Inteldot has over 15 years of experience in the life sciences industry, with allocations across Puerto Rico, the United States, Europe, and Japan. This is a great opportunity for one of our leading clients in Puerto Rico.
Job Description
Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. Focus is on the complex technical issues and scope is typically multi-organizational and/or multi-site and /or involving outside resources.
Administrative shift 8:00am – 5:00pm
Requirements
- Experienced in Method Validation, Method Transfer, Method Qualification.
- Experience in project management.
- Scientific Data Analysis.
- Strong knowledge in Microsoft Excel as a Tool for Data Analysis.
- Sample Management.
- Basic Knowledge on equipment preventive maintenance and troubleshooting.
- Agile on prioritization of critical tasks.
- Ability to develop inspection or qualification protocols in a short timeframe period.
- Strong negotiation skills.
- Good communication skills.
- Able to work with multi-functional Teams.
- Able to communicate effectively in both English and Spanish.
Functions:
- Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between technical groups including following up on and resolving issues that arise.
- Resolve technical issues and troubleshoot for assays as necessary
- Ensure lab compliance which includes Implementing procedures that enhance GMP, GLP and safety.
- Manage existing and/or develop and implement new programs, processes and methodologies.
- Develop, revise and audit various complex controlled documents that may have multi-organizational and/or multi-site impact.
- Approve lab investigations, Lead audit teams
- May serve as subject matter expert to develop technical training.
- May perform routine work in a specific area of responsibility as necessary.
- Represents the department/organization on various teams, independently responsible for following through on multi-site action items.
- May interact with regulatory agencies regarding area(s) of responsibility including written responses.
- May resolve issues with outside resources.
Education:
- Doctorate OR Masters + 2 years of directly related experience OR Bachelors + 4 years of directly related experience OR Scientific background in Biochemistry / Chemistry or Micro (at Bachelors degree).
Skills Required
- Method validation, method transfer, method qualification experience
- Project management experience
- Scientific data analysis
- Strong knowledge of Microsoft Excel for data analysis
- Sample management
- Basic equipment preventive maintenance and troubleshooting
- Ability to prioritize critical tasks and work under pressure
- Ability to develop inspection or qualification protocols rapidly
- Strong negotiation and communication skills
- Ability to work with multifunctional teams and provide technical guidance
- Experience ensuring lab compliance and implementing GMP/GLP and safety procedures
- Experience developing, revising, and auditing controlled documents
- Audit leadership and ability to approve lab investigations
- Ability to communicate effectively in both English and Spanish
- Education: Doctorate OR Masters + 2 years OR Bachelors + 4 years (Biochemistry/Chemistry/Microbiology or related)
What We Do
Inteldot offers custom turn-key systems, systems integration, MES eBR configuration and integration solutions, business intelligence and analytics and technical staffing. We have been providing the Pharmaceutical, Manufacturing and Medical Device industries with services for a variety of applications since 2004
