HireMO

Supervisor, Quality Control - night shift in Springfield, MO

Build your future at Curia, where our work has the power to save lives

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers' therapies from curiosity to cure and ultimately to improve patients' lives.

We proudly offer

- Generous benefit options (eligible first day of employment)

- Paid training, vacation and holidays (vacation accrual begins on first day of employment)

- Career advancement opportunities

- Education reimbursement

- 401K program with matching contributions

- Learning platform

- And more!

This Quality Control Supervisor position will lead evening-shift laboratory operations and a team of Quality Control Analysts who perform analytical testing in support of API manufacturing. This role combines scientific expertise with hands-on leadership to ensure raw materials, in-process samples, finished APIs, stability samples, and special projects are tested safely, accurately, and on schedule. Working closely with Manufacturing, Quality, and other site teams, the supervisor develops team capability, resolves laboratory challenges, and promotes a culture of accountability, collaboration, and continuous improvement. This is an opportunity to make a meaningful impact by helping ensure every product meets the quality standards our customers, and their patients, depend on.

This position primarily supports evening-shift operations and requires flexibility to work outside normal business hours based on operational needs.

Essential Responsibilities

Team Leadership and Development

+ Lead, coach, and develop Quality Control Analysts, creating an environment where employees feel supported, accountable, and empowered to perform their best.

+ Assign and prioritize daily work to meet testing timelines, manufacturing needs, and departmental objectives.

+ Monitor team performance, productivity, and compliance, providing timely feedback, recognition, training, and performance management as appropriate.

+ Ensure employees are properly trained and that required training is documented before independently performing assigned work.

+ Provide technical guidance on laboratory procedures, SOPs, specifications, protocols, controlled forms, investigations, and applicable manufacturing documentation.

Laboratory Operations and Technical Oversight

+ Oversee and, when needed, perform routine and non-routine analytical testing of raw materials, in-process samples, finished APIs, stability samples, and special projects.

+ Review analytical data and documentation to ensure results are accurate, complete, timely, and scientifically sound.

+ Apply strong knowledge of chromatography, including HPLC, UPLC, and GC, as well as other common analytical techniques and instrumentation.

+ Coordinate multiple testing priorities and projects to support established schedules, deadlines, and business needs.

+ Support the maintenance, calibration, qualification, and validation of laboratory instruments and equipment.

+ Provide technical expertise in the evaluation and interpretation of analytical results and laboratory issues.

Quality, Compliance, and Investigations

+ Ensure laboratory activities are performed in accordance with cGMP requirements, approved procedures, data integrity expectations, and applicable company and regulatory standards.

+ Lead or support investigations involving out-of-specification results, deviations, laboratory events, change controls, and CAPAs, ensuring conclusions are scientifically justified and actions are completed on time.

+ Author, review, and revise Quality Control SOPs, test methods, protocols, and other controlled documents.

+ Identify compliance or performance risks, take appropriate action, and escalate significant concerns when necessary.

+ Support audit and inspection readiness by maintaining accurate documentation, compliant laboratory practices, and a well-prepared team.

Safety and Collaboration

+ Promote a safe laboratory environment and ensure compliance with the Chemical Hygiene Plan and all applicable safety procedures.

+ Communicate laboratory results, priorities, risks, and plans clearly and effectively to employees, leadership, cross-functional partners, and customers when appropriate.

+ Partner with Manufacturing, Quality Assurance, Engineering, Maintenance, and other teams to resolve issues, support production schedules, and improve operational performance.

+ Identify and implement opportunities to strengthen laboratory efficiency, quality, safety, and team effectiveness.

+ Perform other duties as assigned.

Good Manufacturing & Documentation Practices

Quality is something we take pride in together. You'll perform your work in alignment with cGMP requirements and Curia's standards, which means:

+ Perform all documentation in compliance with ALCOA++ principles and site SOPs.

+ Adhere to applicable cGMP documents including SOPs, batch records, protocols, change controls, and controlled forms.

+ Keep all required cGMP training current and escalate quality concerns along with proposed solutions to the Quality department.

Qualifications

Required

+ Bachelor's degree in chemistry or another scientific discipline with relevant coursework or professional experience in analytical chemistry.

+ At least 5 years of experience in a GMP- or GLP-regulated laboratory environment.

+ Hands-on experience with chromatography, including HPLC, UPLC, and/or GC, and familiarity with other common analytical instruments and techniques.

+ Strong working knowledge of cGMP requirements, applicable FDA regulations, and compendial standards such as USP and EP.

+ Demonstrated ability to interpret analytical data, troubleshoot laboratory issues, and apply sound scientific judgment.

+ Ability to organize and prioritize multiple activities while meeting changing operational needs and deadlines.

+ Strong written and verbal communication skills, including the ability to communicate technical information clearly and listen effectively.

+ Demonstrated initiative, accountability, and ability to use team resources effectively to achieve results.

+ Proficiency with Microsoft Office applications and other laboratory or quality systems required for the role.

+ Ability and willingness to work an evening-shift schedule and provide support outside normal business hours when operationally necessary.

Preferred

+ Previous experience leading, supervising, training, or mentoring employees in a regulated laboratory environment.

+ Experience supporting pharmaceutical API manufacturing.

+ Experience conducting or leading OOS investigations, deviations, CAPAs, and change controls.

+ Familiarity with FDA regulations applicable to pharmaceutical manufacturing, including 21 CFR Parts 210 and 211.

Physical requirements

This role regularly requires sitting, standing, and using ha...

Apply Externally

Jobs

Supervisor, Quality Control

Summary

You Need a MO Jobs Account First

Jobs

Jobs

Supervisor, Quality Control

Summary

Do You Have a MO Jobs Account?

First, Let's Find Your MO Jobs Account

Create an Account to Apply

You Need a MO Jobs Account First

HireMO Terms of Use

1. Acceptance and Changes

2. A No-Cost Public Workforce Service

3. Eligibility, Youth, and Authority

4. Accounts and Security

5. Accuracy Attestation and Program Information

6. Job Seeker Terms

7. Employer Terms

8. Assessments and Matching

9. Artificial Intelligence Features

10. Public Records and Required Notices

11. User Content and Permissions

12. Acceptable Use

13. Intellectual Property and Government Marks

14. Other Users and Third-Party Services

15. Electronic Communications

16. Suspension, Termination, and Records

17. Disclaimers

18. Limitation of Liability and Sovereign Immunity

19. Employer Indemnification

20. Governing Law and General Terms

21. Contact, Accessibility, and Complaints