Senior Engineer - Juncos, PR

+ Develops quality standards collaborates with engineering manufacturing functions to ensure quality standards are in place. · + +Experience with Risk management documentation: pFMEAsKnowledge in statistics preferably using MinitabKnowledge in designing validation strategies e.g ...

We are seeking a highly skilled and experienced Senior Engineer to lead the development and optimization of packaging systems for biotechnology products including vials prefilled syringes and SureClick autoinjectors. · Packaging Development: Design develop and validate innovative ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Senior Engineer. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the position of Process Development Scientist.To conceive, design, implement and execute specific scientific experiments. · Conceives and designs, executes or evaluates, and i ...

The ideal candidate will have hands-on experience in PLC programming and troubleshooting automated equipment. · In addition to strong expertise in automation systems, · The role will require a combination of advanced technical skills, problem-solving abilities,and a deep understa ...

We are seeking a Principal Validation Engineer to join our team. The ideal candidate will have a Bachelor's Degree and eight years of experience as a senior Engineer in the pharmaceutical or regulated industry. · Bilingual (English & Spanish) with Project Management skills and ex ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · ...

+The Job is to manage the Supply Chain services for a Pharmaceutical or Medical Device industry company. · +Ensure all work is completed with minimal disruption and in compliance with all cGMP guidelines and procedures. · Direct and coordinate daily activities of personnel respon ...

The Supply Chain Manager will ensure all work is completed with minimal disruption and in compliance with all cGMP guidelines and procedures. · ...

Doctorate or Masters + 2 years of Manufacturing and/or Quality support experience or Bachelors + 4 years of Manufacturing and/or Quality support experience or Associates + 8 years of Manufacturing and/or Quality support experience or High school/GED + 10 years of Manufacturing an ...

We are seeking a talented Quality Assurance Specialist to work under the highest ethics standards. Perform duties and responsibilities in support of the Quality Assurance program under minimal supervision and lead site audits. · Review and approve product MPs. · Approve process v ...

To conceive and implement specific scientific experiments under general guidance of supervisor. · -Conceives and designs experimental strategies.-Provides input to new processes to generate robust data.-Designs monitors or conducts experimental strategies with general guidance fr ...

This role involves project management and quality assurance in the biotech or pharmaceutical industry. · Work experience (manufacturing, process development, or quality assurance) in Biotech or pharmaceutical industry with progressively increasing responsibility and demonstrated ...

To conceive, design and implement scientific experiments contributing to the successful completion of goals under general guidance. · ...

We are looking for a Process Development Scientist to join our team in Juncos, PR. The ideal candidate will have a Bachelor's Degree with four years of experience in the pharmaceutical or regulated industry and be bilingual (English & Spanish). They should also have project manag ...

To conceive, design, implement and execute specific scientific experiments... · ...

We are looking for a talented and highly motivated Supply Chain Manager to join our team in Puerto Rico & USA. · ...