qc supervisor

Forsman Farms, Inc.

<div><p>We are seeking a detail-oriented and motivated Quality Control Supervisor to lead our 2nd Shift food safety and quality control efforts at our egg processing plant. In this role, you&rsquo;ll ensure that our products meet the highest standards of food safety and quality, while supporting a culture of continuous improvement. You&rsquo;ll work closely with the Plant Manager, Shift Supervisor, USDA Inspectors, and your Quality team to drive consistency, compliance, and excellence in every process.</p><p><b><br>
Responsibilities</b></p><ul><li>
Oversee and enforce Food Safety, Food Quality, Food Security, and Good Manufacturing Practice (GMP) programs.</li><li>
Train, mentor, and develop team members on job requirements, safety protocols, and continuous improvement practices.</li><li>
Lead and manage the Processing Quality team, including interviewing, hiring, training, and supporting quality employees.</li><li>
Evaluate and document egg quality through sampling; communicate any issues to management and collaborate on solutions.</li><li>
Partner with USDA Inspectors to ensure all processes and finished products are fully compliant.</li><li>
Monitor packaging stages to confirm eggs are properly packaged, labeled, and loaded, with accurate counts for each customer order.</li><li>
Document non-conformances and corrective actions, ensuring timely resolution.</li><li>
Inspect incoming goods and verify compliance through receiving inspections.</li><li>
Calibrate and inspect monitoring equipment to maintain accuracy.</li><li>
Maintain accurate, organized, and complete quality records.</li><li>
Perform food safety and quality testing in the plant lab; track supplies and notify Supervisors of needs.</li><li>
Lead customer complaint resolution and deviation investigations.</li><li>
Support other quality-related initiatives and special projects as assigned.</li></ul><p><b>
Requirements</b></p><ul><li>
Proven ability to work independently while effectively leading and motivating a team.</li><li>
Strong problem-solving skills with the ability to identify issues, propose solutions, implement improvements, and monitor results.</li><li>
Adaptable to changing priorities in a fast-paced production environment.</li><li>
Dependable, self-motivated, and committed to excellence.</li><li>
Excellent communication and interpersonal skills.</li><li>
Previous experience in food manufacturing or quality control preferred.</li><li>
HACCP and SQF training or certification a plus.</li></ul></div><p></p>

2nd Shift QC Supervisor

New Enterprise Stone & Lime Co., Inc.

<div><div><div><div><div>Employment Status:
</div><div><b>Full-Time (&gt;30 hrs/wk)</b></div>
</div>
</div></div><div><p><b>New Enterprise Stone &amp; Lime Co., Inc (NESL)</b> is currently hiring a <b>Quality Control Supervisor (AGG &amp; HMA).</b> This position is responsible for supporting Aggregate and HMA QC Technicians. The QC Supervisor will conduct a variety of tests on AGG &amp; HMA products to verify adherence to standards set by PennDOT, NYSDOT, NYS Thruway Authority, City of Buffalo, and other municipal authorities. This position will support NESL under the direction of the Regional QC Manager, focusing on the safety of coworkers, product quality, cost efficiencies, and industry best practices.</p><p>
The annual salary is $85,000 and candidates maybe be considered for a higher rate based upon experience.</p><div><b>
Quality Control Supervisor (AGG &amp; HMA) - What Will You Do?</b><br>
<ul><li>Drive innovation across operations by leveraging data, collaboration, and lean methodologies to enhance product quality, optimize inventory, and achieve sustainable cost reductions&mdash;while empowering teams to continuously improve the customer experience</li><li>Supervise a small group of QC Technicians, under the guidance the Regional QC Manager.</li><li>Complete all necessary documentation/record-keeping requirements for PennDOT, NYSDOT, and NESL.</li><li>Assist QC Technicians to ensure that AGG and HMA products are produced to the highest industry standards. This includes collaborating with Plant Superintendents on production and escalating any specification issues to the Regional QC Manager as needed.</li><li>Maintain an open line of communication with local, state, and federal materials personnel to stay up to date on changing specifications and regulations.</li><li>Communicate with the sales team to understand job specifications both before and during the bidding process.</li><li>Ensure that all personnel, equipment, and labs maintain required certifications.</li><li>Record results of inspections and report findings of inspections if the required specifications are not met.</li><li>Collect, record, and process any material certifications required for products.</li><li>Input mix designs and test results into specified QC process management system.</li><li>Assist in the hiring of QC personnel.</li><li>Perform other duties as assigned.</li></ul></div><div><b>
Qualifications?</b><br>
<ul><li>Bachelor&rsquo;s Degree in Geology, Engineering, Construction Management, or related field is preferred.</li><li>Minimum of five (5) years of experience in the Construction Materials Industry. QC experience in AGG, HMA or Concrete is preferred.
</li><li>Ability to build professional relationships with leaders and external networks.</li><li>Must have strong interpersonal, verbal, and written communication skills.</li><li>Must be able to work in a fast-paced environment and handle multiple tasks simultaneously.</li><li>Must possess strong attention to detail, good organizational skills with the ability to ensure accurate work.</li><li>Ability to work independently but as part of a team concept.</li><li>Flexibility and the ability to operate under stressful, time-sensitive deadlines.</li><li>Proficient in Microsoft Office (Word, Outlook, Excel, PowerPoint) and related database systems.</li><li>Valid driver&rsquo;s license and compliant with NESL driving standards.</li></ul></div><div><b>
Why Apply?</b><br>
<ul><li>Competitive Benefit Package - Medical, Vision, Dental, 401k, Vacation, Life Insurance &amp; more</li><li>Career Growth - We pride ourselves in developing Coworkers and promoting from within.</li><li>Stable Industry - Our materials are in high demand year over year.</li></ul></div><br>
</div><div><div><div><div><p><b>What Is a NESL Career</b></p><ul><li>
BUILD AMERICA - Our work goes directly toward rebuilding America's infrastructure</li><li>
Contribute to a sustainable future improving the lives of people and communities we serve.</li><li>
Collaborate in an open culture where sound values and dedicated people come together for greater results.</li><li>
Thrive in a people-driven family owned company with countless opportunities to learn and grow.</li></ul><p>
NESL is a privately held family-owned company, priding itself on being Pennsylvania&rsquo;s largest construction materials producer/supplier and not to mention, leader in heavy highway construction. Founded in 1924, NESL boasts over 1,800 coworkers helping To Build America From the Ground Up! Headquartered in New Enterprise, PA, our footprint encompasses 57 quarries, 3 sand deposits, 33 hot mix asphalt plants, 21 fixed and portable ready mix concrete plants and 1 lime distribution center throughout PA and Western NY.
</p><p>And&hellip;we are GROWING!</p><p><i>
New Enterprise Stone &amp; Lime Co., Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristics protected by law. New Enterprise Stone &amp; Lime Co., Inc. is a background screening, drug-free workplace.</i></p><p><i>
All qualified applicants are encouraged to apply.</i></p></div></div></div></div></div><p></p>

Quality Control Supervisor (AGG & HMA)

INCOG BioPharma Services

<div><p>Working closely with the Director of Quality, the Quality Supervisor will serve as an integrated quality leader with accountability spanning both Quality Assurance Operations and Quality Control activities. This role is instrumental in championing INCOG&rsquo;s Quality Mindset and fostering a culture of efficiency, attention to detail, and on-time delivery across manufacturing and laboratory functions.</p>
<p>
The Supervisor will need to successfully navigate and identify operational and quality gaps in both the manufacturing environment and the QC laboratory setting. They will bring a balanced technical depth across GMP manufacturing oversight, contamination control, and laboratory testing operations &mdash; ensuring seamless alignment between QA and QC functions in support of compliant, inspection-ready operations.</p>
<p>
The Quality Supervisor will exemplify excellent interpersonal skills and develop productive, customer-centric working relationships with subordinates, colleagues, customers, suppliers, and partners. The Supervisor will demonstrate excellent written and oral communication skills, with the ability to clearly and concisely articulate complex issues to a range of audiences. The Supervisor will thrive in a team environment but will also work autonomously, leveraging strong self-management and organizational skills. They will value process owners and subject matter experts and will possess a demonstrated ability to influence positive outcomes without direct reporting authority.</p>
<p><b>
This role supervises Weekend shift personnel (Friday&ndash;Sunday). Two shifts are available: Days (7:00 AM&ndash;7:30 PM) and Nights (7:00 PM&ndash;7:30 AM). Candidates must demonstrate availability and flexibility for occasional support outside of their standard shift hours.</b></p><p><b><br>
Essential Job Functions</b></p>
<ul><li>
Recruit, build, and lead an integrated QA Operations team; train and maintain an engaged workforce competent in the theory and application of quality processes across aseptic drug product manufacturing.</li><li>
Maintain an on-floor presence to coach, mentor, and enforce rigorous quality work standards; prioritize and coordinate QA resources to balance production timelines with product quality assurances.</li><li>
Lead development of room/line clearance processes for formulation, aseptic filling, and inspection/packaging areas; train QA personnel on gowning requirements, contamination controls, aseptic line operations, and equipment applications and verifications.</li><li>
Lead QA strategy in partnership with Operations for on-floor batch record review and correction; establish an ongoing state of readiness for rapid decision-making in the evaluation of deviating events, product segregation requirements, and implementation of initial corrective actions.</li><li>
Partner with EH&amp;S and Operations management to communicate safety expectations, assess safety behaviors, practice positive intervention, and enforce best practices aligned to SOPs, compliance requirements, and site goals.</li><li>
Provide technical support, oversight, and team leadership for QC Chemistry, Microbiology, and QC Technical Services; oversee daily QC activities to ensure testing and data review is completed within appropriate timeframes.</li><li>
Deliver daily expectations and assignments to QC personnel; provide in-lab support as needed for routine and on-demand testing.</li><li>
Develop QC team members through mentorship to analysts and data reviewers; communicate with Quality Control Leadership on team performance.</li><li>
Support deviation investigations, laboratory investigations, and CAPA implementation spanning both manufacturing and laboratory quality events; develop and improve current processes to maintain and control general QC functions.</li><li>
Conduct laboratory walk-throughs to ensure inspection readiness and cGMP compliance across all QC laboratory operations.</li><li>
Continuously evaluate processes and procedures across QA and QC functions to create a productive environment while maintaining the highest possible quality standards; ensure all work is carried out in accordance with regulatory requirements, cGMP, and SOPs.</li><li>
Influence the accomplishment of company-wide and team goals; inspire team members while consistently modeling ALP values in all interactions.</li></ul><br>
<p><b>
Special Job Requirements</b></p>
<ul><li>Bachelor's Degree required; Science discipline preferred (Chemistry, Biology, Biochemistry, Microbiology, or related field).</li></ul>
<ul><li>Minimum of 5 years of cGMP experience in biopharma or a similarly regulated industry, including at least 2 years in a Quality Assurance capacity.</li></ul>
<ul><li>Working knowledge of QC Microbiology and/or Chemistry, GxP principles, CAPA/investigation management, data/document review, and relevant quality and regulatory requirements.</li></ul>
<ul><li>Working knowledge of contamination controls, manufacturing processes, and output quality across automated and non-automated systems, including associated data integrity requirements.</li></ul>
<ul><li>Demonstrated experience making risk-based decisions to ensure product quality.</li></ul>
<ul><li>Knowledge of aseptic techniques and processing.</li></ul>
<ul><li>Strong communication and relationship-building skills across all levels of the organization, including operations, quality, and business leadership.</li></ul><p><b><br>
Additional Preferences</b></p>
<ul><li>Advanced Degree.</li></ul>
<ul><li>Certification(s) in Risk Management, Quality Process Analysis, Technical Writing, and/or Quality Investigation.</li></ul>
<ul><li>Hands-on experience with aseptic manufacturing Quality, including isolator based processing.</li></ul>
<ul><li>3 to 5 years of demonstrated working knowledge of GMP laboratory operations (QC Chemistry and/or Microbiology).</li></ul>
<ul><li>2+ years of experience as a people leader or supervisor.</li></ul>
<ul><li>First-hand experience participating in and/or hosting operational floor inspection tours related to Quality Assurance.</li></ul>
<ul><li>Experience building processes and procedures.</li></ul>
<ul><li>Experience with Continuous Improvement, Six Sigma, and/or Lean principles.</li></ul><p><b><br>
Additional Information about INCOG BioPharma Services</b></p>
<p><i>
At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.</i></p>
<p><i>
If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.</i></p>
<p><i>
INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.</i></p>
<p><i>
By submitting your resume and details, you are declaring that the information is correct and accurate.</i></p></div>

Quality Supervisor, Weekend Shift

Black & Veatch

<div><p>We believe real value is powered by the unique skills and experiences of our professionals. The interchange of ideas from a diverse group of people gives our teams an expanded perspective and the ability to find better solutions for our clients.</p><br>
<p></p>
<p><b>
Company : </b>Overland Contracting Inc
</p><p><b>Req Id : </b>114002</p>
<p><b>
Job Title :</b> QC Inspector, Electrical. Monticello Florida 1
</p><p><b>Location :</b> PJMONTICE</p>
<p><b>
Business Unit Sector : </b>OCI-BVOPS-CONSTRUCT EXCL CEFS</p>
<p><b>
Opportunity Type :</b> Craft (non-union)</p>
<p><b>
Relocation eligible :</b> No</p>
<p><b>
Full time/Part time :</b> Full-Time
</p><p><b>Project Only Hire : </b>No</p>
<p><b>
Visa Sponsorship Available:</b> No</p><div><div><div><h2 class="jobSectionHeader"><b>
Job Summary</b></h2>
</div><div><p>
Direct and supervise the visual and physical inspection of solar photovoltaic (PV) systems, including electrical components, on uneven terrain, roofs or other structures in compliance with site assessment and schematics. May include measuring, cutting, torquing structural framing and solar modules supporting systems, testing of wiring, electrical fixtures, apparatus, motors, equipment, and control systems in accordance with all applicable plans, specifications, codes and industry standards. Plan and coordinate the efforts of the QC inspectors under his/her supervision and motivate them to accomplish the work safely, correctly and efficiently.</p>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Key Responsibilities</b></h2>
</div><div><ul><li>Use appropriate hand tools (i.e., crescent wrench, torque wrench, tape measure, screwdriver, laser, etc.) and power tools (i.e., Drills, Impact Wrenches) to perform a variety of functions to inspect photovoltaic (PV) systems in accordance with codes and standards using drawings, schematics, and instructions.</li>
<li>May complete solar electrical inspections.</li>
<li>Inspect structural, mechanical, rack system and PV panels.</li>
<li>Inspect civil installations including ponds, swales, roads, fencing, inverter pads, and backfill.</li>
<li>Supervisor and train QC Inspectors</li>
<li>Train other craft on proper installation practices and processes</li>
<li>Lead and support all safety related processes and programs as requested. Engage with your work team to ensure we achieve zero injuries. No job is so important that your safety and that of your crew will be compromised. Watch for hazards and report any concerns to your supervisor or safety professional. If needed, use your stop work authority until the issue is resolved.</li>
<li>Review crew's timecards for correct hours and phase coding.</li>
<li>Report all accidents and near misses to supervisor. Participate in investigation process as needed. Review accidents and the causes with employees.</li>
<li>Lead, complete, and sign off on daily pre‐job safety planning in the appropriate format. Identify safety hazards you or other employees may be subject to and take all necessary corrective action to eliminate or mitigate hazards. Assure all crew members understand, participate, and sign all pre‐job safety planning tools at start and end of shift.</li>
<li>Understand and respond appropriately to all safety hazards and warning devices (i.e., back‐up alarms, smell of smoke, different colored warning tags, warning sirens).</li>
<li>Understand, support, implement, and follow lockout/tag out procedures. Attend site specific training and assure you follow all procedures as out lined in training.</li>
<li>Follow established safety rules and regulations and maintain a safe and clean work environment.</li>
<li>Use effective verbal and written communication skills. Add, subtract, multiply, and divide whole numbers and fractions rapidly and accurately.</li>
<li>Appropriately communicate with client representatives. Can represent quality in meetings such as POD, client quality meetings, client walk downs, etc.</li>
<li>Listen to other employees and supervisor's suggestions, complaints, problems, safety concerns and recommendations, evaluate each and then devise and implement a plan of action based on that evaluation. Consult with supervisor and if needed HR on any issues.</li>
<li>Coordinate and communicate work with other crafts and co‐workers on the job. As requested by project supervision manage other crafts when needed.</li>
<li>Provide on‐the‐job training to those individuals under his/her supervision.</li>
<li>Train/teach safety practices, policies and procedures related to an employee's assigned tasks.</li>
<li>Perform task planning to safely and efficiently carry out all aspects of that work assigned.</li>
<li>Plan and communicate with supervisor to assure that an adequate supply of tools, materials and equipment are available.</li>
<li>Complete inspections correctly and in a timely manner, meeting requirements of drawings, specifications, and industry standards.</li>
<li>Understand the Project Field Quality Control Plan, Quality Integrated Procedures, Construction Inspection Test Plans, and other contractual quality documents.</li>
<li>Ability to assist construction with the completion of quality checklists, including corresponding photos.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Management Responsibilities</b></h2>
</div><div><div>Individual Contributor</div></div></div><div><div><h2 class="jobSectionHeader"><b>
Preferred Qualifications</b></h2>
</div><div><p>
Previous experience as a supervisor.</p>
<p>One or more of the following certifications:</p>
<ul><li><p>NCCER Concrete Finishing</p>
</li><li><p>NCCER Carpenter</p>
</li><li><p>NCCER Reinforcing Ironwork</p>
</li><li><p>NCCER Rigger</p>
</li><li><p>NCCER Scaffolding</p>
</li><li><p>NCCER Fundamentals of Crew Leadership</p>
</li><li><p>NCCER Project Supervision</p>
</li><li><p>NCCER Project Management</p>
</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>Minimum Qualifications</b></h2>
</div><div><p>
At least 4 years combination of journeyman and QC experience, with at least 1 of those years being QC experience. Prior supervisor experience preferred. Must set standards of excellence in leadership, safety, quality, and productivity for the members of his/her crew. Must have leadership abilities and organizational skills. Must have all necessary tools (see Craft QC Tool List). Must be at least 18 years of age.</p>
</div></div><div><div><h2 class="jobSectionHeader"><b>
Certifications</b></h2>
</div><div><ul><li>NCCER Concrete Finishing</li>
<li>NCCER Carpenter</li>
<li>NCCER Reinforcing Ironwork</li>
<li>NCCER Rigger</li>
<li>NCCER Scaffolding</li>
<li>NCCER Fundamentals of Crew Leadership</li>
<li>NCCER Project Supervision</li>
<li>NCCER Project Management</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Work Environment/Physical Demands</b></h2>
</div><div><ul><li>Typical construction site environment</li>
<li>Requires working in cramped work spaces and getting into awkward positions.</li>
<li>Requires working in very hot (above 90 F degrees) or very cold (below 32F degrees) temperatures and exposure to inclement weather such as dust, wind, snow, rain, etc.</li>
<li>Requires working in extremely bright or low lighting conditions</li>
<li>Includes exposure to sounds and noise levels that are distracting or uncomfortable.</li>
<li>Work around hazardous equipment.</li>
<li>This position is considered a safety sensitive position.</li>
</ul></div></div><div><div><h2 class="jobSectionHeader"><b>Competencies</b></h2>
</div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Salary Plan</b></h2>
</div><div><div>ELC: Electrical</div></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Grade</b></h2>
</div><div><div>200</div></div></div></div><p>
Black &amp; Veatch endeavors to make www.bv.com/careers accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process because of a disability, please contact the Employee Relations Department at +1-913-359-1622 or via our accommodations request form. This contact information is for disability accommodation requests only; you may not use this contact information to inquire about the status of applications. General inquiries about the status of applications will not be returned.</p><br>
<p></p>
<p>
Black &amp; Veatch is committed to being an employer of choice by creating a valuable work experience that keeps our people engaged, productive, safe and healthy.</p><br>
<p></p>
<p>
Our comprehensive benefits portfolio is a key component of this commitment and offers and array of health care benefits including but not limited to medical, dental and vision insurances along with life insurance and a robust wellness program.</p><br>
<p></p>
<p>
To support a healthy work-life balance, we offer paid vacation and holiday time after the eligibility period has been met.</p><br>
<p></p>
<p>
A variety of additional benefits are available to our professionals including, but not limited to, a company matched 401k plan, vendor discounts, AD&amp;D insurance, pre-taxed accounts, voluntary legal plan, identity theft and credit monitoring services, and the B&amp;V Credit Union.</p><br>
<p></p>
<p>
By valuing diverse voices and perspectives, we cultivate an authentically inclusive environment for professionals and are able to provide innovative and effective solutions for clients.</p><br>
<p></p>
<p>
BVH, Inc., its subsidiaries and its affiliated companies, complies with all Equal Employment Opportunity (EEO) laws and regulations. Black &amp; Veatch does not discriminate on the basis of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender Identity and expression, disability, veteran status, pregnancy status or other status protected by law.</p><br>
<p></p>
<p><b>
Notice to External Search Firms</b>: Black &amp; Veatch does not accept unsolicited resumes and will not be obligated to pay a placement fee for unsolicited resumes. Black &amp; Veatch Talent Acquisition engages with search firms directly for hiring needs.</p></div>

QC Inspector, Electrical. Monticello Florida 1

Bureau Veritas

<div><div><p>Purpose of Position</p><p><br>
A Project Quality Supervisor ensures that project deliverables meet established quality standards and compliance requirements.</p><p>
The position performs in line with the Bureau Veritas Quality Assurance System, including the BV Code of Ethics and the BV Group policy.</p><p></p><p><br>
 Major Responsibilities</p><ul><div><ul><li>
Manage a team of the project</li><li>
Review the audit report prior to the client submission
</li><li>Prepare a detailed execution and QHSE plan for the project
</li><li>Assure that the project deliverables have been submitted to client as per the agreed schedule
</li><li>Ensure project / client requirements are met and respected by the project team;</li><li>
Being the focal point of the project<br>
Coordinate with the client representative in order to collect the required data</li></ul></div></ul><p></p><p><br>
Qualification and Experience</p><p></p><ul><li><br>
BSr&rsquo;s in engineering + ISO 9001 lead auditor</li><li>10+ years proven experience in a QA/QC inspection services</li></ul><p><br>
Skills &amp; Qualities:</p><div><ul><li><br>
knowledge of international &amp; SEC standards along with construction, maintenance and material testing procedures</li></ul></div></div></div><p></p>

Project Quality supervisor

NASA Chemicals Pvt Ltd

<p>We are seeking a highly competent and experienced <b>Senior QC Officer</b> to lead and strengthen quality control operations at our Hub Factory. The ideal candidate will ensure that all raw materials, in-process materials, and finished products meet company standards and regulatory requirements while maintaining compliance with ISO and safety standards.</p><p><b>Key Responsibilities (Job Description):</b></p><ul><li>Conduct physical, chemical, and performance testing of raw materials, in-process samples, and finished goods as per approved specifications.</li><li>Ensure implementation and monitoring of Quality Control procedures in line with ISO 9001 standards.</li><li>Supervise laboratory operations and ensure proper calibration of testing equipment and instruments.</li><li>Review and approve batch manufacturing records and QC reports before product release.</li><li>Investigate non-conformities, customer complaints, and quality deviations; recommend corrective and preventive actions (CAPA).</li><li>Maintain proper documentation of test results, COAs, MSDS, and quality records.</li><li>Coordinate with Production, R&amp;D, and Supply Chain departments to resolve quality-related issues.</li><li>Monitor product stability and shelf-life studies where applicable.</li><li>Ensure compliance with local regulatory standards and safety guidelines.</li><li>Train and mentor junior QC staff and lab technicians.</li><li>Participate in internal and external audits.</li><li>Support continuous improvement initiatives to enhance product quality and process efficiency.</li></ul><p><b>Qualification &amp; Experience:</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Chemistry / Applied Chemistry / Chemical Engineering or relevant field.</li><li>Minimum <b>4&ndash;7 years</b> of relevant experience in Quality Control within manufacturing (preferably lubricants, chemicals, paints, polymers, or industrial products).</li><li>Strong knowledge of laboratory testing standards and quality systems.</li><li>Sound understanding of ISO documentation and audit requirements.</li><li>Good analytical, reporting, and problem-solving skills.</li></ul><p><b>Required Skills:</b></p><ul><li>Strong attention to detail</li><li>Leadership &amp; team supervision</li><li>Report writing &amp; documentation skills</li><li>Root cause analysis capability</li><li>Proficiency in MS Office</li><li>Good communication skills</li></ul><p><b>Key Performance Indicators (KPIs):</b></p><ul><li>Product rejection rate</li><li>Compliance with quality standards</li><li>Audit observations closure</li><li>Turnaround time for QC approvals</li><li>Reduction in customer complaints</li></ul><p><b>What We Offer:</b></p><ul><li>Competitive market salary</li><li>Provident Fund</li><li>Medical</li><li>Pick &amp; Drop (Desired Nearest Points)</li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

Senior QC Officer

Julphar

<div></div><div><div><div><div><div><p>At Julphar, we are on a journey of culture transformation &amp; our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.</p>
<p>Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.</p>
<p><b>
Job Summary/Main Purpose</b></p><br>
<p></p>
<p>
The Raw Material Team Leader at Julphar HQ leads quality control processes and a team within the Quality Control division, ensuring compliance with regulatory standards, managing inspections, audits, data analysis, and staff training.</p><br>
<p></p>
<p><b>
Key Responsibilities</b></p>
<ul>
<li>Responsible for the inspection of raw materials to ensure compliance with quality standards and specifications.</li>
<li>Operate various Quality Control (QC) instruments and equipment, depending on the assigned section.</li>
<li>Ensure adherence to Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and safety procedures while maintaining a clean and hygienic laboratory environment.</li>
<li>Enter, review, and verify test data on the SAP system.</li>
<li>Prepare, review, and update Standard Operating Procedures (SOPs) related to raw material testing and inspection activities.</li>
<li>Supervise and follow up with analysts in the raw materials section to ensure accuracy, compliance, and timely completion of activities.</li>
<li>Responsible for the release or rejection of raw materials in SAP according to quality evaluation results.</li>
<li>Coach, guide and train QC staff to ensure a high level of competency and motivation.</li>
<li>Analyze quality data to identify trends and areas for improvement.</li>
<li>Ensure adherence to industry regulations and standards (current regulatory &amp; cGMP requirements).</li>
<li>To adhere with the cGMP principles (premises, personal, equipment, documentation, QMS and audit) and to maintain them in an effective manner.</li>
<li>To check and ensure proper usage of all the QC premises and equipment.</li>
<li>To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.</li>
<li>To ensure the analysis is performed correctly as per applicable procedures and the raw data is checked for correctness, accuracy and compliance.</li>
<li>To perform investigation for the lab incidents, OOS, OOL results, deviations and take appropriate corrective and preventive actions.</li>
<li>Follow up &amp;close all the eQMS actions (CAPA, OOS, Deviations, CC)</li>
<li>To involve and support external and internal audits and to close the audit observations on time.</li>
</ul>
<div></div><ul><li>To handle and close the Quality management system actions like Deviations, OOS, CAPAs, AMS and Change controls using Amplelogic system.</li>
<li>To follow and ensure data integrity and good documentation practices are implemented in the QC labs.</li>
<li>To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.</li></ul><br>
<p></p>
<p><b>
Core Competency</b></p>
<ul>
<li>In terms of Competency, highly oriented with a strong sense of accountability &amp; ownership,</li>
<li>Excellent communication, interpersonal and presentation skills.</li>
<li>Technical Competencies: In-depth knowledge of the industry's standards and regulations guidelines excellent knowledge of reporting procedures and record keeping, must have experience in handling Regulatory Authorities audits and questions and accordingly set up the action plan</li>
<li>Having an Analytical mind with ability to think diversely and understand the big picture, Methodical and diligent with outstanding planning abilities, an analytical mind able to &quot;see&quot; the complexities of procedures and regulations</li>
<li>Strong Manpower handling skills and having effective team communication and motivational skills.</li>
<li>Capable of suggesting ideas in a structured manner and having good Command on English language.</li>
<li>High on communication and collaboration, having an ability to manage multiple stakeholders at a time.</li>
<li>Strong eye for details, having expertise to understand, review and implement the compliance inputs from Quality point of view.</li>
<li>In-depth knowledge of the industry&rsquo;s standards and regulations guidelines, excellent knowledge of reporting procedures and record keeping.</li>
<li>Must be able to manage tasks and priorities and easily adapt to changing situations.</li>
<li>Ability to create cross functional relations and manage conflicts.</li>
<li>Problem Solving and high agility on taking right scientific decisions.</li></ul><br>
<p></p>
<p><b>
Qualifications, Key Experiences / Functional Knowledge Requirements:</b></p><p><br>
</p>
<div></div><ul><li>Minimum 7 years of experience in QC raw materials department.</li>
<li>Must be experienced in managing complex and sensitive operational challenges.</li>
<li>Bachelor&rsquo;s degree in pharmacy</li>
<li>Proven experience in quality control, having leadership skills.</li>
<li>Strong knowledge of regulatory requirements and quality standards relevant to the industry.</li>
<li>Excellent analytical, problem-solving, and decision-making skills.</li>
<li>Strong leadership and team management capabilities.</li>
</ul><p>
We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar</p></div></div></div></div></div><p></p>

Team Leader -QC

Search 9903+ Qc supervisor jobs near you this March. New roles added regularly across leading industries. Apply today.