Quality Assurance Supervisor
Singota Solutions
People & HR, Operations, Quality Assurance
Bloomington, IN, USA
Posted on Mar 2, 2026
About Us
Singota Solutions is a contract development and manufacturing organization (CDMO) focused on getting products to patients faster by being agile, accountable, and transparent. Our team of experts believe in collaboration and customizing our services to assist our clients through the drug development process. Our key services include drug formulation development, analytical testing, aseptic filling, pharmaceutical labeling and kitting, and supply chain management.
Job Description
Job Description # JD221
Job Title: Quality Assurance Supervisor
Department: Quality Assurance
Position Type: Full-time, exempt (Onsite)
Reports to: Senior QA/RA Manager
General Description:
The Quality Assurance Supervisor provides oversight, assistance and guidance in daily quality activities associated with Operations oversight. This encompasses both Manufacturing (sample/dispense, aseptic filling and labeling/packing) and Supply Chain (receiving, storage, shipment) operations. This position also must positively interface with internal key stakeholders, clients and regulatory agencies regarding quality and regulatory issues pertaining to the business unit.
1. Responsible for supporting oversight of quality operations with Manufacturing and Supply Chain Management activities, including the review and approval of records and disposition of materials, as applicable.
2. Perform and/or oversee quality inspections including, but not limited to: labels, components, filled vials, and packaging.
3. Assist in managing Acceptable Quality Limit (AQL) sampling on products and materials in accordance with applicable protocols. Maintain visual inspection qualification.
4. Assist in the review and approval of executed operations supporting documentation, including but not limited to, sampling, dispensing, shipping, and receiving documentation, as applicable.
5. Participate in in-process reviews of manufacturing batch records and protocols.
6. Collaborate internally as well as with applicable suppliers to provide oversight for shipping qualification studies. Oversight includes review and approval of supplier provided protocols and reports.
7. Assist in maintaining material control via electronic inventory management system for materials, goods, and/or finishing product(s), in accordance with defined procedural controls, as applicable.
8. Serve as Subject Matter Expert (SME) on quality aspects of Manufacturing and Supply Chain processes.
9. Become gowning qualified to perform Quality functions within the cleanrooms (line clearances, batch execution support).
10. Author complex deviations, CAPAs, and change controls.
11. Write and review Standard Operating Procedures related to Quality systems within Supply Chain Management and Manufacturing.
12. Perform standard supervisory duties, such as mentoring employees, drafting and delivering performance reviews, delivering disciplinary actions, employee training, creating job descriptions and participating in the hiring process.
13. Responsible for utilizing sound judgement to make decisions regarding complex atypical events.
14. Participate in the development and maintenance of the site’s continuous improvement activities.
15. Perform other duties as assigned by the QA Manager. Perform all responsibilities in accordance with company guidelines and Standard Operating Procedures and appropriate industry and regulatory standards and guidelines.
16. Manage the scheduling/resource allocation for QA operations support.
17. Assist with license compliance
18. Comply with quality and safety management systems including requirements for documentation, training, system use, SOPs, processes, and procedures.
19. Provide support and oversight, as applicable, in the management of manufacturing materials specifications.
Characteristics Required Include:
a. Ability to appropriately communicate to both internal departments and external customers.
b. Demonstration of positive attitude and professional presence.
c. Ability to make independent decisions regarding quality related concerns or issues.
d. Trustworthiness and personal integrity – able to maintain a high degree of confidentiality
e. Excellent time management and organizational skills, ability to manage a diverse workload
Requirements
Education and Work Experience Requirements:
1. Bachelor’s degree or equivalent experience – science-related field preferred.
2. Minimum of 10+ years pharmaceutical experience, preferably in a Quality role.
3. Previous supervisory experience and decision-making experience is desired.
4. Quality certifications (ASQ Quality Auditor, Lean Six Sigma, etc.) are highly desirable
Benefits
- Dental insurance - effective day one of employment
- Health insurance - effective day one of employment
- Vision insurance - effective day one of employment
- Health savings account
- Life & AD&D insurance
- Short & long term disability
- Paid time off & holidays
- Employee Assistance Program
- Tuition assistance
- 401(k) with company match
Singota Solutions is an Equal Opportunity Employer