Administrative Shift Process Improvement

About the RoleIn this position, you will work with a highly enthusiastic team to apply process, operational, scientific expertise, and analytical skills to support manufacturing operations. Your responsibilities will include:SUPPORT THE EXECUTION OF MANUFACTURING/QUALITY SYSTEMS such as non-conformances, process validation, procedures, training, and new...

Job Description Technical Writing (SOP, FORMS) Change Control Process Requirements Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience Alternatively, Bachelor's degree and 5 years of Manufacturing Operations experience Alternatively, Associate's degree and 10 years of Manufacturing Operations experience Alternatively, High...

Company OverviewQuality Consulting Group is a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry. We are committed to excellence in quality and process improvement.

Job Description Engineering (any field) or scientific background (Biology, Microbiology, Biotechnology, Chemistry, etc.)Previous experiences in regulated environment (Biotechnology, Pharmaceutical, Medical Devices, etc.).Experience in Validation with preference in Process Validation.Requirements Doctorate degree OR  Master's degree and 3 years of directly...

Job Description Candidate should have experience providing support to manufacturing activities , preferably knowledge in chromatography and filtration systems.Knowledge in PI historian, statistical analysis and protein purification techniques are recommended.Requirements Master's degree OR Bachelor's degree in Engineering & 2 years of Engineering...

Under general supervision, the Process Engineer provides characterization of process optimization strategies and troubleshooting of operational issues within operations, manufacturing, pilot plant, or capital projects environments.This role applies basic engineering principles to the design and implementation of system modifications, experiments, and/or...

Job Description • Perform Trackwise system queries, deviations • Participate in triage process • Perform oversight of the process and procedures/GMP tasks • Manage Change Controls and deviations for review and approval as QA contact • Work with operations to resolve basic compliance discrepancies • Knowledge in Validations and Laboratory area and...

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities: Support the...

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities: Support the...

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team.In this role, you'll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities: Support the...

Job Description • Strong Technical Writing and excellent written and verbal communication skills in English and Spanish .• Experience in Root Cause Analysis • Understanding of bio-processing unit operations • Compliance/Regulatory knowledge • Experience with standard manufacturing procedures and GMP documentation • Ability to communicate and...

Independently provides and/or directs the technical validation engineering support of process and/or equipment upgrades, replacements, and modifications in the laboratory, manufacturing or manufacturing support environment.Requisitos:Doctorate degree OR Master's degree and 3 years of directly related experience ORBachelor's degree and 5 years of directly...

Qrc Group, LLC">A leader in manufacturing systems, we are committed to delivering exceptional results through innovation, collaboration, and a passion for excellence. As an Associate Manufacturing Systems professional, you will be part of a dynamic team that drives business growth and improves operational efficiency.">Job Summary">This is an exciting...

For scientist services in the Process Development:  Oral & Parenteral Mfg   a rea.WHAT MAKES YOU A FIT:  The Technical Part: Bachelor Degree with six (6) years of exposure in Scientist within the pharmaceutical or regulated industry.Bilingual (English & Spanish).Project Management skills.Shift: Administrative and according to business needs.Experience...

**Job Description:**The successful candidate will be responsible for driving quality and process improvement initiatives in our manufacturing environment.**Key Skills and Qualifications:**Demonstrated expertise in document revision, non-conformance, and change control processes.Strong understanding of manufacturing operations principles and best practices.

For Manufacturing services in the Buffer and Component Prep  area.WHAT MAKES YOU A FIT:  The Technical Part: Bachelor's Degree (preferably in Engineering or Life Sciences) with five (5) years of direct experience as a Quality Professional in the regulated industry.Bilingual (English & Spanish) Project Management skills Shift: Administrative and according...

Job Description Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.Designs sequence of operations and specifies procedures for the fabrication of tools and...

Job Description • Foundation in quality assurance roles focused in Quality Management Systems and GMP documentation (must have) • Support development of new equipment/technology introduction projects, preferably within Packaging Area (must have) • Be knowledgeable about compliance and regulatory aspects for equipment validation, operation and...

JOIN OUR TEAMPharmaLex is a highly successful and growing consulting company for the Healthcare industry around the world.PharmaLex offers professional development, plus a stimulating and collaborative work environment.We are committed to providing exciting career opportunities in an atmosphere that values trust, respect, teamwork, creative talent,...

Under general supervision, the Mfg Systems Engineer provides process optimization strategies and troubleshooting support for operational issues within the operations, manufacturing, pilot plant, or capital projects environment on second shift.The role involves applying basic engineering principles to the design and implementation of system modifications,...