Doentation Control Lead

The Doent Control/QA Specialist will be responsible for maintaining the lifecycle of validation doents within an automated system. This role involves performing quality reviews of validation protocols ensuring compliance with internal and regulatory standards.Key Responsibilities: Manage validation doentation in automated systems including doent control...

The Automation/CSV Lead will manage the qualification of automation systems including DeltaV BMS BAS and EMS as well as CSV for production equipment and ytical instruments. This role requires a deep understanding of automated control systems and experience in computerized systems validation (CSV).Key Responsibilities: Develop and execute protocols for...

The Automation/CSV Lead will manage the qualification of automation systems including DeltaV BMS BAS and EMS as well as CSV for production equipment and ytical instruments. This role requires a deep understanding of automated control systems and experience in computerized systems validation (CSV).Key Responsibilities: Develop and execute protocols for...

We are looking for a CQV Lead with expertise in production equipment such as isolators bioreactors fume hoods BSCs and TCUs. The candidate will be responsible for protocol development and to ensure production equipment meets operational and regulatory standards.Key Responsibilities: Develop and execute commissioning qualification and validation protocols...

We are looking for a CQV Lead with expertise in production equipment such as isolators bioreactors fume hoods BSCs and TCUs. The candidate will be responsible for protocol development and to ensure production equipment meets operational and regulatory standards.Key Responsibilities: Develop and execute commissioning qualification and validation protocols...

Seeking a CQV Lead specializing in facilities and engineering to oversee the qualification of building utilities clean utilities and environmental systems. This individual will be responsible for developing and executing commissioning qualification and validation (CQV) protocols to ensure regulatory compliance and to ensure traceability to design...

Seeking a CQV Lead specializing in facilities and engineering to oversee the qualification of building utilities clean utilities and environmental systems. This individual will be responsible for developing and executing commissioning qualification and validation (CQV) protocols to ensure regulatory compliance and to ensure traceability to design...

We are seeking a Senior Project Manager with extensive experience in managing CapEx projects within the pharmaceutical industry. The role involves overseeing project schedules budgets and reporting for a complex CQV initiative. The Project Manager will work closely with crossfunctional teams ensuring alignment with project milestones and regulatory...

We are seeking a Senior Project Manager with extensive experience in managing CapEx projects within the pharmaceutical industry. The role involves overseeing project schedules budgets and reporting for a complex CQV initiative. The Project Manager will work closely with crossfunctional teams ensuring alignment with project milestones and regulatory...

Hello,One of my clients is looking Role: Documentation Control Lead, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.comRole - Documentation Control LeadLocation: New Brunswick, New Jersey, United StatesDuration: Long-TermNote: NO C2CThe Document Control/QA Specialist will be responsible for...

Hello,One of my clients is looking Role: Documentation Control Lead, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.comRole - Documentation Control LeadLocation: New Brunswick, New Jersey, United StatesDuration: Long-TermNote: NO C2CThe Document Control/QA Specialist will be responsible for...

Job DescriptionThe Document Control Lead will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory standards.Key Responsibilities:Manage validation documentation in automated systems, including...

Job DescriptionThe Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory standards.Key Responsibilities:• Manage validation documentation in automated systems,...

Job Title: QC Team Lead - Regulatory Compliance Experience: Minimum of eight (8) years of experience in pharmaceutical analytical or Quality Control laboratory. Experience with generic pharmaceuticals with significant experience in solid dosage form testing. Strong experience in chromatography (HPLC and GC with Empower data acquisition software). Summary:...

Job Title: Lead, Quality Control ChemistUS Pharma Lab is seeking a highly skilled and experienced Lead, Quality Control Chemist to join our team. As a key member of our Quality Control department, you will be responsible for ensuring the quality and integrity of our products.Responsibilities:Perform routine analysis of samples using HPLC, GC, and other...

Job DescriptionJob DescriptionEmbarking on a career in pest management can be a rewarding experience, offering a unique blend of field and classroom training that equips you with the expertise needed to tackle various challenges. As a pest control technician, you'll become adept at identifying, solving, and preventing pest-related issues, ensuring that...

Job Title: Inventory Control LeadJob Summary:Cenmed Enterprises Inc. is seeking an experienced Inventory Control Lead to join our team. As an Inventory Control Lead, you will be responsible for maintaining the integrity of our inventory counts and reconciling inventory variances, expiry tracking, return track, and short/over picks.Key...

Job Title: Documentation Control LeadThe Documentation Control Lead will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols to ensure compliance with internal and regulatory standards.Key Responsibilities:Manage validation documentation in...

Job Title: Practice ControllerAbout the Role:The Practice Controller will play a key role in driving financial excellence and strategic growth at Astera. This position will be responsible for developing and implementing financial strategies that align with the company's overall objectives, ensuring sustainable growth and financial stability.Key...

Role: Documentation Control LeadLocation: New Brunswick, NJDuration: 24+ MonthsJob Description:The Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory...