IT Quality Assurance Process Consultant jobs in New Bedford, MA

This QA Associate III – Analytical position is an individual contributor role and is a member of InvaGen’s QA Team at the Fall River, MA (Unit IV) site. The position reports to the Site QA Lead. The essential and typically expected job duties for this position include but are not limited to the following:

• Review data generated in the laboratory is accordance with stablished criteria set forth in SOPs and
established specifications
• Assemble quality data to support management review meeting requirements
• Issuing, reviewing, maintaining, and archiving of laboratory logbooks
• Scanning of laboratory approved finalized qualification for easy accessibility by all department
• Training and execution of internal audits, as required
• Review/approval of calibration records for analytical instrumentation and equipment
• Identify and report any non-conformances and/or discrepancies to management if applicable.
• Complete other duties or participate in project work as assigned by management.

• Minimum bachelor’s degree from an accredited college/university in relevant field of study such as Chemistry,
Pharmaceutical Science, or other Life Science discipline.
• Advanced training or education in pharmaceutical quality compliance or related field of study from an
accredited college/university.is preferred.
• Minimum of three (3) years’ experience in quality assurance in a current Good Manufacturing Practice (cGMP)
pharmaceutical work environment.
• Experience in metered dose inhalation (MDI) preferred.
• Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP,
and other business applications.

Job Type: Full-time

Salary: $70,354.60 - $85,620.59 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Experience:

• Pharma: 5 years (Preferred)
• SOP/cGMP: 5 years (Preferred)

Work Location: In person