quality control manager

Leed Insulation & Spray Foam

Job SummaryThe Quality Control Manager plays a critical role in overseeing quality standards within construction and installation services. Reporting directly to the Operations Manager, this role involves conducting thorough inspections, ensuring safety compliance, and addressing any material or installation discrepancies. The manager frequently visits job sites, works independently, and leads training initiatives to enhance installer safety and skills. This position offers valuable opportunities for career advancement and participation in professional training programs.Responsibilities<ul><li>Conduct quality inspections and report issues related to jobs and materials.</li><li>Handle customer complaints and resolve related issues promptly.</li><li>Train installers on safety protocols and quality standards.</li><li>Review material usage to identify discrepancies or misuse.</li><li>Enforce safety compliance on all job sites.</li><li>Maintain detailed reports and documentation of quality findings.</li><li>Collaborate with operations to implement quality improvements.</li></ul>Required Qualifications<ul><li>2+ years of insulation experience</li><li>2+ years of experience in quality control management</li><li>Valid Florida Driver&rsquo;s License</li><li>Strong skills in inspection and safety compliance</li><li>Excellent customer service and problem-solving abilities</li><li>High attention to detail in all quality-related tasks</li><li>Ability to work independently and manage time effectively</li><li>Participation in training programs for skill development</li></ul>Skills<ul><li>Proven experience in construction management with a strong focus on quality control management across diverse projects.</li><li>Expertise in construction regulatory compliance including building codes (structural, plumbing, electrical, mechanical) and energy building codes.</li><li>Proficiency with construction management software for tracking inspections, documentation, and project progress.</li><li>Strong knowledge of construction safety regulations such as federal safety standards applicable to construction sites.</li><li>Excellent analysis skills for interpreting technical drawings, construction plans, and specifications to ensure precise execution.</li><li>Effective team leadership capabilities to guide inspectors and coordinate cross-functional teams toward shared quality goals.</li><li>Skilled in data collection methods related to construction inspection processes for continuous improvement initiatives.</li></ul>Join us as a Quality Control Manager if you are passionate about elevating construction standards through meticulous inspection, innovative problem-solving, and inspiring leadership! Your dedication will help shape safe, compliant structures that stand the test of time while advancing your career in a vibrant industry environment.Pay: $55,000.00 - $65,000.00 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Vision insurance</li></ul>Work Location: In person

Quality Control Manager

Hunter Communications

<div>Description:

Better Careers Start Here!
Join a company that fosters career growth through formal job training and strategic leadership development programs. The amazing career opportunities at Hunter Communications are fueled by our rapidly expanding, state-of-the-art fiber internet and world-class customer service.
At Hunter Communications, all employees are provided a benefits package including medical, dental, vision, disability coverage, life insurance, and an employee assistance program. We offer vacation, sick, and holiday time off, a 401k program with an employer match, and a bonus opportunity.
As a Hunter Communications Contractor Operations &amp; Quality Control Manager you'll be responsible for the successful integration, performance, quality, and operational readiness of Hunter's installation and maintenance contractors. You will serve as the primary liaison between Hunter Communications and our contractor partners, ensuring work is completed safely, efficiently, and in accordance with Hunter standards.
This position is responsible for contractor onboarding, training coordination, quality assurance, billing review, market readiness, inventory coordination, performance management, and operational support. In addition, the role is responsible for conducting quality control reviews of both contractor and internal technician work to ensure consistency in customer experience and installation standards across the company. The successful candidate will regularly travel throughout Hunter's service territory, perform field audits, review operational performance metrics, support market launches, and collaborate with dispatch, engineering, customer service, sales, construction, installation, and other teams to ensure successful service experience. You will find yourself working daily in software systems to support that success. You&rsquo;ll need to excel at communication with our partners, teams, and Employees.
Duties and Responsibilities<ul><li>
Serve as the primary operational point of contact for installation and maintenance contractors</li><li>
Coordinate contractor onboarding and training programs</li><li>
Ensure contractors maintain compliance with Hunter standards, SOPs, contractual obligations, and safety requirements</li><li>
Conduct field audits and quality control inspections on contractor and employee work</li><li>
Track contractor performance metrics and identify opportunities for improvement</li><li>
Review contractor billing for accuracy and compliance with approved scopes of work</li><li>
Coordinate contractor staffing and market deployment activities</li><li>
Support market launches and operational readiness initiatives</li><li>
Develop and maintain contractor scorecards and performance reporting</li><li>
Identify recurring quality, training, or process issues and drive corrective actions</li><li>
Collaborate with dispatch to ensure contractor schedules and capacity align with operational needs</li><li>
Partner with engineering, construction, and operations teams to support service delivery goals</li><li>
Conduct job observations, site visits, quality control, safety, and operational reviews</li><li>
Assist in the development and maintenance of installation, repair, and quality standards</li><li>
Support vendor selection, evaluation, and performance reviews</li><li>
Monitor customer escalations involving contractor-performed work</li><li>
Maintain positive working relationships with contractor leadership and field personnel</li><li>
Ensure consistent customer experience standards across all fulfillment resources</li></ul>
Requirements:
<ul><li>Telecommunications installation, repair, or operations experience</li><li>
Strong understanding of fiber optic service delivery and field operations</li><li>
Experience managing vendors, contractors, or third-party service providers preferred</li><li>
Experience conducting quality assurance and field audits</li><li>
Strong analytical and reporting skills</li><li>
Ability to influence without direct authority</li><li>
Strong communication and relationship management skills</li><li>
Experience working with Salesforce, Microsoft Office, and reporting systems</li><li>
Ability to travel regularly throughout service territory</li><li>
Strong organizational and project management skills</li><li>
Results-driven mindset with strong attention to detail</li><li>
Ability to identify operational risks and develop corrective action plans</li><li>
Comfort with a variety of software applications and a desire to learn new systems</li></ul>
Compensation &amp; Hours
The schedule for this position is 5 days a week (Monday through Friday) with a regular on-call rotation. Evening, weekend work, and travel throughout our service territory may occur. This is an Exempt position, salary determined by experience.
EOE Statement
Hunter Communications provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</div>

Contractor Operations & Quality Control Manager

Allied Universal

<div>Quality Control Manager Bilingual for Federal Contract<h2 class="jobSectionHeader">
Overview</h2><div> 
Company Overview:
</div><div>Allied Universal&reg;, North America&rsquo;s leading security and facility services company, offers rewarding careers that provide you a sense of purpose. While working in a dynamic, welcoming, and collaborative workplace, you will be part of a team that contributes to a culture that positively impacts the communities and customers we serve.</div><h2 class="jobSectionHeader"> 
Job Description</h2><div> 
Allied Universal&reg; is hiring a Quality Assurance / Quality Control (QA/QC) Manager. The Quality Assurance / Quality Control (QA/QC) Manager is a designated Key Personnel position responsible for developing, implementing, and overseeing the Quality Control Program in support of Protective Security Officer (PSO) contracts for a high profile customer. This role ensures full compliance with the Statement of Work (SOW), contractual requirements, and federal security standards through systematic inspections, audits, reporting, and continuous improvement initiatives.</div><div>
The Quality Assurance / Quality Control (QA/QC) Manager serves as the primary authority for quality control activities, working closely with the Contract Manager, supervisory staff, and Government representatives to maintain operational excellence and contractual compliance.</div><div>
</div><div>RESPONSIBILITIES:</div><div>
Quality Control Program Oversight</div><ul><li>
Develop, implement, and maintain the contract-specific Quality Control Plan (QCP) in accordance with SOW requirements</li><li>
Define inspection methods, frequencies, performance metrics, and reporting processes</li><li>
Ensure all quality control activities to address deficiency reporting, discipline procedures, inspection checklists, quality control activity frequency and reporting</li></ul><div>
Inspections and Audits</div><ul><li>
Conduct and/or oversee recurring inspections of PSO performance and post compliance, uniforms, equipment, and certifications, timekeeping, personnel files and training records</li><li>
Ensure inspections are both announced and unannounced, covering all posts and personnel on a recurring basis</li><li>
Utilize inspection tools and systems (e.g., Heliaus or equivalent) for real-time documentation and reporting</li></ul><div>
Compliance Monitoring</div><ul><li>
Ensure all PSOs meet contractual requirements, including licensing and permits, training and certifications, fitness determinations, weapons qualifications</li><li>
Verify compliance with Training Academy Management System (TAMS), Post Tracking System (PTS), and all client systems</li><li>
Identify and mitigate risks that could result in open posts or non-compliance findings</li></ul><div>
Deficiency Identification and Corrective Action</div><ul><li>
Document all deficiencies identified through inspections, audits, or Government feedback</li><li>
Initiate and track corrective actions to closure, including immediate on-site corrections, retraining, disciplinary actions (as appropriate)</li><li>
Notify the Contracting Officers Representative (COR) of deficiencies and corrective actions within required timelines (e.g., within 24 hours)</li></ul><div>
Reporting and Deliverables</div><ul><li>
Prepare and submit required reports, including monthly Quality Control Inspection Reports, deficiency reports and corrective action tracking, trend analysis and performance metrics</li><li>
Ensure reports are submitted to the Contracting Officers Representative no later than the 10th of each month</li><li>
Maintain all Quality Control documentation and make records available to the Government upon request</li></ul><div>
Continuous Improvement and Performance Analysis</div><ul><li>
Analyze inspection results, audit findings, and performance trends</li><li>
Identify systemic issues and implement process improvements</li><li>
Participate in internal quality control reviews/committees to evaluate trends, standardize best practices, improve contract performance</li></ul><div>
Coordination and Communication</div><ul><li>
Serve as liaison between Contract Manager / Task Order Manager, supervisory staff, client Contracting Officers Representative and Protective Security Operations Officer (PSOO)</li><li>
Support Government audits, inspections, and covert testing activities</li><li>
Participate in monthly performance meetings with the client representatives</li></ul><div>
Support to Quality Assurance (Government Oversight)</div><ul><li>
Facilitate Quality Assurance activities, including audits, surveillance, covert testing, tenant feedback reviews</li><li>
Ensure transparency and responsiveness to Government oversight efforts</li></ul><div>
QUALIFICATIONS (MUST HAVE):</div><ul><li>
High school diploma or equivalent</li><li>
Possess, or be able to obtain a Security Clearance up to the Top Secret level</li><li>
Valid driver&rsquo;s license if driving a company or customer owned vehicle</li><li>
Minimum of two (2) years of experience in quality assurance or quality control for personnel-based service contracts</li><li>
Demonstrated experience monitoring contract compliance, inspections, and performance metrics</li><li>
Strong knowledge of government contract relationships to include security operations and personnel compliance</li><li>
Ability to analyze data, identify trends, and implement corrective actions</li><li>
Excellent oral and written communication skills</li></ul><div>
PREFERRED QUALIFICATIONS (NICE TO HAVE):</div><ul><li>
Experience supporting Protective Security Officer (PSO) contracts or similar federal security programs</li><li>
Familiarity with Training Academy Management System (TAMS), Post Tracking System (PTS), government compliance requirements</li><li>
Experience using inspection/reporting technology platforms</li><li>
Background in law enforcement, military, or contract security operations</li></ul><div>
SALARY: $72, 000.24 annually</div><div>
</div><div>BENEFITS:</div><ul><li>
Medical, dental, vision, basic life, AD&amp;D, and disability insurance</li><li>
Enrollment in our company&rsquo;s 401(k)plan, subject to eligibility requirements</li><li>
Eight paid holidays annually, five sick days, and four personal days</li><li>
Vacation time offered at an accrual rate of 3.08 hours biweekly. Unused vacation is only paid out where required by law.</li></ul><h2 class="jobSectionHeader"> 
Closing</h2><div> 
Allied Universal&reg; is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: www.aus.com
</div><div>If you have difficulty using the online system and require an alternate method to apply or require an accommodation, please contact our local Human Resources department. To find an office near you, please visit: www.aus.com/offices.</div><h2 class="jobSectionHeader"> 
Requisition ID</h2> 
2026-1644664</div>

Quality Control Manager Bilingual for Federal Contract

Thermo Fisher Scientific

<div>Work Schedule
First Shift (Days)
Environmental Conditions
Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world&rsquo;s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
How will you make an impact?
The Quality Manager receives assignments in the form of site and functional objectives and determines how to deploy people, time, and resources to meet schedules, quality standards, and business goals. This role provides leadership and guidance to the Quality Control and Quality Assurance organizations within established company policies, recommends improvements to policies and procedures, and ensures effective execution of QC laboratory operations and QA systems. The Quality Manager is accountable for short- to mid-term (1&ndash;2 year) performance, compliance, and continuous improvement results for the quality function, with primary emphasis on QC laboratory excellence while maintaining robust QA systems and compliance.
What will you do?<ul><li>
Translate site and quality function objectives into actionable plans, priorities, and resource allocations to meet operational schedules and quality goals.</li><li>
Provide leadership and direction to the Quality Control team, managing through QC Supervisors as applicable, and ensuring alignment with site priorities.</li><li>
Ensure timely, compliant execution of QC testing, batch record review, and disposition of finished goods.</li><li>
Monitor quality performance metrics, identify trends, and take corrective actions to improve quality, efficiency, and reliability.</li><li>
Guide and support supervisors and individual contributors within established company policies, procedures, and quality systems.</li><li>
Recommend updates to QC and QA policies, procedures, and workflows and establish local procedures that impact the immediate organization.</li><li>
Manage the QA function to create a culture of quality awareness, teamwork, and compliance across the organization.</li><li>
Engage in daily oversight and guidance of nonconforming material investigations, complaint records, corrective and preventive actions, and change controls to drive timely and scientifically sound closure.</li><li>
Provide guidance and direction to stakeholders to ensure ISO 9001 compliance and Quality Management System adherence.</li><li>
Collaborate across functions and sites, leveraging quality and manufacturing expertise to troubleshoot problems, interpret data and determine next steps based on risk-based approach.</li><li>
Manage accuracy, completeness, and timeliness of Quality records.</li><li>
Lead external regulatory inspections and customer audits</li><li>
Oversee internal audits program.</li><li>
Develop quality talent through coaching, feedback, and performance management, with accountability for near-term capability needs, succession planning, and meeting personal career goals while achieving organization goals.</li><li>
Design, plan, and lead Practical Process Improvements (PPI) initiatives focusing on scientific practices, knowledge, best practice, standard work, or quality initiatives.</li></ul>
REQUIREMENTS
Education and Experience<ul><li>
Advanced degree plus 6 years of experience, or Bachelor's degree plus 8 years of experience in regulated pharmaceutical/biotech/medical device industry</li><li>
Preferred Fields of Study: Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, Biotechnology, Engineering, Microbiology, or related scientific field</li></ul><ul><li>
5+ years of people management experience leading QC laboratory teams</li><li>
Strong understanding of analytical testing methods and laboratory operations</li><li>
Knowledge of cGMP regulations, quality systems, and regulatory requirements preferred</li><li>
Demonstrated success implementing and improving quality systems and processes</li><li>
Experience with laboratory information management systems (LIMS) and data integrity requirements</li><li>
Experience leading conversations with customers and auditors and supporting regulatory inspections</li></ul>
Knowledge, Skills, Abilities<ul><li>
Proven understanding of Quality Control Laboratory operating principles and Quality Assurance procedures, processes, and guidelines</li><li>
Leadership experience developing and mentoring staff with ability to affect performance and development of individuals across the Quality department</li><li>
Ability to drive functional, technical, and operational excellence</li><li>
Ability to think strategically with the ability to direct the resolution of technical problems using innovative approaches</li><li>
Project management and organizational skills</li><li>
Clear written and verbal communication skills with ability to analyze data, summarize results, present data, and address feedback</li><li>
Practical application experience in continuous improvement methodologies to improve processes, strengthen quality, and drive efficiency</li><li>
Highly skilled in Quality tools e.g. FMEA, Risk Analysis, Root Cause Analysis</li></ul>
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $112,500.00&ndash;$155,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:<ul><li>
A choice of national medical and dental plans, and a national vision plan, including health incentive programs</li><li>
Employee assistance and family support programs, including commuter benefits and tuition reimbursement</li><li>
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy</li><li>
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan</li><li>
Employees&rsquo; Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount</li></ul>
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards</div>

Quality Manager

AlphaTech Research Corp

Overview We are seeking a highly motivated and experienced Quality Program Manager to lead and support the development, implementation, and maintenance of a quality assurance program compliant with NQA-1 standards within the nuclear industry. The ideal candidate will be a proactive leader with experience in program development, process improvement methodologies, and quality management systems. Join us to drive excellence in quality assurance, foster continuous improvement, and support our commitment to operational integrity and safety.Responsibilities<ul><li>Lead the implementation of a quality assurance program in accordance with ASME NQA-1 standards</li><li>Develop, review, and maintain quality procedures, policies, and work instructions</li><li>Ensure compliance with applicable regulatory, customer, and industry requirements</li><li>Support internal and external audits, including preparation, execution, and corrective action follow-up</li><li>Perform gap analyses and drive closure of identified deficiencies relative to NQA-1 requirements</li><li>Collaborate cross-functionally with engineering, manufacturing, and supply chain teams to ensure quality integration</li><li>Manage document control systems and configuration management processes</li><li>Oversee supplier quality activities, including qualification and audits</li><li>Lead root cause analysis and corrective/preventive action (CAPA) processes</li><li>Provide training and guidance to staff on quality standards and procedures</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Engineering, Quality, or a related technical field</li><li>3&ndash;8+ years of experience in a quality engineering or management role</li><li>Direct experience implementing or maintaining an NQA-1 compliant quality program</li><li>Strong understanding of quality systems, auditing, and regulatory compliance</li><li>Experience with document control, records management, and configuration control</li><li>Familiarity with root cause analysis tools (e.g., 5 Whys, Fishbone, FMEA)</li><li>Strong communication and organizational skills</li></ul>Preferred Qualifications<ul><li>Experience in nuclear, aerospace, defense, or other highly regulated industries</li><li>ASQ certification (e.g., CQE, CQA)</li><li>Lead Auditor certification</li><li>Experience working with suppliers under NQA-1 requirements</li><li>Knowledge of related standards (ISO 9001, 10 CFR 50 Appendix B, etc.)</li></ul>Pay: $65,878.05 - $95,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Relocation assistance</li><li>Vision insurance</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Work Location: In person

Quality Program Manager (NQA-1)

Veros

<div>About Valligent 
Valligent, a Veros Software company, is a leading provider of technology-enabled real estate valuation solutions. The company delivers innovative appraisal, property inspection, and valuation services that help lenders, investors, and mortgage professionals make faster, more informed decisions while improving accuracy, compliance, and the borrower experience. Founded in 2003, Valligent combines industry expertise with advanced technology to modernize the property valuation process. 
Job Summary
The Quality Control Specialist is responsible for reviewing valuation products for accuracy, completeness, compliance, and overall quality before delivery to clients. This role reports to the Vice President of Quality Control and supports valuation review work across the United States and its territories. This is a great fit for someone with real estate valuation or appraisal management company experience who enjoys focused, independent work with limited day-to-day interaction, clear expectations, and measurable results. The ideal candidate has strong self-discipline, excellent attention to detail, and the ability to stay productive while reviewing complex valuation assignments.
What You&rsquo;ll Do
As a Quality Control Specialist, you will help ensure Valligent&rsquo;s valuation products meet internal standards, client requirements, GSE guidelines, and applicable appraisal standards.
Key responsibilities include:<ul><li>
Review incoming valuation products for accuracy, completeness, consistency, and quality</li><li>
Read and evaluate valuation reports to confirm they meet USPAP, GSE, lender, and client requirements</li><li>
Review property characteristics, photos, aerial imagery, street-view imagery, and other available data</li><li>
Identify adverse property, market, location, or report factors that may require additional review or clarification</li><li>
Understand and follow client-specific requirements, GSE guidelines, and internal quality control procedures</li><li>
Review UCDP and EAD Submission Summary Reports, including warnings, indicators, and required corrections</li><li>
Request conditions or revisions from appraisers in a professional, clear, and accurate manner</li><li>
Escalate complex, sensitive, or guideline-driven issues to the appropriate team member or manager</li><li>
Manage multiple assignments while maintaining strong turn times and quality standards</li><li>
Work independently with a strong sense of urgency and accountability</li></ul>
What We&rsquo;re Looking For
We are looking for someone who is analytical, detail-oriented, dependable, and comfortable working in a fast-paced environment. The right person enjoys reviewing reports, identifying issues, solving problems, and producing accurate work with limited supervision.
Qualified candidates should have:<ul><li>
Appraisal management company experience</li><li>
Strong understanding of residential valuation reports, alternative valuations, and appraisal review concepts</li><li>
Excellent attention to detail and ability to identify inconsistencies, missing information, and quality concerns</li><li>
Strong written communication skills, especially when requesting corrections or clarifications</li><li>
Good verbal communication skills when escalation or collaboration is needed</li><li>
Ability to understand and apply USPAP, lender, client, and GSE requirements</li><li>
Ability to review complex assignments and property situations</li><li>
Strong time management and organizational skills</li><li>
Ability to work independently with minimal supervision</li><li>
Strong self-discipline and motivation to meet production and quality goals</li><li>
Ability to multitask in a dynamic, deadline-driven environment</li><li>
Willingness to receive feedback and training to continue improving accuracy, speed, and independence</li><li>
Comfort using computers, valuation platforms, client portals, and productivity tools</li></ul>
Preferred Experience
The following experience is helpful but not required:<ul><li>
Current or previous appraisal license</li><li>
Prior appraisal review or valuation quality control experience</li><li>
Experience reviewing UCDP, EAD, or Submission Summary Report findings</li><li>
Experience working with appraisal management company workflows</li><li>
Familiarity with residential appraisal forms, condition ratings, quality ratings, comparables, adjustments, and report reconciliation</li></ul>
Why Join Valligent?
This role offers the opportunity to use your valuation knowledge in a focused quality control position without the constant client-facing demands of many real estate or appraisal roles. You will be part of a team that values accuracy, consistency, accountability, and strong production performance.
If you have a sharp eye for detail, understand valuation reports, and enjoy independent work where quality and results matter, we would like to hear from you.
Physical Requirements<ul><li>
Must be able to remain in a stationary position for at least 50% of the time</li><li>
Regularly operates a computer and other office productivity equipment, such as a calculator, printer, and related technology</li></ul>
Additional Information
We offer a unique opportunity that encourages innovation and growth along with benefits that include medical, dental, vision, 401K, life, PTO, holidays and more.
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.</div>

Quality Control Specialist

CCL Pharmaceuticals

<div>
 
 
 Who We Are
 
 
 
 
 
 
 CCL Pharmaceuticals is a global life sciences company committed to improving access to trusted healthcare. With a presence in more than 20 countries and six decades of impact, we work to enable Healthy, Happy Lives through science-backed solutions.
 
 
 Our portfolio spans diabetes, cardiovascular, neurology, psychiatry, urology, oncology, immunology, biosimilars, cough and cold, vitamins, minerals, and supplements segments, to name a few. Across all markets, over 3,000 people combine scientific expertise, local insight, and a shared purpose to enhance how individuals live, heal, and care for themselves.
 
 
 Joining CCL Pharmaceuticals means stepping into a collaborative, mission-driven environment where your growth matters as much as your contribution. We enable you to learn, lead, and innovate through every stage of your journey, because the impact we make in healthcare begins with how you Grow with CCL.
 
 
 
 
 
 
 What You'll Do
 
 
 
 In this role, you will lead the planning, execution, and continuous improvement of qualification and validation activities across manufacturing, utilities, facilities, equipment, cleaning processes, analytical methods, and production processes in accordance with the Validation Master Plan (VMP) and global regulatory requirements. You will oversee the development and maintenance the Validation Master Plan, review validation protocols and reports, coordinate qualification activities with Engineering and Manufacturing teams, administer Product Quality Reviews (PQRs), support regulatory inspections and new product registrations, and drive continuous improvements that strengthen compliance, inspection readiness, and operational excellence.
 
 
 
 
 
 
 You Are Good At
 
 
 <ul>
 <li>
 Leading qualification and validation programs across manufacturing operations.
 </li>
 <li>
 Developing and executing Validation Master Plans (VMP).
 </li>
 <li>
 Reviewing validation protocols, reports, and technical documentation with accuracy and attention to detail.
 </li>
 <li>
 Managing cross-functional validation projects and balancing competing priorities.
 </li>
 <li>
 Administering Product Quality Reviews (PQRs) and driving timely follow-up actions.
 </li>
 <li>
 Interpreting GMP, PIC/S, and regulatory requirements to ensure compliant validation practices.
 </li>
 <li>
 Supporting regulatory inspections and validation documentation for product registrations.
 </li>
 <li>
 Building collaborative relationships across Manufacturing, Engineering, Quality Control, and Regulatory Affairs functions.
 </li>
 <li>
 Applying analytical thinking and structured problem-solving to quality and validation challenges.
 </li>
 <li>
 Driving continuous improvement across quality and validation systems.
 </li>
 </ul>
 
 
 
 
 
 What You'll Bring
 
 
 <ul>
 <li>
 Pharm.D, or Master's in Chemistry from and HEC recognized university.
 </li>
 <li>
 7-8 years of experience in Qualification, Validation, or Quality Assurance within a pharmaceutical manufacturing organization.
 </li>
 <li>
 Strong expertise in Validation Master Planning, Process Validation, Cleaning Validation, Analytical Method Validation, Equipment Qualification, Utility Qualification, and Facility Qualification.
 </li>
 <li>
 Sound knowledge of Product Quality Reviews (PQR), cGMP, PIC/S, and international regulatory requirements.
 </li>
 <li>
 Experience supporting regulatory inspections and validation documentation for new product registrations.
 </li>
 <li>
 Proficiency in Microsoft Office and documentation management systems.
 </li>
 <li>
 Strong analytical, leadership, presentation, communication, and stakeholder management skills.
 </li>
 </ul>
 
 
 
 
 
 Who You'll Work With
 
 
 
 This role reports directly to the General Manager Quality Assurance and works closely with teams across Quality Assurance, Manufacturing, Engineering, Quality Control, Regulatory Affairs, Supply Chain, and other operational functions to strengthen validation excellence, regulatory compliance, and quality systems across the organization.
 
 
 
 
 
 The culture you'll experience is shaped by three principles:
 
 <ul>
 <li>
 Transparency in communication, goals, and decision-making.
 </li>
 <li>
 Inclusion in how people are developed, supported, and empowered.
 </li>
 <li>
 Performance-driven mindset that links quality excellence to business outcomes.
 </li>
 </ul>
 
 Our values guide how we work every day:
 
 <ul>
 <li>
 Integrity First &ndash; Doing the right thing, consistently.
 </li>
 <li>
 Collaborate to Win &ndash; Building success together.
 </li>
 <li>
 Passion to Grow &ndash; Continuous learning and development.
 </li>
 <li>
 Innovation to Excel &ndash; Improving impact through better ideas.
 </li>
 </ul>
 
 
 
 
 
 What We Offer
 
 
 
 Opportunity to lead qualification and validation initiatives within a globally growing pharmaceutical organization.
 
 
 Exposure to international regulatory standards, validation practices, and quality systems.
 
 
 Cross-functional leadership opportunities across Manufacturing, Engineering, Quality Control, and Regulatory Affairs.
 
 
 A collaborative workplace focused on innovation, compliance, and continuous improvement.
 
 
 
 
 
 
 Important Notice
 
 
 
 CCL Pharmaceuticals is an equal opportunity employer. All applicants are considered based on merit, qualifications, and organizational need. We are committed to fostering an inclusive environment that respects diverse backgrounds, perspectives, and experiences.
 
 
 
 
 
 For more information about this opportunity and to apply, please visit our website: Sign In - Applicant Portal
 
</div>

Manager Quality Assurance

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