Simtra US LLC
Quality Analyst I - Quality Batch Review
Simtra US LLC, Bloomington, Indiana, United States, 47401
Company Overview
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 – all directly injected into patients worldwide. A strong emphasis on quality and continuous improvement drives our operations.
While our primary focus is cGMP manufacturing, we also provide 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? 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 to 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 and taking on challenges big and small to improve patient health.
The Role The Quality Analyst I is a member of the Quality Assurance Team (QA) reporting directly to the Quality Supervisor, Batch Review. They perform review of all quality documentation generated during filling operations and effectively communicate with customer support departments.
The Responsibilities
Perform batch record review for GMP batches produced at Simtra for accuracy and compliance to procedures based on regulatory requirements and internal guidelines.
Reconcile discrepancies with documentation and/or electronic systems as appropriate.
Facilitate an environment of partnership and communication between Quality Assurance, Production and other support functions to ensure timely Quality review of batch records, meeting internal targets and contractual commitments for batch release.
Initiate nonconformance investigation reports.
Participate in continuous improvement projects to improve department operations, increase efficiency, solve problems, generate cost savings, enhance quality and increase employee and customer satisfaction.
Perform final batch record review, product release/disposition of GMP batches produced at Simtra.
May require client interaction.
Desired Qualifications
Bachelor’s degree required.
Experience in pharmaceutical quality or pharmaceutical manufacturing preferred.
Computer proficiency in Microsoft Word, Excel, Outlook and enterprise software (examples include JDE, BPLM, Pilgrim, Trackwise, etc.).
Physical / Safety Requirements
Duties may require overtime work, including nights and weekends.
Use of hands and fingers to manipulate office equipment is required.
Position may require standing for long periods of time.
Benefits
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/
#J-18808-Ljbffr
Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines – all directly injected into patients worldwide. A strong emphasis on quality and continuous improvement drives our operations.
While our primary focus is cGMP manufacturing, we also provide 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? 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 to 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 and taking on challenges big and small to improve patient health.
The Role The Quality Analyst I is a member of the Quality Assurance Team (QA) reporting directly to the Quality Supervisor, Batch Review. They perform review of all quality documentation generated during filling operations and effectively communicate with customer support departments.
The Responsibilities
Perform batch record review for GMP batches produced at Simtra for accuracy and compliance to procedures based on regulatory requirements and internal guidelines.
Reconcile discrepancies with documentation and/or electronic systems as appropriate.
Facilitate an environment of partnership and communication between Quality Assurance, Production and other support functions to ensure timely Quality review of batch records, meeting internal targets and contractual commitments for batch release.
Initiate nonconformance investigation reports.
Participate in continuous improvement projects to improve department operations, increase efficiency, solve problems, generate cost savings, enhance quality and increase employee and customer satisfaction.
Perform final batch record review, product release/disposition of GMP batches produced at Simtra.
May require client interaction.
Desired Qualifications
Bachelor’s degree required.
Experience in pharmaceutical quality or pharmaceutical manufacturing preferred.
Computer proficiency in Microsoft Word, Excel, Outlook and enterprise software (examples include JDE, BPLM, Pilgrim, Trackwise, etc.).
Physical / Safety Requirements
Duties may require overtime work, including nights and weekends.
Use of hands and fingers to manipulate office equipment is required.
Position may require standing for long periods of time.
Benefits
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/
#J-18808-Ljbffr