Quality Control Chemist

Piramal Pharma•Riverview, MI

2d•Onsite

About The Position

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC) in Riverview, Michigan, is seeking a Quality Control Chemist to provide analytical chemistry support for the facility. The role supports pharmaceutical manufacturing and quality control activities through testing, documentation, laboratory equipment upkeep, and participation in quality unit projects. The position requires a bachelor’s degree in Chemistry, Biochemistry, or equivalent. One year of experience in pharmaceutical quality control or equivalent is preferred. Familiarity with analytical testing and instrumentation is required. The role involves frequent lifting, bending, stooping, squatting, pushing, and pulling; extended periods of standing and walking; and potentially extended periods of sitting, typing, computer entry, or looking at a computer. Work takes place in or near pharmaceutical research or manufacturing equipment and processes, with potential limited exposure to hazardous chemicals. Personal protective equipment such as safety glasses, lab coats, gloves, specialized clothing, and appropriate shoes may be required.

Requirements

Bachelor’s degree in Chemistry or Biochemistry, or equivalent.
Familiarity with analytical testing and instrumentation.
Excellent organizational and planning skills.
Strong written, verbal, and interpersonal communication skills.
High attention to detail.
Demonstrated strong analytical skills and ability to work independently against multiple deadlines.

Nice To Haves

One year of experience in pharmaceutical quality control or equivalent.

Responsibilities

Test raw materials and starting materials as needed to support manufacturing timelines.
Perform cleaning verifications on multi-use equipment using approved methods.
Test reference standards and stability samples.
Document sample preparation, equipment setup, and test results in laboratory notebooks or other appropriate test record forms.
Verify data with a second quality team member as required.
Maintain records required for compliance.
Test intermediates and final products as needed to meet production timelines and client requirements.
Assist with revising documentation as required.
Participate in quality unit projects, including supplier certification, methods development, methods validation, and training quality unit members as appropriate.
Support the maintenance and calibration of laboratory analytical instrumentation.
Maintain the QC laboratory through routine housekeeping and keep personal bench and desk areas organized.
Perform routine testing on the water system, including DI, ice, potable, and QC water, and prepare reports as needed.