Quality assurance specialist jobs in Socastee, SC - 1,841 jobs

Quality Assurance (Auditor) FDA regulated manufacturing environment. ASQ Certified Auditor (CQA) Certification is required. SAP Are you looking to make a career change to a stable company? This exciting opportunity offers a competitive salary plus an excellent benefits package including medical insurance, dental insurance, vision insurance and paid PTO.Does this position match your future career goals? Then this opportunity could be the right fit for you. Why should you apply for this position? A positive workplace culture Competitive Salary Career Advancement opportunities Financial Growth Responsibilities: Ensure proper GMP compliance and SOP procedures are followed SAP experience Maintaining a strong Internal Compliance program ensuring compliance to applicable regulations Document Control and Batch Record Review Apply total quality management tools and approaches to analytical and reporting processes Preparing and periodically reviewing all QC SOPs Supports and participate to all the internal/external audits Schedule and coordinate preparations for product inspections and testing Audit external suppliers (CMO's) Qualifications: Bachelor's degree in Science SAP 5 plus years of industry experience in cGMP environment Knowledge of the Regulations 21CFR Part(s) 210, 211, 507 as well as the Dietary Supplement Regulations 21 CFR 111 is required. ASQ Certified Auditor (CQA) Certification is required. Benefits: A positive workplace culture Competitive Salary Career Advancement opportunities Financial Growth Jasleen Kaur ********************************* Ajulia Executive Search is a search firm specializing in Manufacturing, Finance, IT, Legal and Pharmaceutical positions. This is a confidential search for one of our preferred clients. It is a direct hire position that includes competitive compensation and full comprehensive benefit package. #ZR

The Manager, Quality Management Systems (QMS) is responsible for ensuring compliance with Good Distribution Practices (GDP), 21 CFR regulations, and other applicable standards within a warehouse environment supporting clinical trial supplies. This role leads the implementation, maintenance, and continuous improvement of quality systems to ensure regulatory compliance, operational excellence, and inspection readiness. Essential Duties and Responsibilities Oversee and manage QMS processes, including document control, policy development, and procedure implementation, in alignment with GDP, 21 CFR, and industry standards. Plan, conduct, and manage internal and external audits of warehouse operations to ensure compliance with regulatory requirements, quality guidelines, and standard operating procedures (SOPs). Lead deviation management, including investigations, corrective and preventive actions (CAPAs), change control activities, and risk assessments. Ensure timely vendor and customer qualification and verification activities. Verify accuracy and completeness of quality documentation for all inbound and outbound transactions executed by warehouse operations. Maintain accurate, current, and compliant records within the electronic QMS (eQMS) for all quality-related documentation and activities. Review, approve, and authorize quality-related documents, records, and agreements. Prepare, review, and maintain SOPs, validation documentation, training records, and other quality documents within the eQMS to ensure compliance with regulatory and organizational standards. Support regulatory inspections, internal audits, and customer audits by providing documentation, addressing findings, and ensuring inspection readiness. Monitor QMS performance using metrics and reports to assess effectiveness and identify opportunities for improvement. Develop and deliver training programs for staff on QMS processes, GDP requirements, and regulatory compliance. Collaborate with cross-functional teams, including warehouse operations, logistics, and regulatory functions, to resolve quality issues and implement improvements. Train warehouse operations personnel on quality procedures and compliance expectations. Stay current with evolving regulatory requirements and ensure timely incorporation into QMS practices. Conduct annual reviews of SOPs and update processes as required. Ensure all quality and operational documents are maintained in a controlled, secure, and compliant manner. Work Experience Qualifications Minimum of 5 years of experience in a Quality Management Systems role within the pharmaceutical or life sciences industry. Results-oriented professional with a strong customer service mindset and effective communication skills. Experience with SAP and electronic QMS platforms preferred. High attention to detail with professional verbal and written communication skills. Ability to manage multiple priorities and projects simultaneously in a regulated environment. Willingness and ability to travel for audits, meetings, and industry events. Strong time management, organizational, and problem-solving skills. Self-motivated, accountable, and proactive in driving quality initiatives. Proficient in administrative tools, including MS Office and Google Workspace. Excellent written, verbal, and interpersonal communication skills. Masters is preferred.

In this contingent resource assignment, you may: Consult on complex initiatives with broad impact and large-scale planning for Systems Quality Assurance. Review and analyze complex multi-faceted, larger scale or longer-term Systems Quality Assurance challenges that require in-depth evaluation of multiple factors including intangibles or unprecedented factors. Contribute to the resolution of complex and multi-faceted situations requiring solid understanding of the function, policies, procedures, and compliance requirements that meet deliverables. Strategically collaborate and consult with client personnel. Required Qualifications 5 years of Systems Quality Assurance experience, or equivalent demonstrated through one or a combination of the following: work or consulting experience, training, military experience, education. Comments for Suppliers This position may extend past the 3-month contact. Candidate has proven, strong automation experience moving scripts from Manual to Automated. Proven experience using Selenium, Playwrite, Tosca, HyperExecution, ALM Octane experience in a Commercial Banking UAT environment required. Required Skills & Qualifications Applicants must be able to work directly for the company on W2. Skill 1 - 100% or Must needed with X years of minimum experience. Skill 2 - 100% or Must needed with X years of minimum experience. Skill 3 - 100% or Must needed with X years of minimum experience. Prior experience with the client's industry is a MUST for this position. Education Level - Bachelor's Degree is Mandatory in the field of Computer Science. Preferred Skills & Qualifications Day-to-Day Responsibilities Company Benefits & Culture For immediate consideration please click APPLY.

Pay $31-$33 per hr. Fully Onsite, Shift Work Schedule (includes weekends, and possibly nights) Once shift is determined shifts will be on a stable schedule. Must have: Manufacturing and PQA background Responsibilities: • Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations. • Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls. • Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA)s. • Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements. • Oversee and provide guidance during on-the-floor analytical testing. • Ensure that changes that could potentially impact product quality are assessed according to procedures. • Ensure that deviations from established procedures are investigated and documented per procedures. • Alert senior management of quality, compliance, supply and safety risks. • Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation. • Identification and implementation of continuous improvement opportunities within our processes and systems. • Support and represent PQA during audits and inspections; may directly interact with regulatory agencies during on-site inspections.

We are seeking a Quality Assurance Analyst to join the Loan Operations team here at LoanBoss! LoanBoss is a commercial real estate company specializing in finance software for borrowers and brokers. Our platform simplifies the complexities of real estate finance, providing our clients with the tools they need to successfully manage multi-million-dollar portfolios. The QA Specialist role is responsible for reviewing commercial loan documents and ensuring relevant data is correctly identified and entered into the LoanBoss platform. QA Specialists also help support the Loan Operations team by sharing feedback to help improve quality, digging into any discrepancies in Loan Documents, and helping answer clarifying questions about complex real estate finance concepts. Individuals who excel in this role are great problem solvers and naturally curious. In the coming months, the LoanOps team will be implementing a proprietary AI tool to help streamline operations which will require regular testing from QA Specialists to increase accuracy. If you have a positive mindset and the desire to work hands-on with artificial intelligence, this is the perfect job position for you! Our training involves working hands-on with each team to learn their process and understand a wide array of commercial loan concepts, but is also tailored to fit the individual's learning style. Our team embraces different backgrounds and perspectives, so candidates must fit in with the team and get along well with all types of personalities. You will be a good fit if you have a desire to learn, take initiative and value being challenged. If you bring a strong work ethic and have an appetite for additional responsibilities, you'll find significant opportunities here to advance and grow your career. Location: Our office is located in SouthEnd, right outside of Uptown Charlotte (ability to commute or plan to relocate before starting work) Job Type: Full-time in office Hours: 8:30am - 4:30pm M-F Key Responsibilities: Reviewing commercial loan documents to ensure accurate interpretation Understanding interest rate markets and trends to stay current on market conditions and expectations Communicating feedback to teammates to improve accuracy Collaborating with Product and Customer Service teams to identify bugs and provide client solutions Managing workload independently to ensure deadlines are met Skills: If you have prior experience or knowledge of commercial real estate, that's great. If not, then the #1 qualification will just be intellectual curiosity. Willingness to learn Attention to detail Excellent communication and interpersonal skills Creative problem solving Highly organized Salary: $45,000 - $55,000 per year Benefits: 401k and health insurance, including vision and dental with no premium to employees. No waiting period for eligibility

Location: Greensboro, NC | Full-Time Who We Are We are a trusted leader in the electrical construction industry, known for nearly a century of craftsmanship, safety, and integrity. Headquartered in Greensboro, NC, we've built a reputation for delivering complex, high-quality electrical projects across the Southeast with precision, innovation, and teamwork. Our culture emphasizes collaboration, mentorship, and continuous learning, creating an environment where talented professionals grow their careers while taking pride in the work they do every day. Position Summary We're seeking a QA/QC Technician to support project quality and performance through on-site inspections, documentation, and team coordination. This position plays a critical role in maintaining the company's high standards of consistency, accuracy, and safety. The ideal candidate has hands-on experience in electrical construction, a keen eye for detail, and the ability to communicate effectively across teams and job sites. What You'll Do Conduct field inspections of underground systems, temporary power, switchgear, and equipment installations Review project scopes and QA/QC expectations during kickoff meetings Collaborate with field teams, general contractors, and project managers to ensure compliance with company and client standards Use the QuickBase QA/QC App to record inspections, document issues, and manage nonconformance reports Verify torque and megger testing results and closeout documentation accuracy Promote best practices and consistency across projects Support administrative and documentation tasks as needed Travel to job sites, including occasional out-of-town projects What We're Looking For 5+ years of experience in electrical construction (Foreman or Superintendent experience preferred) Strong knowledge of electrical systems, QA/QC standards, and installation practices Proficient in Microsoft Office Suite and the QuickBase QA/QC App Excellent communication, organization, and reporting skills Comfortable performing physical inspections in active construction environments Dedicated to safety, quality, and teamwork Why You'll Love Working Here A company built on integrity, safety, and technical excellence Collaborative, mentorship-driven culture with advancement opportunities Work on diverse, high-profile projects across multiple industries Competitive pay, benefits, and ongoing professional training If you're ready to join a respected team that values craftsmanship, accountability, and innovation - apply today and help us build what lasts.

Inspire health. Serve with compassion. Be the difference. Performs concurrent medical record reviews to facilitate the highest level of accuracy, quality, and completeness of clinical documentation. This is accomplished by medical record review, query process, and reconciliation process. Participates in the development and delivery of clinical documentation education for providers and health care team members as needed. Serves as preceptor, education resource and second level reviewer for documentation and query justification. May be called on to validate query impact for team. Accountabilities Conducts concurrent medical record reviews of selected patient health records to address clarity, completeness, consistency, and accuracy of clinical documentation. (50%) Employs the query process as needed to provide accurate documentation reflective of patient's severity of illness, risk of mortality, comorbid conditions, length of stay, principal diagnosis, and present on admission (POA) status. (15%) Completes the reconciliation process to ensure accurate coding reflective of patient's severity of illness, risk of mortality, comorbid conditions, length of stay, principal diagnosis, and present on admission (POA) status. (10%) Serves as preceptor, resource, and second level reviewer for appropriate clinical documentation and query justification. (10%) Provides point of care education for providers as relates to accurate capture of patient's severity of illness, risk of mortality, comorbid conditions, length of stay, principal diagnosis, and present on admission (POA) status. (10%) Fulfils all other duties and responsibilities of a CDIS I (5%) Supervisory/Management ResponsibilitiesThis is a non-management job that will report to a supervisor, manager, director or executive.Minimum EducationBachelor's degree in Nursing, Physical Therapy, Respiratory Therapy, Health Information Management, or other healthcare related field. Minimum Experience Four (4) Adult medical/surgical/critical care/ER/PACU nursing coding or related field Clinical documentation improvement experience (2 years) Required Certifications/Registrations/Licenses One of the following certifications: RN, RHIA, RHIT, CCS, or CIC CCDS/CDIP Other Required Experience Computer skills, keyboarding. Strong communication skills with ability to interact with providers and remain tactful. General knowledge of IPPS, ICD10 Coding, MS-DRG/APR-DRG and HCPCS coding systems. Work Shift Day (United States of America) Location Corporate Facility 7001 Corporate Department 70017540 Clinical Documentation Integrity Share your talent with us! Our vision is simple: to transform healthcare for the benefits of the communities we serve. The transformation of healthcare requires talented individuals in every role here at Prisma Health.

Ensures the unit is cosmetically perfect Confirms equipment is functioning to company standards Ensures that the system is complete (accessories, additional components, etc.) Provides feedback to the Senior QA Technician and Warehouse Manager on all discovered issues or defects Maintains record of all testing reports and calibration data Customizes imaging equipment to customer order Requests all necessary components to convert the incoming unit per order Performs all testing tasks and calibration Completes all paperwork on spare parts requested and provides results to the Senior QA Technician/Warehouse Manager Repairs equipment from customer returns Requests all necessary spare parts Completes all paperwork on parts in and out, provides results to the Senior QA Technician/Warehouse Manager Completes the all-final checking procedures per the QA Department standards Maintains a clean work area Collaborates with other departments: Customer Service, RMA, Shipping, and Parts Maintains current knowledge of all company products and all other matters that affect the dental industry Monitors workflow when the manager/supervisor is not available Ensures all processes and protocols are being followed Meets company standards pertaining to quantity and quality of work performed on an ongoing basis, performing all work-related tasks in a manner that is in compliance with all Company policies and procedures Adheres to Company policies, procedures and directives regarding standards of workplace behavior in completing job duties and assignments Repairs, troubleshoots, and updates computers to company standards Performs other duties as assigned MINIMUM QUALIFICATIONS: Training and Experience High School Diploma / GED Warehouse experience Proficient with Computers including Microsoft Office Basic networking skills (preferred) Knowledge, Abilities and Skills Ability to use hand tools and power tools Self-motivated, enthusiastic and willing to learn Proven organizational skills and ability to meet targets, goals, timelines, etc. Excellent verbal and written communication skills Detail-oriented Forklift certified (preferred) If not certified, must become certified within 3-months of hire

Octapharma Plasma offers professional opportunities that make a meaningful difference. We enhance the lives of patients who need our life-saving medicines. We reward the donors who provide the plasma we collect to make them. And we inspire growth and development in the teams at our donation centers, offices, and labs. We invite you to do the same in this role: Onboarding Specialist This Is What You'll Do: Plan and coordinate the logistics of new employee onboarding, including scheduling and preparing materials. Conduct orientation sessions to introduce new hires to the company's culture, values, policies and procedures. Schedule and coordinate onboarding activities, providing guidance and support to new hires throughout the process. Ensuring completion of paperwork and following all legal and administrative compliance when onboarding candidates. Assist new hires with completing the necessary paperwork, including employee forms, benefits enrolment, and IT setup. Processes I-9 and E-Verify requests. Processes background checks and drug screens. This Is Who You Are: Excellent interpersonal skills, strong written and verbal communication skills. Highly ambitious and ability to think outside of the box. Eager to share new ideas and contribute to a team. Self-motivated and willing to assume the initiative. Attentive to every detail. Capable of thriving while working independently. This Is What It Takes: 2+ years of experience in onboarding and recruitment with a proven track record of successful onboarding processes and employee retention. Strong knowledge of onboarding best practices, HR policies and procedures, and employment laws and regulations to ensure compliance during the onboarding process. Strong organizational skills to manage and streamline the onboarding process efficiently. Excellent communication and interpersonal skills to build rapport with new employees and establish a positive onboarding experience. Attention to detail and organizational skills to coordinate and manage multiple onboarding processes simultaneously. Adaptability and flexibility to accommodate the diverse needs and backgrounds of new employees. Ability to collaborate and work effectively with remote team members with prior experience in corporate onboarding. Proficiency in Microsoft Office Suite. Proficiency in using HRIS systems and experience with different applicant tracking systems. May require travel to assist field locations with recruitment. We're widely known and respected for our benefits and for leadership that is supportive and hands-on. Formal training Outstanding plans for medical, dental, and vision insurance Health savings account (HSA) Employee assistance program (EAP) Wellness program 401 (k) retirement plan Paid time off Company-paid holidays Personal time More About Octapharma Plasma, Inc. With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide. We are growing at an impressive pace, and so is the positive impact of our work. Our community relies on teamwork, compassion, and expertise to get things done the right way, while making a meaningful difference in the lives we touch. INNER SATISFACTION. OUTSTANDING IMPACT.

The Outpatient Specialist's main mission is to maintain and grow the current customer base while creating new opportunities through selling the BIOFIRE product line. This includes the sales of instruments, reagents and other services to drive increased adoption and market share within a defined geographical region. The Outpatient Specialist is directly responsible for achieving the territory sales goal through outpatient clinics affiliated with IDNs and clinics not affiliated with IDNs within their assigned territory. Additionally, the Outpatient Specialist will manage both direct sales as well as sales through our distribution partners to achieve high performance in the areas of customer satisfaction, revenue, and profitability. Primary Responsibilities Deliver effective sales call management, opportunity management, pipeline management and forecast accuracy. Identify and establish relationships with key customers and opinion leaders within defined territory. Establish and maintain relationships with our distribution partners to support and advance opportunities and closes. Assess, clarify, validate, and quantify the customer's existing and unmet needs on an ongoing basis. As a part of the Regional Sales team, the Outpatient-Market specialist will identify high value targets within assigned territory and develop strategies to close new business those accounts. Maintain existing customer business to minimize lost business. Work cooperatively in a matrix team and other colleagues to advance and close opportunities. Serve as a liaison between the Outpatient market and Marketing. Channel competitive intel from the field to Marketing and participate as needed in marketing projects and new product launch request. Identify key opinion leaders (KOLs) within defined territory. Manage opportunity pipeline to ensure the timing of closes matches the monthly forecast as it is represented in our CRM tool and related dashboards. Ensure the compliance of business activities meet the most stringent requirements of legal and ethical standards and current company policies. Education and Experience Associates degree and a minimum of 4 years of professional sales experience ORBachelors degree and a minimum of 2 years of professional sales experience required Bachelors degree with 4 years of customer facing experience within the IVD market in lieu of professional sales experience will receive consideration. Strong Knowledge of molecular biology technologies, techniques, and disciplines preferred. In vitro diagnostic (IVD) capital equipment preferred. Point-of-care (POC) sales experience preferred. Distribution-sales experience preferred. Knowledge, Skills, and Abilities Business Skills Functional skills including critical thinking, adaptability, time management, communication, problem-solving and digital literacy. Leading without authority through influence and guidance of others towards a common goal by using expertise, persuasion, and personal qualities to inspire action. Business acumen to understand how a business operates and how to make it successful. Intellectual Horsepower Effective and efficient problem analysis that leads to high-quality decisions. Understand complex information and interpret it accurately, often requiring critical thinking and analysis to grasp the full picture. Manage and meet competing deadlines, requiring careful prioritization and time management to ensure all tasks are completed on time. Creating the New and Different Influence change using skills and relationships to persuade others to adopt new ideas, behaviors, or processes. Perspective to see the world from another person's viewpoint thus gaining new insights and finding creative solutions to challenges. Effectively deal with ambiguity requiring adaptability, critical thinking, and proactive communication to navigate situations with limited details Maintaining Focus Make timely decisions by quickly choosing effective solutions in high-pressure situations for optimal outcomes Priority setting that align with business objectives Thriving in a fast-paced environment by managing tasks, multitasking, and adapting quickly to maintain productivity. Getting Organized Organizing work and resources efficiently to ensure smooth operations Planning objectives and strategies to achieve them within a set timeline Practicing time management to allocate tasks, balance priorities, and meet deadlines efficiently Getting Work Done Through Others Informing others by sharing clear, timely information to ensure alignment. Managing and measuring work by tracking progress, performance, and goal achievement using metrics and KPIs. Managing Work Processes Collect and analyze data to drive informed decision-making to improve performance and identify issues Dealing with Complex Situations Communicates instructions clearly and effectively Demonstrates assertiveness and confidence in the face of a challenge Conflict Management Solution oriented in the face of conflict Comfortable giving clear, direct, and actionable feedback Ability to deal with difficult situations in a timely and bold manner Focusing on the Bottom Line Drive for Results: Drive for Results while successfully removing barriers Action Oriented: Takes action even when facing challenges Being Organizationally Savvy Ability to cooperate with others at all levels including leadership Ability to work cross-functionally allowing for better collaboration and communication when working across teams to achieve shared objectives Communicating Effectively Effective verbal communication skills Written Communications - including the ability to communicate technical data in written form Effective Presentation Skills - including the ability to present technical data Relating Skills Build and maintain positive, productive interactions with colleagues Easily accessible and open to communication Effectively navigate social interactions in the workplace Developing and Inspiring Others Reach mutually beneficial agreements through effective communication and compromise Managing Diverse Relationships Participate in a way that enhances team performance and cohesion. Fosters a culture of inclusiveness among all team members Acting with Honor and Being Open Consistently uphold and reflects the core ethical principles and values that bio Merieux promotes Actively and attentively listen to others, ensuring a clear understanding of their messages, needs, and concerns. Emotional intelligence by having the ability to recognize, understand, and manage one's own emotions, as well as the emotions of others. Maintain composure by having the skill of staying calm, focused, and professional in high-pressure or stressful situations. Working Conditions and Physical Requirements Ability to remain in stationary position, often standing, for prolonged periods. Ability to ascend/descend stairs, ladders, ramps, and the like. Ability to adjust or move objects up to 50 pounds in all directions. Domestic travel required 70% of time Location dependent the selected incumbent will be required to be masked while working in client locations for extended periods when on site in hospitals. Ability to conduct client visits which entails the safe operation of motor vehicles, physically accessing customer facilities and frequent air travel in performance of assigned duties. The estimated salary range for this role is between $87,700 - $140,000. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bio Merieux's bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer.In addition, bio Merieux offers a competitive Total Rewards package that may include: A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options Company-Provided Life and Accidental Death Insurance Short and Long-Term Disability Insurance Retirement Plan including a generous non-discretionary employer contribution and employer match. Adoption Assistance Wellness Programs Employee Assistance Program Commuter Benefits Various voluntary benefit offerings Discount programs Parental leaves #LI-US#biojobs Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bio Merieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bio Merieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site or contact us at [emailprotected]. BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at , by email at [emailprotected], or by dialing 711 for access to Telecommunications Relay Services (TRS).

Food Lion has been providing an easy, fresh and affordable shopping experience to the communities we serve since 1957. Today, our 82,000 associates serve more than 10 million customers a week across 10 Southeastern and Mid-Atlantic states. PRIMARY PURPOSE Provide our customers with a clean, safe, inviting place to shop by maintaining standards in accordance with the standard practice manual. Minimize shrink through proper utilization of standard practice. DUTIES AND RESPONSIBILITIES • Maintain an atmosphere of enthusiastic customer awareness with primary emphasis on fast, friendly, and accurate customer service to create a positive shopping experience • Courteous and helpful to other associates • Sweep and clean floors on nights with no scheduled vendor services • Weekly cleaning of Produce, Market and Deli Departments • Clean and organize the store mop room • Find more efficient ways to do the job and seek to reduce costs and improve labor productivity • Follow QA daily check list and sanitation standards set by Food Lion • Follow current Standard Practices regarding cleanup of Hazardous Waste product • Maintain a complete understanding of and adherence to company guidelines, policies and standard practice • Understand and follow Food Safety and Workplace Safety guidelines and procedures • Observe and correct all unsafe conditions that could cause associate or customer accidents • Report all associate and customer accidents in accordance with established Food Lion procedures to the Manager on Duty • Ensure compliance with local, state and federal regulations • Wear the Food Lion uniform complete with name badge, when on duty, has a neat and clean appearance while adhering to the Food Lion dress code • Successfully complete Computer Based Training (CBT), Training Packet and Training Aid courses • Perform all other duties as assigned QUALIFICATIONS • High school graduate or equivalent preferred • Excellent interpersonal, organizational, communication and customer service skills • Ability and willingness to learn multiple tasks and technical requirements of the job • Ability to use technical information to solve problems • Must meet minimum age requirements to perform specific job functions • Must be able to meet the physical requirements of the position, with or without reasonable accommodations PHYSICAL REQUIREMENTS • Ability to use computers and other communication systems required to perform job functions • Perform repetitive hand and arm motions • Bend and lift products weighing up to 15 lbs. continuously, 25 lbs. frequently, and 50 lbs. on occasion • Pull or push up to 75 lbs. on occasion • Stand 100% of the time, frequently walking short distances • Be able to handle a variety of substances associated with cleaning and packaging materials, fresh fruits, vegetables, house plants/flowers and household cleaners • Use hands to frequently/continuously handle currency (paper and coin) as well as operate a variety of equipment such as cash register, lottery machine (where applicable), scanner, computer, and calculator • Frequent reaching and grasping at waist level: occasionally above shoulder or below waist level • Meet established volume activity standards for the position • Tolerate working in extreme hot/cold temperatures for up to 20 minutes at a time • Have sufficient visual ability to check ID cards, checks, invoices and other written documents Food Lion provides equal employment opportunities to all associates and applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth and related conditions) national origin, age, disability, sexual orientation, veteran status, gender identity or gender expression or any other characteristic protected by law.

The Quality Assurance Assistant is responsible for the inspection of incoming and outgoing products and parts. Ensuring the company's quality standards are met before products reach the customer involves inspections of raw material and incoming goods, in-process parts/product and finished goods prior to shipping. This position requires close communication and coordination with the Quality Management Director and Production Manager. Your tasks Job Summary The Quality Assurance Assistant is responsible for the inspection of incoming and outgoing products and parts. Ensuring the company's quality standards are met before products reach the customer involves inspections of raw material and incoming goods, in-process parts/product and finished goods prior to shipping. This position requires close communication and coordination with the Quality Management Director and Production Manager. Qualifications * Bachelor's Degree or 3+ years of quality experience in manufacture * Certification in quality control is preferred * Verifiable ERP experience, SAP experience preferred * Strong understanding of quality control standards and testing techniques. * Using precision measurement equipment including but not limited to calipers and micrometers * Ability to work with European measurement standards (millimeters, etc.) * Proficient in Microsoft Office 365 using Word, Excel PowerPoint, Teams, Sharepoint and One Note. * Solid attention to detail * Problem-solving abilities * Forklift experience * Excellent communication skills (verbal and written) * Good math and technical skills. Responsibilities * Plan and perform quality inspections of incoming and outgoing products and parts, ensuring they meet the company's quality standards * Conduct in-process quality checks for release of product or for production stops in coordination with production management. * Review of internal and external complaints, sorting complaints and recommending necessary rework with a sense of urgency * Act as a production control catalyst in terms of quality and quantity regarding blocking, releasing, sorting, reworking and scrapping of products and components as needed Your profile Kardex US Manufacturing, LLC is an Equal Opportunity Employer and offers competitive wages and a full benefits package including but not limited to medical, dental, vision, and life insurance, vacation, holidays, and 401K. In this production environment, some PPE is required (provided by the company) when working with equipment in the shop. Ability to bend, lift, push and pull up to fifty (50) pounds is required. As part of our employment selection process, all applicants are subject to both drug testing and to a national background check.

The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. This is a unique opportunity to maintain and further build a strong partnership and learning environment between Manufacturing and Quality staff providing coaching, guidance and direction for manufacturing events, deviations, quality systems and compliance **Key Responsibilities:** + Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations. + Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls. + Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA)s. + Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements. + Oversee and provide guidance during on-the-floor analytical testing. + Ensure that changes that could potentially impact product quality are assessed according to procedures. + Ensure that deviations from established procedures are investigated and documented per procedures. + Alert senior management of quality, compliance, supply and safety risks. + Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation. + Identification and implementation of continuous improvement opportunities within our processes and systems. + Support and represent PQA during audits and inspections; may directly interact with regulatory agencies during on-site **Basic Qualifications:** + High school/GED + 4 years work experience or + Associate + 2 years work experience or + Bachelor + 6 months work **Must Have Skill Sets:** + Previous work on GNP Facilities + PQA or Mfg. preferably Drug Substance Experience + Previous work with Batch records/Deviations/Qa Oversight + Nice to have B.S. degree **Day to Day Responsibilities:** + On the floor guidance/Mfg. support + Oversee compliance in execution + Batch Record Review + SOP review/Approvals + Deviation Review + Help Mfg. Problem solves with Quality mindset **About US Tech Solutions:** US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit *********************** . "US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"

The Quality Assurance Assistant is responsible for the inspection of incoming and outgoing products and parts. Ensuring the company's quality standards are met before products reach the customer involves inspections of raw material and incoming goods, in-process parts/product and finished goods prior to shipping. This position requires close communication and coordination with the Quality Management Director and Production Manager. Your tasks Job Summary The Quality Assurance Assistant is responsible for the inspection of incoming and outgoing products and parts. Ensuring the company's quality standards are met before products reach the customer involves inspections of raw material and incoming goods, in-process parts/product and finished goods prior to shipping. This position requires close communication and coordination with the Quality Management Director and Production Manager. Qualifications Bachelor's Degree or 3+ years of quality experience in manufacture Certification in quality control is preferred Verifiable ERP experience, SAP experience preferred Strong understanding of quality control standards and testing techniques. Using precision measurement equipment including but not limited to calipers and micrometers Ability to work with European measurement standards (millimeters, etc.) Proficient in Microsoft Office 365 using Word, Excel PowerPoint, Teams, Sharepoint and One Note. Solid attention to detail Problem-solving abilities Forklift experience Excellent communication skills (verbal and written) Good math and technical skills. Responsibilities Plan and perform quality inspections of incoming and outgoing products and parts, ensuring they meet the company's quality standards Conduct in-process quality checks for release of product or for production stops in coordination with production management. Review of internal and external complaints, sorting complaints and recommending necessary rework with a sense of urgency Act as a production control catalyst in terms of quality and quantity regarding blocking, releasing, sorting, reworking and scrapping of products and components as needed Your profile Kardex US Manufacturing, LLC is an Equal Opportunity Employer and offers competitive wages and a full benefits package including but not limited to medical, dental, vision, and life insurance, vacation, holidays, and 401K. In this production environment, some PPE is required (provided by the company) when working with equipment in the shop. Ability to bend, lift, push and pull up to fifty (50) pounds is required. As part of our employment selection process, all applicants are subject to both drug testing and to a national background check.

This is a full time, on-site position with a schedule of 12 noon to 12 midnight on a rotating 2-2-3 schedule About This Role The QA Associate III has the working understanding, full knowledge and ability in their primary discipline. They are able to apply technical principles, concepts and understanding of systems and procedures in order to conduct quality and compliance related activities. They are proficient in their understanding of the Biogen Quality Systems. The QA Associate III has working knowledge of GxP regulations and adheres to all regulatory licenses and regulations as well as internal SOPs. The QA Associate III identifies and resolves issues through collaboration with others. They partner with colleagues in identifying and resolving potential compliance concerns. The QA Associate III performs all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures. The QA Associate III should be able to work effectively, independently and within a team framework, across multiple business areas and levels of the organization. What You'll Do Ensure disposition documentation and other documents supporting batch and cell bank disposition are compliant and determine acceptability for use in cGMP production activities and/or release of product for further processing and/or distribution. This includes but is not limited to Review and Approval of executed BPRs, PRCDs/WIs, Formulas, Recipes, Validity Rules (FRRV/BOM), existing/revised MPRs, MSLRs, MSMs, PCDs, PFDs, PARs; on the Manufacturing floor record review and observations, performing WORCs, performing inspection readiness walkthroughs, and oversight of Manufacturing operations. Supports resolution of both technical and compliance issues/gaps of low complexity CAPAs can be assigned and closed based on their understanding of the CAPA intent and review/approval of the associated document (i.e.PRCD ) at Management discretion/oversight. Assists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by Biogen. Provides training within and across functions, as applicable Approximately 50% of time in this position will be spent on the manufacturing floor Other duties as assigned Required Skills Bachelor's Degree required in life sciences or related Minimum of 2 years of experience working in a quality assurance position within a GMP pharma or biotech manufacturing environment Ability to work effectively, both independently and within a team framework across all business areas and levels within the organization locally and globally Excellent written, verbal, and interpersonal communication skills Familiarity with downstream process manufacturing Preferred Skills Previous relevant industry experience in a GMP manufacturing environment Experience with column packing or reviewing column pack binders Job Level: Professional Additional Information The base compensation range for this role is: $69,000.00-$90,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being ; including, but not limited to: Medical, Dental, Vision, & Life insurances Fitness & Wellness programs including a fitness reimbursement Short- and Long-Term Disability insurance A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31) Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar year Paid Maternity and Parental Leave benefit 401(k) program participation with company matched contributions Employee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year Employee Resource Groups participation Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Description & Requirements In today's dynamic regulatory environment, public companies must uphold the highest standards of financial integrity and IT risk management. As an SEC Auditor, you will play a critical role in ensuring compliance with SEC regulations by performing financial statement and IT audits. You will help clients identify and manage business and technology risks, strengthen internal controls, and support the integrity of financial reporting. What You Will Do: * Execute integrated audits of financial statements and IT systems for SEC registrants, ensuring compliance with PCAOB and SEC standards. * Perform audit testing on financial statement accounts such as cash, accounts payable, and fixed assets. * Assess and test internal controls over financial reporting (ICFR), including IT general controls (ITGCs) and application controls, in accordance with SOX 404 requirements. * Conduct walkthroughs and substantive testing of financial statement accounts, disclosures, and related IT processes. * Evaluate the design and operating effectiveness of IT controls for applications, databases, operating systems, networks, and reporting tools. * Collaborate with client teams to understand business processes, IT environments, and control frameworks; obtain audit evidence; and analyze testing results. * Draft audit findings, management letter comments, and recommendations for remediation. * Participate in discussions with clients and leadership regarding audit results and emerging risks. * Stay informed on SEC, PCAOB, and IT risk trends impacting clients. * Deliver an exceptional client experience through timely and responsive communication. Minimum Qualifications: * Bachelor's degree in a related field, preferably in Management Information Systems or Computer Science. * Eligibility to sit for the CPA exam, meeting educational requirements as defined by the applicable state board of accountancy. * Proficiency in Microsoft Office Suite. * Ability to travel for client engagements and internal meetings, including overnight stays. Preferred Qualifications: * Masters degree in a related field, preferably in Management Information Systems or Computer Science. * Prior experience or internships in public accounting with exposure to SEC or IT audits. * Eligibility to sit for the CISA exam or CISA certification. #LI-CLTSP, #LI-CLTU #LI-LS1

We are seeking a dedicated Quality Assurance Senior Associate to join our team. This fully onsite position follows a stable shift schedule that includes weekends and possibly nights. The role requires a background in manufacturing and PQA. As a Sr. Associate in Plant Quality Assurance, you will work directly with plant manufacturing and support groups on bulk drug substance manufacturing and new product introductions. You will facilitate real-time decision-making to ensure adherence to GMP quality requirements and foster a strong partnership between Manufacturing and Quality staff. Responsibilities + Provide ongoing Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other applicable regulations. + Ensure compliance of facilities, equipment, materials, organization, processes, and procedures with applicable regulations and requirements relating to GMP, GDP, Safety, and other controls. + Drive closure and completion of cGMP processes, procedures, documents, and records, including review and approval of deviations, investigations, and corrective/preventative actions (CAPAs). + Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP, and cGMP requirements. + Oversee and provide guidance during on-the-floor analytical testing. + Assess changes that could potentially impact product quality according to procedures. + Investigate and document deviations from established procedures per guidelines. + Alert management of quality compliance, supply, and safety risks. + Provide project management support, leading efforts to achieve timely task completion and develop strategies for system implementation. + Identify and implement continuous improvement opportunities within processes and systems. + Support and represent PQA during audits and inspections, and directly interact with regulatory agencies during on-site inspections. Essential Skills + Quality assurance + Manufacturing + Batch Records + Deviations + QA Oversight + Experience in GNP Facilities + PQA or Manufacturing experience, preferably in Drug Substance Additional Skills & Qualifications + High school diploma/GED with 4 years of work experience or Associate degree with 2 years of work experience or Bachelor's degree with 6 months of work experience or Master's degree Work Environment This is an on-the-floor position providing guidance and support to manufacturing. You will oversee compliance in execution, review batch records, review and approve SOPs, and review deviations. You will also assist manufacturing in problem-solving with a quality mindset. Job Type & Location This is a Contract position based out of Holly Springs, NC. Pay and Benefits The pay range for this position is $31.00 - $34.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Holly Springs,NC. Application Deadline This position is anticipated to close on Jan 29, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Quality Assurance Specialist • Preparing and implementing quality assurance policies and procedures • Performing routine inspections and quality tests • Identifying and resolving workflow and production issues • Meet with and review all workflow and production issues with Regulatory/Compliance Manager weekly/monthly • Meet with and review all workflow and production issues with department employees • Provide additional training where and when needed Responsibilities • Ensure that standards and safety regulations are observed. • Address and discuss issues and proposed solutions with all department management teams and Regulatory/Compliance Manager • Document quality assurance activities and create audit reports. • Make recommendations for improvement. • Create training materials and operating manuals to be approved by Regulatory Compliance Manager • Maintain and update all manuals according to any and all regulatory changes. Requirements and skills • Proven work experience as a Quality Assurance Specialist or similar role • Working knowledge of tools, methods and concepts of quality assurance • Solid knowledge of relevant regulatory standards • Excellent communication skills, both verbal and written • Excellent data collection and analysis skills • Excellent Mathematical skills • Strong attention to detail • Relevant training and/or certifications as a Quality Assurance Specialist Benefits: • Comprehensive benefits (medical, vision, and dental insurance) • 401K plan • PTO and “dream” days • Company events • Education Reimbursement

The Quality Systems Specialist is responsible for supporting the Quality Management System (QMS), including GxP document management and training programs. This role ensures compliance with regulatory standards, maintains the integrity of documentation systems, and collaborates with cross-functional teams to support document and training needs. Essential Duties GxP Document Management Collaborate cross-functionally to generate workflow status reports and support document owners with new document creation and revisions. Review procedural documents for compliance with formatting, metadata, and applicable standards. Initiate periodic review workflows. Serve as workflow owner as needed. Assist document owners in ensuring proper GxP records management. Create document reports to support business processes, including periodic review and stagnant draft reports. Generate document owner, workflow owner, and task owner reports to support offboarding activities and transfer ownership as appropriate. Training Program Support Generate training reports and distribute upcoming and overdue training notifications. Initiate training assessment forms for managers of new personnel. Create learner roles, training requirements, and curricula within the training management system. Quality Management System Support Schedule and facilitate initial and status meetings. Route forms for electronic signature and maintain tracking logs. Upload completed forms into the document management system. Audits and Inspections Prepare for and participate in internal and external audits related to document control and quality systems. Skills & Education Requirements Bachelor's degree in Life Sciences or a related field, or an Associate degree with relevant work experience. Minimum of 5 years of document control experience. Proficiency with electronic document management systems (e.g., Veeva QualityDocs). Experience supporting gene and cell therapy products. Prior experience in a startup or fast-paced environment. Demonstrated integrity, accountability, and strong teamwork skills.