Weil Group

Full Time

The selected resources will provide operational support for document and records management activities at a pharmaceutical manufacturing site. The role is focused on maintaining accurate organized and readily retrievable GMP and business records to support day-to-day operations regula

The selected resources will provide operational support for document and records management activities at a pharmaceutical manufacturing site. The role is focused on maintaining accurate organized and readily retrievable GMP and business records to support day-to-day operations regula

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Full Time

OVERVIEWThe Lead Deviation Investigator is responsible for overseeing conducting and documenting investigations related to deviations nonconformances and quality events. This role ensures timely thorough and compliant investigations that identify true root causes and drive effective c

OVERVIEWThe Lead Deviation Investigator is responsible for overseeing conducting and documenting investigations related to deviations nonconformances and quality events. This role ensures timely thorough and compliant investigations that identify true root causes and drive effective c

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Full Time

The Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment supporting the reliable and compliant manufacture of spray dry dispersion and solid dosage forms at external contract manufacturing groups to predetermined global quality

The Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment supporting the reliable and compliant manufacture of spray dry dispersion and solid dosage forms at external contract manufacturing groups to predetermined global quality

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We are looking for a qualified candidate to Upgrade the Filler Machine Adept Robot System Servo Motion Systems (Including Servo motors and drives) Variable Frequency Drives (VFD) I/O Devices and Safety components with applicable software and hardware products and supported Windows Ope

We are looking for a qualified candidate to Upgrade the Filler Machine Adept Robot System Servo Motion Systems (Including Servo motors and drives) Variable Frequency Drives (VFD) I/O Devices and Safety components with applicable software and hardware products and supported Windows Ope

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Position SummarySenior-level EHS professional responsible for leading safety and environmental compliance activities during construction and capital project execution within an industrial or manufacturing environment. This role requires strong field presence contractor oversight regul

Position SummarySenior-level EHS professional responsible for leading safety and environmental compliance activities during construction and capital project execution within an industrial or manufacturing environment. This role requires strong field presence contractor oversight regul

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Resource Qualifications The assigned resource must meet the following minimum qualifications: Bachelors degree in Engineering Computer Science Information Systems or related field. Minimum five (5) years of experience in pharmaceutical operations or manufacturing environments with p

Resource Qualifications The assigned resource must meet the following minimum qualifications: Bachelors degree in Engineering Computer Science Information Systems or related field. Minimum five (5) years of experience in pharmaceutical operations or manufacturing environments with p

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Full Time

Resources Qualifications BS in electrical computer mechanical engineering and or related fields. Five-(5) years of experience in pharmaceutical operations or Manufacturing processes with proven project management skills which four (4) of the five years experience must be in Process

Resources Qualifications BS in electrical computer mechanical engineering and or related fields. Five-(5) years of experience in pharmaceutical operations or Manufacturing processes with proven project management skills which four (4) of the five years experience must be in Process

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Weil Group

Full Time

Position RequirementHave at least 8 years of experience in the execution of pharmaceutical environment project execution. Have 30HRS OSHA Certification along with other certifications that will qualify the resource above required qualifications.Took the initial EHS Contractor Safety o

Position RequirementHave at least 8 years of experience in the execution of pharmaceutical environment project execution. Have 30HRS OSHA Certification along with other certifications that will qualify the resource above required qualifications.Took the initial EHS Contractor Safety o

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Full Time

Job Title Cyber Resiliency ManagerWork Location: Onsite/ Remotely at ManatiHours: Mon-Fri 8a-5pmPosition SummaryThe Cyber Resiliency Manager for the manufacturing site is responsible for protecting and strengthening the resilience of site-specific IT and OT systems that support pharm

Job Title Cyber Resiliency ManagerWork Location: Onsite/ Remotely at ManatiHours: Mon-Fri 8a-5pmPosition SummaryThe Cyber Resiliency Manager for the manufacturing site is responsible for protecting and strengthening the resilience of site-specific IT and OT systems that support pharm

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Full Time

Paga 11.53 p/h con diferencia lde turno y overtime a dobledisponible para los tres turnos y tiempo extraMAJOR DUTIES AND RESPONSIBILITIES:1. Operates automatic and/or semi-automatic inspection equipment following all established cGMPs and Safety regulation maintaining equipments up ti

Paga 11.53 p/h con diferencia lde turno y overtime a dobledisponible para los tres turnos y tiempo extraMAJOR DUTIES AND RESPONSIBILITIES:1. Operates automatic and/or semi-automatic inspection equipment following all established cGMPs and Safety regulation maintaining equipments up ti

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DUTIES & RESPONSIIBILITITESAccountable for the design and execution of IQ/OQ/PQ studies of process for parenteral and oral solid drug dosages products manufactured at Clients facility. Accountable for designing and executing qualification studies for sterilization/Dehydrogenation/bio-

DUTIES & RESPONSIIBILITITESAccountable for the design and execution of IQ/OQ/PQ studies of process for parenteral and oral solid drug dosages products manufactured at Clients facility. Accountable for designing and executing qualification studies for sterilization/Dehydrogenation/bio-

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Full Time

Experiencia: 0 a 2 añosPaga: 16.28 p/hThe Credit Administrator will be responsible for maintaining accurate financial information and IT systems as well asproviding analytical support and financial information in compliance with corporate policies and governmentregulations. Responsibl

Experiencia: 0 a 2 añosPaga: 16.28 p/hThe Credit Administrator will be responsible for maintaining accurate financial information and IT systems as well asproviding analytical support and financial information in compliance with corporate policies and governmentregulations. Responsibl

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Full Time

We may have a potential need for a Cyber Security Analyst.Education:Bachelors degree in Cybersecurity Computer Science EngineeringCertifications such as CISSP CISM GICSP CRISC is a plusExperience:6 years of experience in cybersecurity OT security or cyber resiliency with at least 3 ye

We may have a potential need for a Cyber Security Analyst.Education:Bachelors degree in Cybersecurity Computer Science EngineeringCertifications such as CISSP CISM GICSP CRISC is a plusExperience:6 years of experience in cybersecurity OT security or cyber resiliency with at least 3 ye

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