What are the responsibilities and job description for the Quality Assurance position at Integrated Resources, Inc ( IRI )?
Job Description: Position Description
Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will be a member of ***’s dedicated and highly effective quality assurance team. You will be responsible for providing Quality Assurance support to GMP clinical manufacturing. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. In addition, this position will perform a range of duties associated with records management to ensure compliance with regulatory requirements and company standards.
How You Will Achieve It
Must-Have
Position Comments visible to Supplier:
Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will be a member of ***’s dedicated and highly effective quality assurance team. You will be responsible for providing Quality Assurance support to GMP clinical manufacturing. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. In addition, this position will perform a range of duties associated with records management to ensure compliance with regulatory requirements and company standards.
How You Will Achieve It
- Review and approve various Good Manufacturing Practices {also cGMP} records (primarily batch records, formulation records).
- Ensure that all documents for batch release are reviewed for completeness and accuracy.
- Support the site relative to a constant state of inspection readiness.
- Recognize when an issue is beyond your sphere of influence and escalate immediately.
- May participate in the release of raw materials, as needed.
Must-Have
- Bachelor's Degree
- Experience in pharmaceutical industry
- Mental agility to handle a large quantity and broad Product of different types of quality assurance work.
- Ability to work independently, problem solve and make recommendations for solutions.
- Role is primarily office-sitting. Position requires walking, sitting, standing, and carrying batch records from one location to another as Andover site is a campus setting.
- 1st Shift, Monday - Friday, typically 8am -5pm (flex on times)
- Work Location Assignment: Andover, MA. On Premise
Position Comments visible to Supplier:
