is seeking a reliable Quality Control Technician to work in an automotive manufacturing facility in South El Monte, CA. The ideal candidate should have at least 1 year of quality control experience and be able to lift up to 35 lbs. without accommodation.Responsibilities:Identify flaws and defects in...