sleep quality specialist - Florham Park - beBeeSleepConsultant

A leading consumer health / cosmetics & skincare manufacturer seeks a Site Quality Specialist to support Quality operations at a GMP manufacturing site. · Support day-to-day site quality operations in a GMP environment. · Review and approve SOPs, deviations, change controls, and ...

In this role, you will support regulatory and quality operations on-site, ensuring compliance with GMP standards while collaborating closely with cross-functional teams. · Support regulatory and quality activities related to site operations in a GMP environmentInitiate, review,/l ...

A leading consumer health/cosmetics & skincare manufacturer is seeking a Site Quality Specialist to support Quality operations at a GMP manufacturing site. · Support day-to-day site quality operations in a GMP environment. · Review and approve SOPs, deviations, change controls, a ...

This role is responsible for managing the drug listing process, including the listing and delisting of products (skincare, cosmetics). The position supports regulatory tasks and regulatory operations as needed. · Reviewing and approving incoming raw material documentation · LIMS ...

This position will support QA oversight of CTLs for CTO Vector External Manufacturing operations. · This role is accountable for oversight of routine Quality responsibilities related to outsourced testing · Deviationss CAPAs Change Controls Certificate of Analysis/Certificate of ...

This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. · ...

The Global Supplier Quality, External QC - Vector will process external deviation and change records from our Contract Test Laboratories (CTL). Other duties may include; Coordinate shipping and testing of samples for lot release, PPQ, · PSQ and will compile vendor documentation t ...

+This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. · +Requires bachelors degree in Science or related discipline. · Minimum 3-5 years of experience working in a regulated GxP environment. · ...

A large CPG client of ours is looking for a regulatory site quality specialist to help with their products OTC drug listing portfolio. · ...

We are seeking a · Regulatory Site Quality Specialist · to support a leading CPG company’s OTC drug listing portfolio. · This role will manage the FDA OTC drug listing process, · including listing and delisting products (skincare · & cosmetics). You will collaborate with cross-fu ...

This position will work independently and with the team in supporting QA oversight of CTLs for CTO Vector External Manufacturing operations. external from our CTLs. · This role is accountable for oversight of routine Quality responsibilities related to outsourced testing, Deviati ...

We are seeking a Regulatory Site Quality Specialist to support a leading CPG company's OTC drug listing portfolio. · Manage OTC drug listing and delisting processes for skincare and cosmetic products. · Collaborate with cross-functional teams to ensure compliance with GMP standar ...

A regulatory site quality specialist is needed for OTC drug listing portfolio management. · Reviewing and approving incoming raw material documentation · GMP batch records review and approval · ...

This individual will provide Quality oversight of the analytical space at our large pharmaceutical client's External Quality team within Advanced Therapeutics. · ,Review and approve nonconformances and deviations out of specification. · ,Interface as liaison internally and extern ...

This job involves providing quality oversight of the analytical space in an External Quality team. The ideal candidate should have experience working in drug substance or pharma manufacturing space with analytical methods. · ...

The Quality Specialist will coordinate the review, investigation, and corrective actions associated with product complaints with the responsible manufacturing facilities in accordance with Corporate and Divisional policies and procedures. · ...

We are looking for a Quality Person In Plant to join the growing External Quality team within Advanced Therapeutics. This individual will be providing Quality oversight of the analytical space. · Bachelor's degree with a concentration in engineering, science, or an equivalent tec ...

+The Quality Control Specialist is responsible for assisting the Quality Control Manager in ensuring the operational soundness of the Bank's customer-facing channels.This individual will work with Direct-to-Consumer management to identify areas of improvement and operational know ...

Job summary:The Quality Assurance eSystem Specialists primary responsibility is to help assure the quality, integrity, and compliance of site Information Technology (IT) systems, · and maintain alignment between business process owners, end users, and other cross functional areas ...

This Quality Assurance role involves performing QA shop floor activities, ensuring manufacturing compliance with applicable procedures and batch records. · ...

This role involves quality assurance monitoring and compliance with standards. · ...