Quality Assurance Associate / Document Control Specialist

Are you ready to play a critical role in ensuring quality and compliance in a fast-paced, regulated environment? As a Quality Assurance Associate focusing on document control, you'll be at the heart of maintaining product integrity and driving operational excellence. If you thrive on precision, collaboration, and making a tangible impact, this opportunity is for you.

Why You Should Apply

• Be a key player in ensuring quality and compliance across manufacturing and quality control.

• Gain hands-on experience managing critical documentation and processes in a regulated industry.

• Collaborate with cross-functional teams to maintain high standards and drive process improvements.

• Enjoy a dynamic work environment where no two days are the same.

What You’ll Be Doing

• Issue and manage controlled manufacturing and testing documents according to production schedules.

• Oversee the equipment program, including calibration, preventive maintenance, and quality assurance sign-offs.

• Coordinate the release of raw materials by reviewing and approving supporting documentation.

• Manage the label program, including developing master labels and maintaining controlled stock.

• Collaborate across departments to ensure timely delivery and adherence to quality standards.

About You

• Be able to do the job as described.

• Strong understanding of cGMP and ISO standards.

• Experience with lab equipment operation and technical documentation.

• Skilled in MS Word, PowerPoint, and Excel for document management.

• Excellent communication skills to interface with all levels of the organization.

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send an email to ccupo@jacobsmgt.com and tell me why you’re interested. Or, if you do have a resume ready, apply here.