QA Manager

We are looking for a Quality Assurance Manager to join the GxP Process Operations Center within the Quality Assurance organization at a large pharmaceutical client based out of Boston, MA. The QA Manager role is broken down into 20% management/coordination and 80% hands-on document control work. On a daily basis, you will help coordinate and distribute the teams project workload between 1-2 other members, assist with managing and updating internal training materials and other internal documentation, and ensuring compliance with regulations and company standards. Other responsibilities of this position include, but are not limited to, the following: Act as a liaison with business departments to implement process improvements. Lead projects for process implementation and training. Serve as the document control lead on cross-functional teams. Author, review, and approve policies, SOPs, and related documentation. Conduct presentations on Quality initiatives and manage client expectations. Provide guidance on process quality and compliance. Document and define business processes and training procedures. Support audits and regulatory inspections. Supervise Quality staff as needed and contribute to departmental metrics and goals.This job posting is for a hybrid 3-day onsite, 40-hour work week starting on a 6 month contract as an employee of Insight Global on assignment at our client with the intention to extend the contract up to 18 months. The individual selected for this role will be offered the role as an employee of Insight Global; compensation, medical benefits, and other terms and conditions of employment shall be presented by Insight Global upon offer. The pay rate range is expected to be $60-67/hr as 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.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com . To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ . Required Skills & Experience-4+ years of experience with document control specifically within a regulated environment-Experience with Veeva (or similar document management systems)-Proficient with MS Word and Outlook-Strong ability to multi-task multiple projects at any given time, detail oriented, and takes initiative Nice to Have Skills & Experience-Pharmaceutical/biotechnology industry experience Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.