Resultados de la búsqueda: 554 vacantes
...international regulations which govern the user's applications.
Reports on the status of validation... ...experience
Experience as Quality Specialist in medical devices of pharmaceutical... ...with rigor and provide guidance where applicable
Support development, review and...
For Engineering support services in the Quality area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and four (4) years of exposure within the Pharmaceutical & Medical Devices Industry.
Bilingual: Spanish and English
Soft Skills...
...Functional Role: Procurement Specialist
Contract Role: Subject Matter Expert
Location... ...management, grants identification and application support, and business continuity... ...Ensure project activity compliance with applicable regulations, laws, policies, and procedures...
...to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.
Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements....
...timely and adequate computerized system validation is performed in conformance with cGMP’s plant procedures, corporate policies, and applicable regulations (FDA, ENEA, DEA, etc.)
Prioritizes projects and schedules as needed.
Provides guidance for determining work...
...Product Introduction
Administrative Shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,,...
...Bristol Myers Squibb (BMS) as the Senior Specialist, Environmental, Occupational Health &... ...adjustments and ongoing support in their roles. Applicants can request a reasonable workplace... ...and conviction records, pursuant to applicable laws in your area.
Any data...
...pharmaceutical products are manufactured, tested, and stored, according to current Good Manufacturing Practices (cGMP) and other applicable regulations. • Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with cGMP practices...
...initiates corrective action of problems and deficiencies to ensure product quality.
Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.
Ensures processes and procedures are in compliance with regulations...
...Investigations Specialist with experience in regulated industries. Strong knowledge of complaints and processes deviations. Will be responsible for performing through, detailed and timely investigations and generation of high quality and timely investigation reports...
...Underwriting Support Specialist American International Group, Inc. (AIG) is a leading global insurance organization. AIG member companies... ...of the accounts and analyze financial statements, application and other documents of underwriting. Request additional information...
Minimum Requirements
Mid-level individual contributor on a project or work team, 3-5 years of experience required.
Bachelor Degree in Engineering
Experience within Medical Devices and/or Pharmaceutical industries.
Experience in equipment IQ, OQ and PQ, Validation...
...Pri General Purpose of the Position
The Onboarding Specialist is responsible for scheduling meetings with new clients to welcome them and establish the communication channel. Onboarding Specialist will be responsible for overseeing active tickets and their completion...
...public events.
Responsible for meeting departmental and center goals and objectives.
Conduct orientation and interview with applicants including parent in case of minors.
Perform applicant files procedures (data entry, scan documents on e- file).
Participate...
...Provide direct support to manufacturing lines.
Ensure Process instructions are accurate, effective and support compliance with applicable regulations.
Develop preventive maintenance strategy and instructions and implement.
Equipment and Process performance...
For Equipment Validation services in the Manufacturing area.
WHAT MAKES YOU A FIT:
The Technical Part:
Bachelor’s Degree in Engineering and five years of experience in Validation Life Cycle within the Medical Device Industry.
Bilingual (English and Spanish)...
...management and compliance.
Administrative shift
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,,...
...highest ethics standards for the following position:
~Permitting Specialist
The Permitting Specialist will play a key role in... ...permitting requirements for projects.
~Prepare and submit permit applications, including gathering necessary documentation and completing...
...Procurement Specialist
JOB SUMMARY : This position is responsible... ...to unlawfully discriminate against any applicant or employee on the basis of race, color... ...military or veteran status or any other applicable legally protected considerations made unlawful...
...evaluate compliance issues.
• Microsoft Office spreadsheet and application skills and presentation knowledge.
• Strong communication (... ...in discrimination complaint-related activities, or any other status protected under applicable federal, state or local law....
