Regulatory Labeling Specialist - Princeton - Integra LifeSciences

Changing lives. Building Careers. · Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making ...

Changing lives. Building Careers. · Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making ...

Changing lives. Building Careers. · Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making ...

Changing lives. Building Careers. · Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making ...

Changing lives. Building Careers. · Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making ...

Shift: 2nd Shift , Sun-Wed 3:30pm-2:00am · Note: Work hours that will change to 6:00pm-6:30pm starting 29-Mar-2026. · The Label Control Specialist at the S-12 Cell Therapy manufacturing facility is responsible for supporting site Label Control activities at S-12 in accordance wit ...

+Job summary · A manufacturing labeling specialist is responsible for packaging and labeling materials project management, strategic and tactical change planning and forecasting of new product markets and indications launches to ensure the Cell Therapy Operations organization mee ...

Job Title: QA CTO Label Specialist · Location: Summit, NJ · Type: Contract · Compensation: $ $34.95/hr · Contractor Work Model: On-Site · Hours: Sun-Wed 3:30pm-2:00am (starting 29-Mar-2026, work hours will change to 6:00pm-6:30pm) · Overview · Global pharma company looking to hir ...

Job Title: QA Label Control Specialist · Pay Rate: $30-$37/hour · Location: Summit, NJ · Duration: 12 months , upto 2 years extension · REQUIRED COMPETENCIES: Knowledge, Skills, and Abilities: · • Must have knowledge and experience with GMP, Quality, and compliance. · • Able to ...

Job Description · The Label Control Specialist at the S-12 Cell Therapy manufacturing facility is responsible for supporting site Label Control activities at S-12 in accordance with policies, standards, procedures and Global cGMPs. Functional responsibilities include performing i ...

Job Number: · Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for a QA CTO Label Specialist for our client in Summit, NJ. · ECLARO's client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medic ...

Job Title: · QA CTO Label Specialist · Location: · Summit, NJ · Type: · Contract · Compensation: · $ $34.95/hr · Contractor Work Model: · On-Site · Hours: · Sun-Wed 3:30pm-2:00am (starting 29-Mar-2026, work hours will change to 6:00pm-6:30pm) · Overview · Global pharma company lo ...

The Quality Assurance Document Control Labeling Specialist supports the cGMP Document Control operations for the client site including the coordination issuance reconciliation and management of production labels and records To succeed in this role you will have a strong attention ...

We are seeking a QA Label Control Specialist- Pharma (Onsite- Summit, NJ) for a global pharmaceutical client. You will be responsible for supporting site Label Control activities at S-12 in accordance with client's policies, standards, procedures and Global cGMPs. Functional resp ...

+Job summary · The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site.+ · +Bachelor's degree or equivalent. · +Supports all activities for the Quality Assurance Label Control group. · ...

This position is a Quality Assurance Document Control (QADC) Labeling Specialist that supports the cGMP Document Control operations for the client site. · ...

Job summary · The Specialist Quality Assurance Labeling Control supports the cGMP Label Control operations for the client site, including the coordination, issuance, reconciliation and management of production labels and records. · ...

The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site, · including the coordination, issuance, reconciliation, and management of production labels and records. · To succeed in this role, you will have a ...

The Principal Specialist is responsible for the strategic global development maintenance and compliance of product labeling throughout drug lifecycle. · Create and execute global labeling strategies from early clinical development through commercialization. · Contribute to writin ...

The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site, including the coordination, issuance, reconciliation and management of production labels and records. · ...

The Quality Assurance Document Control (QADC) Labeling Specialist supports the cGMP Document Control operations for the client site. · Issuing production labels batch records and other controlled documents to support manufacturing operations. · Coordination of work activities to ...