Quality Specialist II

Sunrise Systems, Inc.; Lititz (Lancaster County); On-site; USD 35,817 - 42,705; Part time

Job summary

A leading company in quality assurance is seeking a Quality Specialist II to support Product Review reports and assist with investigations from data collection insights. Responsibilities include communicating trends to management, ensuring timely Product Review submissions, and reviewing Master Data for accuracy. Candidates must have a Bachelor’s Degree, two years in Quality Assurance/Control, excellent analytical and communication skills, and LIMS experience is preferred. This is a contract role located in Lititz, Pennsylvania.

Qualifications

• A minimum of two (2) years related experience with Quality Control or Quality Assurance in a relevant production environment.
• Excellent analytical, prioritization, multi-tasking, and communication skills.
• Ability to work independently without supervision.

Responsibilities

• Communicate observations or trends discovered during data collection.
• Support Product Review completion per scheduled timelines.
• Review Master Data submissions for accuracy.

Skills

Analytical skills

Communication skills

Leadership skills

Multi-tasking

Education

University/Bachelors Degree or higher

Tools

LIMS

Job description

Sunrise Systems, Inc. provided pay range

This range is provided by Sunrise Systems, Inc.. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$26.00/hr - $31.00/hr

Direct message the job poster from Sunrise Systems, Inc.

The Quality Specialist II will be accountable to support Product Review reports and to support investigations pertaining to observations or trends discovered during data collection. The Quality Specialist II will also be accountable for supporting Laboratory Information Management System (LIMS) Master Data changes needed by the Quality Control Laboratory.

Key Responsibilities

• Communicate to Quality Management the observations or trends discovered during the data collection and review of the Product Reviews. Maintain metrics and support management reviews and other presentations.
• Support Product Review completion per scheduled timeline and store in document management system.
• Review Master Data submissions for accuracy and provide feedback as necessary.
• Performs other duties, as assigned.

Qualifications

• A minimum of a University/Bachelors Degree or higher is required.
• A minimum of two (2) years related experience with Quality Control or Quality Assurance in Pharmaceutical, Medical Device, OTC Drug and/or Cosmetic production environment is required
• Excellent analytical, prioritization, multi-tasking, communication, and strong leadership skills and the ability to work independently without supervision is required
• Ability to work effectively on cross functional teams is required
• LIMS experience preferred

Seniority level

• Associate

Employment type

• Contract

Job function

• Quality Assurance
• Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing