Quality Assurance Associate

33072 Pompano Beach, Florida Sysco

Posted 1 day ago

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Job Description

This role starts at 17.00 per hour and the shift will be- 630AM-4PM M-F (alternating Saturdays)

JOB SUMMARY

Responsible for inspecting the product to identify quality issues and assisting with product repacking as needed.

RESPONSIBILITIES

  • Provide technical, customer relations, and personnel management for major programs and projects.

  • Conduct daily walk-through of assigned coolers to check the quality of the product and identify any quality issues.

  • Check dates of product for proper product rotation by date.

  • Remove any distressed product, determine what product needs reworking and what product should be discarded.

  • Rework all distressed/damaged products

  • Communicate quality issues to buyers, management, and associates. Report all lost product or transfers.

  • Assure that all inventory is properly blocked and labeled.

  • Inspects product on production lines; identifies issues and notifies line leads

  • Identifies products according to size, origin, and count

QUALIFICATIONS

Education

Prefer High School or GED

Experience

A minimum of two (2) years related experience (knowledge of produce industry preferred).

Skills

  • Ability to operate warehouse power equipment.

  • Ability to interact with others in a professional manner.

  • Good verbal and written communication skills.

  • General understanding of the shipping procedures of a high volume warehouse operation.

  • Solid understanding of produce varieties handled in a wholesale operation.

Decision Making Authority

Most important decisions made fully independently:

Identifying quality issues, removing the distressed and damaged product

Most important decisions made with review and approval of other individuals or supervisors (include the reviews/approvals required):

All work regularly reviewed by the supervisor and manager.

Physical Demands and Work Environment

Please provide any other information that you think would help us further define the nature and scope of this position.

  • Eliminated Produce QC Inspector title.

  • Some stooping and bending required.

  • Ability to manually inspect produce efficiently for periods of up to or exceeding eight (8) hours.

  • They must be able to move around the work area freely.

  • Frequent lifting of the product up to 50 lbs. during the shift, infrequent lifting up to 80 lbs.

AFFIRMATIVE ACTION STATEMENT:

Applicants must be currently authorized to work in the United States. We are proud to be an Equal Opportunity and Affirmative Action employer, and consider qualified applicants without regard to race, color, creed, religion, ancestry, national origin, sex, sexual orientation, gender identity, age, disability, veteran status or any other protected factor under federal, state or local law. This opportunity is available through Sysco Corporation, its subsidiaries and affiliates.

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Quality Assurance Engineer

Coral Springs, Florida COMPLETE TURBINE SERVICES

Posted 7 days ago

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Job Description

Job Details

Job Location
CTS Engines Coral Springs - Coral Springs, FL

Description

Responsibilities

The Quality Assurance Engineer reports to the VP of QA and is responsible for assisting with the development, implementation, and continuation of organizational training and Quality Assurance processes in accordance with regulatory, statutory, customer, and organizational requirements. Other duties may be assigned as conditions warrant.

Duties

Duties of the Quality Assurance include the following:
  1. Support on assigned task by the VP of QA related to Quality Assurance.
  2. Control and evaluation of vendor/supplier quality as per Part 145.217.
  3. Control and analysis of FOD & Tool Program.
  4. Coordinate with the Technical Instructor the training of personnel including, initial, recurrent, specialized, and remedial training, and update and maintain the training records.
  5. Documenting, recording, and maintaining personnel training records.
  6. Ensure employee assessments are signed and completed in the employee training files.
  7. Control, entry, and coordination of OJT Program.


Authority & Delegation

The VP of QA may delegate additional quality-related duties to the Quality Assurance. However, delegation of duties does not relieve the VP of QA of his/her responsibilities under this manual or other regulatory requirements.

Continuity

In the absence of the Quality Assurance the Technical Instructor and /or QA Specialist will assume his/her duties and responsibilities or assign them to another qualified individual.

GENERAL COMMITMENT FOR ALL EMPLOYEES
  • Commitment to company values and complies with department norms, policies, directives, and procedures.
  • Strive for continuous improvement to processes and procedures.
  • Honors and protects confidential and proprietary documents and information.
  • Satisfies work schedule requirements.
  • The job description is not designed to cover or contain a comprehensive listing of all activities, duties or responsibilities that are required by the employee. Performs other duties as assigned.

**You must be a citizen or permanent resident to be considered. We do not have sponsorship plans at this time.**
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Quality Assurance Associate

33072 Pompano Beach, Florida BioStem Technologies

Posted 10 days ago

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Job Description

BioStem Technologies, founded in 2014 and located in South Florida , is a leading medical technology company focused on advanced wound care and regenerative medicine. We develop and commercialize placental tissue allografts, cutting-edge wound care products, and surgical solutions aimed at improving patient outcomes. As we continue our rapid growth and expansion, we seek a Quality Assurance Associate to join our Quality Team.

The Quality Assurance Associate plays a key role in supporting daily QA operations within a regulated tissue banking manufacturing environment. This entry-level position is responsible for executing routine quality assurance tasks such as document review, controlled material inspections, logbook audits, and ensuring compliance with internal procedures and applicable regulatory requirements (e.g., 21 CFR 1271, AATB Standards).

This is an excellent opportunity for individuals looking to start a career in quality assurance, regulatory compliance, or biotech manufacturing. The QA Associate works closely with experienced QA staff and cross-functional departments to ensure high standards of quality and regulatory adherence are maintained throughout tissue processing operations.

Essential Duties and Responsibilities

Include but are not limited to the following, other duties may be applied;
  • Perform routine review of batch records, logbooks, and other documentation for completeness, accuracy, and compliance.
  • Assist with line clearances, room releases, and real-time QA checks in processing and manufacturing areas.
  • Create product and process labels based on approved templates and specifications.
  • Verify accuracy of labels prior to printing and application, ensuring correct donor, lot, expiration, and regulatory information is displayed.
  • Conduct inspections of incoming materials and supplies for conformance to specifications and documentation requirements.
  • Support document control processes including routing, tracking, and archiving of SOPs, forms, and records.
  • Verify proper documentation practices (GDP) are followed throughout operations.
  • Assist in data entry, file maintenance, and preparation of quality metrics or audit materials.
  • Support deviation tracking, non-conformance documentation, and QA-related investigations as assigned.
  • Participate in internal audits, quality meetings, and training sessions.
  • Escalate observed issues, errors, or deviations to QA leadership in a timely and accurate manner.
  • Comply with gowning, cleanroom, and environmental control procedures as needed.
Requirements

Required Qualifications:
  • Bachelor's degree in Life Sciences, Biology, Biotechnology, or a related field preferred.
  • Associate degree with relevant experience in a regulated industry may be considered.
  • 0-2 years of experience in a quality, regulatory, or laboratory role in a tissue bank, pharmaceutical, medical device, or biotech environment.
  • Internship or co-op experience in a regulated manufacturing setting is a plus.
  • Basic knowledge of Good Documentation Practices (GDP) and regulatory requirements (e.g., FDA, AATB, 21 CFR 1271) is desirable.
  • Familiarity with label printing systems and verification workflows preferred.
  • Strong attention to detail, organizational skills, and willingness to learn.
  • Ability to follow written procedures and work instructions with consistency and accuracy.
  • Strong communication and teamwork skills.
  • Proficiency in Microsoft Office (Word, Excel, Outlook); experience with electronic documentation systems is a plus.


BioStem Technologies, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
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Quality Assurance Associate

33066 Pompano Beach, Florida Sysco

Posted today

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Job Description

**This role starts at 17.00 per hour and the shift will be- 630AM-4PM M-F (alternating Saturdays)**
**JOB SUMMARY**
Responsible for inspecting the product to identify quality issues and assisting with product repacking as needed.
**RESPONSIBILITIES**
+ Provide technical, customer relations, and personnel management for major programs and projects.
+ Conduct daily walk-through of assigned coolers to check the quality of the product and identify any quality issues.
+ Check dates of product for proper product rotation by date.
+ Remove any distressed product, determine what product needs reworking and what product should be discarded.
+ Rework all distressed/damaged products
+ Communicate quality issues to buyers, management, and associates. Report all lost product or transfers.
+ Assure that all inventory is properly blocked and labeled.
+ Inspects product on production lines; identifies issues and notifies line leads
+ Identifies products according to size, origin, and count
**QUALIFICATIONS**
**Education**
Prefer High School or GED
**Experience**
A minimum of two (2) years related experience (knowledge of produce industry preferred).
**Skills**
+ Ability to operate warehouse power equipment.
+ Ability to interact with others in a professional manner.
+ Good verbal and written communication skills.
+ General understanding of the shipping procedures of a high volume warehouse operation.
+ Solid understanding of produce varieties handled in a wholesale operation.
**Decision Making Authority**
Most important decisions made fully independently:
Identifying quality issues, removing the distressed and damaged product
Most important decisions made with review and approval of other individuals or supervisors (include the reviews/approvals required):
All work regularly reviewed by the supervisor and manager.
**Physical Demands and Work Environment**
Please provide any other information that you think would help us further define the nature and scope of this position.
+ Eliminated Produce QC Inspector title.
+ Some stooping and bending required.
+ Ability to manually inspect produce efficiently for periods of up to or exceeding eight (8) hours.
+ They must be able to move around the work area freely.
+ Frequent lifting of the product up to 50 lbs. during the shift, infrequent lifting up to 80 lbs.
AFFIRMATIVE ACTION STATEMENT:
Applicants must be currently authorized to work in the United States. We are proud to be an Equal Opportunity and Affirmative Action employer, and consider qualified applicants without regard to race, color, creed, religion, ancestry, national origin, sex, sexual orientation, gender identity, age, disability, veteran status or any other protected factor under federal, state or local law. This opportunity is available through Sysco Corporation, its subsidiaries and affiliates.
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Bilingual Quality Assurance EngSpa

Miramar, Florida 5TH HQ

Posted 9 days ago

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Job Description

We're seeking for a Quality Assurance Inspector in Miramar, FL. who will be responsible for monitoring, inspecting and proposing measures to correct or improve final products in order to meet established quality standards. The ideal candidate must have a very positive attitude, energetic, very organized, detailed orientated, handle pressure well, and excel in a fast paced and highly dynamic environment. Must be fully bilingual English- Spanish.

Schedule: 2:30pm-11pm

Salary $18

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:

  • Performs the inspection of in-process product, and gathering the appropriate documentation
  • Assures cGMP compliance at all times on the production floor
  • Performs Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP's, Safety initiatives, Company policies, FDA and DEA regulations documenting all work performed, ensuring accuracy and thoroughness informing management of any deviations from established internal and regulatory standards/procedures
  • Inspects and approves rooms, lines and equipment prior to use by manufacturing and R&D personnel
  • Approves components for in-process operations
  • Monitors manufacturing and packaging areas for compliance with internal SOPs, cGMPS and FDA/DEA regulations
  • Documents all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance
  • Samples in-process items, and finished products, performing required inspections and testing of in-process items and finished products.
  • Processes and distribute samples to different departments
  • Reviews cGMP compliance records for accuracy and thoroughness and good documentation practices.
  • Applies disposition status to components and in-process materials
  • Issues QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage

QUALIFICATIONS:

  • Associate degree or equivalent work experience
  • 1-3 years experience in quality control of a manufacturing environment
  • Bilingual (English and Spanish) required
  • Knowledge in cGMP regulations and FDA guidelines
  • Detailed oriented
  • Basic computer and math skills.
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Quality Assurance Inspector III

33024 Tamarac, Florida VSE

Posted 9 days ago

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Job Description

COMPANY OVERVIEW: Turbine Controls MRO, a VSE Aviation Company ("TC MRO") is a globally recognized maintenance, repair and overhaul facility with over 180 employees and more than 45 years of expertise in engine component and accessory repair services. Our locations in Bloomfield, Connecticut and Miramar, Florida service original equipment manufacturers, airlines, engine centers, asset managers and government agencies supporting components and LRU's for commercial, military, airframe and industrial applications. Our focus on customer satisfaction, process improvement, quality, delivery and competitive pricing has made TC MRO a recognized leader in the aerospace industry.SUMMARY: The Quality Inspector III performs inspection of aviation accessories in accordance with the current technical data provided in the Component Maintenance Manuals, Services Bulletins, Service Information Letters, Airworthiness Directives, Regulations and Quality procedures acceptable to or approved by the FAA. Quality Inspection is performed to ensure product integrity is maintained to all requirements and to ensure that customer requirements have been fully complied with prior to completion of inspection function. DUTIES & RESPONSIBILITIES: Responsibilities include, but are not limited to: Completes first run articles with support from engineering. Ensure shelf life is monitored and expired chemicals are properly segregated throughout department. Verify all maintenance and repair tasks have been performed correctly and in accordance with technical manuals, engineering drawings, and regulatory requirements. Ensure traceability and accuracy of all documentation required for regulatory compliance. Work closely with production teams to address and resolve quality concerns in real-time. Conduct thorough inspections of aviation accessories to ensure compliance with FAA regulations, industry standards, and company quality assurance procedures. Perform thorough inspections of incoming & in-process and final inspections of accessories to verify adherence to specifications and quality standards. Use precision measuring instruments and testing equipment to inspect parts and assemblies for defects, wear, and deviations from specifications. Document inspection results, non-conformances, and corrective actions in accordance with company procedures and regulatory requirements. Review and interpret technical documents/drawings and CMM's to ensure accurate inspections. Collaborate with engineering, production, and quality teams to address and resolve quality issues. Other duties as assigned. MINIMUM REQUIREMENTS: 5+ years of inspection/relevant experience. OR Associate's degree in lieu of 2 years of experienceDemonstrated understanding of unit functionality. Ability to determine product configuration at the piece part level based off technical documents, product design, training and past knowledge as required for configuration management. Exercise decisiveness on product acceptance. Proficiency in using precision measuring instruments (micrometers & calipers) and inspection equipment. Strong ability to read and interpret technical documents/drawings and CMM"s. Excellent attention to detail and organizational skills. Ability to exercise decisiveness on product acceptance. Willingness to learn and take on new challenges. Excellent communication skills, both verbal and written. Demonstrated track record of dependability and accountability. Maintain a positive attitude, show resilience, and the ability to adapt to changing priorities. Demonstrated ability to work collaboratively within a team environment. Ability to meet vision standards for near and distance visual acuity. Must understand, read, and write English. PREFERRED REQUIREMENTS): 6+ years of experience in quality inspection in aviation industry with a focus on MRO. Experience in quality management systems. Prefer Certified Repairman. Perform prefinal inspection, typing of release documents, and final release of documents if performing final inspection. OTHER: The selected applicant will be subject to a background check and drug testing.VSE is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law. At VSE, we don't just hire employees; we nurture careers and champion well-being. We understand that our success is driven by the people who make up our incredible team, and that's why we're committed to providing a workplace that goes beyond just a job-it's a place where you can truly flourish. When you choose VSE, you're choosing a company that prioritizes YOU. Let us tell you why: Time Off: Enjoy Paid Time Off to relax and recharge. Family Support: We offer Paid Maternity Leave and Paid Bonding Leave, along with access to our Employee Assistance Program, ensuring your family's well-being. Education: Pursue your educational goals with Tuition Reimbursement for Undergrad, Technical, and Graduate Programs. Financial Security: We offer a 401(k) and Employee Stock Purchase Plan to secure your financial future. Healthcare: Your health is essential, and we provide Health, Dental, and Vision Care. Flexible Spending: Take advantage of HSA, FSA, and Dependent Care plans for added flexibility. Insurance: We've got you covered with Short-Term and Long-Term disability insurance. Competitive Salaries: Your hard work is rewarded with competitive salaries. Ready to be part of a company that values you as much as your skills and expertise? Join VSE and let's take your career to new heights while ensuring your well-being every step of the way. Come grow with us. Your future begins here. Apply TODAY!

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Food Quality Assurance Associate

33024 Tamarac, Florida Sysco

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Company: US1490 North Star Seafood, LLCSales Territory: NoneZip Code:33178Travel Percentage: 0COMPENSATION INFORMATION:The pay range provided is not indicative of Sysco’s actual pay range but is merely algorithmic and provided for generalized comparison. Factors that may be used to determine rate of pay include specific skills, work location, work experience and other individualized factorsMonday - Friday 9:30am to 6pmPay $20.25/ hourlyCome join our Team! Be a part of a dynamic organization by working for one of Sysco’s specialty meat companies where we provide custom-cut fresh steaks and other meat, seafood and poultry, giving customers dependable quality, selection and freshness. BENEFITS· Competitive pay· Ongoing job skills training, leadership development training· Career growth opportunities – we promote from within!· PTO and Paid holidays· Comprehensive healthcare benefits· Generous retirement benefits· Employee discount· Healthcare programs· Tuition Reimbursement· Safety programs· Service recognitions and employee rewards· Cross training opportunities· More benefits, too many to nameJOB SUMMARYMonitor Food Safety & Quality Assurance (FSQA) support/evaluation programs and inspection/audit procedures to ensure compliance of products and processes to corporate and regulatory requirements at a Sysco Specialty Meat and/or Seafood Company.RESPONSIBILITIESMonitoring of FSQA programs including HACCP Program, sanitation standard operating procedures, pest control, good manufacturing practices, approved supplier program, foreign material control, plant sanitation, chemical control, product quality assurance, FSQA Customer complaints, food defense and securityAssist in Employee Training of FSQA Programs, Policies, and ProceduresAssist in Implementation of Independent FSQA Audit Program – SQF AuditsAssist when necessary for product evaluations, plant visits, and supplier/customer communication to assist other staff members. Assist as needed in any manner capable of during emergencies the plant President or GM (general manager) determines are paramount to the business.Frequently interacts with the following: SSMC/SSSC Personnel, Operations, Sales, Transportation and Maintenance as well as Sysco Operating Companies, and supplier/customer personnel at the line level.QUALIFICATIONSEducationFormal job training in TQM principles, SPC, HACCP concepts, CFIA/FDA regulations would be beneficial.Formal quality and sensory analysis training would be helpful.ExperienceOne to 3 years of meat and/or seafood industry (as appropriate) experience at a federal CFIA/FDA meat and/or seafood processing plant (as appropriate).Raw meat or seafood industry the only experience will be accepted instead of combined experienceProfessional SkillsDemonstrate the ability to write reports, basic business correspondence, as well as to effectively present information and respond to questions from managers.Demonstrate the ability to add, subtract, multiply, and divide into all units of measure, using whole numbers, common fractions, and decimals.Demonstrate the ability to define problems, collect data and establish facts.Demonstrate the ability to interpret basic technical instructions.Ability to use personal computer, lab equipment, food preparation equipment and office communication equipment.Certifications, Licenses and/or RegistrationsValid driver’s license.Physical DemandsRegularly required to talk or hear.Frequently is required to use hands to finger, handle, or feel objects, tools, or controls.Occasionally required to stand; walk; sit; reach with hands and arms; stoop, kneel, crouch, or crawl; and taste or smell.Occasionally lift and/or move up to 100 pounds.Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.Plant audits and inspections may require lifting of products up to 100 pounds and inspection requires working in a production environment on a moving line, lifting cartons, and visual inspection.Corrected vision required for sensory analysis to identify color, clarity.Warehouse and plant audit also requires close and distance vision to judge GMPs; peripheral vision and depth perception mandatory for safety.Work EnvironmentFrequently exposed to fumes or airborne particles.Occasionally works near mechanical parts and in high, precarious places and is occasionally exposed to wet and/or humid conditions, extreme cold, and risk of radiation.The noise level in the work environment is usually moderate and operating in a refrigerated environment is common.Plant audits/inspections and working at remote in-transit processing facilities and Sysco Operating Companies contain both moderate/loud noise and exposure to fumes and mechanical hazards.BENEFITS INFORMATION:For information on Sysco’s Benefits, please visit is the global leader in foodservice distribution. With over 71,000 colleagues and a fleet of over 13,000 vehicles, Sysco operates approximately 333 distribution facilities worldwide and serves more than 700,000 customer locations.We offer our colleagues the opportunity to grow personally and professionally, to contribute to the success of a dynamic organization, and to serve others in a manner that exceeds their expectations. We’re looking for talented, hard-working individuals to join our team. Come grow with us and let us show you why Sysco is at the heart of food and service.AFFIRMATIVE ACTION STATEMENT:Applicants must be currently authorized to work in the United States.We are proud to be an Equal Opportunity and Affirmative Action employer, and consider qualified applicants without regard to race, color, creed, religion, ancestry, national origin, sex, sexual orientation, gender identity, age, disability, veteran status or any other protected factor under federal, state or local law.This opportunityis available through Sysco Corporation, its subsidiaries and affiliates.

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Quality Assurance Auditor I

33329 Davie, Florida Teva Pharmaceuticals

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Job Description

Quality Assurance Auditor I
Date: Jul 5, 2025
Location:
Davie, United States, Florida, 33326
Company: Teva Pharmaceuticals
Job Id: 61820
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The opportunity**
This position is responsible for leading and maintaining the site Internal Audit Program and providing support during business partner audits and regulatory inspections. This position supports teams using trend and investigational data to create value through process improvements and failure reduction activities and provides representation for quality department on cross functional teams. In addition, provide support to monthly quality metrics, Site Quality Council, Compliance Gap Assessments, Inspection Readiness, Deviations, CAPAs, Complaints and other miscellaneous quality projects.
**How you'll spend your day**
All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.
- Compliance with Internal Audit Program schedule
- Generate, Collect and Upload Monthly & Quarterly Metrics for Quality Council and Site Quality Risk Map
- Prepare supporting documentation, facilitate and attend the Site Quality Council, present area results and prepare meeting minutes
- Prepare Site Quality Councils presentation on time
- Provide High quality support for Compliance CAPAs and investigations. Help develop and conduct the site Internal Audit Program.
- Provide support during Teva's GRA Audits, Third Party Audits and outside Regulatory Inspections (e.g. FDA, MHRA, EU, Anvisa, etc.).
- Provide support to Site Inspection Readiness activities.
- Support Complaint investigations
- Assign, monitor and close audit and Compliance CAPAs in the Quality System.
- Perform gap assessments to ensure compliance with regulations.
- Provide support for site investigations.
- Prepares and submits reports, standards, and other documents as required.
- Engage in and promote Quality & Operational Excellence.
- Coordinate with other departments and perform investigations, and process change controls.
- Prepare APR contributions for complaints, investigations to show product performance and determine compliance
- Coordinate with other departments to complete investigations and reports
- Review and approve protocols, reports and change controls
- Provide guidance and coaching to employees on GMP, inspection readiness and quality systems
- Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
- Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies, procedures, state, federal and local laws, Good Manufacturing Practices (cGMP's), and Standard Operating Procedures (SOP's) instructions.
- Responsible for performing additional related duties as assigned or required by business needs.
**Your experience and qualifications**
Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.
Education/Certification/Experience:
- Requires Bachelor's Degree in Science, Engineering or related field from an accredited college or university.
- Minimum of five years relevant progressive QA experience in the pharmaceutical or a related industry or an equivalent combination of education and experience
- Requires experience in a solid dose manufacturing environment.
- Requires experience with and an in-depth knowledge of cGMP and other applicable industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.
- Requires experience with the handling of deviations, investigations, and CAPA's.
- Experience with Manufacturing/Quality systems such as TrackWise, Glorya, Veeva, LIMS/Labware, SAP, Learning Management Systems and statistical software preferred.
- Knowledge of CGMPs, SOPs, FDA, and other regulatory compliance regulations and standards required
- ASQ/CQE/CQA Certification preferred.
Skills/Knowledge/Abilities:
- Strong Project Management and organizational skills.
- Analyzing and troubleshooting problems, identifying solutions, recommending and implementing methods, procedures and or/techniques for resolutions.
- Responding to technical inquiries from management, peers, and regulatory agencies.
- Operating scientific and personal computers.
- Managing multiple projects, duties, and assignments.
- Interpreting and applying Federal, state, and local policies, procedures and regulations.
- Establishing and maintaining cooperative working relationships with others.
- Pharmaceutical principles, practices, and their application.
- FDA, SOP, cGMP and other pertinent regulatory compliance and requirements.
- Pertinent Federal and State laws related to personnel administration.
- Business English usage, spelling, grammar, and punctuation.
- Principles of safety, worker's compensation, OSHA, and related principles and practices.
- Business, scientific and personal computer hardware and software applications.
- Skill levels in MS Office including proficiency in Word, PowerPoint, Excel, Teams and SharePoint.
- Must be able to maintain the highest levels of confidentiality, integrity and discretion.
- Excellent verbal, written, and interpersonal skills required.
Problem Solving:
- Proactively works on problems of a moderate to complex scope where evaluation of contributing factors requires the analysis of situations or data and an in-depth knowledge and evaluation of various known and unknown factors.
- Acts independently and proactively to recommend and administer methods and procedures for problem resolution.
- Able to identify solutions to general problems through collaboration and creativity.
TRAVEL REQUIREMENTS
- N/A
**Enjoy a more rewarding choice**
We offer a competitive benefits package, including:
Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.
Retirement Savings: 401(k) with employer match, up to 6% and an annual 3.75% Defined Contribution to the 401k plan.
Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.
Life and Disability Protection: Company paid Life and Disability insurance.
Additional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible , Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more?
The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment?
**Already Working @TEVA?**
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site ( internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
**Important notice to Employment Agencies - Please Read Carefully**
Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
EOE including disability/veteran
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Senior Quality Assurance Manager

33388 Plantation, Florida Chewy

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**Our Opportunity:**
Chewy is looking for a **Senior Quality Assurance Manager** to join our Chewy Private Brands Team. We make boring, interesting and fun as we represent the voice of the Customer. If you love to paint the big picture and enjoy driving high impact change, talk to us!
We are looking for a self-motivated individual who can be the voice of the Customer, is data driven/analytical, can develop deep insights, and take the lead to drive continuous improvement of quality for our hard good products within Private Brands. The ideal candidate will be someone who loves pets and has experience with the manufacture of a variety of hard good products (hard lines, soft lines and electronics) that serve the needs of pets and their pet parents.
**What you'll do:**
+ Complete on-site supplier review of facilities
+ Ensure Commissioning process is successful during launch of new products by facilitating initial production runs
+ Develop and maintain Product Specifications and testing requirements for hard goods products
+ Assess and evaluate supplier factories' capability and quality assurance processes, request and drive supplier quality improvements
+ Ensure vendors' cooperation according to Chewy.com's Quality and Compliance policies
+ Maintain current Quality and Social Audit documentation for all vendors
+ Responsible for developing testing protocols and coordinating with third party labs for product testing
+ Manage data analysis and execution of corrective actions for non-conforming issues for internal facilities and suppliers
+ Develop third party pre-shipment inspections by improving detail and operating at depth based on product type
+ Act as subject matter expert for product quality, safety and regulatory within owned product categories
+ Mentor QA team members at manufacturing sites to identify and correct production and product issues
+ Remain current on applicable regulations (ex: Prop 65, CARB compliance, etc.)
+ Knowledge of metals, fabrics, printing, color matching, and drop tests, transit tests, etc.
+ Own development of production methods and provide solutions when manufacturing issues arise
+ Host training sessions to teach partners about how complex products are made and how they function
+ Coach QA team members on technical evaluation process of design/construction and provide feedback
+ Able to analyze data and create actionable next steps
+ Able to partner and direct cross-functional teams to ensure team success
+ Building continuing education for the team to become highly knowledgeable on products
**What you'll need:**
+ Degree in Textile Science/Technology (softlines/toys), Industrial Engineering, or related science degree
+ 10+ years working in manufacturing/consumer products (non-consumable items)
+ Prior auditing/co-manufacturing experience required
+ Understand and have prior experience with hard good and/or soft line production in China
+ Multi-functional team leadership and project management skills
+ Strong statistical knowledge and analytical and problem solving skills
+ Excellent communication skills, both verbal and written
+ Proficiency in Microsoft Office Suite (Word, Excel, Outlook)
+ Ability to drive process improvement
+ Commitment to professional growth and development as the scope of the position increases
+ Demonstrated integrity, maturity, professionalism, and sensitivity
+ Ability to have late night calls with factories, agents and QA Contractors in China when needed
+ Ability to travel approximately 30%-40% (includes overseas travel)
**Bonus:**
+ Ability to speak mandarin a plus
**Chewy is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, ancestry, national origin, gender, citizenship, marital status, religion, age, disability, gender identity, results of genetic testing, veteran status, as well as any other legally-protected characteristic. If you have a disability under the Americans with Disabilities Act or similar law, and you need an accommodation during the application process or to perform these job requirements, or if you need a religious accommodation, please contact** ** ** **.**
**To access Chewy's Customer Privacy Policy, please click here ( .**
**To access Chewy's California CPRA Job Applicant Privacy Policy, please click here ( .**
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Coder Quality Assurance Auditor

33388 Plantation, Florida Akumin

Posted today

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Job Description

The **Coder** **Quality Assurance Auditor** ensures that services which are billed retail have compliant documents that support accurate coding, helping to support the submission of clean claims in an effort to increase reimbursement and decrease DSO.
**Specific duties include, but are not limited to:**
+ Conducts reimbursement reviews based on denial information from insurance carriers. Performs quality assurance testing under the direction of a Retail Revenue Services Supervisor/ Manager, in order to ensure accuracy, timeliness, and compliance. Conducts regularly scheduled as well as random testing and audits.
+ Analyzes data and utilizes business software to create compelling, informative and persuasive communications to Operations teams and sites.
+ Develops and maintains workflow documentation for system and work processes related to billing/collections and reimbursement.
+ Works with the collections team to create first/second level appeals.
+ Reviews data to ensure A/R and DSO are at appropriate levels.
+ Reviews work results, logs, forms, reports and other documents to analyze and track department performance. Resolves workflow issues and/or makes recommendations to Retail Revenue Services Supervisor/Manager to maximize productivity and workflow while ensuring accuracy, timeliness, and compliance.
+ Executes special projects as assigned by the RRS Supervisor/Manager.
+ Other job duties as needed.
**Position Requirements:**
+ High School Diploma or equivalent experience.
+ Certified Coder through AAPC or AHIMA.
+ 1-2 years of healthcare experience or in a healthcare setting.
+ All candidates who accept an offer for employment will be required to successfully complete a pre-employment background check and drug screen as a condition of employment.
**Preferred:**
+ Associate's Degree.
+ Previously worked in a revenue cycle management environment focusing on A/R resolution.
+ 1-2 years of experience in coder auditing experience.
+ Multi-specialty and/or Radiology experience.
**Physical Requirements:**
Standard office environment.
More than 50% of the time:
+ Sit, stand, and walk.
+ Repetitive movement of hands, arms and legs.
+ See, speak and hear to be able to communicate with patients.
Less than 50% of the time:
+ Stoop, kneel or crawl.
+ Climb and balance.
+ Carry and lift 10-20 Lbs.
The stated pay range for this posting is an average and may not be reflective of your individual circumstances. The pay range for this role takes into account a wide range of factors that are considered in making compensation decisions, including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs.
The base pay for this position ranges from **$16.18 per hour in our lowest geographic market up to $32.36 per hour in our highest geographic market** .
Akumin Operating Corp. and its divisions are an equal opportunity employer and we believe in strength through diversity. All qualified applicants will receive consideration for employment without regard to, among other things, age, race, religion, color, national origin, sex, sexual orientation, gender identity & expression, status as a protected veteran, or disability.
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