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$114.56k - $171.84k
...brilliant and diverse minds to make a real difference, there’s only one choice.Associate Principal Bioprocess Automation Engineer - cGMP PURPOSE:The Associate Principal Automation Engineer is responsible for defining & applying automation strategies for equipment and facilities...SuggestedWork experience placementLocal areaRemote workRelocation package$116k - $258k
...healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.Job TitleSenior Automation Engineer (cGMP) - Project FarmaLocation(s)Customer Site - AL, Customer Site - CO, Customer Site - DC, Customer Site - FL, Customer Site - GA,...SuggestedFull timeRemote workWork visa$65.5k - $96.41k
cGMP HVAC Mechanic Job ID: req4651 Employee Type: nonexempt full-time Division: Vaccine Clinical Materials Program Facility: Frederick: G-WAY Location: 7116 Geoffrey Way, Frederick, MD 21704 USA The Frederick National Laboratory is operated by Leidos Biomedical Research...SuggestedFull timePart time- An established industry player is seeking a dynamic Training Specialist to enhance organizational effectiveness through strategic training initiatives. This role involves conducting training needs analysis, designing impactful programs, and collaborating with various departments...Suggested
- At Houston Methodist, the Current Good Manufacturing Practice (cGMP) Specialist position is responsible for adherence to Standard Operating Procedures (SOPs) and cGMP regulations pertaining to the manufacture of therapeutics and devices. Additionally, this position will...Suggested
- ...producing solutions and media per SOPs, training manufacturing operations staff, and supporting production runs. You will work in a cGMP environment, handle unit operations, and drive improvements in daily practice while maintaining quality records. Candidates should have...Suggested
- A prominent IT staffing company is seeking a Manufacturing Technician in Sanford, North Carolina. In this role, you will operate and maintain production equipment, ensure compliance with regulatory requirements, and clean facilities according to Good Manufacturing Practices...Suggested
- Bristol Myers Squibb is seeking a Bioprocess Associate to support commercial manufacturing of therapeutic proteins at Devens, MA. You will follow documented procedures and cGMPs to ensure quality and compliance in daily production tasks. The role involves operating bioreactors...Suggested
- ...Medicine, Department of Medicine, seeks a QC Specialist to oversee quality control testing for cell and gene therapy products in a cGMP facility. You will design and implement QC testing, review batch records, and support technology transfer from pre-clinical to cGMP....Suggested
$131k - $165k
...Compliance Manager is a hands-on leader and change agent responsible for building, implementing, and sustaining a compliant, scalable IVD cGMP Quality Management System (QMS) across Cytek facilities. This role develops practical processes, strengthens documentation...SuggestedShift work- Cytek Biosciences in Fremont is seeking a QMS Compliance Manager to lead the development and implementation of a compliant IVD cGMP Quality Management System. This role requires expertise in regulatory environments, process improvement, and team leadership. The ideal candidate...Suggested
$90k - $100k
SOFIE in Totowa, NJ is seeking a Sr Radiochemist, RCM Project Lead to develop and validate manufacturing methods for diagnostic and therapeutic radiopharmaceuticals. This role involves ensuring compliance with regulatory standards and leading a team in quality control procedures...Suggested- Sr. Current Good Manufacturing Practices (cGMP) Specialist At Houston Methodist, the Sr. Current Good Manufacturing Practices (cGMP) Specialist is responsible for adherence to Standard Operating Procedures (SOPs) and cGMP regulations pertaining to the manufacture of therapeutics...Suggested
- A leading IT staffing company is seeking a candidate with 0-3 years of GMP manufacturing or QA experience for a role in compliance and quality assurance. Responsibilities include ensuring adherence to regulatory requirements, coordinating batch records, and approving documents...Suggested
$87.58k - $92k
...biologics and drugs for cell and gene therapy of internal/external users in the university's current Good Manufacturing Practices (cGMP) facility. The Quality Control (QC) Specialist is responsible for designing, developing, evaluating, and implementing quality control...SuggestedFixed term contractWork experience placementLocal area- Experic is seeking a Project Manager to oversee assigned pharmaceutical clients under minimal supervision. You will plan resources, assemble or lead the project team, manage time, budget, scope, quality and satisfaction, and monitor risk and progress. You will coordinate...
$85k - $100k
...quality systems to support Quality Assurance activities. Qualifications Minimum 5 years of Quality Assurance auditing experience in a cGMP environment with a minimum of 5 years of external vendor/supplier compliance auditing experience within an FDA regulated industry....- Gift of Life Marrow Registry is seeking a Quality Assurance Coordinator based in Boca Raton, Florida. This role assists with oversight of the Quality Management System, ensuring compliance with federal and state regulations involving quality culture throughout the organization...Full timeFlexible hours
$87.58k - $92k
...Control (QC) Specialist to support manufacturing of biologics and cell and gene therapy products in its Good Manufacturing Practices (cGMP) facility. The role includes designing, developing, evaluating, and implementing quality control testing, assays, and procedures for...- Hims & Hers in California is seeking a Quality Specialist to join our sterile injectable manufacturing team. You will execute day-to-day quality oversight on the floor and within the QMS, ensuring products meet identity, strength, quality, and sterility standards in alignment...
- Anika in Bedford, MA is seeking a Shift Lead to oversee day-to-day manufacturing operations in a cGMP environment. You will lead the team in executing production activities, ensuring compliance with safety and quality standards. The ideal candidate has at least 6 years...Shift work
- ...staffing firm is seeking a Technical Document Writer for its Marlborough location. The candidate will focus on writing and reviewing cGMP documentation, contributing to project success. Key responsibilities include maintaining standard procedures and collaborating...Contract work
- ...engagement with a pharmaceutical client. The role involves on-site support for sample handling, inventory control, and compliance with cGMP; a strong candidate will manage LIMS data, coordinate logistics for vaccines/biologics, and contribute to audit readiness. Education...
- ...role (9 AM-5 PM PT). Responsibilities include performing basic to moderate tests, routine sample testing, and lab maintenance in a cGMP environment. Opportunities for training and teamwork are available. Qualifications include a B.S./B.A. in a relevant science and 0-5...
- ...seeking a Production Chemist in Torrance, CA to support the manufacture of high-quality Active Pharmaceutical Ingredients (APIs) in a cGMP-regulated environment. The role spans from executing batch production to maintaining compliance with safety and quality standards....
- ...seeking a qualified leader to oversee QA and QC operations in New Brunswick, New Jersey. The position requires ensuring compliance with cGMP standards and managing quality goals aligned with global objectives. Applicants should have a Bachelor's degree in a related field,...
$16.68 - $22.26 per hour
...Responsibilities include establishing inventory controls, monitoring materials, and coordinating efficient movement, ensuring compliance with cGMP standards. Candidates should have a high school diploma, preferably an associate degree, and experience in inventory management or...- Bora Pharmaceuticals is seeking a Quality Associate to support cGMP documentation, batch review, and final disposition in manufacturing and packaging operations. This role emphasizes rigorous documentation and adherence to quality procedures within FDA-regulated processes...
- Concordance Healthcare Solutions LLC is seeking a Quality Coordinator to support cGMP compliant quality programs at our Edison, NJ location. This full-time role will involve managing MasterControl for quality management while collaborating closely with various managers...Full timeWork at office
- Charles River Laboratories in Wayne, PA, seeks an experienced Training Specialist to develop and coordinate technical training for a cGMP laboratory workforce. You will manage training programs, ensure compliance with SOPs, and support the learning management system to...Hourly pay