Glp Jobs in Mainz

Greensboro, NC AREACompetitive salary + BonusRelo: YesOur client company seeking an expert in separations sciences and chromatography methods development supporting product regulatory requirements and submissions to develop robust methods and innovations to meet global deliverables.Yo More...

JOB SUMMARY: ToxicologyThe candidate will provide scientific oversight and strategic guidance for nonclinical safety evaluation programs from late-stage research through all phases of the drug development process including market application. reporting to the Senior Director Noncli More...

o Ensures customer requirements/specifications and service requirements are compiled for all airlines/customers. This includes airline equipment standards, airline equipment inventory, GLP, and quality assurance controls. o Manage all aspects of inventory management to ensure financi More...

NAMSA pioneered the industry, NAMSA was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the in More...

Senior Validation Engineer Contract Woburn, Massachusetts The Senior Validation Engineer will support a diverse variety of Quality Control and Manufacturing instrumentation, including analytical and microbiological instruments, maintaining the validated state of the instruments fro More...

Ridgefield, CT Contract Duration: 12-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Scientist III in the Ridgefield, CT area. Support critical reagent quality control, characterization, stability testing Currently seeking a talented and innovati More...

The Laboratory Animal Technician will perform responsibilities in compliance with all applicable SOPs, study protocols, GLP guidelines, and other Federal, State, and corporate policies and guidelines.The Laboratory Animal Technician must have AALAS certification as a Laboratory Animal More...

Job Title: Quality Control Technician Location (On-site, Remote, or Hybrid?): Gurnee, IL, (On-site) Contract Duration: Contract until 03/31/2023 Work Hours:2:00PM 10:00PM Description: This is a NonExempt position Summary Perform a wide variety of activities to support the Qualit More...

Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Coordinate with cross-functional proje More...

NAMSA pioneered the industry, NAMSA was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the in More...

Director, Quality Assurance Location: San Diego, CAIndustry: Pharmaceutical / BiotechSummary:Responsible for all aspects of GCP compliance, including inspection readiness. Establish and execute quality plans, policies and quality system elements related to GCP activities. This positio More...

Duration: 6 – 12 Months Responsibilities:* Sample management and tracking, including the receiving and sending ofshipments.* Handling of human clinical samples - FFPE and frozen tissues, blood, PBMCs.* RNA/DNA/protein extraction, QC and downstream biomarker assays.* Manage elect More...

We are looking for a well-established expert in the area of Quality, with emphasis on Quality Control and with strong scientific credentials who are aligned with our noble mission. The candidate should be driven to attain the highest standards of success with integrity. The role o More...

Job title: GXP-Validation Analyst; Location: Chicago/Nearshore CST time Purpose of the position Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facil More...

Job Summary Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples finished product and stability samples in accordance with (GMP, GLP, DEA and company policies and procedures. Assists in writing and perfo More...

B SUMMARY: Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples finished product and stability samples in accordance with (GMP, GLP, DEA and company policies and procedures. Assists in writing and per More...

[Position Summary]: - DOA (Defective on arrival) Specialist is responsible for providing key weekly and monthly reporting of DOA operations and inspection results to be shared with management through the executive level. The candidate will also be responsible for creating and tracking More...

Purpose of the position Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Coordinate More...

Purpose of the position Consult project/client needs wrt validation and 21 CFR Part 11 GXP compliance testing procedures Performing Compliance evaluation of procedures and systems wrt equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Coordinate wi More...

Hours: 2nd shift: 2pm to 12:30am Summary: The Quality Lab Associate II will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all sta More...