78 Manufacturing jobs in Zephyrhills
Senior Quality Control Engineer (Manufacturing)
Posted today
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Senior Quality Control Specialist - Manufacturing
Posted today
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Manufacturing Team Leader
Posted today
Job Viewed
Job Description
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
Objectives/Purpose of Job:
Coordinates the production activities for filling lines, packaging lines, sterilization preparation, and compounding. Receives directions from the area manager on the production plan and daily schedule. Place customer service and accountability to the customer as the constant goal. Coordinate closely with other departments on operational and planning issues related to meeting the production plans and company goals. Evaluates product quality issues with the QA/QC representative. Assures proper logbook completion and review. Requires three to five years of previous leadership experience.
Filling
Coordinates the operation of aseptic filling equipment including ointment fillers, gel fillers, solution/suspension fillers, RABS, line and equipment cleaning, line clearance, equipment disinfection, and proper documentation practices.
Packaging
Coordinates the operation of packaging equipment including manual case labeling, visual inspections, bundling, cartoning, labeling, banding, line and equipment cleaning, line clearances, serialization, and proper documentation practices.
Aseptic Prep
Coordinates the operation of sterilization equipment including autoclave, dry heat oven, and skids. Schedules equipment and area disinfection and assures proper documentation practices.
Compounding
Coordinates the operation of bulk compounding equipment including nonsterile and sterile kettles, ball mill, and slurry vessels. Schedules area and equipment cleaning/disinfection and proper documentation practices.
Key Activities/Responsibilities:
* Maintains production area to prevent cross-contamination (line/area clearance).
* Assigns tasks for manufacturing operations and support associates.
* Supervise, develop, provide feedback, and coach employees.
* Complete performance reviews as scheduled.
* Performs and assists employees with time keeping transactions.
* Coordinates the turnaround, set-up, and changeover of manufacturing equipment.
* Verifies component readiness, reject verification, and product returns.
* Review weekly production schedule and work with the Planning department on capacity and scheduling issues.
* Coordinate activities to support the production schedule. Participate in process related issues using thorough technical process knowledge to make timely decisions to ensure that efficiency and other business goals are achieved.
* Provides feedback to Managers regarding associate performance and behaviors.
* Ensures that manufacturing equipment operates efficiently at or above target line speeds while minimizing line downtime and product reject.
* Responsible for maintaining OEE (system entry and standards).
* Completes all batch record and inventory documentation accurately (review batch records/ERPLx transactions/CAMS/CPMS).
* Assists with nonconformance investigations, material variance review, line efficiency standards, and improvement opportunities.
* Liaison with MQA Quality Control and QC Microbiology EMPS departments.
* Meets and maintains all required training during the year (SOP, EHS, and HR).
* Support operational excellence and EHS initiatives.
* Assume responsibility for the GMP, ISO, EHS awareness and compliance within the respective area.
* Attend and participate in OpEx improvement initiatives such as reducing costs and OEE improvements.
* All other duties, as assigned.
Qualifications/Training:
* HS diploma required. AA/AS degree preferred.
* 8+ years of production leadership.
* Demonstrated exceptional people management and leadership skills.
* Detail oriented.
* Problem solving, facilitator and management skills. Self-initiative.
* Exceptional communication and documentation skills. Demonstrated analytical skills. Must be results oriented on a continual basis.
* Computer literacy.
* Must be able to read, write, and speak English and possess basic math skills.
This position may be available in the following location(s): US - Tampa, FL
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Our Benefit Programs: Employee Benefits: Bausch + Lomb
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Manufacturing Team Leader
Posted 8 days ago
Job Viewed
Job Description
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
Objectives/Purpose of Job:
Coordinates the production activities for filling lines, packaging lines, sterilization preparation, and compounding. Receives directions from the area manager on the production plan and daily schedule. Place customer service and accountability to the customer as the constant goal. Coordinate closely with other departments on operational and planning issues related to meeting the production plans and company goals. Evaluates product quality issues with the QA/QC representative. Assures proper logbook completion and review. Requires three to five years of previous leadership experience.
Filling
Coordinates the operation of aseptic filling equipment including ointment fillers, gel fillers, solution/suspension fillers, RABS, line and equipment cleaning, line clearance, equipment disinfection, and proper documentation practices.
Packaging
Coordinates the operation of packaging equipment including manual case labeling, visual inspections, bundling, cartoning, labeling, banding, line and equipment cleaning, line clearances, serialization, and proper documentation practices.
Aseptic Prep
Coordinates the operation of sterilization equipment including autoclave, dry heat oven, and skids. Schedules equipment and area disinfection and assures proper documentation practices.
Compounding
Coordinates the operation of bulk compounding equipment including nonsterile and sterile kettles, ball mill, and slurry vessels. Schedules area and equipment cleaning/disinfection and proper documentation practices.
Key Activities/Responsibilities:
- Maintains production area to prevent cross-contamination (line/area clearance).
- Assigns tasks for manufacturing operations and support associates.
- Supervise, develop, provide feedback, and coach employees.
- Complete performance reviews as scheduled.
- Performs and assists employees with time keeping transactions.
- Coordinates the turnaround, set-up, and changeover of manufacturing equipment.
- Verifies component readiness, reject verification, and product returns.
- Review weekly production schedule and work with the Planning department on capacity and scheduling issues.
- Coordinate activities to support the production schedule. Participate in process related issues using thorough technical process knowledge to make timely decisions to ensure that efficiency and other business goals are achieved.
- Provides feedback to Managers regarding associate performance and behaviors.
- Ensures that manufacturing equipment operates efficiently at or above target line speeds while minimizing line downtime and product reject.
- Responsible for maintaining OEE (system entry and standards).
- Completes all batch record and inventory documentation accurately (review batch records/ERPLx transactions/CAMS/CPMS).
- Assists with nonconformance investigations, material variance review, line efficiency standards, and improvement opportunities.
- Liaison with MQA Quality Control and QC Microbiology EMPS departments.
- Meets and maintains all required training during the year (SOP, EHS, and HR).
- Support operational excellence and EHS initiatives.
- Assume responsibility for the GMP, ISO, EHS awareness and compliance within the respective area.
- Attend and participate in OpEx improvement initiatives such as reducing costs and OEE improvements.
- All other duties, as assigned.
Qualifications/Training:
- HS diploma required. AA/AS degree preferred.
- 8+ years of production leadership.
- Demonstrated exceptional people management and leadership skills.
- Detail oriented.
- Problem solving, facilitator and management skills. Self-initiative.
- Exceptional communication and documentation skills. Demonstrated analytical skills. Must be results oriented on a continual basis.
- Computer literacy.
- Must be able to read, write, and speak English and possess basic math skills.
This position may be available in the following location(s): US - Tampa, FL
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement.
Our Benefit Programs: Employee Benefits: Bausch + Lomb
Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Manufacturing Team Leader
Posted 8 days ago
Job Viewed
Job Description
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
**Objectives/Purpose of Job:**
Coordinates the production activities for filling lines, packaging lines, sterilization preparation, and compounding. Receives directions from the area manager on the production plan and daily schedule. Place customer service and accountability to the customer as the constant goal. Coordinate closely with other departments on operational and planning issues related to meeting the production plans and company goals. Evaluates product quality issues with the QA/QC representative. Assures proper logbook completion and review. Requires three to five years of previous leadership experience.
**Filling**
Coordinates the operation of aseptic filling equipment including ointment fillers, gel fillers, solution/suspension fillers, RABS, line and equipment cleaning, line clearance, equipment disinfection, and proper documentation practices.
**Packaging**
Coordinates the operation of packaging equipment including manual case labeling, visual inspections, bundling, cartoning, labeling, banding, line and equipment cleaning, line clearances, serialization, and proper documentation practices.
**Aseptic Prep**
Coordinates the operation of sterilization equipment including autoclave, dry heat oven, and skids. Schedules equipment and area disinfection and assures proper documentation practices.
**Compounding**
Coordinates the operation of bulk compounding equipment including nonsterile and sterile kettles, ball mill, and slurry vessels. Schedules area and equipment cleaning/disinfection and proper documentation practices.
**Key Activities/Responsibilities:**
1. Maintains production area to prevent cross-contamination (line/area clearance).
2. Assigns tasks for manufacturing operations and support associates.
3. Supervise, develop, provide feedback, and coach employees.
4. Complete performance reviews as scheduled.
5. Performs and assists employees with time keeping transactions.
6. Coordinates the turnaround, set-up, and changeover of manufacturing equipment.
7. Verifies component readiness, reject verification, and product returns.
8. Review weekly production schedule and work with the Planning department on capacity and scheduling issues.
9. Coordinate activities to support the production schedule. Participate in process related issues using thorough technical process knowledge to make timely decisions to ensure that efficiency and other business goals are achieved.
10. Provides feedback to Managers regarding associate performance and behaviors.
11. Ensures that manufacturing equipment operates efficiently at or above target line speeds while minimizing line downtime and product reject.
12. Responsible for maintaining OEE (system entry and standards).
13. Completes all batch record and inventory documentation accurately (review batch records/ERPLx transactions/CAMS/CPMS).
14. Assists with nonconformance investigations, material variance review, line efficiency standards, and improvement opportunities.
15. Liaison with MQA Quality Control and QC Microbiology EMPS departments.
16. Meets and maintains all required training during the year (SOP, EHS, and HR).
17. Support operational excellence and EHS initiatives.
18. Assume responsibility for the GMP, ISO, EHS awareness and compliance within the respective area.
19. Attend and participate in OpEx improvement initiatives such as reducing costs and OEE improvements.
20. All other duties, as assigned.
**Qualifications/Training:**
1. HS diploma required. AA/AS degree preferred.
2. 8+ years of production leadership.
3. Demonstrated exceptional people management and leadership skills.
4. Detail oriented.
5. Problem solving, facilitator and management skills. Self-initiative.
6. Exceptional communication and documentation skills. Demonstrated analytical skills. Must be results oriented on a continual basis.
7. Computer literacy.
8. Must be able to read, write, and speak English and possess basic math skills.
This position may be available in the following location(s): ((location_obj))
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement ( .
Our Benefit Programs:Employee Benefits: Bausch + Lomb ( must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Manufacturing Technician II
Posted 3 days ago
Job Viewed
Job Description
DescriptionPosition: Manufacturing Technician II Schedule: Monday-Friday (2:45 pm - 11:15 pm) & (6:30 am - 3:00 pm) Fluent is a premier medical cannabis company with cultivation, processing, and retail locations in Florida, Texas, Pennsylvania, and New York. Our purpose is to compassionately provide patients access to the highest level of medical cannabis in an unrivaled, professional healthcare environment with outstanding customer service. Patient care always comes first at Fluent, and our standards, practices, and performance is unmatched. We are looking for leaders who want to work alongside great talent and create a positive work experience for their team. We are focused on continuous improvements, which creates development opportunities, engaged feedback, and increased contributions towards our goals as a leader in the medical cannabis industry.Find out more at . Follow us on LinkedIn. ROLE SUMMARY:The Manufacturing Technician II supports, measures, and guides daily and weekly manufacturing operations through the conversion of raw materials into finished products at a medical cannabis facility. The Manufacturing Tech II ensures the production schedule and facility compliance in their assigned manufacturing area. Activities may span the entire manufacturing cycle of cannabis products, from botanical preparation to final product packaging. The ideal candidate will excel as a team leader with expertise in food/pharmaceutical manufacturing and solid attention to detail. The role demands heavy amounts of documentation, supervising personnel, and time management. Duties are completed individually and in small teams, under the indirect supervision of Manufacturing Tech IIIs and Supervisors. The position is structured around a required training program and expected function.KEY RESPONSIBILITIES:All candidates must be able to work in an environment with a safety culture. Extended standing, bending, reaching, and high dexterity functions are required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions, including but not limited to: Training and guiding other team members on proper protocols and methods Maintaining the labor and production cycle timelines set by management Capturing, tracking, and reporting data metrics from work areas and activities Ensuring consistent quality of work is achieved Coordinating work patterns and directives from Tech IIIs and Supervisors Maintaining working inventory of necessary equipment for tasks Ensuring scheduled manufacturing tasks are completed and documented Taking direction, staying organized, and keeping detail-oriented with good judgement Collaborating effectively with coworkers when assigned group work and maintaining a culture of continuous improvement as a cohesive team Maintaining a clean and organized work environment Inputting documentation as required Following state and company guidelines, Standard Operating Procedures (SOP), Good Agricultural Collection Practices (GACP), and Good Manufacturing Practices (GMP) Participating individually and in small teams for general manufacturing duties, such as dispensing, packaging, equipment breakdowns, moving products, inventory audits, labeling, cleaning and sanitation of equipment, post-harvest processing, and other general duties around the manufacturing areas as they relate to the upkeep of compliance and production Completing coursework designated in the "Fluent Sessions" training programQUALIFICATIONS: 1-3 years working in a manufacturing environment Minimum of one year of supervisory experience, with proven ability to effectively lead and organize a team. Hold above average interpersonal and communication skills Adaptability for changes at last minute Capable of working without supervision Understanding of applicable federal, state, and local laws and regulations as they pertain to the Grow operation Ability to work both in a team and independently Ability to accurately follow multi-layered instructionsSKILLS / INTERESTS: Medical device or Active Pharmaceutical Ingredient manufacturing Food safety Strong attention to detail Ethical Conduct Leadership skills Ability to work in a fast-paced environment Work in a safe, efficient manner, adhering to company safety policies Basic written and verbal communication skills Self-driven, hard-working, and able to communicate effectively High degree of flexibility, with a strong work ethic Effectively manage time and meet all specified deadlines Excellent organizational skills Strong team player Ability to climb, squat, bend, twist, and stand for long periods of time Able to work in an environment with varying temperatures Basic computer skillsSUPERVISORY RESPONSIBILITIES:This position has supervisory responsibility of the team.REQUIRED EDUCATION and EXPERIENCE:Bachelor's degree in business administration/Management preferred.Two plus years of supervisory experienceADDITIONAL REQUIREMENTS:Must have reliable transportation and a valid driver licensePer state law, must be at least 21 years of age.Must successfully complete a comprehensive background check.Must pass a drug screening.WORK ENVIRONMENT:This position operates in cultivation and manufacturing environments. This role routinely uses cultivation processing equipment and standard office equipment such as computers, phones, photocopiers, filing cabinets, and fax machines.PHYSICAL DEMANDS:The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. While performing the duties of this job, the employee is regularly required to speak and hear. The employee frequently is required to stand for extended periods; walk; use hands to handle or feel objects, tools or controls; reach with hands and arms. Ability to work on desktop or laptop computer for extended periods of time reading, reviewing/analyzing information, and providing recommendations, summaries and/or reports in written format. Must be able to effectively communicate with others verbally and in writing. Employee may be required to occasionally lift and/or move moderate amounts of weight, typically less than 20 pounds. Regular and predictable attendance is essential.POSITION TYPE / EXPECTED HOURS OF WORK:This position regularly requires long hours and frequent weekend work.TRAVEL:Travel is primarily local during the business day, although some out-of-the-area and overnight travel may be expected.OTHER DUTIES:Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.AAP/EEO Statement:Fluent is an equal opportunity employer and we welcome applications from all backgrounds regardless of race, color, religion, sex, ancestry, age, marital status, sexual orientation, gender identity, disability or any other classification protected by PANY BENEFITS:Fluent provides comprehensive benefits offerings to all full-time employees. Our benefits include medical, dental and vision and supplemental insurance, paid time-off program and non-matching 401k plan. FLUENT participates in E- Verify to ensure a legal workforce. All applicants must be legally authorized to work in the United States and will be required to submit proof of such eligibility. Please note: Only shortlisted candidates will be contacted.
Manufacturing Technician I
Posted 17 days ago
Job Viewed
Job Description
Position: Manufacturing Technician I
Reporting Location: Tampa, FL 33610 (Near Busch Gardens)
Schedule: 1st Shift: (6:30 AM - 3 PM); 2nd Shift: Mon-Fri (2:45 PM - 11:15 PM)
Key Responsibilities: Participating individually and in small teams for general manufacturing duties, such as dispensing, packaging, equipment breakdowns, moving products, inventory audits, labeling, sanitation, post-harvest processing, and other general duties around manufacturing as they relate to production.
Fluent is a premier medical cannabis company, with cultivation, processing and retail locations in Florida, Texas, Pennsylvania, and New York. Our purpose is to compassionately provide patients access to the highest level of medical cannabis in an unrivaled, professional healthcare environment with outstanding customer service. Patient care always comes first at Fluent and our standards, practices, and performance is unmatched.
We are looking for leaders who want to work alongside great talent and create a positive work experience for their team. We are focused on continuous improvements, which creates development opportunities, engaged feedback, and increased contributions towards our goals as a leader in the medical cannabis industry.
Find out more at Follow us on LinkedIn.
ROLE SUMMARY
The Manufacturing Technician I supports the day-to-day manufacturing operations through the conversion of raw materials into finished products at a medical cannabis facility. The Manufacturing Tech I is responsible for ensuring their work meets all quality and efficiency standards. Activities may span the entire manufacturing cycle of cannabis products, from botanical preparation to final product packaging. The ideal candidate will excel in repetitious tasks, with expertise in food/pharmaceutical manufacturing, and a strong attention to detail. The role demands heavy amounts of documentation, and time management. Duties are completed individually and in small teams, under the indirect supervision of Manufacturing Technician IIs and department leads. The position is structured around a required training program and expected function.
KEY RESPONSIBILITIES
All candidates must be able to work in an environment with a safety culture. Extended periods of standing, bending, reaching, and high dexterity functions are required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions, including but not limited to:
• Participating individually and in small teams for general manufacturing duties, such as dispensing, packaging, equipment breakdowns, moving products, inventory audits, labeling, sanitation, post-harvest processing, and other general duties around manufacturing as they relate to production
• Collaborating effectively with coworkers when assigned group work, and maintain a culture of continuous improvement as a cohesive team
• Inputting documentation as required
• Maintaining a clean and organized work environment
• Maintaining an ability to execute techniques consistently
• Maintaining compliance with worker protection standards (WPS)
• Inputting documentation as required
• Following state and company guidelines, Standard Operating Procedures (SOP), Good Manufacturing Practices (GMP), and food safety standards
QUALIFICATIONS
• 1-3 years working in a manufacturing environment
• Interpersonal and communication skills
• Adaptability for changes at last minute
• Ability to work both in a team and independently
• Ability to accurately follow multi-layered instructions
SKILLS / INTERESTS
• Medical device or Active Pharmaceutical Ingredient manufacturing
• Food safety
• Strong attention to detail
• Ethical Conduct
• Ability to work in a fast-paced environment
• Work in a safe, efficient manner, adhering to company safety policies
• Basic written and verbal communication skills
• Self-driven, hard working, and able to communicate effectively
• High degree of flexibility, with a strong work ethic
• Effectively manage time and meet all specified deadlines
• Excellent organizational skills
• Strong team player
• Ability to climb, squat, bend, twist, and stand for long periods of time
• Able to work in environment with varying temperatures
SUPERVISORY RESPONSIBILITIES
This position has no supervisory responsibility.
REQUIRED EDUCATON and EXPERIENCE
High School diploma or GED
ADDITIONAL REQUIREMENTS
Must have reliable transportation and a valid driver license
Per state law, must be at least 21 years of age.
Must successfully complete a comprehensive background check.
Must pass a drug screening.
WORK ENVIRONMENT
This position operates in cultivation and manufacturing environments. This role routinely uses cultivation processing equipment and standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to speak and hear. The employee frequently is required to stand for extended periods; walk; use hands to handle or feel objects, tools or controls; reach with hands and arms. Ability to work on desktop or laptop computer for extended periods of time reading, reviewing/analyzing information, and providing recommendations, summaries and/or reports in written format. Must be able to effectively communicate with others verbally and in writing. Employee may be required to occasionally lift and/or move moderate amounts of weight, typically less than 20 pounds. Regular and predictable
attendance is essential.
POSITION TYPE / EXPECTED HOURS OF WORK
This position regularly requires long hours and frequent weekend work.
TRAVEL
Travel is primarily local during the business day, although some out-of-the-area and overnight travel may be expected.
OTHER DUTIES
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or
responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any
time with or without notice.
AAP/EEO Statement
Fluent is an equal opportunity employer and we welcome applications from all backgrounds regardless of race, color,
religion, sex, ancestry, age, marital status, sexual orientation, gender identity, disability or any other classification
protected by law.
COMPANY BENEFITS
Fluent provides comprehensive benefits offerings to all full-time employees. Our benefits include medical, dental and
vision and supplemental insurance, paid time-off program and non-matching 401k plan
FLUENT participates in E- Verify to ensure a legal workforce. All applicants must be legally authorized to work in the United States and will be required to submit proof of such eligibility.
Please note: Only shortlisted candidates will be contacted.
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Manufacturing Team Leader

Posted today
Job Viewed
Job Description
Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.
**Objectives/Purpose of Job:**
Coordinates the production activities for filling lines, packaging lines, sterilization preparation, and compounding. Receives directions from the area manager on the production plan and daily schedule. Place customer service and accountability to the customer as the constant goal. Coordinate closely with other departments on operational and planning issues related to meeting the production plans and company goals. Evaluates product quality issues with the QA/QC representative. Assures proper logbook completion and review. Requires three to five years of previous leadership experience.
**Filling**
Coordinates the operation of aseptic filling equipment including ointment fillers, gel fillers, solution/suspension fillers, RABS, line and equipment cleaning, line clearance, equipment disinfection, and proper documentation practices.
**Packaging**
Coordinates the operation of packaging equipment including manual case labeling, visual inspections, bundling, cartoning, labeling, banding, line and equipment cleaning, line clearances, serialization, and proper documentation practices.
**Aseptic Prep**
Coordinates the operation of sterilization equipment including autoclave, dry heat oven, and skids. Schedules equipment and area disinfection and assures proper documentation practices.
**Compounding**
Coordinates the operation of bulk compounding equipment including nonsterile and sterile kettles, ball mill, and slurry vessels. Schedules area and equipment cleaning/disinfection and proper documentation practices.
**Key Activities/Responsibilities:**
1. Maintains production area to prevent cross-contamination (line/area clearance).
2. Assigns tasks for manufacturing operations and support associates.
3. Supervise, develop, provide feedback, and coach employees.
4. Complete performance reviews as scheduled.
5. Performs and assists employees with time keeping transactions.
6. Coordinates the turnaround, set-up, and changeover of manufacturing equipment.
7. Verifies component readiness, reject verification, and product returns.
8. Review weekly production schedule and work with the Planning department on capacity and scheduling issues.
9. Coordinate activities to support the production schedule. Participate in process related issues using thorough technical process knowledge to make timely decisions to ensure that efficiency and other business goals are achieved.
10. Provides feedback to Managers regarding associate performance and behaviors.
11. Ensures that manufacturing equipment operates efficiently at or above target line speeds while minimizing line downtime and product reject.
12. Responsible for maintaining OEE (system entry and standards).
13. Completes all batch record and inventory documentation accurately (review batch records/ERPLx transactions/CAMS/CPMS).
14. Assists with nonconformance investigations, material variance review, line efficiency standards, and improvement opportunities.
15. Liaison with MQA Quality Control and QC Microbiology EMPS departments.
16. Meets and maintains all required training during the year (SOP, EHS, and HR).
17. Support operational excellence and EHS initiatives.
18. Assume responsibility for the GMP, ISO, EHS awareness and compliance within the respective area.
19. Attend and participate in OpEx improvement initiatives such as reducing costs and OEE improvements.
20. All other duties, as assigned.
**Qualifications/Training:**
1. HS diploma required. AA/AS degree preferred.
2. 8+ years of production leadership.
3. Demonstrated exceptional people management and leadership skills.
4. Detail oriented.
5. Problem solving, facilitator and management skills. Self-initiative.
6. Exceptional communication and documentation skills. Demonstrated analytical skills. Must be results oriented on a continual basis.
7. Computer literacy.
8. Must be able to read, write, and speak English and possess basic math skills.
This position may be available in the following location(s): ((location_obj))
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.
To learn more please read Bausch + Lomb's Job Offer Fraud Statement ( .
Our Benefit Programs:Employee Benefits: Bausch + Lomb ( must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
Manufacturing Process Engineer
Posted today
Job Viewed
Job Description
Manufacturing Plant Supervisor
Posted today
Job Viewed