Job description
mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services include the assessment and validation of automation equipment, network infrastructures and business processes, as well as the involved project management.
Job Description
Education
Preferred Qualifications
This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.
Job Description
- Development & Execution of projects and protocols of Laboratory.
- Development of Laboratory documentation.
- Review Laboratory documentation.
- Laboratories Testing and Equipment Validations.
- Facilities Qualifications.
- Promote and support activities required to assure validation state of the Facility.
- Coordinate department tasks, protocols and special projects.
- Lead, Coordinate and collaborate in the preparation and execution of Validation packages of processes, equipment, method and systems assigned.
- Assure compliance to specified procedures and regulations.
- Participate, and perform as required, in the preparation of changes packages to specifications and procedures.
- Development, execution and approval of plant protocols including coordination within the R&D and Engineering Groups.
- Maintain a positive outlook toward ergonomics, Health, Safety, Security and support activities related to this matter.
- Validate testing methods as required.
- Clear understanding of all Manufacturing & Quality Processes, Systems & Metrics.
- Critical Systems Request Documentation (CSR’s) Handling.
- Environmental testing Documentation Handling.
- Perform laboratory testing, when required.
- Regulatory compliance with our environmental, energy, health and safety policy.
- Other responsibilities as assigned by the Supervisor.
Education
- Bachelor's Degree in related scientific field chemistry and related experience within applicable regulated laboratory required in the Pharmaceutical Industry or medical devices the equivalued required.
Preferred Qualifications
- Chemical Laboratory: 5 years
- IQ/OQ/PQ: 2 years
- Analytical Method Validations: 2 years
- From zero (0) to two (2) years of experience in Chemical Laboratory.
- Demonstrated track record in effective laboratory techniques, including compliance, technical excellence and laboratory processes.
This Company is an equal employment opportunity employer. We adhere to a policy of making employment decisions without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age or disability. We assure you that your opportunity for employment with this Company depends solely on your qualifications.
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