Technical Services Associate I (Risk Management) at Simtra BioPharma Solutions

Bloomington, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Jan, 26

Salary

0.0

Posted On

21 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Risk Management, Regulatory Compliance, Statistical Analysis, Technical Expertise, Change Control, Non-Conformance Investigations, Deviation Reports, Process FMEA, Quality Assurance, Pharmaceutical Manufacturing, Engineering Support, Client Interaction, Cross-Functional Collaboration, Problem Solving, Documentation, Continuous Improvement

Industry

Pharmaceutical Manufacturing

Description

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. Why join Team Simtra? Because we: Make it HAPPEN – We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER – We work as one, respecting each voice and tapping into our unique strengths across teams—so we can solve problems in new ways. Make it RIGHT – We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT – We take pride in our day-to-day work, knowing the impact we make – taking on challenges big and small to improve patient health. This role: The Technical Services Associate I (Risk Management) is responsible for risk management activities associated with non-conformances, complaints, equipment validation, qualification and change control activities at the BPS site. This position interacts with clients, regulatory agencies and cross-functional teams (Engineering, Technical Services, Manufacturing, etc.) to ensure timely approval of all associated documents. This position reports to the Technical Services Validation Sr. Manager. The responsibilities: Provide guidance and technical expertise of regulatory and Baxter requirements in Risk Management strategies and processes. Assess risk associated with non-conformances complaints, audits, change control etc. and update the site process FMEA with new risks as needed. Approve risk forms submitted with newly identified risk submitted via non-conformance investigations, complaints, audits, change control etc. Author and/or approve applicable risk assessment documents for equipment and manufacturing process related changes. Author and/or approve applicable deviation reports for product and process related deviations. Help lead Risk Management activities for sustaining Engineering/Manufacturing projects Provide SME input to risk remediation activities. Support risk assessment of new processes to be validated. Uses statistical tools to analyze data. Performs annual reviews of all process FMEAs. Participates in regulatory inspections. Desirable qualifications: Bachelor’s degree required, preferably in a science or engineering related field Pharmaceutical industry experience in parenteral manufacturing a plus American Society of Quality (e.g., CQE, CMQ/OE, etc.) and/or Six Sigma certification a plus. Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, Pilgrim, Trackwise, etc.) Physical / Safety Requirements: Must be able to wear appropriate personal protective equipment. Duties may require overtime work, including nights and weekends Use of hands and fingers to manipulate office equipment is required Position requires sitting for long hours but may involve walking or standing for periods of time. Must be able to gown for Grade C area In return, you’ll be eligible for [1]: Day One Benefits Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance Spouse Life Insurance Child Life Insurance Short and Long-Term Disability 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 Additional Benefits 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 [1] Current benefit offerings are in effect through 12/31/25 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. Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/

Responsibilities

The Technical Services Associate I (Risk Management) is responsible for risk management activities associated with non-conformances, complaints, equipment validation, qualification, and change control activities. This role involves interacting with clients, regulatory agencies, and cross-functional teams to ensure timely approval of all associated documents.