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Terrestrial Bio
QA Engineer Lead/Manager, EQ Validation and Metrology
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What they do
A Quality Assurance Manager focuses on prevention of mistakes and defects in manufacturing products. Develops procedures to ensure that quality standards are maintained. Manages all steps related to quality assurance as part of the quality management strategy of a company. May involve leadership of a team of quality assurance supervisors, specialists, and other associated staff members.
$115,452 / year median in Massachusetts
-0% projected decline
Job Description
QA Engineer Lead/Manager, EQ Validation and Metrology Terrestrial Bio Woburn, MA Job Details Full-time $100,000 - $140,000 a year 4 hours ago Qualifications Manufacturing facility experience Full Job Description About Terrestrial Bio, Inc. Terrestrial is transforming the delivery of next-generation therapies, starting with GLP-1. Terrestrial's proprietary Tacterra microarray patch (MAP) and applicator platform consists of a patch resembling an adhesive bandage, which is applied with a preloaded applicator and removed after a few minutes. Once applied, each patch delivers bioactive tips into the skin, which dissolve quickly into the body, rapidly releasing their therapeutic payload. Designed for self-administration, the temperature-stable Tacterra platform enables precise, controlled delivery of a wide range of therapeutics without medical sharps or refrigeration. Terrestrial has generated strong clinical and in-vivo proof of concept across multiple molecules. For more information, visit www.terrestrialbio.com. Why this role The Quality Assurance Engineer Lead/Manager role will manage Terrestrial Bio's Equipment and Metrology program in support of the testing and manufacture of Terrestrial's combination products, with a strong focus on the calibration, re-certification, preventative maintenance, and qualification for critical equipment and instruments. Reporting to the Head of Quality and Compliance, this role works cross-functionally with Manufacturing, Process Development, Quality Control, and Facilities by scheduling and/or performing the calibration and preventative maintenance of critical equipment and instruments to ensure critical equipment/instrumentation is operating within expected operating parameters to include qualification for intended use. What you'll do Oversee calibration schedules and procedures for equipment and instrumentation used in the manufacture, testing, and storage of cGMP products. Ensure that all work aligns with Good Manufacturing Processes (cGMP), Good Documentation Practices (GDP) and 21 CFR Part 11, Electronic Record Standards as applicable. Lead root cause investigations for equipment and analytical instruments deviations and implement Corrective and Preventative Actions (CAPA) as needed. Author, review, approve, and revise Standard Operating Procedures (SOPs) and equipment related protocols such as Installation Qualifications, Operating Qualifications, and Performance Qualifications (IQOQPQ). Act as the subject matter expert (SME) on the calibration and preventative maintenance of all equipment/instruments partnering with Facilities, Manufacturing and Quality Control to ensure cGMP compliance. How you'll impact Improve, Develop and Manage the Metrology program which may include the management of personnel with the QA Equipment Validation and Metrology Program Establish positive relationships across all departments as an advocate for stakeholders to accomplish their agendas. Provide professional service oriented support in support of Terrestrial Bio's Quality Assurance objectives. Who you are A minimum of BS in Mechanical Engineering, Electrical Engineering, Chemical Engineering, Physics, or related technical field required Minimum of BS with 6+ / MS with 3+ years working in a regulated manufacturing environment (Pharma, Biotech, or Medical Device) Strong mechanical skills and a good grasp of analytical instrumentation, measurement systems, and manufacturing equipment Working knowledge of cGMP requirements and International Standards (ISO/IEC17025)