Manufacturing Validation Expert

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.

GMP Manufacturing ExpertiseMentor Technical Group provides expert guidance and support to the life sciences industry, ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. As a GMP Manufacturing Expert, you will play a critical role in helping our clients navigate the complex regulatory landscape 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.

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...

**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...

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...

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.

**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...

**Job Description:**We are seeking a highly skilled Pharmaceutical Operations Expert to join our team at Quality Consulting Group. In this role, you will be responsible for ensuring the efficient and reliable operation of our manufacturing processes.Key Responsibilities:Develop and implement process optimization strategies to improve equipment availability...

**Company Overview**QUALITY CONSULTING GROUP is a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry.We are seeking a highly motivated Manufacturing Process Engineer to contribute to our world-class manufacturing team in Puerto Rico & USA.Main Responsibilities:Designs manufacturing processes, procedures, and production layouts...

Job Description Experience in Document Revision, Non Conformance and Change Control.Requirements Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience OR Bachelor's degree and 5 years of Manufacturing Operations experience or Associate's degree and 10 years of Manufacturing Operations experience or High school diploma / GED...

Company Overview: Quality Consulting Group, a leading provider of quality assurance services in the pharmaceutical, biotech, and medical devices industry, seeks an experienced professional to join our team.">Job Description: As a key member of our quality team, you will be responsible for supporting the execution of manufacturing/quality systems, including...

Mentor Technical Group provides technical support and solutions for the FDA-regulated industry. Our team has extensive knowledge and experience in ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.Our MissionWe strive to deliver high-quality services that meet the needs of our clients. Our focus areas...

We are seeking a skilled and proactive Manufacturing/Quality Systems Specialist to join our team.This role requires minimal supervision and involves supporting the execution of manufacturing and quality systems, including non-conformance management, process validation, procedural development, training, and new product introductions.The ideal candidate will...

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 in...

Job Description:Mentor Technical Group is a leading provider of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, we have the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines.We are seeking a...

Key ResponsibilitiesThe successful candidate will be responsible for managing manufacturing operations, ensuring compliance with regulatory requirements, and implementing process improvements.

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 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...

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...