Quality Assurance Specialist II

Description:

Quality Assurance Specialist II is an intermediate level position with hands-on QA experience. Under moderate supervision, the individual will be working primarily on quality systems, the reserve sample program and incoming attribute inspections. The individual will also assist in quality operations area, such as batch record and quality control data review, line clearances, AQL inspection, and will be interacting with cross-functional groups such as Quality Control, Manufacturing and Regulatory Affairs.

ESSENTIAL DUTIES:

• Perform a wide variety of quality assurance activities to ensure compliance with procedures, applicable US and international regulatory requirements for biologic drug substances and drug products under clinical development.
• Manage the reserve sample program.
• Perform incoming quality attribute inspections.
• Coordinate and track closure of the change controls, deviations, quality investigations and CAPAs.
• Prepare quality system metrics.
• Review and disposition of incoming raw materials.
• May support quality operations, as needed (e.g., review executed records such as batch records/ quality control data or equipment qualifications; perform line clearance and product inspection; review other records under supervision such as change control requests, deviations, lab investigations, environmental monitoring excursions, proposed CAPAs).
• Support continuous improvement of quality systems. Author new, revise existing department procedures and/or forms.
• Assist in internal compliance audits as needed.
• Provide inspection readiness support and assist during inspections by regulatory authorities or other third parties.
• Other duties as assigned.

Skills:

Batch Record Review, capa, audit, document control, quality assurance, quality control, batch record

Additional Skills & Qualifications:

• Minimum 4 year’s experience performing quality functions in pharmaceutical and/or biotech related fields.
• Some working knowledge of quality systems cGMP standards applicable to clinical biologics DS and DP.
• Works under moderate supervision.
• Ability to independently analyze and reconcile simple issues.
• Ability to organize and manage multiple tasks in a fast-paced environment, with minimal instruction on routine work and moderate instructions on new assignments.
• Good verbal and written communication and interpersonal skills.

PREFERRED ADDITIONAL SKILLS (I.E., COMPUTER):

• Proficient with commonly used word processing, database systems and other software.

Education:

• BA or equivalent in biology, chemistry or related science or equivalent experience

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $43