Quality Assurance Specialist II

Commercial stage biotechnology company focused on innovative aesthetic, therapeutic and financial technology offerings, setting a new standard in healthcare

The 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.

Perform a wide variety of quality assurance activities to ensure compliance with Revance procedures, applicable US and international regulatory requirements for biologic drug substances and drug products under clinical development.

Assist in the management of the reserve sample program.

Perform incoming quality attribute inspections.

Review, approve, 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.

WORK ENVIRONMENT and PHSYICAL DEMANDS:
This section of the job description is required by the American with Disability Act, (ADA)
The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job
The ADA prohibits employers from discriminating against a “qualified individual with a disability” in all aspects of the employment relationship
A “qualified individual with a disability” is “an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.”

Prolonged periods of sitting at a desk and working on a computer.

Must be able to lift up to 10 pounds at times.

We are an equal opportunity employer
We are a company where diverse backgrounds, experiences and viewpoints are valued
Revance does not discriminate in practices or employment opportunities on the basis of an individual's race, color, national or ethnic origin, religion, age, sex, gender, sexual orientation, marital status, veteran status, disability, or any other prohibited category set forth in federal or state regulations.

Skills:
EXPERIENCE:

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:

BS or equivalent in biology, chemistry or related science or equivalent experience.

#TB_PH