Resultados de la búsqueda: 21 vacantes
...Responsibilities:
• Independently design, execute and interpret critical experiments to answer scientific questions for manufacturing technical evaluation, new product introduction, or continuous process improvement initiatives. Understand the broad objectives of the...
...&S management system requirements and compliance obligations, promote continuous improvement, and consider EH&S aspects during the design and change process.
Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and disposal...
...Five (5) years of experience in computerized system validation of pharmaceutical or biopharmaceutical industry.
Experience in:
Design and execution of compliant and efficient validation strategies for system and equipment supporting the Manatí Site.
Development...
...EHS management system requirements and compliance obligations, promote continuous improvement, and consider EH&S aspects during the design and change process. Comply with all EHS procedures and policies including incident reporting, use of PPE, waste management and...
...Independently design, execute and interpret critical experiments to answer scientific questions for manufacturing technical evaluation, new product introduction, or continuous process improvement initiatives. To apply visit our site or send your resume to ******:Bachelor...
$20 - $27 por hora
...Conduct comprehensive time studies on manufacturing processes to identify bottlenecks, reduce waste, and increase efficiency.
Design, test, and implement lean manufacturing techniques to optimize production flow and minimize production time.
Collaborate with cross...
...in method development/transfer of biomolecules.
#Experience designing, executing and evaluating method development protocols for new... ...dosage forms.
#Knowledge of Statistical Process Control, and Design of Experiments with demonstrated analytical and problem-solving...
...equipment can handle all current products configuration components and will determine whether it can support proposed changes.
Justify, design, specify, purchase, test, install and validate any new equipment purchases.
Manage project timetables for new and ongoing...
...interest. Run daily reports (number of arrivals, departures), identify any special requests, and check reports for accuracy. Complete designated cashier and closing reports in the computer system. Cash guests' personal checks and traveler's checks. Count bank at the...
...affinity diagrams, brainstorming, etc.). Applies critical thinking to discern relevant information to the investigation report.
Design CAPAs aligned to root cause that are effective in preventing recurrences. Assign CA-PA with reasonable timeframes, track due dates,...
...barriers that affects project scope and/or schedule.
Requirements
# Knowledge and experience of Rockwell Automation products
# Design and programing of CompactLogix PLCs (Required)
# Design and programing of FactoryTalk View SE applications (Required)
#...
...Type Non-Management
POSITION SUMMARY
Assign room according to guest request and preferences whenever possible. Pre-register designated guests and prepare key packets. Organize and coordinate check-in/pre-registration procedures for arriving groups. Review/Track/...
...even to the environment, you might just be what we’re looking for!
AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)
Designs, executes and evaluates method development protocols to ascertain the required degree of validation for new and existing methods...
...Facilitates pastry classes for customers and the community.
Verifing Culinary Standards and Responsibilities are Met
• Develops, designs, or creates new ideas and items for pastry kitchen.
• Follows proper handling and right temperature of all food products.
•...
...support proposed changes in packaging components.
Support, assist and /or justify packaging capital projects help research, such as designs, specifies, purchases, tests, installs, and validates any new equipment purchases
BEING A FITS PIECE COMES WITH PERKS:
~ One...
...process and analytical and microbiology laboratory.
Review/Approve equipment/facilities/system validation documents such as Users design Specifications (URS), Design Specifications(DQ), Risk Assessment(RA), Data Mapping/Data Flow/data Integrity, Audit Trail Review...
...knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
~Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
~SDLC, Risk Assessment...
...proposed changes.
#Supports, assists and /or justifies inspection technology/operations capital projects help research.
#Justifies, designs, specifies, purchases, tests, installs and validates any new equipment purchases.
#Plans, coordinates, and executes projects to...
...Engineering.
~Experience in pharmaceutical facilities and equipment qualifications in a manufacturing environment.
~Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
~SDLC, Risk Assessment...
...knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
~Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.
~SDLC, Risk Assessment...