cgmp

**RESPONSIBILITIES:** The cGMP Compliance Handler is typically scheduled on eight hour shifts five days a week.  cGMP Compliance Handler must have the flexibility to work on other shifts or overtime when needed. The cGMP Handler must be able to perform job duties with minimal direct supervision and is required to follow an established performance protocol...

DescriptionDescriptionCSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical...

Company DescriptionA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every...

About the Role Catalent Pharma Solutions is seeking a Manufacturing Operator to support its pharmaceutical production operations in a cGMP-regulated environment. This role plays a critical part in ensuring high-quality softgel manufacturing, inspection, and packaging while maintaining strict safety and quality standards. You will work in a clean, safe, and...

Description: The employee will be responsible for cleaning and sanitizing the batching department using the appropriate equipment and processes. The areas will consist of the floors, outside of the tanks, mezzanines, walls, etc. The employee is required to comply with departmental safety requirements, contribute to the quality improvement process and...

**Job ID** REQ20180371 **Category** Support Services The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the “Trojan Family,” which is...

Job Title - Training SpecialistLocation - Greenfield, IN (no relocation available and no VISA candidates or C2C/C2H or W2)The Training Coordinator IV is an advanced-level, site-focused training role responsible for establishing, maintaining, and continuously improving the training program for a regulated warehouse operation that stores pharmaceutical...

CSBio is seeking a Supervisor of cGMP Peptide Manufacturing at its Milpitas facility. You will lead production operations, oversee SPPS, purification, lyophilization, and packaging for clinical and commercial campaigns, reporting to the Head of Manufacturing.This is a hands-on leadership role with responsibility for schedule, quality, and compliance. You...

Company DescriptionEngineeringJob DescriptionJob Title- Specialist QALocation- Woburn, MADuration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs, Change Bio-pharma space / Biologics . M-F onsite•    Knowledge in cGMP / GMP manufacturing and technical knowledge in validation of...

The cGMP Specialist Project Specialist drives the successful execution of manufacturing projects within the Office of Translational Production and Quality, serving as the primary liaison between our clients and internal operations. This role encompasses a variety of responsibilities, including developing project plans, tracking and reporting on project...

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 be responsible for assisting senior team members with aspects of compliance associated...

Randstad - - Responsibilities: Manufacture lyophilized formulations on production lines

The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the “Trojan Family,” which comprises the faculty, students and staff that make the university...

20bloc, Inc. is seeking a hands-on Head of Engineering and Facilities to lead CQV and site readiness as we finalize our cGMP manufacturing space in Thousand Oaks.You will own transfer of processes, equipment qualification, and manufacturing readiness, while supporting the MSAT function with a pragmatic, execution-focused approach. The role requires deep cGMP...

🧪 QC Laboratory Chemist I | cGMP | FDA📍 Charlotte Metro Area💰 Salary range $70k - $80k plus discretionary bonus potential up to 12% 🕰️ Hours: Monday – Thursday 3:30pm – 11:30pm & Friday 1:30pm – 9:30pm🚨 US Citizens or Green Card Holders only | No C2CImmediate opening for a QC Laboratory Chemist I to join an industry-leading health and...

SUMMARY:The Global Head of cGMP Training is a corporate quality position responsible for strengthening the effectiveness of cGMP training across Sharp’s global network, with an immediate focus on improving shop floor and operational training.This role is accountable for raising the quality, relevance, and consistency of training for GMP‑impacting roles,...

The University of Southern California (USC), founded in 1880, is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC, you will be a part of a world-class research university and a member of the “Trojan Family,” which is comprised of the faculty, students and staff that make the...

Leidos Biomedical Research, Inc. at the Frederick National Laboratory seeks a Calibration Specialist to support initial compliance and ongoing QA processes for cGMP manufacturing in a vaccine program.The role focuses on calibration, testing, documentation, and cross-functional collaboration within a regulatory framework. Ideal candidates have 5+ years in...

🧪 QC Laboratory Chemist | cGMP | FDA(Must have at least 2 years' of INDUSTRY experience in a cGMP Laboratory and a BS in CHEMISTRY only).📍 Charlotte Metro Area💰 Salary range $70k - $80k plus discretionary bonus potential up to 12% 🕰️ Hours: Monday – Thursday 3:30pm – 11:30pm & Friday 1:30pm – 9:30pm🚨 US Citizens or Green Card Holders...

Samsung Biologics is seeking an Automation Engineer to support process control systems, manufacturing equipment, building systems, and plant utilities at the Rockville, MD facility. The role focuses on automation and control system engineering for manufacturing operations, facilities, validation activities, and capital projects while ensuring cGMP and...