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Job Description

Our pharmaceutical client is looking for a QA Specialist to join their team. This person will demonstrate sufficient depth of knowledge within own work area in order to perform hands-on routine QA tasks. This role supports Operations including batch record review, document review, and disposition activities. Resolve routine quality issues related to product manufacture and testing with guidance/coaching. Project work, as needed, will also be expected.

• Provides ongoing site-based Operations support for both start up and ongoing product manufacturing.

• Competently reviews simple batch records and associated simple deviations and simple analytical investigations. (Cal OOTs, RAAC, CIS and Events)

• Able to resolve less challenging quality issues and make simple batch disposition decisions with guidance and coaching.

• Able to review and approve documents in PDOCS with quality mindset.

• Uses established QA procedures and methodologies to propose solutions for straight forward problems with guidance and coaching.

• Makes decisions that require knowledge of quality systems.

• Represents QA on various Teams with direction from management.

• Exercises judgment in resolving simple quality issues.

• Able to review executed batch documentation for technical content within own subject area and reference to applicable GMPs and regulatory expectations, make value-added comments.

• Manages own workload with oversight by manager/peer.

• Represents their quality records with Board of Health inspectors, with support of management, as needed.

• Maintains inspection readiness and supports internal/external audits as needed.

• Supports QA on the floor rotation.

• Manage own time to meet agreed targets and develop plans for work activities on own projects within a team.

• Review and approve Manufacturing records to ensure that the information and documentation conforms to company policy and cGMP's.

• Ensure that all documents received in the batch release area reviewed for completeness and accuracy.

• Maintain inspection readiness, support inspections from regulatory agencies & customers and improve quality assurance systems.

• Participate in Green/Black belt projects, Right First Time (RFT) Improvement projects, Corrective Action / Preventative Action Effectiveness, etc. as appropriate.

• Assist and support the manufacturing/packaging staff in detecting and solving compliance errors in real time during manufacturing operations.

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 [email protected] 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/.

Skills and Requirements

1-3 years of related experience

Experience working in cgmp environment