MV01-011326 Engineering Technical Lead (ETL) - Juncos, PR

The Engineering Technical Lead – Biotech Facilities Design is responsible for providing technical leadership and coordination in the design of biotechnology and pharmaceutical facility projects. · ...

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

+Job summary · Under general direction, functions as the technical specialist for testing and development in areas of molecular biology and microbiology. · +Responsible for providing technical guidance, provide reports, data analysis and ensure flow of communication between techn ...

The job requires leading the drafting, review, and execution of validation protocols. · ...

The Specialist Tech Engineering will provide technical engineering support on all system/equipment optimization strategies, upgrades, replacements and modifications ensuring that all of the maintenance team operations are maintained in compliance with current corporate policies i ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · The C&Q Lead – Filling Operations: responsible for planning, executing, and managing all Commissioning and Qualification (C&Q) activities associated ...

This position is for a Validation Specialist to work under the highest standards of ethics with expertise in Packaging Validation. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: · Cleaning Validation Scientist.Bachelor's Degree in Science or Engineering. · Minimum of 3 years of experience in direct pharmaceutical, medical devi ...

+We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: Engineer - Packing. · +<ul style= ...

The Quality Specialist will review and approve product MPs, · approve process validation protocols and reports for manufacturing processes, · request Quality on incident triage team.The candidate should have a Bachelor's Degree with four (4) years of experience within the pharmac ...

+Job summary · +Review and approve product MPs, process validation protocols and reports for manufacturing processes, · +Request Quality on incident triage team, Environmental Characterization reports. ...

Job summary · A leading services supplier is seeking a Commissioning & Qualification Lead to oversee commissioning, qualification and validation activities for upstream and downstream process equipment in a biotech GMP manufacturing facility. · ...

+We are seeking a talented, dedicated individual committed to working under the highest ethical standards for the following position: · +Engineer · + ...

We are seeking a talented Process Development Scientist. Requirements include a Doctorate degree or Master degree with 5 years of Scientific experience. Qualifications include process validation previous experience and English speaking and writing skills. · Skills required are ad ...

We are looking for a Quality Specialist to join our team. The ideal candidate will have a Bachelor's degree in sciences and four years of experience in the regulated industry. · ...

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position: CIP/SIP CQV Lead for Biotech. · The CIP/SIP CQV Lead is responsible for the planning, coordination and execution of all Commissioning Qualification and ...

+Job summary · We are seeking a Manufacturing Specialist for our Quality Systems area. The ideal candidate will have a Bachelor's Degree and five years of experience in the pharmaceutical or regulated industry. · +QualificationsBachelor's Degree with five (5) years of experience ...

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

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 ...

With minimal supervision support the execution of manufacturingquality systems such as nonconformances process validation procedures training and new product introductions. · Initiate revise and approve manufacturing procedures ensure all procedures reflect current operations ser ...