Quality Control Supervisor

Simtra BioPharma Solutions (Simtra) is a world‑class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre‑filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder‑filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines – which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life‑changing medicines to patients worldwide. The role: The Quality Control Metrology Supervisor manages the activities in the QC Metrology department and the analysts that perform instrument maintenance and instrument projects in support of the company’s quality program. This role works as part of the quality control function, training and leading others within the laboratory. This position reports to the Quality Control Chemistry Manager. The responsibilities: Manages the daily activities of the QC Metrology department. Ensure timely Metrology support to Production, QC Chemistry, QC Microbiology, QC Critical, Incoming Quality Control and other cGMP production areas where analytical instruments are deployed. Manage new instrument projects to ensure timely and compliant installation and qualification. Calibrate analytical instruments for conformance to established government, commercial and specification standards. Develop and execute validation protocols (Installation Qualification / Operational Qualification / Performance Qualification) for analytical instruments. Manage standard operating procedures (SOPs) on new and existing instruments. Responsible for instrument re‑certification with outside standard laboratories, performing incoming inspections and documentation reviews on these instruments. Write, revise and review SOPs. Participate in continuous improvement functions (Lean initiatives) that increase efficiency, solve problems, generate cost savings, improve customer service activities and improve quality. Perform/assist in internal assessments and investigations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude. Serve as a technical resource for process and/or product development activities. Participate in client and regulatory audits and respond to audit observations. Serve as project subject‑matter expert on lab instruments and processes. Understands advanced biological and chemical assays requiring precise analytical skills and an understanding of biology and chemistry principles. Can operate advanced laboratory equipment (HPLC, UV, Karl Fischer, pH meter, etc.). Has a thorough knowledge of US and EU pharmacopeias and a working knowledge of JP pharmacopeia. Ensure that data integrity requirements are maintained. Initiate and author laboratory investigation reports. Perform general laboratory/personal area clean‑up. Identify and lead special projects that involve new methods, instrumentation and technologies. The requirements: Bachelor’s degree required, preferably in a physical science related field. Minimum of 5 years of experience with QC instruments. Previous leadership experience preferred. Computer proficiency in Microsoft Word, Excel, Outlook and the ability to use enterprise software. Knowledge of instrument, software and documentation repair and calibration systems required. Knowledge and navigation skills of QC documentation required. Physical / Safety Requirements: Must be able to wear personal protective equipment. Duties may require overtime work, including nights and weekends. Use of hands and fingers to manipulate office equipment is required. Position may require sitting or standing for long periods of time. Requires handling of laboratory chemicals. Must be able to qualify for 20/40 corrected vision. In return, you’ll be eligible for: Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance (Spouse Life Insurance, Child Life Insurance) 401(k) Retirement Savings Plan with Company Match Time Off Program (Paid Holidays, Paid Time Off, Paid Parental Leave and more) Adoption Reimbursement Program Education Assistance Program Employee Assistance Program Community and Volunteer Service Program Employee Ownership Plan Additional Benefits (Short and Long‑Term Disability Insurance) Voluntary Insurance Benefits (Vision Coverage, Accident, Critical Illness, Hospital Indemnity Insurance, Identity Theft Protection, Legal and more) Onsite Campus Amenities (Workout Facility, Cafeteria, Credit Union) Disclaimer This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. Equal Employment Opportunity Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. #J-18808-Ljbffr