Fda Gmp Jobs

Field-based sales leader sought to manage and grow a regional Practice Development team for Allergan Aesthetics, driving consumable utilization and key account integration across the Mid East region from a Charlotte, NC home base.

QRC Group is hiring a bilingual Technical Writer in Gurabo to produce and maintain GMP- and regulatory-compliant documentation supporting pharmaceutical development, manufacturing, and inspections.

Lead a large QC laboratory organization at AbbVie's Waco facility, directing lab operations, compliance, and technical projects to support manufacturing and product quality.

Experienced QA professional needed to lead inspection readiness and regulatory response activities for a consultancy supporting pharmaceutical and medical device clients.

Experienced engineering technician to support equipment optimization, MAXIMO data maintenance, and regulatory-compliant maintenance operations for a pharma/medical device consulting client.

Experienced QA-focused scientist needed to perform GMP/GLP audits, review analytical data and batch records, and support quality systems at Eurofins' San Diego lab.

QRC Group seeks a Specialist Tech Engineering in Juncos to support equipment optimization and maintenance compliance for regulated pharmaceutical/medical device environments.

QRC Group seeks an experienced Quality Systems Specialist to manage and improve quality systems, support investigations, and ensure compliance with GMP, FDA 21 CFR Part 11 and data integrity requirements.

NeuroLogica seeks a Logistics & Inventory Manager in Danvers, MA to lead warehouse operations, inventory control, and logistics for our medical imaging manufacturing and service organization.

Lead and scale Tovala’s food safety and quality assurance programs across manufacturing, supply chain, and product development to ensure regulatory compliance and exceptional product quality.

Senior leader accountable for end-to-end Supply Chain Center performance, safety, and leadership development at a leading global pizza company.

Turner & Townsend is hiring a Director of Project Management to lead delivery and growth of life sciences and manufacturing construction services while managing multidisciplinary teams and client relationships.

Cala Health is hiring a remote Therapy Access Intake Specialist (contractor) to handle patient intake, document/fax processing, CRM entry, and benefit verification to support therapy access operations.

Senior QA executive needed to lead Sirtex's global quality management system, drive FDA and international regulatory approvals for device and drug products, and manage a cross-functional QA organization from the Woburn hybrid office.

Lead global regulatory strategy and submissions for Telix’s radiopharmaceutical portfolio, driving IND/BLA/MAA filings and agency interactions to support product approvals and international roll-out.

Senior quality executive needed to lead Irvine and global laboratory operations, standardize best-in-class systems, and ensure regulatory compliance across the organization.

Serve as Associate General Counsel, Senior Director of Regulatory Compliance & Privacy to lead Oura’s global regulatory, privacy, and corporate compliance programs for wearable and digital health products.