The Chemistry Manufacturing Controls Manager will support the execution of multi-product global regulatory CMC for marketed products. This role contributes to the preparation and submission of regulatory CMC documentation, including clinical trial submissions, and provides regulatory support to various cross-functional teams with a focus on Biologics.
Key Duties and Responsibilities: Execute commercial Lifecycle Management (LCM) strategy and submissions with a focus on US/CA/EU. Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions Participates effectively on cross-functional teams and may serve as the primary regulatory CMC contact for assigned products and projects Required Education Level & Experience Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field Typically requires 4 years of experience in the pharmaceutical industry or related field, or the equivalent combination of education and experience Required Knowledge/Skills Strong interpersonal skills to exchange complex information with others and to guide others Proficiency in regulatory (FDA, EMA, Health Canada, and ICH) guidelines Strong problem-solving skills Ability to collaborate and communicate in an open, clear, complete, timely, and consistent manner Strong sense of planning and prioritization, and the ability to work with all levels of management Sound knowledge of cGMP, FDA, EMA, ICH Pay Range $75-$80/HR Requisition Disclaimer This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements

Also on the board Same function, level within a rung

Level

Senior

Salary

$75.00 - $80.00 per hour

Location

East Boston, MA

Occupation

Regulatory Affairs Managers

Industry

Pharmaceutical Preparation Manufacturing

Posted

yesterday

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