LL01-260108 Calibration Documentation & Planning Specialist - Juncos

We are seeking a Computer System Validation (CSV) Specialist with more than five years of experience in the biotech industry to support validation activities for regulated computerized systems. · Support planning, execution, and documentation of computer system validation activit ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CQV Specialist - Smoke Testing / Airflow Visualization. · Plan and execute smoke studies (airflow visualization) for cleanrooms, RABS, isolators, filli ...

We're seeking a Specialist QA to work for one of our top Biotechnology Industry clients at Juncos, PR. · Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

We are seeking Specialists QA (multiple positions) to work for one of our top biotechnology industry client at Juncos, · PR. · MS degree and 2 years of directly related experience OR BS degree and 4 years of directly related experience (Sciences or Engineering) · ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities is responsible for ensuring the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems, water systems (e.g. ...

The Commissioning and Qualification (C&Q) Specialist for Utilities and Facilities ensures the qualification and validation of critical utility systems and facility infrastructure in a GMP-regulated environment. · This includes HVAC systems, water systems (e.g., WFI, RO/DI), clean ...

We are seeking a talented individual committed to working under high ethics standards for the position of CQV Specialist. · The ideal candidate will have prior experience with biotech processes, familiarity with regulatory standards (FDA/EU Annex 15), and ability to work cross-fu ...

The Commissioning and Qualification (C&Q) Specialist for Laboratory Systems in QC is responsible for ensuring the successful implementation, validation, and qualification of laboratory systems used in Quality Control environments. · ...

Job summary:This is a manufacturing engineer position at Quality Consulting Group in Puerto Rico & USA. The successful candidate will work with a highly enthusiastic team contributing to the world-class manufacturing industry. · Responsibilities :Assesses impact of IT reports/app ...

We are seeking a skilled Computer System Validation (CSV) Specialist to support a fully onsite project.The ideal candidate will have strong experience in validating GxP-regulated systems. · ...

The Commissioning and Qualification (C&Q) Specialist for Process Equipment will lead and execute the commissioning and qualification activities for syringe filling lines in a regulated GMP environment. · The role requires expertise in process equipment validation, · including fil ...

We are seeking a talented Quality Professional with Manufacturing Process Audit experience. · Review and approve product MPs. · Approve process validation protocols and reports for manufacturing processes. · ...

Join Amgen's Mission of Serving Patients · At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. · As a member of the Amgen team, you'll help make a lasting impac ...

We are seeking a skilled Computer System Validation (CSV) Specialist to support a fully onsite project with one of our key clients. · Develop, review, and execute validation deliverables. · Evaluate systems according to client and regulatory requirements. · ...

We are seeking Specialist QA to work in the east region of PR. This job might be an outstanding fit if you have a degree in Life Science or Engineering and experience in QA processes. · Doctorate OR Master degree in Life Science or Engineering + 2 years of directly related experi ...

The Senior Engineering Specialist independently leads process optimization,troubleshooting,and engineering initiatives within manufacturing,pilot plant,operational or capital project environments. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · Sr Engineer · 1st shift, but it will be required to work 2nd or 3rd shift during the CIP Cycle development activities. · Experience in Pharmaceutical ...

Provides characterization of process optimization strategies and/or troubleshooting of operational issues in operations, manufacturing, pilot plant environment. · ...

We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you. · ...

Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. · ...