Data Quality Specialist - New Brunswick

We are a fast-growing startup operating in specialized alternative markets, where every detail matters. As a Quality Assurance Specialist, you will serve as the checkpoint for accuracy and consistency across our workflows. · ...

We are seeking a Senior Specialist in Documentation Management to join our team. This role is responsible for ensuring compliance within the organization as it pertains to documentation and records management. The ideal candidate will have a minimum of 4 years of quality experien ...

We're looking for someone who takes pride in precision, thrives in structured environments, and enjoys ensuring that systems and processes perform exactly as intended.About this role: · Verify workflows and task completion against established SOPs · Conduct pre- and post-executio ...

We are recruiting Quality/Compliance Specialist for one of our clients. · ...

Provides Quality support to Contract Manufacturing Operations (CMOs) within a cross functional team and Product Disposition reviews for drug products manufactured/packaged by CMOs. · In addition, to ensure that products released from CMOs comply with Client internal and governmen ...

The Quality Assurance Specialist will oversee manufacture, testing and distribution of clinical supplies to assure quality and compliance with Good Manufacturing Practices (GMP/GDP) and other applicable regulations. · Batch disposition (release/reject decision) · Audit of interna ...

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. · We offer a wide variety of competitive benefits services and programs that provide employees with resources to pursue goals both at work personal lives Read more: · ...

Ensure that products manufactured at packaging facilities are manufactured tested released according to established specifications. · ...

Provides quality support to contract manufacturing operations within a cross-functional team and product disposition reviews for drug products manufactured/packaged by CMOs. · ...

Challenging. Meaningful. Life-changing. · Bachelor of Science degree in chemistry, pharmacy or biology or a related pharmaceutical science. · ...

This role will develop processes and procedures for the supplier quality management system. · B.S. in Natural Sciences, Chemistry, Microbiology, Biology or Pharmacy · ...

This role involves providing quality oversight during Clinical Supply Operations drug product and packaging manufacturing activities. · Provide Quality on the floor in-Process support during manufacturing operations. · Assure the quality of manufactured products complies with all ...

Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. · Bristol Myers Squibb is anything but usual. · Here, uniquely interesting work happens every day, · in every department.From optimizing a production line to the latest breakthrough ...

Global Pharma company looking to hire experienced quality professional to assist with SAP projects of full end to end system lifecycle. · SAP Quality Management consultant · ...

We are looking for an experienced quality professional to assist with SAP projects of full end-to-end system lifecycle in our Global Pharma company. · SAP Quality Management consultant to support SAP projects of full end-to-end system lifecycle; including analysis, testing, proce ...

Challenging. Meaningful. Life-changing. · Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. · ...

We are seeking a Documentation Management Specialist to support our ClientDocs initiative. This individual will be responsible for testing new system prototypes, user acceptance testing, migration mapping from current systems to ClientDocs, and assisting with training activities. ...

This role involves performing independent review and approval of initial Commissioning Qualification and Validation lifecycle documents subsequent changes reviewing periodic reviews requalification decommissioning retirement plans protocols summary reports providing instruction g ...

+The candidate will manage commercial specifications and methods to ensure clear documentation. · Review change proposals for GTS documents. · Perform quality approval of GTS documents. · +Manage commercial specifications and methods. · +Qualifications + Bachelor degree requiredB ...

This is an opportunity to work with a unique organization where challenging and meaningful tasks happen every day. You will have the chance to grow through uncommon opportunities alongside high-achieving teams. · Perform independent review and approval of initial Commissioning, Q ...