Quality Control Job Vacancies in Madhya Pradesh

We are looking for a Pharmaceutical Quality Assurance Executive to ensure that our products meet the highest standards of quality and safety. This role is ideal for recent graduates or those with up to five years of experience in the pharmaceutical industry.Key Responsibilities:1. **Quality Audits**: Conduct routine inspections and audits of production processes to ensure compliance with quality standards and regulatory requirements.2. **Document Control**: Manage and maintain quality documentation, including standard operating procedures (SOPs) and quality manuals, ensuring all records are up to date and accurate.3. **Product Testing**: Collaborate with laboratory teams to perform sample testing and analyze results, guaranteeing that products meet established quality specifications before release.4. **Problem Resolution**: Identify quality issues, investigate root causes, and recommend corrective actions to prevent recurrence and enhance overall product quality.5. **Training and Support**: Assist in training staff on quality assurance processes and regulatory requirements, fostering a quality-first culture within the organization.Required Skills and Expectations:Candidates must possess a relevant graduate degree. Strong attention to detail and excellent analytical skills are essential for identifying and resolving quality issues. Clear communication abilities are necessary to effectively collaborate with various teams. A proactive attitude, along with a willingness to learn and adapt in a fast-paced environment, is crucial for success in this role. Familiarity with quality assurance principles and regulatory guidelines in the pharmaceutical sector is a plus.

We are looking for a Beverage Supervisor to oversee our beverage operations in Guna, India. This role requires an individual with at least two years of experience in the beverage industry and a passion for providing excellent service.Key Responsibilities:1. **Supervision of Beverage Staff**: You will lead and manage the beverage team, ensuring everyone adheres to company standards and provides top-notch customer service.2. **Inventory Management**: You will monitor beverage stock levels, place orders, and ensure that all supplies are adequately managed to prevent shortages.3. **Quality Control**: You will conduct regular checks to ensure all beverages meet our quality standards, and any issues are addressed promptly.4. **Training and Development**: You will be responsible for training new staff and providing ongoing education to existing employees about beverage preparation and service standards.5. **Customer Interaction**: You will engage with customers to enhance their beverage experience, responding to feedback and resolving any complaints professionally.Required Skills and Expectations:Candidates must have at least a 12th-grade education and two years of relevant experience. Strong communication and interpersonal skills are essential for interacting with both customers and team members. A keen attention to detail is important for maintaining quality and cleanliness. The ideal candidate must be able to work in a fast-paced environment and possess effective problem-solving skills.

We are seeking an experienced Production professional to join our team in Indore, India. The ideal candidate will have 5 to 10 years of experience in a production environment, effectively managing processes and ensuring high-quality output.Key Responsibilities:1. **Production Planning**: Develop and implement efficient production schedules to meet project deadlines while optimizing resource use.2. **Quality Control**: Monitor production processes to ensure that products meet quality standards and take corrective actions when necessary.3. **Team Management**: Supervise and lead production staff, providing guidance, training, and support to ensure smooth operations and foster a productive work environment.4. **Inventory Management**: Oversee inventory levels, ensuring that materials are available for production while minimizing waste.5. **Process Improvement**: Identify areas for improvement in production processes and suggest ideas for enhancing efficiency and quality.6. Must have Knowlede about sortex machine and processing chana plantRequired Skills and Expectations:Candidates should have a deep understanding of production processes and techniques, with strong analytical and problem-solving skills. Excellent communication skills are essential for effectively collaborating with team members and other departments. The ability to manage multiple tasks and adapt to changing situations will be critical. Candidates must be detail-oriented and possess strong decision-making abilities, ensuring timely and efficient production in a dynamic workplace setting. A graduate degree is required, and male candidates are preferred for this role.

Need FARO CMM Operator for indore pithampur location

We are seeking a Finishing Supervisor to oversee the final stages of production in Indore, India. Your key responsibilities will include inspecting finished products for quality, ensuring all finishing processes are completed correctly, and supervising a team of finishing workers.You will be responsible for ensuring that all finishing work meets company standards and customer specifications. This includes coordinating with other departments to ensure timely completion of projects, maintaining accurate records of production data, and troubleshooting any issues that may arise during the finishing process.The ideal candidate will have strong attention to detail, excellent communication skills, and the ability to work well under pressure. Prior experience in a supervisory role and knowledge of finishing techniques and equipment are preferred. A 12th pass education level is required for this position, and candidates with 0-3 years of experience will be considered. This is a full-time, work-from-home position that offers the opportunity for growth and advancement within the company.

Designation :- QC Officer/Senior OfficerQualification:- MSc/B. Pharma Experience :- 4 Years To 8 YearsSalary:- As Per Interview Gender:- MaleJob Responsibilities:- i)RM (Raw Material) Analysisii) FG (Finished Goods) Analysisiii) AMT / AMV Analysisiv)Strong knowledge of QC proceduresJob Location:- Indore,MPIndustry:- Reputed Manufacturing Industry

We req manufacturing ex to oversee manufacturing activities for our plant manufacturing machining components and fabricated assemblies

Designing on solidworks & Autocad. Inspection of jobs on machine. New job study & production setup. Job record of machines. Final inspection report of jobs & packaging

Key ResponsibilitiesQuality AssuranceDevelop, implement, and maintain Quality Management Systems (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable standards.Conduct internal audits, CAPA (Corrective & Preventive Action), and risk assessments to ensure ongoing compliance.Monitor production processes and verify adherence to SOPs, specifications, and quality standards.Quality ControlPerform in-process inspections, final product testing, and release of products.Review and approve batch records, test reports, and other QC documentation.Manage calibration and preventive maintenance schedules for testing and measuring instruments.Investigate non-conformities and implement corrective actions.Regulatory ComplianceEnsure compliance with national and international medical device regulations (FDA, CDSCO, CE, ISO).Support preparation of regulatory submissions (510(k), PMA, CE Marking, etc.).Communicate with regulatory authorities to resolve compliance issues.Process ImprovementIdentify areas of process improvement to enhance product quality and operational efficiency.Implement Lean Six Sigma/continuous improvement methodologies to reduce defects and improve productivity.Supplier Quality ManagementConduct supplier audits and ensure raw material/component quality.Collaborate with vendors for corrective actions and quality improvement initiatives.Documentation & ReportingPrepare and maintain technical files, Device Master Records (DMR), and Device History Records (DHR).Maintain up-to-date documentation to support internal audits, external inspections, and certifications.Generate quality reports and present trends to management for decision-making.Required Skills & KnowledgeStrong understanding of QA/QC principles in the medical device industry.Knowledge of ISO 13485, ISO 14971, GMP, and FDA 21 CFR Part 820.Hands-on experience with quality audits, validation, and verification processes.Familiarity with regulatory submissions and compliance requirements.Excellent documentation, analytical, and problem-solving skills.Ability to train and guide cross-functional teams on quality and compliance. WhatsApp: +91 9266682964

Job Title:Medical Device Regulatory Affairs SpecialistBhopal LocationCompany: Intense Medical & Dental System Pvt Ltd Bhopal.Job Brief:We are looking for a skilled Regulatory Affairs Specialist to manage and coordinate regulatory compliance for our medical devices. This role requires strong communication with channel partners, collaboration with documentation teams, and ensuring all products meet regulatory standards for both domestic and international markets.______________Key Responsibilities:* Ensure medical devices comply with all applicable national and international regulatory requirements and standards* Prepare and submit regulatory submissions, including 510(k), PMA, and other global market registrations* Communicate with regulatory authorities (such as the FDA, CDSCO) to handle queries and support approval processes* Monitor and interpret changes in medical device regulations and assess their impact on the company* Provide regulatory guidance and training to cross-functional teams including R&D, QA/RA, and Product Development* Develop and implement regulatory strategies to support new product development and market expansion* Maintain organized, up-to-date documentation to demonstrate compliance and support audits* Collaborate with channel partners and internal documentation specialists to ensure consistent regulatory alignment______________Requirements:* Bachelors degree in Biomedical Engineering, or B.E electronic commination. or a related discipline* 34 years of experience in medical device regulatory affairs* Strong knowledge of domestic and international medical device regulations (FDA, EU MDR, ISO 13485, CDSCO, etc.)* Excellent verbal and written communication skills* High attention to detail, analytical thinking, and problem-solving ability* Experience working collaboratively across multiple teams______________Preferred Qualifications:* Regulatory Affairs Certification (RAC)* Experience with Class II or III medical devices* Familiarity with quality systems (e.g., ISO 13485, FDA QSR)Key Responsibilities: Quality Assurance and Control Regulatory Compliance Process Improvement Supplier Quality Management Key Documentation and Reporting

Candidates should be relevant experience in sheet metal fabrication industry Should be good in English languages

Officer/SrOfficer Quality ControlAMV, HPLCAnalysis, FP/RM/PM Analysis & GLP

We are seeking a dedicated Production Officer to join our team in Pithampur, Indore. This role is ideal for recent graduates or those with up to six years of experience who are looking to grow in a dynamic production environment. Key Responsibilities: - **Monitor Production Processes:** Oversee daily production activities to ensure efficiency and adherence to quality standards. This involves checking equipment performance and making necessary adjustments. - **Cooperate with Team Members:** Collaborate with other staff, including engineers and quality control personnel, to promote a smooth production workflow and resolve any issues that arise. - **Maintain Records:** Keep accurate records of production output, materials used, and any discrepancies. This data will help improve future production processes. - **Enforce Safety Standards:** Ensure that all safety regulations are followed to create a safe working environment for all employees and minimize the risk of accidents. - **Report to Management:** Provide timely updates to supervisors about production status, challenges faced, and suggestions for improvements.Required Skills and Expectations: Candidates should have a strong understanding of manufacturing processes and the ability to work effectively in a team. Good communication skills are essential, as is the ability to solve problems creatively. Attention to detail and a commitment to quality and safety are crucial for success in this role. A proactive attitude and willingness to learn will help the candidate thrive in a fast-paced production environment.

- Monitor and oversee the finishing processes: The finishing supervisor is responsible for supervising and ensuring that all finishing processes are carried out efficiently and according to standards.- Train and guide finishing team members: It is the duty of the finishing supervisor to train new team members on finishing techniques and procedures, as well as to provide guidance and support to existing staff.- Inspect finished products for quality: The finishing supervisor must conduct regular inspections of finished products to ensure they meet quality standards and specifications before further processing or shipping.- Maintain records and reports: Keeping track of production records, quality assurance reports, and other relevant documentation is essential for the finishing supervisor to maintain smooth operations.- Coordinate with other departments: Collaboration with different departments, such as production, quality control, and logistics, is crucial for the finishing supervisor to ensure a seamless workflow.The ideal candidate for the finishing supervisor position should have a high school diploma or equivalent, with 0-3 years of experience in a similar role. They should have strong attention to detail, excellent communication skills, and the ability to work independently. A good understanding of finishing techniques and processes is required, as well as the ability to multitask and prioritize tasks effectively. Additionally, proficiency in basic computer skills for data entry and reporting purposes is necessary.