Validation Expert

Company OverviewEQVAL Group, Inc. provides expert services to the manufacturing industry, serving clients in Medical Devices, Pharmaceuticals, and Biotechnologies.Job DescriptionWe are seeking a skilled Manufacturing Engineer to join our team. The ideal candidate will have experience in Medical Device or Pharmaceutical industries and will be responsible for...

Job OverviewWe are seeking a highly skilled Sr Validation Scientist to join our team at Qrc Group Llc. This role requires expertise in validation processes, particularly in regulated environments such as Biotechnology, Pharmaceutical, and Medical Devices.The ideal candidate will have experience in independently providing technical validation engineering...

Overview: At Qrc Group Llc, we are seeking a Quality Engineering and Validation Expert to join our team. As a key member of our quality assurance team, you will be responsible for ensuring that our products meet the highest standards of quality.Responsibilities:Lead quality assurance efforts for new product introductionsDevelop and implement quality...

We are seeking a highly skilled and independent Validation Engineer to provide technical support for process and equipment upgrades, replacements, and modifications in laboratory, manufacturing, or manufacturing support environments.The ideal candidate will possess advanced validation expertise and demonstrate exceptional problem-solving, leadership, and...

**Job Summary**We are seeking a highly skilled Quality Control Expert to join our team. In this role, you will be responsible for implementing and maintaining quality control procedures across various aspects of our business.This includes process validation, product disposition, cleaning validations, and quality aspects of the manufacturing process.

Job OverviewIntegrated Services For Productivity & Validation, Inc seeks an experienced Manufacturing Specialist to join their team. This role requires expertise in document revision, non-conformance, and change control.

About UsAt QUALITY CONSULTING GROUP, we strive to deliver exceptional results by providing expert consulting services to our clients. Our team of professionals is dedicated to ensuring compliance with federal regulations and providing high-quality services.ResponsibilitiesThis role involves conducting compliant validation processes for quality information...

**Biopharma Consulting Jad Group** is seeking an experienced Validation Scientist to join our team. As a key member of our consulting group, you will be responsible for providing technical support for process and equipment upgrades, replacements, and modifications in laboratory, manufacturing, or manufacturing support environments.The ideal candidate will...

About the Role">The validation engineer will be responsible for developing and implementing validation strategies for laboratory instruments and equipment. This includes designing and executing qualification protocols, assessing data integrity, and ensuring compliance with regulatory requirements.">Key Responsibilities">">Design and execute qualification...

**About Us**Biopharma Consulting Jad Group is a leading consulting firm specializing in biopharmaceutical development and manufacturing. We offer expert services in validation and compliance management, helping our clients navigate the complexities of regulatory requirements and industry standards.We are committed to delivering high-quality services that...

Overview of Mentor Technical GroupWe are a global provider of life science engineering and technical solutions. Our comprehensive portfolio includes technical support and solutions for the FDA-regulated industry.We have a strong presence in various markets, including the United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South...

Key ResponsibilitiesThe successful candidate will be responsible for performing Trackwise system queries, deviations, and triage processes. They will also oversee process and procedures/GMP tasks, manage Change Controls and deviations, and work with operations to resolve basic compliance discrepancies.

Job SummaryWe are seeking a highly skilled Biopharma Process Improvement Expert to join our team. The successful candidate will be responsible for process optimization, capital projects, and equipment troubleshooting.Key Responsibilities:Apply basic engineering principles to resolve technical issues of moderate scope and complexityEvaluate, select, and apply...

Job Summary:Flexible & Integrated Technical Services, LLC is seeking a highly skilled Regulated Industry Expert to join our team. In this role, you will be responsible for ensuring compliance with regulatory requirements and validating manufacturing processes.Responsibilities:Review and validate product MPRsDevelop and implement process validation...

We're looking for a skilled Regulatory Compliance Expert to lead our quality assurance efforts in the Inspection area. As a member of our team, you will play a key role in ensuring regulatory compliance and maintaining the highest quality standards.About This RoleThis position requires a strong background in regulatory compliance and quality assurance. The...

Job DescriptionWe are looking for an experienced Data Scientist to join our team at Integrated Services For Productivity & Validation, Inc. The successful candidate will have a strong background in data analysis and interpretation, as well as excellent communication and interpersonal skills.About the RoleThe primary responsibility of this role will be to...

**Job Description**We are seeking a highly skilled and independent Validation Engineer to provide technical support for process and equipment upgrades, replacements, and modifications in laboratory, manufacturing, or manufacturing support environments.The ideal candidate will possess advanced validation expertise and demonstrate exceptional problem-solving,...

**Job Responsibilities:The ideal candidate will have experience in planning and executing commissioning, qualification, and validation (CQV) activities. They will also have excellent communication and influencing skills to ensure that all necessary CQV activities are completed on time and according to the validation program. **Working Conditions:The...

The RoleKey responsibilities include:Conducting compliant validation processes for quality information technology systems.Coordinating activities with clients, programmers/developers, and operating personnel.Identifying current and anticipated requirements for compliant computerized operations.Suggesting methods for identification and implementation of...

Requirements and QualificationsTo be considered for this position, applicants must possess a Doctorate degree or Master's degree with 3 years of experience in manufacturing operations, or Bachelor's degree with 5 years of experience, or Associate's degree with 10 years of experience, or High school diploma/GED with 12 years of experience.