Manufacturing Operations Supervisor; Weekend Night Shift
Listed on 2026-01-26
-
Manufacturing / Production
Pharmaceutical Manufacturing
Overview
The Manufacturing Operations Supervisor is responsible for overseeing production operations, ensuring that all work completed is within appropriate time frames, delivering daily expectations and assignments. Providing on floor support and review of MBRs, providing coaching and feedback to the operations team. Involvement in manufacturing deviation investigations and CAPA implementation. Influencing the accomplishments of company wide and team goals and objectives as well as inspiring team members while consistently modeling ALP values in all interactions.
The individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs). The Manufacturing Operations Supervisor will constantly evaluate internal processes and procedures and work to create a productive space while maintaining high quality standards.
This position is vital to lead our weekend night-shift operations on Friday-Sunday, 12-hour shifts.
Essential Job Functions- Provide technical support, oversight and team leadership in manufacturing batch activities.
- Coordinate the development of individual team members with routine one-on-ones, training oversight and training opportunities.
- Develop and improve current processes to maintain and control the formulation and filling operations.
- Assure compliance with cGMP requirements (current good manufacturing practices).
- Perform GEMBA walks and checks for process improvements.
Job Requirements
- Knowledge of process control, quality engineering, sampling requirements, statistical techniques, and process capability
- Familiarity with relevant quality and regulatory requirements and trends and cGMPs
- Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders.
- Knowledge of aseptic techniques and processing
- 1-2 years demonstrated working knowledge of aseptic manufacturing operations.
- 1-2 years in a people leadership role
INCOG Bio Pharma has built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.
INCOG Bio Pharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG Bio Pharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate.
We will not tolerate discrimination or harassment based on any of these characteristics.
By submitting your resume and details, you are declaring that the information is correct and accurate.
#J-18808-Ljbffr(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).