Now Hiring an Data Reviewer

Pay: $25hr - $35hr

Location: Must be local to the state of Minnesota

Job Description:

This individual will be responsible for reviewing data, batch records, work orders before it goes to the quality assurance team. They will also be looking at temperature locks, QC data, make sure that there are no process mishaps,

• Responsible for auditing analytical data to ensure testing is completed according to appropriate test methods and standard operation procedures.

• Responsible for reviewing analytical documentation and data for release, stability, and R&D testing in order to ensure data quality standards are met. Ensure that all testing is conducted according to appropriate test methods and standard operating procedures..

• Verifies calculations are correct. Ensures that all final results are accurate prior to batch disposition.

• Verifies that all equipment used has been calibrated. Ensures that all appropriate documentation for the equipment used is completed appropriately.

• Verifies that all reagents, standards, test solutions, and volumetric solutions used during testing were prepared correctly and used within their expiry.

• Responsible for identifying and communicating errors found in testing documentation. Works towards a quick resolution and data corrections with laboratory personnel.

• Responsible for communicating atypical and out-of-specification results to laboratory management.

• Performs the review of equipment/system maintenance and calibration on analytical instrumentation (e.g. dishwashers, balances, coagulation systems etc.) as required.

• Understands cGMP documentation requirements.

Skills & Qualifications:

• Associate degree or higher in a relevant field such as biochemistry or chemistry

• Minimum one year of related experience in a laboratory environment.

• Basic understanding of cGMP principals.

• Strong attention to detail and protocol.

• Experience with Microsoft software – Outlook, Excel, Word.

• GMP QC laboratory experience for pharmaceutical, biotechnology or medical devices industry highly preferred.

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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.