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The Research Associate II conducts laboratory experiments supporting biopharmaceutical development, including in-process testing and data analysis, while ensuring safety and proper chemical handling.

The Process Engineer will support manufacturing processes, collaborate with teams on equipment issues, and ensure compliance with cGMP operations. Responsibilities include equipment commissioning, specification, and project management.

The Director of Program Control leads internal business functions, manages a program control team, and ensures compliance with policies while overseeing project planning, tracking, and reporting.

The QA Specialist II ensures compliance review of GMP data, provides QA oversight, and collaborates with internal and external teams for quality assurance in biopharmaceutical testing.

The Program Control Senior Manager oversees program performance, develops plans, mentors junior staff, manages budgets, and ensures compliance with financial standards.

The QA Specialist II ensures compliance through reviewing and approving GMP data, method qualifications, validations, and laboratory investigations in biopharmaceutical development.

The Senior QA Specialist leads Quality support for client projects, ensuring compliance with Quality Systems, regulatory requirements, and facilitating client interactions, troubleshooting issues, and supporting audits and investigations for pharmaceutical manufacturing processes.

Supervise microbiological programs, manage employee development, ensure quality testing, and maintain compliance with regulations in a laboratory environment.

The Proposal Development Manager writes and edits technical proposals for biopharmaceutical services, collaborates with teams, and ensures proposal accuracy and quality.

The In-Process Support Associate will perform cGMP in-process analytical support, testing drug substances and conducting data analysis while adhering to safety requirements.