At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.
2025. All right reserved.
SGS_JOB_2321
Contract - 12 Months
The Data Assurance Associate (GPV) plays a vital role in ensuring the accuracy, compliance, and quality of case processing activities within Pharmacovigilance. This role involves active communication with internal teams, external partners, and vendors to address case-related queries, oversee case corrections, and support training initiatives. The associate will contribute to maintaining the highest standards in pharmacovigilance operations while driving process improvements and compliance with global regulatory requirements.
Location (mandatory): Portsmouth NH • We are seeking a QC Analyst III will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed.
Location - Marana, AZ The global sub-chapter Production Engineering - Change Services is part of the global Engineering Chapter responsible for cost efficient, reliable and lean Change Control Management (ECRs). The scope of this team is mainly on Product Care topics for established products and introduction of new products from pilot phase to commercial production. The sub-chapter brings in technical expertise to deliver successful material, system, process and product changes.
Location : Vacaville CA Under moderate supervision, QC Specialist is expected to support planning, managing, and executing projects related to the product portfolio for Vacaville Quality Control. These projects include analytical transfers, control system updates, regulatory filings and other activities associated with the life-cycle of a product.
Location - Vacaville California Responsible for support and execution of QC laboratory equipment qualification activities while in full compliance with current cGMP regulations and Roche/Genentech corporate principals, quality policies, standards and core values. Maintains company’s right to operate, supply to patients, and cost effectiveness by actively participating in continuous improvement projects
Location: Westborough MA 01752. The primary purpose of the Analyst I position is to Support Quality Control Microbiological testing of drug substances, raw materials and process intermediates in support of clinical development and commercial programs under cGMP and GLP guidelines, address excursions and conduct investigations.
Location (mandatory): Marlborough, MA 01752 (Onsite) The engineer will be responsible for leading customer engagements, troubleshooting, running experiments, and analyzing data using techniques such as electrochemistry, SEM, and HPLC. The role involves close collaboration with global teams, preparing technical reports, and ensuring strict adherence to safety protocols.
At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.