Quality Control Chemist I

Cencora • Columbus, OH

2d • Onsite

About The Position

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details This role is in support of American Health Packaging, a Cencora business offering pharma packaging services in the US. Under the general direction of the Senior Manager of Regulatory Affairs & Stability, the QC/Stability Chemist will focus on stability and release testing, as required, of products repackaged at AHP and work closely with other departments within the Quality Unit to ensure drug product meets all standards. Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable. Ensure compliance with local and corporate policies and procedures. Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable. Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations. Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable. Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately. Prepare lab reports as required. Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests. Maintain Quality System records and ensure completeness and accuracy. Coordinate with department management to identify and implement compliant process improvements. Clarify regulations, policies, and procedures to internal teams as applicable. Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections. Conduct follow-up checks on the effectiveness of corrective actions Performs other duties to support Quality Systems and Regulatory Affairs department as assigned.

Requirements

• Bachelor’s degree in chemistry or related field required
• Three or more years’ experience within a pharmaceutical manufacturing (cGMP) laboratory environment
• Should have a working knowledge of pharmaceutical manufacturing requirements, Quality System principles (Documentation, Training, Investigations/CAPA, Change Control, etc), and global Quality Control regulations
• Good oral, written, communication, and interpersonal skills
• Ability to develop and maintain cooperative working relationships with others
• Effectively interfaces with multiple levels of associates within the organization, including management and plant associates
• Ability to work independently
• Ability to handle a variety of tasks simultaneously
• Attention to detail
• Familiarity with concepts of electronic documentation management systems (EDMS)
• Physical activity requiring reaching, bending, kneeling, stooping, lifting, finger dexterity, grasping, feeling, repetitive motions, talking and hearing
• Ability to lift up to 50 lbs
• Visual requirement is for close vision, distance vision, peripheral vision and ability to adjust focus
• Associate is required to stand, walk (or otherwise be mobile)
• Ability to deal with stressful situations as they arise

Nice To Haves

• Experience with MasterControl or other electronic quality management system preferred

Responsibilities

• Focus on stability and release testing, as required, of products repackaged at AHP
• Work closely with other departments within the Quality Unit to ensure drug product meets all standards
• Ensure stability and release testing activities are compliant with FDA, DEA, other regulatory body requirements as applicable
• Ensure compliance with local and corporate policies and procedures
• Perform stability and release testing for drug products in accordance with compendial and global requirements, as applicable
• Develop, revise, and review standard operating procedures (SOPs), work instructions (WIs), and test method documents to ensure compliance with applicable compendia and regulations
• Assist in the support of manufacturing operations including process validation, environmental monitoring, and utilities as applicable
• Perform review and release of stability and release tests for compliance to SOPs and regulatory requirements and ensure data is reported accurately
• Prepare lab reports as required
• Assist with root cause investigations for quality incidents related to chemical analysis for stability and release tests
• Maintain Quality System records and ensure completeness and accuracy
• Coordinate with department management to identify and implement compliant process improvements
• Clarify regulations, policies, and procedures to internal teams as applicable
• Coordinates with departmental leaders to develop appropriate corrective actions resulting from investigations, internal audits, and facility inspections
• Conduct follow-up checks on the effectiveness of corrective actions
• Performs other duties to support Quality Systems and Regulatory Affairs department as assigned

Benefits

• In addition to traditional offerings like medical, dental, and vision care, we also provide a comprehensive suite of benefits that focus on the physical, emotional, financial, and social aspects of wellness.
• This encompasses support for working families, which may include backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, paid parental leave, and paid caregiver leave.
• To encourage your personal growth, we also offer a variety of training programs, professional development resources, and opportunities to participate in mentorship programs, employee resource groups, volunteer activities, and much more.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees