Do you have experience in a high-volume food manufacturing environment, an eye for detail, and a commitment to safety and cleanliness? If so, we want to talk to you!<\/p>
<\/p>
Villari Foods is currently seeking Quality Control Technicians for our Warsaw, NC warehouse location. The right candidate will have a strong work ethic, leadership skills, and impeccable organizational skills. Our Quality Control team is responsible for ensuring our company meets or exceeds quality control programs designed to result in continuous production of products consistent with established standards. This includes training new employees on these procedures, as well.<\/p>
Job duties:<\/b><\/p> - Ensure HACCP CCPs are verified and documented based on regulatory guidelines.
- Slaughter CCPs are met for milk, ingesta and fecal and offal CCPs are met<\/li>
- Ensure RTE cook and chilling CCPs are met<\/li>
- Ensure heat treated not fully cooked (HTNFC) chilling CCPs are met<\/li>
- Ensure raw intact and raw non-intact CCPs are met<\/li> <\/ul><\/li>
- Conduct quality audits on product temperatures, label checks, metal detection, packaging checks, weight control, verify brine formulation and pump checks, blending of ingredients and restricted ingredients.<\/li>
- Adhere to product specifications during harvesting and on finished packaged products.<\/li>
- Ensure segregation is followed throughout each step of special claims handling.<\/li>
- Ensure all GMPs are followed.<\/li>
- Comply with all SSOP guidelines and quality manual policies.<\/li>
- Perform monthly internal audits at the direction of the SQF Practitioner.<\/li>
- Communicate quality and facility issues to QC Supervisor.<\/li>
- Maintain a safe work environment following company procedures and safety regulations<\/li>
- Perform other tasks as directed<\/li> <\/ul>
To qualify for this job you must have:<\/b><\/p> - GED or High school diploma<\/li>
- 1-year experience in related field (high-volume food manufacturing preferred)<\/li>
- Excellent plant regulatory and HACCP skills<\/li>
- Excellent communication skills - both written and oral<\/li>
- Ability to read and write in English<\/li>
- Ability to perform basic arithmetic functions such as addition, subtraction, multiplication, and division using whole numbers, common fractions, and decimals<\/li>
- Familiarity with Microsoft Office Suite, AS400, and Lotus Notes<\/li>
- Strong attention to detail<\/li>
- Ability to meet deadlines and work well under pressure<\/li>
- Slaughter and animal humane experience preferred.<\/li> <\/ul>
<\/p>
What Villari Food Group offers you:<\/b><\/p> - Competitive compensation<\/li>
- Opportunity to earn overtime hours<\/li>
- Medical, dental, and vision Insurance<\/li>
- Company-paid life insurance<\/li>
- 401K<\/li>
- Paid vacation days and holidays<\/li>
- Employee discounts on Villari meat products<\/li>
- Opportunities for employee recognition<\/li>
- Opportunities for promotion from within; more than 80% of our leaders started in an entry-level position at Villari Foods!<\/li>
- Employment with a great team and a highly experienced supervisor<\/li> <\/ul>
<\/p>
How Villari Foods is different:<\/b><\/p> - As a family-owned and operated business, were more connected with our team members and truly consider each employee a member of the Villari family.<\/li>
- Were a people-focused culture. Team members are not only known but also cared for by peers, leaders, and owners. You arent just a number.<\/li>
- The experience each employee has working at Villari is important to us. Thats why we strive for a better quality of work-life with a slower pace that avoids eventual burnout.<\/li> <\/ul>
<\/p>
Physical requirements and work environment: <\/b> The work environment characteristics and physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<\/p> - The work environment will include cold temperatures between 50F to 10F (non-weather related), working near moving mechanical parts, exposure to fumes or airborne particles, and chemicals. Villari Foods will provide cold-weather gear to you.<\/li>
- The noise level in the work environment is usually moderate but can be loud.<\/li> <\/ul>
- Frequently lift and\/or move up to 50 pounds, occasionally up to 100 pounds<\/li>
- Able to drive a registered motor vehicle to satisfy daily requirements<\/li>
- Specific vision abilities required include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus<\/li>
- Able to speak and hear for safety and productivity<\/li>
- Use scanners, tablets, radios, phones, and other warehouse machinery<\/li>
- Frequently required to stand, use hands and\/or fingers to grasp, handle, feel, reach, and pull<\/li>
- Occasionally required to climb or balance, stoop, kneel, crouch, or crawl<\/li> <\/ul>
<\/p>
More about Villari Foods:<\/b> Founded in 1925 by Sam Villari, Villari Foods is still a family-owned business with a rich history. As a teenager, Sam came to America from Italy, instilled with the value his native culture placed on pure, good food as an integral part of the family and social life. Today, at Villari Foods, we combine our unwavering commitment to Old World quality with our capacity to keep pace with evolving customer demands and exceed expectations for great taste, good health, variety, value, convenience, and creativity in the kitchen. With the fourth Villari generation now entering the business, our family remains dedicated to ensuring an exceptional experience for all who enjoy our products.<\/p>
We offer a wide variety of quality pork and other meat products for retail, food service, and export markets. We understand and are responding to consumer preferences for meat products that are locally sourced, humanely raised, organic, and free of antibiotics, hormones, and steroids. And were well known for our smoked products.<\/p>
As part of Villari Foods, we also have our own livestock and trucking operations, which allows for greater quality control and extraordinary customer service, including superior delivery options. We partner with local farms and are committed to environmental sustainability.<\/p>
EEO Statement:<\/b><\/p>
Villari Food Group is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, gender identity, protected veterans status, status as a disabled individual, or any other protected group status or non-job characteristic as directed by law.<\/p><\/div>
<\/p><\/div><\/body><\/html>","company":"Villari Foods","city":"Warsaw","inferred_city":"Warsaw","inferred_city_with_inferred_state":"North carolina | Warsaw","inferred_cbsa":null,"fips":null,"is_metropolitan":null,"state":"NC","inferred_state":"North carolina","country":"US","inferred_country":"United states","created":"2024-12-21T05:30:21.427995+00:00"},"sort":[1734566400000]},{"_index":"job__2024_12_13__09_47_17","_type":"_doc","_id":"EEGm3ZMB2bT-PlfHcW7B","_score":null,"_source":{"unique_id":"0b238837-9115-5fa2-9994-c7e2ee357aa9","key":"cb6a1bf8a660fa15790159edfca375bc","title":"Quality Assurance System Specialist","inferred_title":"Quality assurance system specialist","salary_offered":"$69,000 - $111,550 a year","inferred_salary_from":69000,"inferred_salary_to":111550,"inferred_salary_yearly_from":69000,"inferred_salary_yearly_average":90275,"inferred_salary_yearly_to":111550,"inferred_salary_yearly_range_spread":0.62,"inferred_salary_currency":"USD","inferred_salary_time_unit":"yearly","inferred_max_experience":8,"inferred_average_experience":8,"inferred_min_experience":8,"inferred_seniority_level":"Entry Level","sign_on_bonus":null,"url":"https:\/\/www.indeed.com\/viewjob?jk=260d92252c80b95a","type":"Full Time","category":null,"board":"indeed","post_date":"2024-12-17","is_remote":false,"html_description":"
Full job description<\/h2><\/div> Johnson & Johnson is currently seeking a Quality Assurance System Specialist to join our Johnson & Johnson Innovative Medicine Supply Chain organization located in Wilson, North Carolina.<\/p>
While this role will ultimately support the site operations located in Wilson NC, this role will also be required to support the project phase across both design & construction. For the project design phase, the role will require you to be present with our design teams in the Greater Philadelphia region. Once the design phase is completed, this role will support the construction and operational start-up of the site. For this, you will be required to be on site in Wilson, NC. Based on your current location the hiring team will work with you to determine travel and relocation arrangements. In steady state, we expect travel to be less than 10%.<\/p>
J&J is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients. The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience. J&Js significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations.<\/p>
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https:\/\/www.jnj.com\/.<\/p>
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the worlds most pressing healthcare challenges.<\/p>
We know that the success of our business and our ability to deliver meaningful solutions depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.<\/p>
At Johnson & Johnson, we all belong.<\/p>
We are currently seeking a highly qualified individual to join our Quality System team as a Quality System Specialist at our new Large Molecule Drug Substance Manufacturing facility. In this key role, you will be responsible for carrying out tasks and projects related to Quality Systems activities as required by Good Manufacturing Practice (GMP). These activities include change control, nonconformance investigation, complaints and CAPA system, Specifications, Quality Agreements and Gap Assessments management within the scope of the organization, Training, Management review (QSMR), documentation management, annual product review and validation compliance activities, among others.<\/p>
Essential Job Duties and Responsibilities:<\/p>
- Provides support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met following the J&J Standards.<\/li>
- Partners with other Departments to ensure that compliance systems are implemented in an efficient manner.<\/li>
- Develops and implements processes, procedures, forms, work instructions and tools related to the implementation of compliance systems at the site.<\/li>
- Carries out tasks related to the administration of site nonconformance management, change control and training systems and its applicable Electronic Tracking System (ETS).<\/li>
- Develops and implements processes, procedures and tools related to the implementation of compliance systems at the site.<\/li>
- Assist Specifications, Quality Agreements and Gap Assessment management activities within the scope of the organization.<\/li>
- Support Management review (QSMR), documentation management, annual product review and validation compliance activities, as required.<\/li>
- Responsible for managing the assigned Quality Systems Metrics and supporting the implementation of all quality policies, procedures, and systems to assure compliance with Regulatory and Company requirements.<\/li>
- Provides training in Good Documentation Practice (GDP) and GMP to site personnel as directed as directed by the Quality Systems Manager.<\/li>
- Develops and maintains training materials for provision of GDP and GMP training to site personnel of applicable systems.<\/li>
- Supports Inspection readiness at the site as Quality Systems SME.<\/li> <\/ul>
Required:<\/p>
- Bachelor's degree in a scientific, engineering or technical discipline.<\/li>
- Minimum of 8 years of experience working in a quality, manufacturing, validation or compliance role within the biological and\/or pharmaceutical industry.<\/li>
- Knowledgeable of FDA\/HPRA\/EMEA regulatory requirements applicable to biologics and\/or pharmaceuticals.<\/li>
- Ability to apply GMP regulations and other FDA and international guidelines to all aspects of the position.<\/li> <\/ul>
Preferred:<\/p>
- Experience in development\/and or evolution of GMP systems and\/or start up experience highly desirable.<\/li>
- An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements.<\/li>
- Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.<\/li>
- Proven ability to manage multiple priorities and work independently with minimal supervision.<\/li>
- Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements.<\/li>
- Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.<\/li>
- Ability to build and nurture strong and positive relationships.<\/li>
- The ability to work in a team environment and interact with all levels of the organization.<\/li> <\/ul>
Note: This position description is a general guideline; it does not purport to be an exhaustive list of all elements of the position. Management reserves the right to modify this position description at any time, or to vary the duties and responsibilities of the position to meet production, scheduling or other business needs.<\/p>
If you are passionate about quality systems, GMP, documentation in the pharmaceutical industry and possess the necessary skills and experience, we invite you to apply for this exciting opportunity as a Quality System Specialist. Join our team and contribute to the development of life-saving therapies in a dynamic and rewarding environment.<\/p>
This job posting is anticipated to close on 12\/31\/2024. The Company may however extend this time-period, in which case the posting will remain available on https:\/\/www.careers.jnj.com to accept additional applications.<\/p>
The anticipated base pay range for this position is $69,000 to $111,550. The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.<\/p>
Employees and\/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).<\/p>
Employees are eligible for the following time off benefits:<\/p>
- Vacation up to 120 hours per calendar year<\/li>
- Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington up to 56 hours per calendar year<\/li>
- Holiday pay, including Floating Holidays up to 13 days per calendar year<\/li>
- Work, Personal and Family Time - up to 40 hours per calendar year<\/li> <\/ul>
For additional general information on Company benefits, please go to: https:\/\/www.careers.jnj.com\/employee-benefits<\/p>
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.<\/p>
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.<\/p><\/div><\/div><\/body><\/html>","company":"Johnson & Johnson","city":"Wilson","inferred_city":"Wilson","inferred_city_with_inferred_state":"North carolina | Wilson","inferred_cbsa":"Wilson, NC","fips":"48980","is_metropolitan":false,"state":"NC","inferred_state":"North carolina","country":"US","inferred_country":"United states","created":"2024-12-19T05:30:22.036446+00:00"},"sort":[1734393600000]},{"_index":"job__2024_12_13__09_47_17","_type":"_doc","_id":"HUGp3ZMB2bT-PlfHYIfJ","_score":null,"_source":{"unique_id":"642f7a34-a33a-532c-9d39-be3e706ae3c4","key":"b849e45e19304dae8d3490ca0f8e344d","title":"2nd Shift Quality Assurance Technician\/T\u00e9cnico de Control de Calidad 2-Turno","inferred_title":"Quality assurance technician \/ control","salary_offered":"$13 - $14 an hour","inferred_salary_from":13,"inferred_salary_to":14,"inferred_salary_yearly_from":27040,"inferred_salary_yearly_average":28080,"inferred_salary_yearly_to":29120,"inferred_salary_yearly_range_spread":0.08,"inferred_salary_currency":"USD","inferred_salary_time_unit":"hourly","inferred_max_experience":1,"inferred_average_experience":1,"inferred_min_experience":1,"inferred_seniority_level":"Entry Level","sign_on_bonus":null,"url":"https:\/\/www.indeed.com\/viewjob?jk=6ca9b835c11e5662","type":"Full Time","category":null,"board":"indeed","post_date":"2024-12-17","is_remote":false,"html_description":"
Full job description<\/h2><\/div> Do you have experience in a high-volume food manufacturing environment, an eye for detail, and a commitment to safety and cleanliness? If so, we want to talk to you!<\/p>
<\/p>
Villari Foods is currently seeking three Quality Control Technicians for our Warsaw, NC warehouse location. The right candidate will have a strong work ethic, leadership skills, and impeccable organizational skills. Our Quality Control team is responsible for ensuring our company meets or exceeds quality control programs designed to result in continuous production of products consistent with established standards. This includes training new employees on these procedures, as well.<\/p>
Job duties:<\/b><\/p> - Ensure HACCP CCPs are verified and documented based on regulatory guidelines.
- Slaughter CCPs are met for milk, ingesta and fecal and offal CCPs are met<\/li>
- Ensure RTE cook and chilling CCPs are met<\/li>
- Ensure heat treated not fully cooked (HTNFC) chilling CCPs are met<\/li>
- Ensure raw intact and raw non-intact CCPs are met<\/li> <\/ul><\/li>
- Conduct quality audits on product temperatures, label checks, metal detection, packaging checks, weight control, verify brine formulation and pump checks, blending of ingredients and restricted ingredients.<\/li>
- Adhere to product specifications during harvesting and on finished packaged products.<\/li>
- Ensure segregation is followed throughout each step of special claims handling.<\/li>
- Ensure all GMPs are followed.<\/li>
- Comply with all SSOP guidelines and quality manual policies.<\/li>
- Perform monthly internal audits at the direction of the SQF Practitioner.<\/li>
- Communicate quality and facility issues to QC Supervisor.<\/li>
- Maintain a safe work environment following company procedures and safety regulations<\/li>
- Perform other tasks as directed<\/li> <\/ul>
To qualify for this job you must have:<\/b><\/p> - GED or High school diploma<\/li>
- 1-year experience in related field (high-volume food manufacturing preferred)<\/li>
- Excellent plant regulatory and HACCP skills<\/li>
- Excellent communication skills - both written and oral<\/li>
- Ability to read and write in English<\/li>
- Ability to perform basic arithmetic functions such as addition, subtraction, multiplication, and division using whole numbers, common fractions, and decimals<\/li>
- Familiarity with Microsoft Office Suite, AS400, and Lotus Notes<\/li>
- Strong attention to detail<\/li>
- Ability to meet deadlines and work well under pressure<\/li> <\/ul>
<\/p>
What Villari Food Group offers you:<\/b><\/p> - Competitive compensation<\/li>
- Opportunity to earn overtime hours<\/li>
- Medical, dental, and vision Insurance<\/li>
- Company-paid life insurance<\/li>
- 401K<\/li>
- Paid vacation days and holidays<\/li>
- Employee discounts on Villari meat products<\/li>
- Opportunities for employee recognition<\/li>
- Opportunities for promotion from within; more than 80% of our leaders started in an entry-level position at Villari Foods!<\/li>
- Employment with a great team and a highly experienced supervisor<\/li> <\/ul>
<\/p>
How Villari Foods is different:<\/b><\/p> - As a family-owned and operated business, were more connected with our team members and truly consider each employee a member of the Villari family.<\/li>
- Were a people-focused culture. Team members are not only known but also cared for by peers, leaders, and owners. You arent just a number.<\/li>
- The experience each employee has working at Villari is important to us. Thats why we strive for a better quality of work-life with a slower pace that avoids eventual burnout.<\/li> <\/ul>
<\/p>
Physical requirements and work environment: <\/b> The work environment characteristics and physical demands described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.<\/p> - The work environment will include cold temperatures between 50F to 10F (non-weather related), working near moving mechanical parts, exposure to fumes or airborne particles, and chemicals. Villari Foods will provide cold-weather gear to you.<\/li>
- The noise level in the work environment is usually moderate but can be loud.<\/li> <\/ul>
- Frequently lift and\/or move up to 50 pounds, occasionally up to 100 pounds<\/li>
- Able to drive a registered motor vehicle to satisfy daily requirements<\/li>
- Specific vision abilities required include close vision, distance vision, peripheral vision, depth perception, and the ability to adjust focus<\/li>
- Able to speak and hear for safety and productivity<\/li>
- Use scanners, tablets, radios, phones, and other warehouse machinery<\/li>
- Frequently required to stand, use hands and\/or fingers to grasp, handle, feel, reach, and pull<\/li>
- Occasionally required to climb or balance, stoop, kneel, crouch, or crawl<\/li> <\/ul>
<\/p>
More about Villari Foods:<\/b> Founded in 1925 by Sam Villari, Villari Foods is still a family-owned business with a rich history. As a teenager, Sam came to America from Italy, instilled with the value his native culture placed on pure, good food as an integral part of the family and social life. Today, at Villari Foods, we combine our unwavering commitment to Old World quality with our capacity to keep pace with evolving customer demands and exceed expectations for great taste, good health, variety, value, convenience, and creativity in the kitchen. With the fourth Villari generation now entering the business, our family remains dedicated to ensuring an exceptional experience for all who enjoy our products.<\/p>
We offer a wide variety of quality pork and other meat products for retail, food service, and export markets. We understand and are responding to consumer preferences for meat products that are locally sourced, humanely raised, organic, and free of antibiotics, hormones, and steroids. And were well known for our smoked products.<\/p>
As part of Villari Foods, we also have our own livestock and trucking operations, which allows for greater quality control and extraordinary customer service, including superior delivery options. We partner with local farms and are committed to environmental sustainability.<\/p>
EEO Statement:<\/b><\/p>
Villari Food Group is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, gender identity, protected veterans status, status as a disabled individual, or any other protected group status or non-job characteristic as directed by law.<\/p><\/div>
<\/p><\/div><\/body><\/html>","company":"Villari Foods","city":"Warsaw","inferred_city":"Warsaw","inferred_city_with_inferred_state":"North carolina | Warsaw","inferred_cbsa":null,"fips":null,"is_metropolitan":null,"state":"NC","inferred_state":"North carolina","country":"US","inferred_country":"United states","created":"2024-12-19T05:30:22.036446+00:00"},"sort":[1734393600000]},{"_index":"job__2024_12_13__09_47_17","_type":"_doc","_id":"WUGm3ZMB2bT-PlfHcW7B","_score":null,"_source":{"unique_id":"b8f50854-e63e-538e-97de-ded182f087eb","key":"cf6deedefbfada1edf2fb001cf828e95","title":"Quality Assurance Specialist II","inferred_title":"Quality assurance specialist","salary_offered":null,"inferred_salary_from":71000,"inferred_salary_to":100000,"inferred_salary_yearly_from":71000,"inferred_salary_yearly_average":85500,"inferred_salary_yearly_to":100000,"inferred_salary_yearly_range_spread":0.41,"inferred_salary_currency":"USD","inferred_salary_time_unit":"yearly","inferred_max_experience":2,"inferred_average_experience":2,"inferred_min_experience":2,"inferred_seniority_level":"Entry Level","sign_on_bonus":null,"url":"https:\/\/www.linkedin.com\/jobs\/view\/quality-assurance-specialist-ii-at-affirm-4102052077","type":"Full Time","category":"Quality Assurance","board":"Linkedin","post_date":"2024-12-17","is_remote":false,"html_description":"
Affirm is reinventing credit to make it more honest and friendly, giving consumers the flexibility to buy now and pay later without any hidden fees or compounding interest.
At Affirm, our Customer Operations Team is growing rapidly! We have a network of external providers and internal teams that need a top rate Quality Assurance and Training and Development culture that can keep up.
Our Quality Assurance (QA) Team sits within Shared Services. This team is responsible for ensuring that our Customer Care and Merchant Operations Teams are providing the highest quality, most delightful experiences to our customers. As a key member of our Quality Assurance Team, you will work with our cross-functional partners such as Process Excellence, Training, Workforce Management, Vendor Management and our Compliance Teams in order to ensure our teams are providing a phenomenal overall customer experience!
What you'll do
- Evaluate and provide feedback on how Customer Operations Teams interact with customers by monitoring, reviewing and auditing calls, emails and chats <\/li>
- Coordinate and participate in calibration sessions with Vendor Partners and Operations Teams to ensure consistent application of quality standards <\/li>
- Act as a subject matter expert to ensure all Customer Operations team members are meeting our quality expectations and providing a positive experience for all customers <\/li>
- Collaborate with team members, recommend, develop, and implement process improvements based on collected data that can be used as benchmark measurements <\/li>
- Work cross functionally with partners on addressing identified agent and interaction opportunities <\/li>
- Create all necessary documentation and SOPs for program details <\/li>
- Create dashboards and reporting for QA metrics\/KPIs <\/li> <\/ul>What we look for
- 2+ years of experience in a Quality Assurance role <\/li>
- Intermediate Excel\/Google Sheets skills for data analysis and reporting <\/li>
- Prior experience working in the financial services or fintech space a plus <\/li>
- Focused, self-motivated and reliable with ability to multi-task and work both in a team setting and independently <\/li>
- Possesses a positive attitude with excellent interpersonal skills and the ability to interact and build solid working relationships with all levels of the organization <\/li>
- Ability to work in a team environment and adapt to changing workload and circumstances effectively as well as respond to new information quickly <\/li> <\/ul>Pay Grade - EEquity Grade - 3Employees new to Affirm typically come in at the start of the pay range. Affirm focuses on providing a simple and transparent pay structure which is based on a variety of factors, including location, experience and job-related skills.Base pay is part of a total compensation package that may include equity rewards, monthly stipends for health, wellness and tech spending, and benefits (including 100% subsidized medical coverage, dental and vision for you and your dependents.)USA base pay range (CA, WA, NY, NJ, CT) per year: $80,000 - $100,000USA base pay range (all other U.S. states) per year: $71,000 - $91,000Please note that visa sponsorship is not available for this position.Affirm is proud to be a remote-first company! The majority of our roles are remote and you can work almost anywhere within the country of employment. Affirmers in proximal roles have the flexibility to work remotely, but will occasionally be required to work out of their assigned Affirm office. A limited number of roles remain office-based due to the nature of their job responsibilities.Benefits<\/strong>Were extremely proud to offer competitive benefits that are anchored to our core value of people come first. Some key highlights of our benefits package include:
- Health care coverage - Affirm covers all premiums for all levels of coverage for you and your dependents <\/li>
- Flexible Spending Wallets - generous stipends for spending on Technology, Food, various Lifestyle needs, and family forming expenses<\/li>
- Time off - competitive vacation and holiday schedules allowing you to take time off to rest and recharge<\/li>
- ESPP - An employee stock purchase plan enabling you to buy shares of Affirm at a discount <\/li> <\/ul>We believe Its On Us to provide an inclusive interview experience for all, including people with disabilities. We are happy to provide reasonable accommodations to candidates in need of individualized support during the hiring process.[For U.S. positions that could be performed in Los Angeles or San Francisco] Pursuant to the San Francisco Fair Chance Ordinance and Los Angeles Fair Chance Initiative for Hiring Ordinance, Affirm will consider for employment qualified applicants with arrest and conviction records.By clicking \"Submit Application,\" you acknowledge that you have read Affirm's Global Candidate Privacy Notice and hereby freely and unambiguously give informed consent to the collection, processing, use, and storage of your personal information as described therein. <\/div><\/body><\/html>","company":"Affirm","city":"Charlotte","inferred_city":"Charlotte","inferred_city_with_inferred_state":"North carolina | Charlotte","inferred_cbsa":"Charlotte-Concord-Gastonia, NC-SC","fips":"16740","is_metropolitan":true,"state":"NC","inferred_state":"North carolina","country":"US","inferred_country":"United states","created":"2024-12-19T05:30:22.036446+00:00"},"sort":[1734393600000]},{"_index":"job__2024_12_13__09_47_17","_type":"_doc","_id":"E0Gm3ZMB2bT-PlfHr3FL","_score":null,"_source":{"unique_id":"5058c65a-0217-5d20-b9c9-fe4a2037ab37","key":"6e19ea42c939a5e2dae2f1a20dde15a4","title":"Quality Assurance, C&Q Specialist","inferred_title":"Quality assurance specialist","salary_offered":"$91,000 - $147,200 a year","inferred_salary_from":91000,"inferred_salary_to":147200,"inferred_salary_yearly_from":91000,"inferred_salary_yearly_average":119100,"inferred_salary_yearly_to":147200,"inferred_salary_yearly_range_spread":0.62,"inferred_salary_currency":"USD","inferred_salary_time_unit":"yearly","inferred_max_experience":4,"inferred_average_experience":4,"inferred_min_experience":4,"inferred_seniority_level":"Entry Level","sign_on_bonus":null,"url":"https:\/\/www.indeed.com\/viewjob?jk=92e2afdb2bf3921f","type":"Full Time","category":null,"board":"indeed","post_date":"2024-12-17","is_remote":false,"html_description":"
Full job description<\/h2><\/div> Johnson & Johnson is currently seeking a Quality Assurance, C&Q (Commissioning & Qualifications) Specialist to join our Johnson & Johnson Innovative Medicine Supply Chain organization located in Wilson, North Carolina.<\/p>
While this role will ultimately support the site operations located in Wilson NC, this role will also be required to support the project phase across both design & construction. For the project design phase, the role will require you to be present with our design teams in the Greater Philadelphia region. Once the design phase is completed, this role will support the construction and operational start-up of the site. For this, you will be required to be on site in Wilson, NC. Based on your current location the hiring team will work with you to determine travel and relocation arrangements. In steady state, we expect travel to be less than 10%.<\/p>
J&J is expanding our manufacturing capacity with $2 billion investment to support strong portfolio growth and continue delivering breakthrough innovation and transformational medicines for patients. The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience. J&Js significant supply chain investment ensures a resilient and reliable future supply of medicines to meet accelerating demand for our current portfolio of medicines and our future innovations.<\/p>
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https:\/\/www.jnj.com\/.<\/p>
For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the worlds most pressing healthcare challenges.<\/p>
We know that the success of our business and our ability to deliver meaningful solutions depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.<\/p>
At Johnson & Johnson, we all belong.<\/p>
We are currently seeking a highly qualified individual to join our Quality team as a Quality Assurance, C&Q Specialist at our new Large Molecule Drug Substance Manufacturing facility in Wilson, North Carolina. We are seeking a talented and passionate professional who thrives in a fast-paced environment and is committed to ensuring the highest standards of quality throughout our organization. If you have a keen eye for detail, exceptional problem-solving skills, and a proven track record in quality assurance, this is the perfect opportunity for you to make a lasting impact.<\/p>
As Quality Assurance, C&Q Specialist, you will be responsible for ensuring compliance with regulatory requirements and company policies while overseeing commissioning, qualification, and validation activities for equipment, utilities, and facilities following current Good Manufacturing Practices, Johnson & Johnson Policies and internal procedures to ensure compliance with regulatory requirements and industry standards supporting project and commercial stages of the new Site.<\/p>
Essential Job Duties and Responsibilities:<\/p>
- Ensure the site validation program has been developed and maintained in compliance with all regulatory and corporate requirements and Master Plans.<\/li>
- Works with the applicable qualification teams representing Quality Assurance in the requirement, design review, construction, qualification and leveraging documentation strategies, cleaning development\/validation and implementation of project.<\/li>
- Review and approve commissioning and qualification documentation, including URS (User Requirements Specifications), IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols and reports, SOPs, Work Instructions and any other technical document.<\/li>
- Review and approves validation protocols and reports (analytical, cleaning, process, etc.)<\/li>
- Provide quality oversight for C&Q and validation execution activities to ensure compliance with GMP, FDA, EMA, and other regulatory requirements.<\/li>
- Support the development and implementation of C&Q and validation plans, ensuring alignment with project timelines and deliverables.<\/li>
- Participate in the risk assessment process for equipment, utilities, and systems to define qualification\/validation requirements.<\/li>
- Perform QA reviews of system impact assessments and categorization of equipment and utilities.<\/li>
- Ensure compliance with company quality standards, including SOPs, work instructions, and quality policies.<\/li>
- Act as the QA point of contact for deviations, CAPAs, and change controls related to C&Q and validation activities.<\/li>
- Provide recommendations for process improvements to enhance compliance and efficiency in C&Q and validation activities.<\/li>
- Reviews\/approves Technology Transfer documents assuring they meet regulatory and J&J requirements.<\/li>
- Collaborate with cross-functional teams, including engineering, validation, and manufacturing, to address quality issues.<\/li> <\/ul>
Required:<\/p>
- Bachelor's degree in a scientific or engineering discipline is required.<\/li>
- A minimum of 4 years of work experience within the biological and\/or pharmaceutical industry and knowledge in compliance of commissioning, qualification and validation of GMP processes and systems.<\/li>
- Strong understanding of cGMP, FDA, EMA, ICH guidelines, and ISPE Baseline Guides. Hands-on experience with qualification\/validation lifecycle (URS, FAT, SAT, IQ, OQ, PQ) and cleaning\/process validation.<\/li>
- Familiarity with ISPE guidelines, including GAMP 5, ASTM E2500, and validation lifecycle principles.<\/li>
- Strong understanding of risk-based approaches to commissioning and qualification\/validation.<\/li>
- Proficiency in technical writing for validation and quality documents.<\/li>
- Strong communication and interpersonal skills for cross-functional collaboration.<\/li>
- Proven expertise as a Subject Matter Expert in C&Q for regulated industries.<\/li>
- Proficiency in risk management methodologies such as FMEA and HACCP.<\/li> <\/ul>
Preferred:<\/p>
- Knowledge working with utilities (water for injection, clean steam, process gases, HVAC, SIP\/CIP), fridges, freezers, LAF, BSC units, autoclaves and isolators as well as Process Equipment Bioreactors, UF\/DF, centrifuge, Chromatography systems.<\/li>
- Experience in development\/and or evolution of C&Q strategies and\/or start up experience highly desirable.<\/li>
- An unquestionable level of integrity and commitment to operating ethically and within the boundaries of regulatory requirements.<\/li>
- Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams.<\/li>
- Proven ability to manage multiple priorities and work independently with minimal supervision.<\/li>
- Detail-oriented mindset, with a keen eye for identifying opportunities for process improvements.<\/li>
- Proven ability to prioritize tasks and meet deadlines in a dynamic manufacturing environment.<\/li>
- Ability to build and nurture strong and positive relationships.<\/li>
- The ability to work in a team environment and interact with all levels of the organization.<\/li> <\/ul>
Note: This position description is a general guideline; it does not purport to be an exhaustive list of all elements of the position. Management reserves the right to modify this position description at any time, or to vary the duties and responsibilities of the position to meet production, scheduling or other business needs.<\/p>
If you are passionate about quality, GMP, qualification\/validation in the biotech\/pharmaceutical industry and possess the necessary skills and experience, we invite you to apply for this exciting opportunity as a C&Q QA Specialist. Join our team and contribute to the development of life-saving therapies in a dynamic and rewarding environment.<\/p>
The anticipated base pay range for this position is $91,000 to $147,200. The compensation and benefits information set forth in this posting applies to candidates hired in the United States. Candidates hired outside the United States will be eligible for compensation and benefits in accordance with their local market.<\/p>
This job posting is anticipated to close on 12\/31\/2024. The Company may however extend this time-period, in which case the posting will remain available on https:\/\/www.careers.jnj.com to accept additional applications.<\/p>
Employees and\/or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Employees may be eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).<\/p>
Employees are eligible for the following time off benefits:<\/p>
- Vacation up to 120 hours per calendar year<\/li>
- Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington up to 56 hours per calendar year<\/li>
- Holiday pay, including Floating Holidays up to 13 days per calendar year<\/li>
- Work, Personal and Family Time - up to 40 hours per calendar year<\/li> <\/ul>
For additional general information on Company benefits, please go to: https:\/\/www.careers.jnj.com\/employee-benefits<\/p>
Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.<\/p>
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com.<\/p><\/div><\/div><\/body><\/html>","company":"Johnson & Johnson","city":"Wilson","inferred_city":"Wilson","inferred_city_with_inferred_state":"North carolina | Wilson","inferred_cbsa":"Wilson, NC","fips":"48980","is_metropolitan":false,"state":"NC","inferred_state":"North carolina","country":"US","inferred_country":"United states","created":"2024-12-19T05:30:22.036446+00:00"},"sort":[1734393600000]}]-->
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