5,117 Inspector Vi jobs in the United States
Supervisor, Parenteral (Product Inspection)
Posted 6 days ago
Job Viewed
Job Description
**Organization Overview:**
At Lilly, we serve an extraordinary purpose. We make a difference for people around the globe by discovering, developing and delivering medicines that help them live longer, healthier, more active lives. Not only do we deliver breakthrough medications, but you also can count on us to develop creative solutions to support communities through philanthropy and volunteerism.
**Responsibilities:**
Lilly is entering an exciting period of growth and we are committed to delivering innovative medicines to patients around the world. Lilly is investing over $1 Billion to build a completely new, inspiring, environmentally conscious, and highly automated campus in Concord, North Carolina. This brand-new campus will utilize the latest technology to increase the company's capacity in parenteral (injectable) medications, device assembly, and packaging operations. This is an exciting and once-in-a-lifetime opportunity to build and operate a new site. If you ever wanted to have a direct impact building a team's culture and in how the team operates, now is the perfect opportunity!
During the project phase, the Operations Supervisor will have responsibility of supporting start-up activities to bring the Parenteral (PAR) area into service. The PAR department will have ownership of product formulation, aseptic isolator barrier filling, and visual inspection operations. Activities will include coordinating start-up support amongst self and team to; train on the use of the equipment and develop technical proficiency, develop a diverse and inclusive culture, and lead operational readiness activities.
Once the facility is turned over to operations, the Supervisor role is responsible for leadership of the team that operates the multiple PAR. They will develop an inclusive culture and technical expertise of manufacturing team and employees. This individual will ensure that the lines are adequately staffed with trained & qualified employees. Strict adherence to safety and quality rules and procedures is expected. Direct line supervision for this role includes line leaders and operators. As a site leader and expert at our growing site, you'll have significant opportunities for growth into future leadership and technical roles.
**Integrity**
+ Leading by examples with a Safety first, Quality Always mindset. Comfortable with exercising and encouraging "Stop Work Authority" for all employees if there is a perceived unsafe or product impacting situation.
+ Responsible for maintaining a safe work environment, exemplifying safe working practices, and being accountable for supporting HSE goals.
+ Act as both administrator and technical leaders for operations. Set a good example through demonstrated knowledge of procedures, compliance with quality systems, and teaching of proper techniques.
**Excellence**
+ Collaborate with area supervisors to ensure a high standard of; communication, best practice sharing, and consistency across the groups and different shifts.
+ Responsible for shop floor execution as it relates to business plan, cGMP conformance, and Operational Standards for Manufacturing Excellence.
+ Striving and encouraging a mindset of continuous improvement. Gathering ideas for improvement, articulating their business value, and working with support team to implement the ideas with highest objective value.
+ Ensures there are enough adequately trained and compliant personnel staffed to meet production goals. Reviews and updates training plans as needed to maintain compliance and excellence.
+ Develop area documentation (procedures, work instructions, job aides, etc.) with team to support start-up, training, and operation.
+ Originate & Investigate deviations, operational quality issues, and support determination of root cause. Support implementation of corrective actions to ensure consistent quality.
**Respect for People**
+ Support the site in building a diverse, empowered, and capable team.
+ Responsible for managing several direct reports working across multiple manufacturing lines on responsible shift.
+ Responsible for the coaching, development, and performance evaluation of operators.
+ Communicate cross functionally with support team if there are quality, equipment, operational concerns.
**Basic Requirements**
+ High School Diploma or equivalent
+ Prior supervisory experience
+ Basic computer skills (desktop software, MS Office) are required.
+ Previous experience in operations or directly supporting a manufacturing operation (Pharma, Food, Clean-room, or other applicable).
+ Excellent interpersonal, written, and oral communication skills
+ Strong organizational skills and ability to handle and prioritize multiple requests.
+ Strong technical aptitude and ability to train and mentor others.
+ A valid driver's license.
**Time Commitments and Work Authorization**
+ Ability to work overtime as required
+ Ability to wear safety equipment (glasses, shoes, gloves, etc)
+ Ability to work and gown in a cleanroom (Grade C, ISO 8) environment.
+ Ability to work 12 hour shifts once in production.
+ Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.
**Experience with, completion of, or understanding of:**
+ 4+ years in manufacturing/operations with 2+ years in supervisory role
+ cGMP standards and FDA (or other industry) guidelines for production
+ STEM degree or certification
+ Aseptic filling, single use assemblies, isolator technology.
+ Formulation, dispensing, material preparation.
+ Automated, semi-automated, and/or manual inspection.
+ Highly automated equipment (inspection, packaging, filling, assembly, etc.)
+ Manufacturing Execution Systems and SAP or other electronic business systems
+ Continuous improvement methodologies and mindset - lean, six sigma, etc.
+ Root cause analysis and implementing corrective actions
+ Ability to organize and motivate teams
+ Facility, Equipment, Systems, Start-up
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$5.33 - 51.83
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
#WeAreLilly
Product Inspection Operator - Night Shift
Posted today
Job Viewed
Job Description
Job Description
Description:
This position will work Monday through Friday from 10:00pm to 6:00am for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30pm - 5:30am . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:30pm to 5:30am will receive a 10% shift differential.
The Role and Responsibilities
As a Product Inspection Operator, you play a vital role in ensuring the success and efficiency of our production operations. Your responsibilities include monitoring production quality through visual inspections and assisting with basic troubleshooting to keep operations running smoothly. By following established standards and executing reaction plans, you address challenges such as excessive rejects and machine downtime promptly and effectively. Your meticulous attention to detail ensures accurate documentation of machine performance, while your proactive communication during shift changeovers promotes seamless transitions and continuity. By consistently adhering to company policies, safety standards, and procedures, you contribute to achieving production goals and reinforcing our commitment to delivering high-quality products.
Your Key Areas of Impact
Machine Operations and Troubleshooting: You assist in the operation of inspection units within your designated zones, ensuring adherence to the Standards of Operations (SOPs) and Total Productive Maintenance (TPM) procedures. Monitoring production closely and conducting visual inspections helps identify and remove defective products before final stacking, preserving the quality of finished goods. Troubleshooting basic machine issues and escalating complex problems to the Production Supervisor or Line Lead minimizes downtime and maintains production flow. These efforts contribute to steady and efficient operations, reducing defects and optimizing machine performance.
Documentation and Communication: Accurate and detailed record-keeping forms a vital part of what you do. Downtimes, reject rates, and inspection findings are meticulously documented, creating a clear and accountable record of production processes. This information provides valuable insights into trends and machine performance, supporting proactive decision-making. During shift changeovers, you communicate effectively with your relief, ensuring they are fully informed of machine conditions, recent issues, and updates on production progress. The seamless transfer of information prevents errors and maintains operational continuity, keeping production efficient and on schedule.
Quality Assurance and Continuous Improvement: You focus on consistently meeting quality standards by monitoring defect rates and identifying root causes of issues. Reaction plans are executed promptly to address any problems, safeguarding the quality of the final product. With a focus on supporting production goals, such as achieving output targets, you help drive team success. Participation in workshops, problem-solving meetings, and the refinement of work instructions fosters innovation, efficiency, and waste reduction. These efforts not only uphold product quality but also enhance teamwork and contribute to operational excellence.
You’ve received your high school diploma and have at least two (2) years of experience in a manufacturing environment where you utilize visual product inspection and measurement systems to ensure products meet required specifications. You may have experience in statistical process control (SPC). You have strong attention to detail, effective communication skills, and the ability to work both independently and collaboratively as part of a team. You work with a high level of integrity, confidentiality, organization, and time management.
This position will work Monday through Friday from 10:00pm to 6:00am for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30pm - 5:30am . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:30pm to 5:30am will receive a 10% shift differential.
The Work Environment, Physical Demands, and Travel
Your work is conducted in a dynamic manufacturing setting, requiring ability to work in production floor environments, where exposure to noise, dust, fumes, and varying temperatures is common, necessitating the use of appropriate personal protective equipment and adherence to safety protocols. This job requires remaining in a stationary position 70% of the time, whether standing or sitting, and moving about inside the facility. This job requires manual dexterity, as it involves operating machinery, tools, or controls, and handling or manipulating objects. The job involves both close-up work and monitoring processes from a distance, as well as identifying and distinguishing colors. The ability to discern various sounds and alarms is crucial for maintaining safety and operational efficiency. This job requires operating a computer 20% of the time. This job requires the ability to be able to lift to 35 lbs.
This Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee for this seat. Duties, responsibilities, and activities may change at any time with or without notice.
Employee must be able to perform the essential functions of the position satisfactorily. In alignment with the Americans with Disabilities Act (ADA), if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. This commitment to providing accommodations underscores our dedication to creating an inclusive work environment where all employees have the opportunity to succeed and contribute effectively. Employees in need of such accommodations are encouraged to contact our Human Resources department to discuss their specific needs.
Product Inspection Operator - Night Shift
Posted today
Job Viewed
Job Description
Job Description
Description:
This position will work Monday through Friday from 2:00pm to 10:00pm for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30pm - 5:30am . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:30pm to 5:30am. will receive a 10% shift differential.
The Role and Responsibilities
As a Product Inspection Operator, you play a vital role in ensuring the success and efficiency of our production operations. Your responsibilities include monitoring production quality through visual inspections and assisting with basic troubleshooting to keep operations running smoothly. By following established standards and executing reaction plans, you address challenges such as excessive rejects and machine downtime promptly and effectively. Your meticulous attention to detail ensures accurate documentation of machine performance, while your proactive communication during shift changeovers promotes seamless transitions and continuity. By consistently adhering to company policies, safety standards, and procedures, you contribute to achieving production goals and reinforcing our commitment to delivering high-quality products.
Your Key Areas of Impact
Machine Operations and Troubleshooting: You assist in the operation of inspection units within your designated zones, ensuring adherence to the Standards of Operations (SOPs) and Total Productive Maintenance (TPM) procedures. Monitoring production closely and conducting visual inspections helps identify and remove defective products before final stacking, preserving the quality of finished goods. Troubleshooting basic machine issues and escalating complex problems to the Production Supervisor or Line Lead minimizes downtime and maintains production flow. These efforts contribute to steady and efficient operations, reducing defects and optimizing machine performance.
Documentation and Communication: Accurate and detailed record-keeping forms a vital part of what you do. Downtimes, reject rates, and inspection findings are meticulously documented, creating a clear and accountable record of production processes. This information provides valuable insights into trends and machine performance, supporting proactive decision-making. During shift changeovers, you communicate effectively with your relief, ensuring they are fully informed of machine conditions, recent issues, and updates on production progress. The seamless transfer of information prevents errors and maintains operational continuity, keeping production efficient and on schedule.
Quality Assurance and Continuous Improvement: You focus on consistently meeting quality standards by monitoring defect rates and identifying root causes of issues. Reaction plans are executed promptly to address any problems, safeguarding the quality of the final product. With a focus on supporting production goals, such as achieving output targets, you help drive team success. Participation in workshops, problem-solving meetings, and the refinement of work instructions fosters innovation, efficiency, and waste reduction. These efforts not only uphold product quality but also enhance teamwork and contribute to operational excellence.
You’ve received your high school diploma and have at least two (2) years of experience in a manufacturing environment where you utilize visual product inspection and measurement systems to ensure products meet required specifications. You may have experience in statistical process control (SPC). You have strong attention to detail, effective communication skills, and the ability to work both independently and collaboratively as part of a team. You work with a high level of integrity, confidentiality, organization, and time management.
The Work Environment, Physical Demands, and Travel
Your work is conducted in a dynamic manufacturing setting, requiring ability to work in production floor environments, where exposure to noise, dust, fumes, and varying temperatures is common, necessitating the use of appropriate personal protective equipment and adherence to safety protocols. This job requires remaining in a stationary position 70% of the time, whether standing or sitting, and moving about inside the facility. This job requires manual dexterity, as it involves operating machinery, tools, or controls, and handling or manipulating objects. The job involves both close-up work and monitoring processes from a distance, as well as identifying and distinguishing colors. The ability to discern various sounds and alarms is crucial for maintaining safety and operational efficiency. This job requires operating a computer 20% of the time. This job requires the ability to be able to lift to 35 lbs.
This position will work Monday through Friday from 2:00pm to 10:00pm for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30pm - 5:30am . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:30pm to 5:30am. will receive a 10% shift differential.
This Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee for this seat. Duties, responsibilities, and activities may change at any time with or without notice.
Employee must be able to perform the essential functions of the position satisfactorily. In alignment with the Americans with Disabilities Act (ADA), if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. This commitment to providing accommodations underscores our dedication to creating an inclusive work environment where all employees have the opportunity to succeed and contribute effectively. Employees in need of such accommodations are encouraged to contact our Human Resources department to discuss their specific needs.
Product Inspection Operator - Day Shift
Posted today
Job Viewed
Job Description
Job Description
Description:
This position will work Monday through Friday from 2:00pm to 10:00pm for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30am - 5:30pm . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:30pm to 5:30am will receive a 10% shift differential.
The Role and Responsibilities
As a Product Inspection Operator, you play a vital role in ensuring the success and efficiency of our production operations. Your responsibilities include monitoring production quality through visual inspections and assisting with basic troubleshooting to keep operations running smoothly. By following established standards and executing reaction plans, you address challenges such as excessive rejects and machine downtime promptly and effectively. Your meticulous attention to detail ensures accurate documentation of machine performance, while your proactive communication during shift changeovers promotes seamless transitions and continuity. By consistently adhering to company policies, safety standards, and procedures, you contribute to achieving production goals and reinforcing our commitment to delivering high-quality products.
Your Key Areas of Impact
Machine Operations and Troubleshooting: You assist in the operation of inspection units within your designated zones, ensuring adherence to the Standards of Operations (SOPs) and Total Productive Maintenance (TPM) procedures. Monitoring production closely and conducting visual inspections helps identify and remove defective products before final stacking, preserving the quality of finished goods. Troubleshooting basic machine issues and escalating complex problems to the Production Supervisor or Line Lead minimizes downtime and maintains production flow. These efforts contribute to steady and efficient operations, reducing defects and optimizing machine performance.
Documentation and Communication: Accurate and detailed record-keeping forms a vital part of what you do. Downtimes, reject rates, and inspection findings are meticulously documented, creating a clear and accountable record of production processes. This information provides valuable insights into trends and machine performance, supporting proactive decision-making. During shift changeovers, you communicate effectively with your relief, ensuring they are fully informed of machine conditions, recent issues, and updates on production progress. The seamless transfer of information prevents errors and maintains operational continuity, keeping production efficient and on schedule.
Quality Assurance and Continuous Improvement: You focus on consistently meeting quality standards by monitoring defect rates and identifying root causes of issues. Reaction plans are executed promptly to address any problems, safeguarding the quality of the final product. With a focus on supporting production goals, such as achieving output targets, you help drive team success. Participation in workshops, problem-solving meetings, and the refinement of work instructions fosters innovation, efficiency, and waste reduction. These efforts not only uphold product quality but also enhance teamwork and contribute to operational excellence.
You’ve received your high school diploma and have at least two (2) years of experience in a manufacturing environment where you utilize visual product inspection and measurement systems to ensure products meet required specifications. You may have experience in statistical process control (SPC). You have strong attention to detail, effective communication skills, and the ability to work both independently and collaboratively as part of a team. You work with a high level of integrity, confidentiality, organization, and time management.
This position will work Monday through Friday from 2:00pm to 10:00pm for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30am - 5:30pm . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:3pm to 5:30am will receive a 10% shift differential.
The Work Environment, Physical Demands, and Travel
Your work is conducted in a dynamic manufacturing setting, requiring ability to work in production floor environments, where exposure to noise, dust, fumes, and varying temperatures is common, necessitating the use of appropriate personal protective equipment and adherence to safety protocols. This job requires remaining in a stationary position 70% of the time, whether standing or sitting, and moving about inside the facility. This job requires manual dexterity, as it involves operating machinery, tools, or controls, and handling or manipulating objects. The job involves both close-up work and monitoring processes from a distance, as well as identifying and distinguishing colors. The ability to discern various sounds and alarms is crucial for maintaining safety and operational efficiency. This job requires operating a computer 20% of the time. This job requires the ability to be able to lift to 35 lbs.
This Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee for this seat. Duties, responsibilities, and activities may change at any time with or without notice.
Employee must be able to perform the essential functions of the position satisfactorily. In alignment with the Americans with Disabilities Act (ADA), if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. This commitment to providing accommodations underscores our dedication to creating an inclusive work environment where all employees have the opportunity to succeed and contribute effectively. Employees in need of such accommodations are encouraged to contact our Human Resources department to discuss their specific needs.
Product Inspection Operator - Day Shift
Posted today
Job Viewed
Job Description
Job Description
Description:
This position will work Monday through Friday from 6:00am to 2:00pm for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30am - 5:30pm . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:30pm to 5:30am will receive a 10% shift differential.
The Role and Responsibilities
As a Product Inspection Operator, you play a vital role in ensuring the success and efficiency of our production operations. Your responsibilities include monitoring production quality through visual inspections and assisting with basic troubleshooting to keep operations running smoothly. By following established standards and executing reaction plans, you address challenges such as excessive rejects and machine downtime promptly and effectively. Your meticulous attention to detail ensures accurate documentation of machine performance, while your proactive communication during shift changeovers promotes seamless transitions and continuity. By consistently adhering to company policies, safety standards, and procedures, you contribute to achieving production goals and reinforcing our commitment to delivering high-quality products.
Your Key Areas of Impact
Machine Operations and Troubleshooting: You assist in the operation of inspection units within your designated zones, ensuring adherence to the Standards of Operations (SOPs) and Total Productive Maintenance (TPM) procedures. Monitoring production closely and conducting visual inspections helps identify and remove defective products before final stacking, preserving the quality of finished goods. Troubleshooting basic machine issues and escalating complex problems to the Production Supervisor or Line Lead minimizes downtime and maintains production flow. These efforts contribute to steady and efficient operations, reducing defects and optimizing machine performance.
Documentation and Communication: Accurate and detailed record-keeping forms a vital part of what you do. Downtimes, reject rates, and inspection findings are meticulously documented, creating a clear and accountable record of production processes. This information provides valuable insights into trends and machine performance, supporting proactive decision-making. During shift changeovers, you communicate effectively with your relief, ensuring they are fully informed of machine conditions, recent issues, and updates on production progress. The seamless transfer of information prevents errors and maintains operational continuity, keeping production efficient and on schedule.
Quality Assurance and Continuous Improvement: You focus on consistently meeting quality standards by monitoring defect rates and identifying root causes of issues. Reaction plans are executed promptly to address any problems, safeguarding the quality of the final product. With a focus on supporting production goals, such as achieving output targets, you help drive team success. Participation in workshops, problem-solving meetings, and the refinement of work instructions fosters innovation, efficiency, and waste reduction. These efforts not only uphold product quality but also enhance teamwork and contribute to operational excellence.
You’ve received your high school diploma and have at least two (2) years of experience in a manufacturing environment where you utilize visual product inspection and measurement systems to ensure products meet required specifications. You may have experience in statistical process control (SPC). You have strong attention to detail, effective communication skills, and the ability to work both independently and collaboratively as part of a team. You work with a high level of integrity, confidentiality, organization, and time management.
This position will work Monday through Friday from 6:00am to 2:00pm for an estimated duration of two months. Following this period, the role will transition to a 12-hour 3-4-4-3 shift schedule, including weekends, working 5:30am - 5:30pm . Under this schedule, employees work 3 days the first week and 4 days the next, repeating on a rotating basis. All hours worked between 5:3pm to 5:30am will receive a 10% shift differential.
The Work Environment, Physical Demands, and Travel
Your work is conducted in a dynamic manufacturing setting, requiring ability to work in production floor environments, where exposure to noise, dust, fumes, and varying temperatures is common, necessitating the use of appropriate personal protective equipment and adherence to safety protocols. This job requires remaining in a stationary position 70% of the time, whether standing or sitting, and moving about inside the facility. This job requires manual dexterity, as it involves operating machinery, tools, or controls, and handling or manipulating objects. The job involves both close-up work and monitoring processes from a distance, as well as identifying and distinguishing colors. The ability to discern various sounds and alarms is crucial for maintaining safety and operational efficiency. This job requires operating a computer 20% of the time. This job requires the ability to be able to lift to 35 lbs.
This Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities required of the employee for this seat. Duties, responsibilities, and activities may change at any time with or without notice.
Employee must be able to perform the essential functions of the position satisfactorily. In alignment with the Americans with Disabilities Act (ADA), if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. This commitment to providing accommodations underscores our dedication to creating an inclusive work environment where all employees have the opportunity to succeed and contribute effectively. Employees in need of such accommodations are encouraged to contact our Human Resources department to discuss their specific needs.
Quality Assurance/Quality Control Manager
Posted today
Job Viewed
Job Description
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
- Develop and implement quality assurance policies and procedures to ensure compliance with ISO standards and regulatory requirements.
- Manage and lead the quality assurance and quality control team to ensure effective testing and quality checks.
- Conduct regular audits of processes and products to identify areas for improvement and ensure adherence to quality standards.
- Oversee the development and execution of testing protocols, including manual and automation testing.
- Utilize root cause analysis to investigate quality issues and implement corrective actions to prevent recurrence.
- Collaborate with cross-functional teams to promote quality awareness and ensure quality practices are integrated into all aspects of production and development.
- Analyze quality data and metrics to identify trends, risks, and opportunities for process improvement.
- Facilitate training sessions for staff on quality standards, documentation, and best practices in quality control.
- Bachelor's degree in Quality Assurance, Engineering, or a related field.
- Minimum of 5 years of experience in quality assurance and quality control roles, with at least 2 years in a management position.
- Strong knowledge of ISO standards and regulatory compliance requirements.
- Proven experience in testing methodologies, including software testing, automation testing, and manual testing.
- Excellent analytical and problem-solving skills with a focus on continuous improvement.
- Strong documentation skills with the ability to create and maintain quality manuals and policies.
- Experience in risk management and root cause analysis.
- Ability to work collaboratively in a team environment and communicate effectively with all levels of the organization.
- Full Benefits
- 3 Weeks PTO
- Company vehicle
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
- Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : RC L784 -- in the email subject line for your application to be considered.***
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
Quality Assurance/Quality Control Manager
Posted today
Job Viewed
Job Description
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
- Develop and implement quality assurance policies and procedures to ensure compliance with ISO standards and regulatory requirements.
- Manage and lead the quality assurance and quality control team to ensure effective testing and quality checks.
- Conduct regular audits of processes and products to identify areas for improvement and ensure adherence to quality standards.
- Oversee the development and execution of testing protocols, including manual and automation testing.
- Utilize root cause analysis to investigate quality issues and implement corrective actions to prevent recurrence.
- Collaborate with cross-functional teams to promote quality awareness and ensure quality practices are integrated into all aspects of production and development.
- Analyze quality data and metrics to identify trends, risks, and opportunities for process improvement.
- Facilitate training sessions for staff on quality standards, documentation, and best practices in quality control.
- Bachelor's degree in Quality Assurance, Engineering, or a related field.
- Minimum of 5 years of experience in quality assurance and quality control roles, with at least 2 years in a management position.
- Strong knowledge of ISO standards and regulatory compliance requirements.
- Proven experience in testing methodologies, including software testing, automation testing, and manual testing.
- Excellent analytical and problem-solving skills with a focus on continuous improvement.
- Strong documentation skills with the ability to create and maintain quality manuals and policies.
- Experience in risk management and root cause analysis.
- Ability to work collaboratively in a team environment and communicate effectively with all levels of the organization.
- Full Benefits
- 3 Weeks PTO
- Company vehicle
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
- Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : RC -- in the email subject line for your application to be considered.***
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
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Director Quality Assurance Quality Control
Posted today
Job Viewed
Job Description
QA/QC Director – Fairfield, NJ
Summary:
The QA/QC Director is primarily responsible for the development and implementation of quality management systems. Establishing quality standards and procedures as well as monitor compliance and regulatory requirements.
Responsibilities
- To ensure that the production facility is operating at a high operational and compliance standard.
- Lead, coach and manage a team of chemists to ensure data integrity and performance to meet business objectives
- Monitor each department’s operations to ensure that all procedures are being adhered to and that only approved products or services are being delivered to the company’s clients.
- Oversee the entire department, ensuring that proper procedures are being followed when approving each product or service.
- Ensure that deadlines are met
- Train and develop colleagues
- Assist employees to solve problems, using quality management techniques
- Consult with the quality managers and other personnel to design quality strategies and goals for the department, which will be implemented by employees
- Help to promote the implementation of quality systems throughout the company
- Develop and implement policies relating to all operations in accordance with company objectives. Ensure these policies are adhered to by personnel under your supervision and that appropriate records are kept for future reference
- Keep management informed on product quality and any concerns that may influence this measure, such as complaints from customers or suppliers, etcetera
- Other duties assigned by Management
Education:
- Bachelor’s degree in a scientific discipline with a minimum of 10 years’ experience in quality management
Experience Requirements:
- Experienced with liquid manufacturing and packaging of Rx products.
- Experience with Empower 3
- Experience working in an FDA regulated environment
- Experience with ANDA and NDA submissions
- Experience with validations of processes, cleaning, analytical methods, facilities and equipment
- Knowledge of CFR & ICH Regulatory Guidelines
- Knowledge of cGMP processes and GDP.
Computer Skills:
- Microsoft Word
- Microsoft Excel
- Empower 3
Other Requirements:
- Has significant technical knowledge of quality management principles.
- In depth knowledge of all laboratory equipment, practices, and procedures
- Ability to think logically and independently
- Demonstrated managerial abilities
- Problem analysis, solving and resolution skills
- Has excellent oral and written skills
- Has excellent interpersonal skills
- Is self motivated
- Has a very high attention to detail
- Has a positive attitude
- Must speak, read, and write in English
Quality Assurance/Quality Control Manager
Posted today
Job Viewed
Job Description
You must be able to work in the U.S. without sponsorship. No C2C or 3rd parties, please.
We're hiring an experienced QA/QC Manager to support a greenfield data center construction project in New Albany, OH. This is a high-impact role for someone who understands the complexity of electrical installations and thrives in a detail-driven, fast-paced construction environment.
This is an on-site role focused on maintaining and overseeing all aspects of the project's quality assurance and control plan. You’ll report directly to the Project Manager and coordinate with on-site and off-site teams, subcontractors, and stakeholders to ensure compliance, safety, and precision across the board.
Key Requirements:
- Hands-on experience with high voltage electrical projects
- Strong command of construction quality regulations
- Exceptional attention to detail and documentation
- Ability to communicate effectively with all levels – from tradespeople to leadership
- Previous experience in greenfield or data center construction strongly preferred
- Skilled in electrical inspections, walk-downs, and system testing
- Comfortable with tools like Excel, Word, and QA documentation systems
What You'll Be Doing:
- Implement and manage the project’s QA/QC plan
- Oversee subcontractor compliance and coordinate inspections
- Lead documentation processes – from submittals and logs to final as-builts
- Conduct walk-downs, material tracking, shop drawing reviews, and 4-phase inspections
- Maintain testing records, rework lists, and support third-party audits
- Actively ensure the project stays on track, safe, and within quality specs
Additional Info:
- Must be able to read and interpret blueprints, specs, and system documentation
- Prior work with systems like CSA, CX mapping, Bus Duct, Cable Bus, and MV/LV gear
- Physical ability to move around large construction sites and wear PPE daily
- 15+ years in QA/QC for heavy industrial construction preferred
If you're someone who takes pride in doing it right the first time, keeps quality at the forefront, and is ready for a major project, let’s talk.
Manager, Quality Assurance & Quality Control
Posted 1 day ago
Job Viewed
Job Description
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System ( which makes everything possible.
The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.
This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.
In this role, you will have the opportunity to:
+ Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.
+ Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.
+ Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.
+ Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.
+ Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.
+ Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.
+ Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.
The essential requirements of the job include:
+ Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD
+ Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations
+ Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues
+ Track record of collaborating with technical groups to identify product improvement opportunities
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Travel requirements <5% of the time, domestic and international
+ Overnight travel may be required
+ Be able to occasionally lift and/or move up to 40 pounds.
+ Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
+ This position will occasionally require travel by car and flying in and out of airports with possible long wait times
It would be a plus if you also possess previous experience in:
+ Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.
+ Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.
+ Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.
+ Experience and/or knowledge of NCRs
The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
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Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
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We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .