QC Chemist I (1st shift/Group B)
Quality, Service, Collaboration, Courage. Do you exhibit these values and wish to be around others that do too? Are you interested in making a difference in your community and the world? Are you looking for a place where you can grow and learn in a diverse, community-minded culture? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day.
Shift Details: 1st shift (6:00 am to 5:00 pm). Wednesday thru Saturday (Group B). Overview of this Position: The QC Chemist supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. Non-Negotiable Requirements:- Bachelor's degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology).
- Minimum of 1-3 years pharmaceutical or testing experience.
- Qualification for use of a full-face respirator is required.
- Proficient computer skills in Microsoft Word, Excel, and Outlook.
Preferred Requirements:
- Excellent written and verbal skills; Ability to communicate effectively with management, staff, and regulatory agencies by exhibiting excellent interpersonal skills.
- Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Responsibilities Include (but are not limited to):
- Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients, excipients and finished pharmaceutical products.
- Prepare standards and samples for analysis.
- Run instrumentation independently including, but not limited to, HPLC, FTIR, UV VIS, and physical testing on pharmaceutical products according to client/compendia procedures and departmental SOPs.
- Review laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
- Process data, generate reports, and evaluate data.
- Perform all job responsibilities in compliance with cGMPs, company SOP's, and current industry practice.
Full available during formal interview process.
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