quality assurance specialist

Sheffield Pharmaceuticals

<div>Join Sheffield Pharmaceuticals as a Full-Time Quality Assurance Specialist in New London, CT, and be a key player in our commitment to innovation and excellence. This onsite position offers a dynamic work environment where your problem-solving skills will shine as you contribute to customer-centric projects. This role not only allows you to advance your career but also makes a real impact on product quality and safety. Experience a relaxed yet high-performance culture that values integrity and encourages you to grow. You'll be surrounded by dedicated professionals who share a passion for delivering top-notch pharmaceutical solutions.
You will be provided great benefits such as Medical, Dental, Vision, 401(k), Life Insurance, Health Savings Account, and Paid Time Off. Take the opportunity to be part of a team that champions excellence and embodies a flexible work approach while driving industry standards forward. Join us today and shape the future of healthcare!
<h3 class="jobSectionHeader">Your role as a Quality Assurance Specialist</h3>
As a Quality Assurance Specialist at Sheffield Pharmaceuticals, your daily responsibilities will revolve around ensuring that our products meet the highest industry standards. You will conduct thorough inspections and tests on raw materials and finished goods to identify any deviations from quality specifications. Collaborating closely with the production and development teams, you will document and report non-conformities and recommend corrective actions.
Regularly participating in quality audits and safety assessments will be part of your routine, helping to maintain compliance with regulatory requirements. Additionally, you will assist in the development and implementation of quality assurance processes while staying updated on industry best practices. Your role will also involve continuous learning and adapting to new technologies and methodologies to enhance quality management practices within the organization.
<h3 class="jobSectionHeader">What matters most</h3>
To thrive as a Quality Assurance Specialist at Sheffield Pharmaceuticals, you'll need a keen eye for detail and strong analytical skills to identify potential quality issues effectively. Excellent communication abilities are crucial for collaborating with cross-functional teams and conveying findings clearly. A solid understanding of pharmaceutical regulations and quality control principles is essential, alongside a problem-solving mindset to address challenges proactively. You should possess strong organizational skills to manage multiple tasks and maintain precise documentation.
Being adaptable and open to learning will help you keep pace with changing industry standards and practices. Additionally, fostering a customer-centric approach will enable you to align quality initiatives with the needs of our clients. A passion for safety and excellence will also set you apart as you contribute to our mission of delivering high-quality pharmaceutical products.
<h3 class="jobSectionHeader">Ready to join our team?</h3>
If you think this role will suit your needs, great! Applying is a piece of cake. Good luck - we're excited to meet you!</div>

Quality Assurance Specialist

Aditi Consulting

<div>
 
 
 
 
 Payrate:
 
 
 
 
 
 $43.00 - $43.00/hr.
 
 
 
 &nbsp;
 
 
 
 
 Summary:
 
 
 
 
 
 
 The San Diego Clinical and Specialty Services (CSS) Quality Assurance Specialist I supports clinical trial projects, ensuring all work is performed in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs). They are responsible for implementing and maintaining quality assurance processes throughout the product lifecycle. This involves ensuring that all documentation is accurate, up-to-date, and properly maintained in accordance with regulatory requirements.
 
 
 
 &nbsp;
 
 
 
 
 Education and Experience:
 
 
 
 <ul>
 <li>
 
 
 Bachelor&rsquo;s degree required or equivalent relevant work experience.
 
 
 </li>
 <li>
 
 
 5-7 years of relevant work experience in a GMP environment, or comparable pharmaceutical knowledge and experience.
 
 
 </li>
 <li>
 
 
 JD Edwards or comparable ERP systems preferred.
 
 
 </li>
 <li>
 
 
 Minimum of 3 years of customer service experience.
 
 
 </li>
 <li>
 
 
 Proficient knowledge of MS Office software and query-based systems activities (e.g., Pivot Tables, VLOOKUP&rsquo;s, Excel Formulas, building presentations in PowerPoint, etc.).
 
 
 </li>
 </ul>
 &nbsp;
 
 
 
 
 Skills Requirements:
 
 
 
 <ul>
 <li>
 
 
 Receives instruction, guidance and direction from others
 
 
 </li>
 <li>
 
 
 Uses existing procedures to solve routine problems
 
 
 </li>
 <li>
 
 
 Proactive to address work issues at the individual level
 
 
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 <li>
 
 
 Ability to follow a variety of instructions furnished in written, oral, diagram, or schedule form
 
 
 </li>
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 Mathematical and scientific reasoning ability
 
 
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 Ability to identify aberrant data and potential quality/compliance concerns escalating to management
 
 
 </li>
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 Ability to work effectively under pressure to meet deadlines
 
 
 </li>
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 Sufficient skills and knowledge in the use of computers and associated computer technology (Microsoft Office Software = Outlook, Word, Excel, OneNote, PowerPoint)
 
 
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 <li>
 
 
 Computer technology relates to both the hardware and software used in performing common computing tasks. (JDE, TrackWise, Smartsheets).
 
 
 </li>
 <li>
 
 
 Proficient in Adobe Acrobat
 
 
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 Proficiency in all QS I items
 
 
 </li>
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 Proficient in JDE
 
 
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 Able to create Certificate of Analysis independently
 
 
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 Inspection of bulk drug and finished product
 
 
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 Adhere to GMP standards routinely with limited errors and limited guidance
 
 
 </li>
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 Able to help with investigations
 
 
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 Able to communicate to other teams about requirements
 
 
 </li>
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 Perform effective rapid response
 
 
 </li>
 <li>
 
 
 Subject Matter Expert in JDE related to MMQC processes
 
 
 </li>
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 Inspection of all incoming material types
 
 
 </li>
 <li>
 
 
 Investigation and Deviation writing proficient
 
 
 </li>
 <li>
 
 
 Authoring/Updating documents related to MMQC
 
 
 </li>
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 Approval of GSA jobs
 
 
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 Independent release of labels for use
 
 
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 Approve label prints
 
 
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 Approve external label request forms
 
 
 </li>
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 Verify variable data
 
 
 </li>
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 Perform effective rapid response
 
 
 </li>
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 Subject Matter Expert in JDE related to label release
 
 
 </li>
 <li>
 
 
 Investigation and Deviation writing proficient
 
 
 </li>
 <li>
 
 
 Authoring/Updating documents
 
 
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 <li>
 
 
 One Approach
 
 
 </li>
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 Assist with DME training for new associates
 
 
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 Reviewing/approving Deviations and Complaints
 
 
 </li>
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 Perform effective rapid response
 
 
 </li>
 <li>
 
 
 Attend/prepare for BRMs
 
 
 </li>
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 Client comment resolutions with assistance
 
 
 </li>
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 Drive effective rapid responses
 
 
 </li>
 <li>
 
 
 Complaint assessment
 
 
 </li>
 <li>
 
 
 Presentation of Quality items to clients and ELT
 
 
 </li>
 <li>
 
 
 Assist with other site/global quality items
 
 
 </li>
 <li>
 
 
 Authoring/Updating documents
 
 
 </li>
 <li>
 
 
 Train QS I and II associates
 
 
 </li>
 <li>
 
 
 Reviewing / approving engineering studies
 
 
 </li>
 <li>
 
 
 Review/ approval of Periodic reviews and requalification
 
 
 </li>
 <li>
 
 
 Reviewing /approving change controls and change actions
 
 
 </li>
 <li>
 
 
 Perform effective rapid response
 
 
 </li>
 <li>
 
 
 Presentation of Quality items to clients
 
 
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 <li>
 
 
 Assist with other site/global quality items
 
 
 </li>
 </ul>
 &nbsp;
 
 
 
 
 Pay Transparency:
 
 
 
 
 
 
 The typical base pay for this role across the U.S. is:
 
 $43.00 - $43.00/hr.
 
 &nbsp; Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select.&nbsp; Full-time employees are eligible to select from different benefits packages.&nbsp; Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.
 
 
 
 
 &nbsp;
 
 
 
 
 Consent to Communication and Use of AI Technology: By submitting your application for this position&nbsp;and providing your email address(es) and/or phone number(s), you consent to receive text (SMS), email, and/or voice communication whether automated&nbsp;(including auto telephone dialing systems or automatic text messaging systems), pre-recorded,&nbsp;AI-assisted, or individually initiated from Aditi Consulting, our agents, representatives, or affiliates&nbsp;at the phone number and/or email address you have provided. These communications may include information about potential opportunities and information. Message and data rates may apply. Message frequency may vary.
 
 
 
 
 &nbsp;
 
 
 
 
 You represent and warrant that the email address(es) and/or telephone number(s) you provided to us belong to you and that you are permitted to receive calls, text (SMS) messages, and/or emails at these contacts.&nbsp;You also acknowledge and agree to Aditi Consulting LLC&rsquo;s use of AI technology during the sourcing process, including calls from an AI Voice Recruiter. AI is used solely to gather data and does not replace human-based decision-making in employment decisions.&nbsp; Calls may be recorded.
 
 
 
 
 &nbsp;
 
 
 
 
 Consent is not a condition of purchasing any property, goods, or services. You may revoke your consent at any time by replying &ldquo;STOP&rdquo; to messages or by contacting
 
 
 
 
 
 
 privacy@aditiconsulting.com
 
 
 
 
 
 
 .
 
 
 
 
 &nbsp;
 
 
 
 
 For information about our collection, use, and disclosure of applicant's personal information as well as applicants' rights over their personal information, please see our
 
 
 
 
 
 
 Privacy Policy
 
 
 
 
 &nbsp;
 
 
 
 #AditiConsulting
 
 
 
 
 
 
 #
 
 
 
 
 
 
 26-01083
 
 
 
 
 &nbsp;
 
</div>

SIMPLi

<div>
 
 
 About Us
 
 
 
 
 SIMPLi is an award-winning, leading regenerative food brand on a mission to connect people around the world through the joy of food. Founded in 2020, SIMPLi co-founders Sarela Herrada and Matt Cohen sought to bring the best single-origin ingredients from around the world directly to you in a way that equally benefits people, producers, and the planet. SIMPLi partners directly with farmers to source the finest ingredients and make them accessible to consumers nationwide in stores, restaurants, and online.
 
 
 
 
 If you&rsquo;re passionate about food, sustainability, and making a difference, then SIMPLi is the place for you!
 
 
 
 
 
 
 
 The Role
 
 
 
 We are seeking a detail-oriented and collaborative
 
 Quality Assurance Specialist
 
 to support certification, compliance, and quality system implementation across our supply chain. This role ensures products meet regulatory, certification, and internal standards while working cross-functionally with operations, suppliers, and customers.
 
 
 
 
 
 The ideal candidate combines technical knowledge with strong communication skills and proactively contributes to continuous improvement. This candidate must have prior experience in the food industry and be able to commute to our Philadelphia office 3 days a week.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 Quality Systems &amp; Documentation
 
 
 <ul>
 <li>
 Develop, maintain, and improve SOPs and quality documentation
 </li>
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 Support implementation and monitoring of internal quality standards
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 Maintain organized records for audits and compliance verification
 </li>
 <li>
 Maintain organized tracking of complaints.
 </li>
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 Maintain organized tracking of sales and operational support requirements.
 </li>
 </ul>
 
 
 
 
 
 Inspection &amp; Compliance
 
 
 <ul>
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 Conduct physical inspections and verification activities at copackers and warehouses.
 </li>
 <li>
 Ensure product compliance with certifications and regulatory requirements (e.g., Organic, Kosher, GFSI, FDA, etc.)
 </li>
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 Support certification processes and audit preparation
 </li>
 </ul>
 
 
 
 
 
 Supplier &amp; Co-packer Coordination
 
 
 <ul>
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 Coordinate onboarding of co-packers, warehouses and suppliers.
 </li>
 <li>
 Monitor day-to-day quality performance and issue resolution
 </li>
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 Communicate requirements and follow up on corrective actions
 </li>
 </ul>
 
 
 
 
 
 Customer &amp; Stakeholder Support
 
 
 <ul>
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 Address quality-related requests from customers
 </li>
 <li>
 Prepare specs, CoA and supporting documentation
 </li>
 <li>
 Participate in cross-functional problem solving
 </li>
 </ul>
 
 
 
 
 
 Product Evaluation
 
 
 <ul>
 <li>
 Conduct sensory analysis when required for shelf-life validation or approval.
 </li>
 <li>
 Assist with product quality reviews and decision-making support.
 </li>
 </ul>
 
 
 
 
 
 Continuous Improvement
 
 
 <ul>
 <li>
 Identify risks and propose process improvements
 </li>
 <li>
 Support root cause analysis and corrective/preventive actions
 </li>
 </ul>
 
 
 
 
 
 Qualifications
 
 
 
 
 Required
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Food Science, Food technology, Biology, Quality, or related field
 </li>
 <li>
 4+ years experience in quality assurance, food/ag supply chain, or certifications
 </li>
 <li>
 Familiarity with certification frameworks (Organic, GFSI, etc.)
 </li>
 <li>
 Strong documentation and organizational skills
 </li>
 <li>
 Professional communication and teamwork mindset
 </li>
 </ul>
 
 
 Preferred
 
 
 <ul>
 <li>
 Experience with FDA regulation
 </li>
 <li>
 Experience working with customers and distributors
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 <li>
 Sensory evaluation exposure
 </li>
 <li>
 Audit preparation experience
 </li>
 </ul>
 
 
 
 
 
 Key Competencies
 
 
 <ul>
 <li>
 Accountability and respect for reporting structure
 </li>
 </ul>
 
 
 
</div>

Alimentiv

<div>
 
 Responsible for providing senior support in planning, organizing and/or evaluating the day-to-day delivery of global quality assurance (QA) services. Responsible for supporting the business in quality assurance, policy planning and development, ongoing quality improvement through clinical audit and liaison with other business units and external partners. Will also provide support, expertise, and industry best practice guidance.
 
 
 
 
 
 
 Quality Assurance Implementation
 
 <ul>
 <li>
 Implement quality assurance plans and processes and identify indicators needed to assess product/service quality levels.
 </li>
 <li>
 Collaborating with management/functional experts or Sponsors to identify requirements of the organization in order to conduct internal audits, site audits, vendor assessments and vendor audits.
 </li>
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 Oversee the development of Quality System documents including policy, procedure, instruction, guidance and form and template development in collaboration with departments and senior management.
 </li>
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 Develop QA processes, train and oversee junior QA staff.
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 Liaise with the Human Resources department to ensure that all staff are qualified.
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 Remain current on and ensure internal awareness of regulatory trial conduct standards and requirements.
 </li>
 <li>
 Identify changes to standards and regulations governing Clinical Research and provide recommendations for implementation as required
 
 </li>
 </ul>
 
 
 
 
 Regulatory, Ethical Conduct and Audit Monitoring
 
 <ul>
 <li>
 Remain current on, interpret and communicate changes to regulatory trial conduct standards and requirements.
 </li>
 <li>
 Identify, implement and/or develop policies, processes, and/or training to meet these standards.
 </li>
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 Plan/lead/facilitate Sponsor and regulatory inspections and audit activities including preparation of staff, oversight of proceedings and ensure findings addressed are resolved.
 </li>
 <li>
 Perform internal audits and vendor assessments, ensuring that all observations are appropriately addressed and resolved.
 </li>
 <li>
 Communicate audit findings to internal stakeholders and provide guidance to teams regarding the development of Root Cause Analysis and Corrective Preventive Actions.
 </li>
 <li>
 Liaise with other departments in the completion of Sponsor requests for information.
 </li>
 <li>
 Support internal departments with privacy related questions or inquiries
 
 </li>
 </ul>
 
 
 
 
 Product/Service Consulting
 
 <ul>
 <li>
 Provide guidance during product/service enhancements cycles or during times of organizational change around quality compliance and cross-functional process requirements and organization efficiency gains.&nbsp;
 
 </li>
 </ul>
 
 
 
 
 Qualifications
 
 <ul>
 <li>
 The successful candidate will possess either an undergraduate degree with 4-6 years of related experience and on the go training, or a College Diploma with 7-9 years of related experience and training.
 </li>
 <li>
 Life Sciences, Clinical Research, Information Technology or Clinical Quality Assurance specialty preferred. Strong analytical, critical thinking and problem-solving skills required. Knowledge of ICH GCP, global regulations governing Clinical Research and global privacy regulations
 
 </li>
 </ul>
 
 
 
 
 
 
 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
 
</div>

WBM PVT LTD

Job Description:We are looking for a detail-oriented and responsible Quality Assurance (QA) Officer to join our team. The ideal candidate will be responsible for monitoring and improving product/service quality, ensuring company standards are met, and maintaining compliance with internal policies.Responsibilities:<ul><li>Monitor daily operations to ensure quality standards are maintained</li><li>Conduct inspections and quality checks</li><li>Identify process improvements and suggest corrective actions</li><li>Prepare quality reports and documentation</li><li>Ensure compliance with company policies and safety standards</li><li>Coordinate with different departments to maintain quality performance</li></ul>Requirements:<ul><li>Bachelor&rsquo;s degree (preferred)</li><li>Proven experience in Quality Assurance or related field</li><li>Strong attention to detail</li><li>Good communication and reporting skills</li><li>Ability to analyze data and identify issues</li><li>Knowledge of quality control standards and procedures</li></ul>Skills:<ul><li>Problem-solving skills</li><li>Time management</li><li>Team coordination</li><li>Microsoft Office proficiency</li></ul>Benefits:<ul><li>Competitive salary</li><li>Professional growth opportunities</li><li>Supportive work environment</li></ul>How to Apply:Interested candidates can apply through Indeed.Job Type: Full-timePay: Rs30,000.00 - Rs50,000.00 per monthWork Location: In person

<div>
 
 JOB SUMMARY:
 
 
 
 The
 
 Quality Assurance Specialist
 
 performs routine monitoring work and uses statistical sampling, auditing, and observation of work to ensure consistent compliance with policies and procedures.
 
 
 
 ESSENTIAL FUNCTIONS:
 
 
 
 <ul>
 <li>
 Conducts monitoring and makes recommendations for improvement and maintains documentation on program reviews.
 </li>
 <li>
 Compiles required monitoring documents and submits responses to Continuous Improvement Manager.
 </li>
 <li>
 Provides technical assistance on workforce services programs.
 </li>
 <li>
 Maintains knowledge on current and future programs to ensure compliance with laws and regulations.
 </li>
 <li>
 Performs other related duties as assigned.
 
 
 </li>
 </ul>
 
 REQUIRED SKILLS/ABILITIES:
 
 
 
 <ul>
 <li>
 Knowledge of workforce development, economic development, business intelligence and trends, and project management.
 </li>
 <li>
 Knowledge of effective management techniques and practices to include planning, strategy development and implementation, assessment of outcomes and accountability.
 </li>
 <li>
 Knowledge with applicable federal, state, and local laws and regulations.
 </li>
 <li>
 Knowledgeable with the Integrated Service Principles.
 </li>
 <li>
 Knowledge of quality control, auditing, or performance monitoring,
 </li>
 <li>
 Knowledge of word processing, spreadsheet, technology, and computer skills.
 </li>
 <li>
 Exceptional customer service and interpersonal skills.
 </li>
 <li>
 Excellent problem-solving and critical thinking skills, organizational skill, and detail oriented.
 </li>
 <li>
 Excellent verbal and written communication skills.
 </li>
 <li>
 Ability to analyze and interpret information and data and provide relevant feedback for action.
 
 
 </li>
 </ul>
 
 EDUCATION AND EXPERIENCE:
 
 
 
 <ul>
 <li>
 High School Diploma or GED required.
 </li>
 <li>
 Associates or Undergraduate degree preferred.
 </li>
 <li>
 (1-2) Years of relevant experience required.
 </li>
 <li>
 Additional relevant work experience may be considered in lieu of required education.
 </li>
 <li>
 Valid driver&rsquo;s license and proof of insurance with good driving record.
 </li>
 <li>
 Bilingual in English and Spanish preferred.
 
 
 </li>
 </ul>
 
 PHYSICAL DEMANDS:
 
 
 
 Physical requirements include lifting to 10 pounds occasionally. Subject to standing, sitting, bending, and walking to perform job scope. Requires visual acuity, speech, and hearing. Working conditions are primarily in an office environment. Occasional driving and travel required. Flexible hours may be required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
 
 
 
 COMPANY OVERVIEW:
 
 
 
 C2 Global Professional Services (C2 GPS) is an industry leader providing innovative workforce and career services to Texans, Floridians, and Nevadans. C2 GPS has a reputation for outstanding customer service, building relationships in our local communities, and providing career services to enable job seekers to find meaningful work and grow their careers.
 
 
 Our company values of Respect, Communication, Customer Engagement, and Ingenuity are embedded in every facet of how we work to deliver a standard of excellence that is unmatched by our competitors. Fueled by unprecedented growth, our service delivery model currently spans several counties in Texas, Florida, and Nevada.
 
 
 C2 GPS&rsquo; guiding principle is to successfully navigate workforce development solutions. Our employees must be passionate about providing superior customer service to all our customers and supporting the communities where we live and work.
 
 
 Join a team of talented professionals dedicated to transforming lives for the better. Not only will you collaborate with a passionate and committed group, but you&rsquo;ll also gain access to a competitive benefits plan that enhances your work-life balance. Let&rsquo;s make a difference together!
 
 
 <ul>
 <li>
 Health Insurance (with no-cost options for employee-only plans)
 </li>
 <li>
 Wellness Reimbursement
 </li>
 <li>
 Generous Paid Time Off
 </li>
 <li>
 Paid Parental Leave
 </li>
 <li>
 401(K) with 100% Employer Match up to 6% of individual contributions
 </li>
 <li>
 Dental
 </li>
 <li>
 Vision
 </li>
 <li>
 Life Insurance
 </li>
 <li>
 Short and Long Term Disability
 </li>
 <li>
 Pet Insurance
 
 
 </li>
 </ul>
 
 EEO/AA
 
 
 
 C2 Global Professional Services, LLC reaffirms its commitment to the principles of equal opportunity and diversity. Our policy prohibits employment decisions based on race, color, religion, sex, gender, gender identity, sexual orientation, ancestry, pregnancy, medical condition, age, marital status, national origin, citizenship status, disability, genetic information, veteran status, or any other protected status in accordance with the requirements of all federal, state, and local laws.
 
 
 Further, the company takes affirmative action to ensure that applicants are employed, and employees are treated during employment without regard to any of these characteristics. Employment decisions can include hiring, firing, compensation, benefits, promotion, training selection, or other statuses or conditions of employment. All employment decisions will be made based on individual skills, knowledge, abilities, job performance, and other appropriate qualifications.
</div>

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