quality compliance officer

SAPANA POLYWEAVE PVT LTD AURANGABAD

Position Title : Quality Manager &amp; Compliance OfficerDepartment : Quality Assurance &amp; ComplianceLocation : AurangabadReport To : Plant HeadExperience Required: 5&ndash;8 Years Education: B.E./B.Tech in Mechanical, Textile, or Industrial EngineeringAbout the Company Sapana Polyweave Pvt. Ltd. is a leading manufacturer of PP mats and woven products, catering to global retailers and brands. The company is committed to maintaining high standards of product quality, sustainability, and ethical compliance through continuous improvement and innovation. We are seeking an experienced and dedicated Quality Manager &amp; Compliance Officer to strengthen our Quality and Compliance systems and ensure adherence to international standards.Position Overview The Quality Manager &amp; Compliance Officer will be responsible for developing, implementing, and maintaining the Quality Management System (QMS) across departments. The role includes leading internal and external audits, driving corrective and preventive actions (CAPA), and ensuring compliance with GRS, SEDEX, BSCI, GoodWeave, FCCA, SCAN, and other buyer-specific requirements. The ideal candidate must possess strong leadership, documentation, and analytical skills with the ability to coordinate across multiple departments and meet buyer expectations.Key ResponsibilitiesQuality Management<ul><li>Implement and maintain QMS as campare ISO standards, ensuring process adherence across all departments.</li><li>Prepare and update SOPs, Work Instructions, PFMEA, Process Flow Charts, and Control Plans.</li><li>Conduct incoming, in-process, and final inspections of materials and finished goods.</li><li>Monitor rejection trends, quality KPIs, and drive continuous improvement initiatives.</li><li>Lead root cause analysis (RCA), CAPA, and 8D problem-solving for customer and internal complaints.</li><li>Coordinate with production and to eliminate recurring process deviations.</li><li>Manage calibration, equipment validation, and inspection record systems for QA instruments.</li></ul>Audit &amp; Compliance Management<ul><li>Plan and lead internal, customer, and certification audits &mdash; ISO, GRS, SEDEX, BSCI, GoodWeave, SCAN, FCCA.</li><li>Ensure closure of non-conformities and timely submission of corrective action reports.</li><li>Maintain documentation and evidence for all social, environmental, and technical compliance audits.</li><li>Manage traceability and mass balance systems as per GRS (Global Recycled Standard) requirements.</li><li>Coordinate buyer audits and 3rd party inspections (Target, Walmart, Kingfisher, etc.) ensuring zero major NCs.</li><li>Handle warehouse compliance &mdash; FIFO, material segregation, hygiene, and pest control norms.</li></ul>Training &amp; Development<ul><li>Plan and conduct regular training programs on quality awareness, compliance standards, PPE, fire safety, and first aid.</li><li>Organize audit preparedness sessions for staff and vendors.</li><li>Maintain training records, attendance logs, and feedback assessments as per audit protocols.</li></ul>Documentation &amp; Reporting<ul><li>Maintain and control QA records, test certificates, inspection reports, buyer documents, and traceability logs.</li><li>Prepare monthly QA performance reports, trend analysis, and continuous improvement reports.</li><li>Ensure documentation compliance with customer-specific quality and compliance standards.</li></ul>Required Skills &amp; Competencies<ul><li>Strong understanding of GRS, SEDEX, BSCI, GoodWeave, FCCA, SCAN standards.</li><li>Hands-on experience in CAPA, FMEA, 8D, RCA, PPAP, and Control Plan preparation.</li><li>Excellent command over quality documentation and audit processes.</li><li>Effective communication and interpersonal skills for buyer and auditor interaction.</li><li>Leadership ability to manage a team of quality inspectors and cross-functional coordination.</li><li>Proficiency in MS Office (Excel, Word, PowerPoint) and report generation.</li><li>Ability to work under pressure and meet multiple audit deadlines.</li></ul>Why Join Us<ul><li>Exposure to leading international buyer compliance systems.</li><li>Opportunity to lead end-to-end Quality and Compliance functions.</li><li>Continuous professional growth through audit experience and training programs.</li><li>Supportive management with a focus on process excellence and innovation.</li></ul>Job Type: Full-timePay: &#8377;30,000.00 - &#8377;50,000.00 per monthWork Location: In person

Quality Manager & Compliance Officer

Julphar

<div></div><div><div><div><div><div>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.
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.
<h3 class="jobSectionHeader">
Job Purpose / Summary</h3>

The role is responsible for ensuring full compliance with cGMP, GSP, and GDP standards across all Julphar warehouses, including Raw Materials (RM), Packaging Materials (PM), and Finished Products (FP). The incumbent will oversee quality compliance during receiving, storage, and shipping activities, conduct investigations into deviations, manage CAPA and market complaints, and support continuous improvement of warehouse operations in line with regulatory and company requirements.

<h3 class="jobSectionHeader">Key Responsibilities</h3>
<h4 class="jobSectionHeader">1. cGMP and Quality Compliance</h4>
<ul>
<li>Ensure consistent implementation of cGMP principles across all warehouse operations (RM, PM, and FP).
</li>
<li>Oversee compliance with Good Storage Practices (GSP) and Good Distribution Practices (GDP) during receiving, handling, and shipping activities.
</li>
<li>Conduct periodic inspections and ensure adherence to FDA, WHO, and other regulatory requirements.
</li>
<li>Ensure that all incoming materials are properly labeled, inspected, and stored according to SOPs and quality guidelines.
</li>
</ul><h4 class="jobSectionHeader">2. Warehouse Operations and Documentation</h4>
<ul>
<li>Review and approve all records related to the receipt, storage, handling, and shipment of materials and finished products.
</li>
<li>Verify that materials and products are managed as per product-specific storage requirements, including temperature and humidity controls.
</li>
<li>Ensure timely documentation and closure of all deviations and CAPAs related to warehouse activities.
</li>
<li>Monitor warehouse logbooks and enforce Good Documentation Practices (GDP).
</li>
</ul><h4 class="jobSectionHeader">3. Investigations and Corrective Actions</h4>
<ul>
<li>Lead and document investigations into deviations, temperature excursions, mishandling, or inventory discrepancies.
</li>
<li>Ensure prompt implementation of corrective and preventive actions (CAPA) to address any non-compliance.
</li>
<li>Manage market complaint investigations and handle change controls related to warehouse operations.
</li>
<li>Review and evaluate CAPAs associated with deviations and complaints to ensure effective closure.
</li>
</ul><h4 class="jobSectionHeader">4. Shipment and Transfer Compliance</h4>
<ul>
<li>Oversee compliance of finished product processes&mdash;from receiving to shipment&mdash;in line with approved procedures.
</li>
<li>Review and approve temperature data logger reports for shipments in case of excursions.
</li>
<li>Review and validate product transfer requirements between consignees.
</li>
<li>Ensure compliance of shipping and release processes with approved standards.
</li>
</ul><h4 class="jobSectionHeader">5. Material Handling and Rejection Management</h4>
<ul>
<li>Oversee the handling and documentation of rejected, obsolete, blocked, and expired materials and finished products.
</li>
<li>Verify and approve gate passes related to shipping.
</li>
<li>Conduct continuous inspections of all warehouses to drive process improvement and compliance.
</li>
</ul><h4 class="jobSectionHeader">6. SOPs and System Management</h4>
<ul>
<li>Prepare, review, and update Standard Operating Procedures (SOPs) related to warehouse quality functions.
</li>
<li>Execute QMS-related actions for warehouses and ensure timely completion of all quality-related tasks.
</li>
<li>Support system audits, KPI tracking, and improvement initiatives.
</li>
</ul><h3 class="jobSectionHeader">Core Competencies</h3>
<ul>
<li>Strong knowledge of GMP, GSP, GDP, and other global regulatory standards (FDA, WHO, etc.).
</li>
<li>Results-driven with a strong sense of accountability, ownership, and attention to detail.
</li>
<li>Excellent problem-solving, analytical, and decision-making abilities.
</li>
<li>Effective team leadership, collaboration, and communication skills.
</li>
<li>Proficient in planning, prioritization, and time management under pressure.
</li>
<li>Demonstrates solution-oriented thinking and process compliance.
</li>
<li>Organized, self-motivated, and committed to continuous improvement.
</li>
</ul><h3 class="jobSectionHeader">Qualifications and Experience</h3>
<ul>
<li>Bachelor&rsquo;s degree in Science, Pharmacy, or a related healthcare discipline (Master&rsquo;s degree preferred).
</li>
<li>3&ndash;4 years of experience in a similar role within the pharmaceutical, healthcare, or medical industry.
</li>
<li>Proven experience in quality systems, vendor management, and deviation/CAPA handling.
</li>
<li>Strong knowledge of QMS systems and good computer proficiency (especially MS Word and Excel).
</li>
<li>Excellent command of English (written and verbal).
</li>
<li>Demonstrated success in process compliance, KPI development, and system implementation.
</li>
</ul>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</div></div></div></div></div>

Specialist - QA Warehouse Oversight

GE Vernova

<div><h1 class="jobSectionHeader">Job Description Summary</h1>
Lead and execute verification of Green tagged blades to understand effectiveness of Firewall process and closely work with manufacturing plants to bridge the gaps in the process and product deviations. Continuous improvement of Quality processes, training, certification, audit and implementation of quality inspections and measurements in all GE Manufacturing plants globally.<h1 class="jobSectionHeader">
Job Description</h1>
Key responsibilities include:
Competency Development &amp; Resource Adequacy:<ul><li>
Responsible for monitoring and improving effectiveness of Quality Controllers certification program in the region.</li><li>
Responsible to improve the competence level of quality staff in plants as per GE Vernova competency model.</li><li>
Audit and track the certification database to ensure only certified resources performing inspection in the plants.</li></ul>
Measurement and Inspection Methods (Visual inspection and Measurements):<ul><li>
Execute and support Firewall inspection on the green tagged blades as per the sampling plan and provide constructive feedback to the plants to improve the process and product Quality.</li><li>
Test, validate and provide feedback and needed inputs to respective team to improve the inspection methods, Acceptance Criteria and Measurement methods.</li><li>
Conduct Periodic MSA and validation of inspection and measurement methods (both variable and attribute methods).</li><li>
Leading and support implementation of new inspection methods, new technologies and new Acceptance Criteria.</li><li>
Act as Global standard and work towards bringing down the variation between Quality Controllers within and across the manufacturing facilities.</li></ul>
Quality Compliance<ul><li>
Plan and perform process audit in plants (IPE, Crawler) for critical processes as per defined frequency.</li><li>
Drive improvements in the audit process to make it is lean and effective.</li><li>
Follow up on audit findings closure.</li><li>
Bring improvement in BMS process and tools related to process audits</li></ul>
Operational process and support:<ul><li>
Take ownership of Visual inspection processes and methods, challenge current setup and make the process lean and efficient.</li><li>
Support customer or third part inspections and provide clear report to the management team.</li><li>
Own and drive improvement of Quality KPIs related to inspection effectiveness and escapements.</li><li>
Tracking, monitoring, and improving performance of gauge R &amp; R in plants.</li><li>
Training and implementation of new AC</li></ul>
Required Qualifications:
<ul><li>Technical associate degree or equivalent with minimum 5 years of blade manufacturing and specifically working with Quality inspections and measurement.</li><li>
Candidates with LM/GE Vernova blades inspections and level 2 or above certifications would add additional strength.</li><li>
International experience and cultural awareness covering Americas, Europe, Canada, India and China.</li><li>
Knowledge of blade manufacturing is preferable, combined with explicit knowledge on Quality tools, Systems and Processes, Audits, Six Sigma, PFMEA, Control plans, PPAP.</li><li>
Strong English language skill (verbal and writing).</li><li>
Preferable to have an ISO 9001 internal auditor certification and relevant audit experience.</li><li>
Flexible travelling across LM business units for execution of job and support.</li><li>
Good with MS office tools such as Excel, Word and PPT.</li></ul>
Desired Characteristics<ul><li>
A person with a quality mindset and strong believer of data-oriented approach and continuous improvement.</li><li>
Able to demonstrate GE Vernova way and integrity values.</li><li>
A person with self-motivation and encourages others to take responsibility.</li><li>
Communication: Effectively communicate beyond own area at all levels. Initiates or improves the way to communicate, facilitate, negotiate resulting in increased impact and commitment.</li><li>
Decision making: Sets goals and regularly follow up on these goals. Takes decisions and monitors results.</li></ul><h1 class="jobSectionHeader">
Additional Information</h1><div><div><div><div><div><div><div>
Relocation Assistance Provided: Yes</div></div></div></div></div></div></div></div>

Quality Specialist-Visual inspection and Measurements

Bunge

<div>Location : Rajpura
City : Rajpura
State : Punjab (IN-PB)
Country : India (IN)
Requisition Number : 40450
Job Title &ndash; 2P /3P Operation &ndash; Contract Manufacturing 
Department &ndash; Technical 
Job Grade &ndash; Sr. Executive 
Reporting to (job title) &ndash; AGM Contract Manufacturing 
Overall purpose of job: Ensure Food Safety, Quality Compliance &amp; timely Production of Bunge Products manufactured at 2P/3P sourcing unit. Product should be consistent as per Bunge requirement.<div> 
Tasks and Responsibilities: 
<ul><li>Production/ Dispatch execution as per plan by coordinating with 2P units and all other concerned stake holders.</li><li>Highlight the challenges on time in meeting the monthly plan for corrective action.</li><li>Need to inform PM suppliers for tentative requirement of PM during the month so that suppliers can arrange raw material for PM accordingly.</li><li>Follow up to get necessary Crude oil on time in 3P units for production based on Monthly production plans from RKM</li><li>Monitor and control inventory of packaging materials in units and reorder of PM.</li><li>Follow up with procurement team for rate card of different PM SKUs in concerned unit.</li><li>Issue necessary Packaging material POs to vendors by coordinating with Mohali team.</li><li>Follow up with PM suppliers for timely PM delivery in unit.</li><li>Production Planning in 3p units based on dispatch requirements from supply chain and follow up with units</li><li>Quality checking &ndash; Check and ensure that product quality is as per Bunge specs /Legal specs in chemical analysis and PCRO.</li><li>Need to ensure that all PM receipt should be as per Bunge specifications.</li><li>Get necessary dispatch plans from supply chain dept, coordinate with logistics team for trucks and with units for timely loading and dispatch</li><li>Ensure that units are filling all log sheets from material receipts to FG dispatch as per Bunge systems</li><li>Ensure that standards are followed in filling machines, log sheets entered, and preventive maintenance taken care</li><li>QA systems- provide specs, procedures, training in Bunge standards. Ensure all records kept properly for traceability requirements.</li><li>Need to ensure that counter samples are sent from unit to nearest own unit for cross checking the analysis being done in sourcing units. Corrective action in case of any variation in results.</li><li>Keep people management skills and ensure proper coordination between Bunge and units without any frictions affecting the production and dispatch</li><li>Attend quality complaints and follow up units for action plans and necessary closure.</li><li>Provide continuous training for unit people to improve standards of production, process, QA, loading , Housekeeping and other food safety standards.</li><li>Reporting of production/ dispatch/ available stock/ Ready stock for dispatch - details as per the standard MIS report.</li><li>Coordination with unit and Mohali team to get the PM receipt / Oil receipts entries done in SAP.</li><li>Coordination with unit and Mohali team for production entry in SAP.</li><li>Follow up with unit and Mohali team to provide details and get invoice to CFA and STNs for direct dispatch.</li><li>Monthly physical stock count for FG/ Oil and PM stocks. Agree the difference with unit for debit note and clearance of the same without any dispute.</li><li>Follow up with supplier and procurement for implementing any change in PM artwork/ design or Size.</li></ul></div> 
Interface: 
1. Build relationship with 2P unit management and maintain good rapport to ensure that we get the product as per Bunge requirement from 2P unit. 
2. Should have leadership skill and sound subject knowledge to train the persons concerned in 2P/3P units. 
Education, qualifications, special training, experience and skills:
1. Should be a Oil Technologist having 2-3 Years of experience working in Edible oil field. 
2. Sound knowledge about different oils, processing, packing and quality checks techniques/ Basic knowledge of statutory requirement like FSSAI / Weights &amp; Measure etc. 
3. Sound knowledge of Packing material quality and check points to ensure right quality PM receipts in plant to pack. Should have leadership quality to educate/ train the persons in unit to ensure receipts as per Bunge need. 
4. Good at Leadership and coordination skills to handle all internal &amp; external stake holders. Computer knowledge to generate daily reports and e-mailing related to daily activities. 
5. Travel to market &amp; customer point on need basis for complaint handling, product improvements etc</div>

Senior Executive - Contract Manufacturing

Almas Nursing College

Job Title: Assistant Legal Officer TraineeLocation: Almas Hospital, Kottakkal, Malappuram, Kerala Department: Legal / Compliance Reporting To: Legal Officer / Hospital AdministrationAbout Almas HospitalAlmas Hospital is a multi-specialty healthcare institution committed to providing exceptional patient care with a focus on quality, safety, and compliance. We are expanding our legal and compliance team to support our growing operations and ensure that all legal and regulatory requirements are met.Job SummaryWe are looking for a motivated Assistant Legal Officer Trainee to support the legal and compliance functions of the hospital. This role offers hands-on experience in healthcare law, regulatory compliance, contract management, and corporate legal matters. The trainee will work closely with the Legal Officer and hospital administration to ensure legal and ethical standards are maintained.Key Responsibilities<ul><li>Assist in drafting, reviewing, and maintaining contracts, agreements, and legal documents.</li><li>Support the Legal Officer in regulatory compliance, including healthcare laws, labor laws, and hospital-specific regulations.</li><li>Conduct research on legal issues affecting hospital operations.</li><li>Assist in handling internal compliance audits and documentation.</li><li>Maintain records of legal cases, notices, and correspondence.</li><li>Support the hospital in policy drafting and updating SOPs to meet legal requirements.</li><li>Liaise with external legal advisors, government authorities, and regulatory bodies when required.</li></ul>Qualifications &amp; Requirements<ul><li>Bachelor&rsquo;s Degree in Law (LLB) from a recognized university.</li><li>Fresh graduates or candidates with up to 1 year of relevant experience may apply.</li><li>Knowledge of healthcare regulations, corporate law, and labor laws is a plus.</li><li>Strong analytical, research, and drafting skills.</li><li>Excellent communication and interpersonal skills.</li><li>Attention to detail and ability to maintain confidentiality.</li></ul>Training &amp; Growth<ul><li>Structured training under the guidance of the Legal Officer.</li><li>Exposure to hospital management, compliance, and legal processes.</li><li>Opportunity to grow into a full-fledged Legal Officer role based on performance.</li></ul>Job Type: Full-timePay: &#8377;10,000.00 - &#8377;20,000.00 per monthEducation:<ul><li>Bachelor's (Preferred)</li></ul>Work Location: In person

Assistant Legal Officer Trainee

HSE Contractors Inc

Quality Assurance Officer &amp; Quality Control Analyst:(Pharmacy Degree)Multinational company seeks a quality Assurance Officer/ Quality Control Analyst for a 6-month contract in 6th of October City.Responsibilities: Oversee sampling, audits, GMP/ISO/EDA compliance, investigate quality issues, and validate methods.Requirements: Pharmacy degree, 3+ years in QA or pharmaceutical manufacturing, GMP &amp; gas chromatography knowledge, strong English.Living in 6th of October City is preferred.Apply now: Rec.uni2@uni-serve.meJob Type: Temporary Contract length: 6 monthsPay: E&pound;13,000.00 - E&pound;20,000.00 per month

Quality Assurance Officer & Quality Control Analyst:(Pharmacy Degree)

Cigalah Gulf Medical

Job Opening: Regulatory Affairs Officer / CoordinatorLocation: Kingdom of BahrainWe are looking for a Regulatory Affairs Officer / Coordinator to join our growing pharmaceutical team. The ideal candidate will play a key role in ensuring our company&rsquo;s full compliance with NHRA regulatory requirements, supporting product registrations, renewals, and quality-related operations.Qualifications &amp; Requirements:<ul><li>Bachelor&rsquo;s Degree in Pharmacy (BS Pharmacy)</li><li>Must possess a valid NHRA license (Bahrain)</li><li>4&ndash;5 years of proven experience in Regulatory Affairs within the pharmaceutical industry</li><li>Solid understanding of NHRA and GCC regulatory guidelines and procedures</li><li>Experience in Quality Assurance (QA), Quality Systems, and Regulatory Compliance</li><li>Excellent knowledge of dossier preparation, submission, and tracking</li><li>Strong organizational and documentation skills with keen attention to detail</li><li>Good communication and interpersonal skills</li><li>Must be currently residing in Bahrain</li><li>Able to join immediately</li></ul>Key Responsibilities:<ul><li>Prepare, compile, and review regulatory dossiers for product registration, renewals, and variations in compliance with NHRA/GCC requirements</li><li>Liaise effectively with NHRA officials and other health authorities to ensure timely approvals</li><li>Maintain and update product licenses, certificates, and technical documentation</li><li>Ensure regulatory compliance for all marketed pharmaceutical products</li><li>Support internal and external audits, quality reviews, and inspection readiness activities</li><li>Collaborate with cross-functional departments (QA, Supply Chain, Production, etc.) to ensure adherence to company and regulatory standards</li><li>Stay up to date with changing regulations, guidelines, and industry trends affecting product registration and compliance</li></ul>Job Type: Full-time

Regulatory Coordinator

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