Quality Associate I - Filling (2nd Shift) at Simtra BioPharma Solutions

Bloomington, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

22 Jan, 26

Salary

0.0

Posted On

25 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, cGMP, Aseptic Processing, Regulatory Compliance, Batch Records, Nonconformance Reports, Corrective Action, Preventative Action, SOP Revisions, Team Collaboration, Internal Audits, External Audits, Manufacturing Oversight, Process Improvement, Safety Standards, Documentation

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. The role: The Quality Associate I, Line Operations is a member of the Quality Assurance Line Operations Team reporting directly to the Quality Supervisor. They maintain quality oversight of the manufacturing areas by working closely with manufacturing personnel and performing various checks during manufacturing processes. They also assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Simtra Standard Operating Procedures. This position strives for continuous improvement of processes and contributes to creating an environment where teamwork, efficiency, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product. This position supports 2nd Shift: Monday-Thursday 2:00pm-12:30am. The shift may be flexible based on business needs. The responsibilities: Ensures compliance with all worldwide regulatory agency requirements and company-specific regulations related to quality of product and employee safety. In-process review of records to ensure they are complete, accurate and follows current Good Manufacturing Practices (cGMP) requirements. Records include batch records and other documents involved in the aseptic processing of drug product. Reports errors, deficiencies, discrepancies and observations to management. May stop operations when product safety is or may be compromised. Performs Quality functions in classified areas, including production oversight, manufacturing process assessments, and aseptic intervention oversight. Works in collaboration with management teams to prepare for internal and external audits. Assists with timely closure of audit observations and CAPAs. Initiates and authors Nonconformance Reports and corrective and preventative action responses. Conducts bi-annual inspections of classified areas in preparation for facility shutdown periods. Initiates standard operating procedure (SOP) revisions as needed to support continuous improvement. Ensures that SOPs are current and effective and that staff performs routine tasks according to SOP through direct observation. Desired qualifications: Bachelor’s degree (preferred science field), or Associate’s degree with at least three years of Pharmaceutical Quality/Manufacturing or other GXP regulated industry experience, or high school diploma/GED with at least six years Pharmaceutical Quality/Manufacturing or other GXP regulated industry experience Computer proficiency in Microsoft Word, Excel, and Outlook, and the ability to use enterprise software (examples include: Veeva, Trackwise, etc.) Physical / Safety Requirements Must wear appropriate PPE as required for various manufacturing areas Must be able to gown qualify for Grade A/B areas. Duties will require overtime work, including scheduled weekend shifts Position requires standing for long hours, but may require sitting for periods of time. 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 Employee Ownership Plan 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 Quality Associate I maintains quality oversight of manufacturing areas by working closely with personnel and performing various checks during processes. They assess regulatory and quality risks according to agency rules and company procedures.