To Go Specialist Jobs in Juncos

DescriptionAt Cheniere we provide the world with safe reliable energy. But more than that we provide opportunities for our talented employees to impact their communities every day. Our diversity is key to our continued success and forges a path where our culture supports greater equity and inclusion...

Quality Professional with experience in Quality System and addition some knowledge or to be familiar with in PASx/MES application MAXIMO SAP LIMS QMTS and Veeva. Available during weekends and holidays as requested always available to be on site. RequirementsDoctorate OR Masters 2 years of experien...

We are seeking a C&Q Specialist to support a critical shutdown tied to a robotic arm replacement and motion control upgrades (servos/VFDs pneumatic safety interlocks) within a highly automated production system. This role will be responsible for executing and documenting Installation Qualification (...

Knowledge and experience in: Process Safety Pre-Start Up Safety Reviews Process Safety Management (PSM) High Risk Processes Hazardous/Compressed Gases Combustible Dust Risk Assessments and Machine Safeguards.RequirementsMaster degree or Bachelor degree & 2 years of directly related experience Associ...

Deviations documentation and Change Control Management.Requirements-Doctorate OR-Masters 2 years of Manufacturing Operations experience OR-Bachelors 4 years of Manufacturing Operations experience OR-Associates 8 years of Manufacturing Operations experience OR-High school/GED 10 years of Manufact...

Experience (manufacturing process development or quality assurance) in Biotech or pharmaceutical industry with progressively increasing responsibility and demonstrated experience in compliance problem solving critical thinking project management and quality systems. Proficient and experienced in ow...

Execute Quality disposition (approval or rejection) of bulk drug substances. Provide Quality oversight to ensure that operations for clinical and licensed pharmaceutical Drug Substance (API) are manufactured tested stored and managed according to current Good Manufacturing Practices (cGMP) Good Lab...

Responsible of performing finance partnering activities to support capital site strategy.Responsible for developing implementing and maintaining the financial plans and policies of the capital organization. In charge of establishing fiscal controls preparing financial reports advising management on...

SummaryThe Quality Applications Specialist supports quality systems and product transfer activities by ensuring compliant validation of computerized systems and manufacturing processes. The role focuses on sterilization equipment process validation and quality system compliance in regulated environm...

Expericence in Quality and ComplianceExperience with validation protocols and reports for clean utilities manufacturing processes cleaning processes equipment computerized systems change control records deviationsetc. Experience in biological processes is desired.RequirementsDoctorate OR Masters 2...

QRC Group is a leading provider of consulting engineering validation quality and talent solutions for the pharmaceutical biotechnology and regulated manufacturing industries. Our mission is to connect top-tier talent with essential projects that drive innovation quality and operational excellence fo...

Aseptic Process NPI Change Control FATs Validation and PPQsRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Life...

Change Control Documentation Review Validation PPQRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Bachelor Degr...

Lead and execute Computer System Validation (CSV) activities for Quality Information Technology systems in compliance with FDA GxP ISO and global regulatory requirements.Conduct and maintain formal validation documentation including Validation Plans Risk Assessments IQ OQ PQ protocols and reports an...

NPI Change Control Documentation Review Validation C&Q PPQ FATRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.S...

Aseptic Process NPI Change Control FATs Validation and PPQsRequirements-Doctorate OR-Masters 2 years of directly related experience OR-Bachelors 4 years of directly related experience OR-Associates 8 years of directly related experience OR-High school/GED 10 years of directly related experience....

NPI Change ControlFATsValidationPPQsRequirementsDoctorate OR Masters 2 years of directly related experience ORBachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Life Science or Engineering

NPIChange ControlDocumentation ReviewValidationPPQFATRequirementsDoctorate OR Masters 2 years of directly related experience OR Bachelors 4 years of directly related experience ORAssociates 8 years of directly related experience ORHigh school/GED 10 years of directly related experience.Bachelor...

Experience with: VeevaTrackwiseCAPAChange ControlRequirementsDoctorate degree OR Masters degree and 3 years of Manufacturing Operations experience ORBachelors degree and 5 years of Manufacturing Operations experience ORAssociates degree and 10 years of Manufacturing Operations experience ORHigh scho...

Experience in deviations DQMS experience in leading multidisciplinary teamsRequirements-Doctorate OR Masters 2 years of Manufacturing Operations experience OR Bachelors 4 years of Manufacturing Operations experience OR-Associates 8 years of Manufacturing Operations experience OR-High school/GED...