The Production Supervisor is a Direct Supervisor of Union Operators and Technicians in the mixing, granulation, formulation, compression and packaging of pharmaceutical products. Responsible for ...
The Production Supervisor is a Direct Supervisor of Union Operators and Technicians in the mixing, granulation, formulation, compression and packaging of pharmaceutical products. Responsible for ...
The Production Supervisor is a Direct Supervisor of Union Operators and Technicians in the mixing, granulation, formulation, compression and packaging of pharmaceutical products. Responsible for ...
The Production Supervisor is a Direct Supervisor of Union Operators and Technicians in the mixing, granulation, formulation, compression and packaging of pharmaceutical products. Responsible for ...
Pharmaceutical Manufacturing or other FDA regulated industry * Experience in processing powders ... The main focus will be Oral Solid Dose (granulation, compression) process optimization. Additional ...
Pharmaceutical Manufacturing or other FDA regulated industry * Experience in processing powders ... The main focus will be Oral Solid Dose (granulation, compression) process optimization. Additional ...
Pharmaceutical Manufacturing or other FDA regulated industry * Experience in processing powders ... The main focus will be Oral Solid Dose (granulation, compression) process optimization. Additional ...
Pharmaceutical Manufacturing or other FDA regulated industry * Experience in processing powders ... The main focus will be Oral Solid Dose (granulation, compression) process optimization. Additional ...
Pharmaceutical Compression Operator information
What is a pharmaceutical compression operator?
Pharmaceutical Compression Operators are professionals responsible for operating and maintaining tablet compression machines used in the production of pharmaceutical tablets. They ensure that tablets are manufactured to precise specifications, including weight, thickness, and hardness, by monitoring and adjusting machinery during the production process. These operators also perform routine equipment checks, troubleshoot issues, and maintain strict adherence to safety and quality standards. Their role is essential in ensuring that medications are produced efficiently and meet regulatory requirements.
What are the key skills and qualifications needed to thrive as a pharmaceutical compression operator?
To thrive as a Pharmaceutical Compression Operator, you need knowledge of pharmaceutical manufacturing processes, attention to detail, and a high school diploma or equivalent. Familiarity with tablet press machines, Good Manufacturing Practices (GMP), and quality control systems is typically required. Strong problem-solving, teamwork, and communication skills help operators address production issues and maintain safety standards. These skills ensure consistent product quality, regulatory compliance, and efficient operation in pharmaceutical production environments.
What are the most common challenges faced by pharmaceutical compression operators during production runs?
Pharmaceutical Compression Operators often encounter challenges such as maintaining consistent tablet quality, troubleshooting mechanical issues with compression machines, and adhering to strict GMP (Good Manufacturing Practice) protocols. Variations in raw material properties or environmental factors like humidity can affect tablet compression, requiring quick problem-solving and close attention to detail. Additionally, operators must work efficiently within a team to meet production targets while ensuring safety and compliance at all times.
What is the difference between Pharmaceutical Compression Operator vs Pharmaceutical Tablet Press Operator?
| Aspect | Pharmaceutical Compression Operator | Pharmaceutical Tablet Press Operator |
|---|---|---|
| Credentials | High school diploma, on-the-job training, sometimes certifications | High school diploma, specialized training, certifications often preferred |
| Work Environment | Manufacturing floors, cleanroom settings, machinery operation | Manufacturing lines, tablet pressing machinery, controlled environments |
| Industry Usage | Commonly used term in pharmaceutical manufacturing | Often used interchangeably, but more specific to tablet pressing |
| Search & Comparison | Primary job title searched for manufacturing roles | Related role, often compared for specific equipment operation |
Both roles involve operating tablet pressing machinery in pharmaceutical manufacturing. The term 'Pharmaceutical Compression Operator' is broader, encompassing various compression processes, while 'Pharmaceutical Tablet Press Operator' specifically refers to operating tablet presses. They share similar credentials and work environments, but the terminology may vary by employer or region.
What are popular job titles related to Pharmaceutical Compression Operator jobs in Missouri?
For Pharmaceutical Compression Operator jobs in Missouri, the most frequently searched job titles are:
What job categories do people searching Pharmaceutical Compression Operator jobs in Missouri look for?
The top searched job categories for Pharmaceutical Compression Operator jobs in Missouri are:
What cities in Missouri are hiring for Pharmaceutical Compression Operator jobs?
Cities in Missouri with the most Pharmaceutical Compression Operator job openings:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 17 days ago
Job description
Experiencing together a unique human adventure
Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business.
Pharmaceutical Production Supervisor - 2nd Shift
Virbac Animal Health is seeking a Pharmaceutical Production Supervisor for our 2nd Shift Production Team. The Production Supervisor is a Direct Supervisor of Union Operators and Technicians in the mixing, granulation, formulation, compression and packaging of pharmaceutical products. Responsible for operational mastery, safety, quality, productivity, regulatory compliance, continuous improvement, cost improvements and employee training. This position will be Monday through Friday from 3:00 pm to 11:30 pm .
The Pharmaceutical Production Supervisor will be responsible for maintaining the motivation, development, and performance of the team and collaborators. Will maintain performance of production to meet the customer demand, while keeping employees working within regulations, standards, and procedures.
Qualified candidates must possess a BS in Chemistry/Engineering with a minimum of 5 years in the Pharmaceutical Industry or at least 10 years of experience in the Pharmaceutical industry with part of the experience as a Supervisor. cGMP experience along with writing deviations that include corrective actions are also a necessity for this position.
This exciting position will work in Bridgeton, MO. It comes with an excellent benefits package including generous time off including 13 Holidays, Floating Holidays, Vacation, Sick time. 401k + match, life, medical, dental, and vision benefits, and more!
Responsibilities
Area of responsibility 1: Team Management
Expected results: Guarantees motivation, development and performance of team and collaborators. Maintains a good atmosphere and working conditions.
Area of responsibility 2: Productivity
Expected results: Guarantee performance of production to meet customer demand.
Area of responsibility 3: Regulatory Compliance/Quality
Expected results: Ensure employees work within regulations, standards and procedures
Area of responsibility 4: Continuous Improvement
Expected results: Improve production performance, quality, safety delivery and customer service.
Area of responsibility 5: Troubleshooting
Expected results: Ensure deviations are investigated and resolved in a timely manner.
Area of responsibility 6: Safety
Expected results: Improve safety by increasing collaborator involvement and working conditions.
Area of responsibility 7: Training
Expected results: Ensure all collaborators have the training required to perform the functions of their positions.
Requirements (Diploma and experience)
BS in Chemistry/Engineering with a minimum of 5 years in the pharmaceutical industry or at least 10 years of experience in the pharmaceutical industry with part of the experience as a Supervisor.
Skills
Must have prior operational pharmaceutical experience. Knowledge of chemical safety and advanced analytical troubleshooting; must have supervisory and continuous improvement. Experience supervising in a union environment is beneficial.
Pass prerequisite test assessments.
Virbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension.
Joining Virbac means joining dynamic teams ambitious for success.
Add Your Talent to Ours!
Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal health also means listening to them and helping them to acquire new skills, preparing them for the challenges of tomorrow and encouraging them to contribute to an ever more responsible approach to our business.
Pharmaceutical Production Supervisor - 2nd Shift
Virbac Animal Health is seeking a Pharmaceutical Production Supervisor for our 2nd Shift Production Team. The Production Supervisor is a Direct Supervisor of Union Operators and Technicians in the mixing, granulation, formulation, compression and packaging of pharmaceutical products. Responsible for operational mastery, safety, quality, productivity, regulatory compliance, continuous improvement, cost improvements and employee training. This position will be Monday through Friday from 3:00 pm to 11:30 pm .
The Pharmaceutical Production Supervisor will be responsible for maintaining the motivation, development, and performance of the team and collaborators. Will maintain performance of production to meet the customer demand, while keeping employees working within regulations, standards, and procedures.
Qualified candidates must possess a BS in Chemistry/Engineering with a minimum of 5 years in the Pharmaceutical Industry or at least 10 years of experience in the Pharmaceutical industry with part of the experience as a Supervisor. cGMP experience along with writing deviations that include corrective actions are also a necessity for this position.
This exciting position will work in Bridgeton, MO. It comes with an excellent benefits package including generous time off including 13 Holidays, Floating Holidays, Vacation, Sick time. 401k + match, life, medical, dental, and vision benefits, and more!
Responsibilities
Area of responsibility 1: Team Management
- Lead, direct, train and provide support to shift personnel
- Assure employees understand duties, responsibilities, policies and procedures including product batch record instructions
- Set and achieve objectives, both departmental and team
- Empower and motivate team members
- Foster dialogue and relationships
- Participate in recruitment
Expected results: Guarantees motivation, development and performance of team and collaborators. Maintains a good atmosphere and working conditions.
Area of responsibility 2: Productivity
- Pre shift preparation
- Organize team's activities in relation to production schedule
- Ensures availability of supplies and of equipment according to production needs
- Maintain inventory of miscellaneous production supplies and parts
- Monitor and assess department work flow and daily task activities
- Monitor KPIs
- Enhance productivity and product quality levels
- Support to new product introductions by participating in operational mastery and corresponding training
Expected results: Guarantee performance of production to meet customer demand.
Area of responsibility 3: Regulatory Compliance/Quality
- Ensure the operational and pharmaceutical mastery of their units and processes
- Direct supervision of production in compliance with our SOPs and regulating agencies' rules.
- Reviews product batch records for accuracy of entries, compliance to established limits, specifications and presence of all verification signatures
- Provide hands-on leadership to ensure Quality and Compliance
- Participate in writing and/or updating GMP documentation in coordination with QA
- Write and/or update local operating procedures
- Participate in qualification and validation in the unit
Expected results: Ensure employees work within regulations, standards and procedures
Area of responsibility 4: Continuous Improvement
- Propose, participate and/or lead kaizen events
- Perform their operating system through Gemba walk
- Continuously identify and lead improvements in their units and processes
- Participate in waste reduction in order to increase effectiveness and efficiency of manufacturing operations
Expected results: Improve production performance, quality, safety delivery and customer service.
Area of responsibility 5: Troubleshooting
- Participate in detecting deviations in collaboration with their team
- Perform a thorough root cause analysis and understand other kinds of root cause analysis tools
- Lead deviation investigations and participate in CAPA with QA
- Manage deviations and exceptions in collaboration with QA, process engineer
Expected results: Ensure deviations are investigated and resolved in a timely manner.
Area of responsibility 6: Safety
- Ensure compliance with Safety Program
- Ensure employees work safely in accordance with regulations, standards and procedures
- Eliminate unreasonable risk to health and the environment
- Report all safety and/or environmental incidents to Safety Manager
Expected results: Improve safety by increasing collaborator involvement and working conditions.
Area of responsibility 7: Training
- Identify and anticipate team's skill requirements and propose training programs
- Coordinate individual training for their team in accordance to the required curricula
Expected results: Ensure all collaborators have the training required to perform the functions of their positions.
Requirements (Diploma and experience)
BS in Chemistry/Engineering with a minimum of 5 years in the pharmaceutical industry or at least 10 years of experience in the pharmaceutical industry with part of the experience as a Supervisor.
Skills
Must have prior operational pharmaceutical experience. Knowledge of chemical safety and advanced analytical troubleshooting; must have supervisory and continuous improvement. Experience supervising in a union environment is beneficial.
Pass prerequisite test assessments.
Virbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension.
Joining Virbac means joining dynamic teams ambitious for success.
Add Your Talent to Ours!