Band 5 Compliance Specialist II

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Pharma Services |Viral Vectors | 5 Commerce Drive, Plainville, MA |100% Onsite Days How will you make an impact? This role makes an impact by leading and owning manufacturing investigations; utilizing root cause analysis tools, as required, to identify root causes and contributing factors; supporting and developing consistent manufacturing/quality standards and processes for Deviations and CAPAs in Quality Systems; and conducting complex document revisions and/or document management, including batch production records and manufacturing procedures.

Investigation / CAPA Conduct and Assemble GxP Deviation Investigation Identify event impact and communicate/present findings to Manufacturing and Quality. Define, own, and/or support corrective and preventive actions (CAPAs) in alignment with Manufacturing requirements. Utilize manufacturing process knowledge and investigational skills to identify and resolve manufacturing issues and drive continuous improvement in process operations. Edit cGMP documents and process them through workflow for creation of quality-approved documentation. Collaborate cross-functionally with Manufacturing and other supporting groups. Support Manufacturing during internal and external observations, as required. Practice and promote safe work habits while adhering to safety procedures and guidelines.   Support and develop consistent manufacturing/quality standards and/or processes for Deviations and CAPAs in Quality Systems. Support document revisions and/or document management, including batch production records and manufacturing procedures. Own and maintain tracking systems for manufacturing compliance priorities. Work collaboratively with others to meet group and organizational goals. Participate in initiatives that support innovation and continuous improvement activities. Improve compliance with quality procedures, policies, and regulations. Participate in client and planning meetings as requested, including presentation and document preparation. Support Manufacturing change control.

Minimum High School Diploma required with 6–8 years’ industry related experience 4–6 years’ industry related experience with an Associate’s Degree 2–4 years’ industry related experience with a Bachelor’s Degree Strong interpersonal and communications skills; written and oral.

2-4 years of BioPharma Deviation Investigation Experience Knowledge, Skills, Abilities Must be skilled in the use of a personal computer and related software applications. Must have strong interpersonal and communication skills and the ability to work effectively with a wide range of constituencies in diverse areas. Must be skilled in meetings and interviews to eliciting technical details from subject matter specialists. Must be able to provide effective written or verbal communication to peers, senior associates, and area management within their operational group. Must be able to develop logical structure for technical documents, content and illustrations. Must be detail oriented while proofreading documents. Must be able to recognize, understand and respond to situations requiring further evaluation and report these events (process, safety, personnel, etc.) to senior specialists or area management. Must be able to understand operational documents for GMP compliance, accuracy and completeness.•  Ability to gown aseptically and/or sterile gown as needed.•  Ability to write, read, and review written documentation for extended periods of time.•  Ability to function in a fast-paced, dynamic environment with multiple priorities simultaneously.•  Strong planning, organization, and multitasking skills.•  Strong interpersonal and communication skills, with the ability to work effectively with a wide range of constituencies in a diverse community. Work Environment/Physical Requirements Standard office