Find & Apply For Quality Control Analyst Jobs in Worcester, Massachusetts

To Discuss more about this job opportunity, please reach out to Anwesha Mohapatra (LinkedIn URL

• Anwesha Mohapatra
• Collabera | LinkedIn ), email your updated resume at Email
• anwesha.

mohapatra@collabera.com . Thank you!

Pay Range:

$23/hr to $28/hr

Job Title:

Quality Assurance Quality Control (QA QC)

Inspector II Location:

Worcester, MA 01604

Work Type:

Onsite Contract Duration:

6

Months, Possible Extension Job Summary:

The QA QC Inspector II will support data review operations within a fast paced GMP pharmaceutical environment. This role involves reviewing laboratory testing records, maintaining accurate documentation, and supporting data archiving activities. The individual will work closely with the data review team to ensure timely and accurate completion of assigned tasks. Responsibilities include reviewing laboratory data, supporting compliance with GMP requirements, and maintaining records within established quality systems. The ideal candidate will demonstrate strong organizational skills, attention to detail, and effective time management.

Key Responsibilities:

Perform routine reviews of laboratory testing data, including on the floor and off the floor reviews for low complexity test methods. Archive laboratory data and documentation within the RIMS system. Support data review activities across raw materials, environmental monitoring, in process testing, final bulk, stability, and validation. Review laboratory records and ensure documentation complies with GMP requirements and established procedures. Maintain a safe working environment by following applicable safety procedures and guidelines. Support administrative activities, including logbook management, scanning, filing, and document organization. Assist with data mining projects and other assigned data review activities. Complete assigned tasks within established timelines while maintaining accuracy and quality standards. Collaborate with team members to support daily operations and maintain a productive working environment. Support the training of other employees through practical demonstrations of established processes.

Required Qualifications:

Bachelor's degree in a relevant discipline or equivalent educational background. Alternatively, a High School Diploma with at least 5 years of combined experience in pharmaceutical or biologics manufacturing, Quality Assurance, or Quality Control. Experience working in a GMP regulated environment. Strong organizational and time management skills. Ability to review, maintain, and archive laboratory documentation accurately.

Preferred Qualifications:

Experience working with RIMS systems. Working knowledge of Empower and A280. Experience with laboratory data review and documentation management. Exposure to pharmaceutical or biologics laboratory operations.

Benefits :

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually

• AS Applicable)