Quality Control Job Vacancies in Uttarakhand

Key Responsibilities:Raw & Packaging Material Quality: Inspect incoming durum wheat semolina, water, additives, and packaging materials to ensure they match internal standards .In-Process Quality Control (IPQC): Monitor critical control points during mixing, extrusion, drying, and cooling (e.g., moisture content, cooking time, breaking rate, and strand uniformity).Food Safety & Compliance: Maintain systems like HACCP, GMP, GHP, and ISO 22000 / FSSC 22000, ensuring complete alignment with local food authorities. Finished Goods Release: Conduct physical, visual, and analytical testing on finished pasta before approving batches for market dispatch .Audits & Documentation: Lead internal/external quality audits, maintain accurate lab records, and manage traceability documentation. Team Leadership & Training: Supervise shift quality controllers and lab analysts, providing continuous training on safety, hygiene, and testing protocols.

Handle customer inspections (PGCIL, Railways, NTPC, BHEL, TPI, Govt. & Export)Prepare GTP, QAP, inspection reports, and quality documentationManage NABL, BIS & IMS audit documentationEnsure product quality, process control, and finished goods testingHandle customer complaints, CAPA, and type test coordinationMaintain document control and traceability

We are seeking a QC Executive with 3 to 5 years of experience to join our team in Joshimath. The ideal candidate will be responsible for ensuring the quality of our products and processes, playing a key role in maintaining high standards.Key Responsibilities:1. Quality Inspection: Conduct regular inspections of products and processes to ensure they meet established quality standards. This includes testing materials and finished products.2. Documentation: Maintain detailed records of inspections, tests, and quality metrics. This will involve compiling reports to track quality issues and improvements.3. Problem Resolution: Identify and analyze quality issues, and work to develop solutions and corrective actions. This may also involve coordinating with other departments to address concerns.4. Process Improvement: Assist in reviewing and refining existing quality control processes to enhance efficiency and effectiveness. Propose recommendations based on inspection findings.5. Compliance: Ensure that all quality control practices comply with industry regulations and standards. Stay updated with changes in regulations to implement necessary adjustments.Required Skills and Expectations:The successful candidate should have a bachelors degree and a strong background in quality control. Attention to detail and strong analytical skills are essential for identifying issues and implementing solutions. Proficiency in using quality control tools and software is important. Additionally, effective communication and teamwork skills are necessary, as the role involves collaborating with various teams. The candidate should possess a proactive attitude towards maintaining high-quality standards and be willing to take ownership of responsibilities.

Candidate should be familiar with all the sheet metal fabrication process

Improve profitability through strategic planning, ensure smooth daily operations across all departments, implement efficient processes to boost productivity, maintain high service and quality standards motivate the team, conduct performance reviews and support staff development, build and maintain strong client relationships, ensure high customer satisfaction.

Manufacturing industry

We have vacant of 2 Quality Control Analyst Pharma Jobs in Rudrapur, Uttarakhand, for Freshers Educational Qualification : B.Sc, B.Pharma, M.Pharma, M.Sc Skill Chemical analysis, Instrumental analysis, Sample preparation. Equipment maintenance. etc.Candidates with prior experience in pharmaceutical quality control environment will be preferred.

Hiring for Production Head for Nicotine Manufacturing CompanyExp:15 Plus YearsJob Purpose:The Production Head will be responsible for overseeing, managing, and optimizing the end-to-end production activities of the nicotine manufacturing facility. This role ensures that production targets are achieved with strict compliance to quality, safety, statutory, and regulatory standards. The incumbent will drive process improvements, enhance productivity, and maintain alignment with Good Manufacturing Practices (GMP) and global industry regulations.Key Responsibilities:Production & Operations Management:- Plan, organize, and control all production activities to meet business targets.- Ensure continuous, efficient, and cost-effective production of nicotine and related products.- Monitor production processes and adjust schedules as needed to meet demand and timelines.- Implement best practices in manufacturing and ensure adherence to Standard Operating Procedures (SOPs).Quality, Safety & Compliance:- Ensure strict compliance with GMP, ISO, FDA, and other global regulatory requirements.- Maintain product quality by enforcing quality control checks and coordination with the QA/QC teams.- Drive a culture of safety, ensuring adherence to EHS (Environment, Health & Safety) guidelines.- Liaise with regulatory bodies during audits, inspections, and certifications.People & Team Management:- Lead, mentor, and develop the production team to achieve high performance.- Allocate manpower effectively to optimize productivity.- Conduct regular training and skill development sessions for team members.Process Improvement & Cost Control:- Monitor and control production costs, wastages, and downtime.- Identify and implement process improvement initiatives to maximize efficiency.- Ensure optimal utilization of resources including raw materials, manpower, and machinery.Cross-functional Collaboration:- Work closely with Quality Assurance, Supply Chain, R&D, and Maintenance teams.- Support new product development trials and technology transfer activities.- Collaborate with procurement for timely availability of raw materials and consumables.Key Skills & Competencies:- Strong knowledge of nicotine/chemical/pharmaceutical manufacturing processes.- In-depth understanding of GMP, ISO, and regulatory requirements (FDA, REACH, WHO, etc.).- Proven ability in process optimization, productivity enhancement, and cost reduction.- Leadership, decision-making, and problem-solving skills.- Strong communication and cross-functional collaboration.- Analytical mindset with ability to work under pressure.Qualifications & Experience:- B.E./B.Tech / M.Sc. / M.Tech in Chemical Engineering, Industrial Chemistry, or related field.- 15 to 20 years of experience in chemical / pharmaceutical / nicotine / API manufacturing industry.- Minimum 5 years in a leadership role managing plant or large-scale production operations.- Experience with high-compliance and safety-driven manufacturing setups preferred

Conducting visual inspections of products or materials to identify defects or inconsistencies. Assisting with the execution of quality control tests and procedures. Using quality control equipment and software to analyze and improve standards. Documentation and Record Keeping:Accurately documenting inspection results and test data. Maintaining records of quality control activities and findings. Adhering to Quality Standards:Ensuring that products and processes meet established quality standards and specifications. Identifying and reporting any deviations or non-conformances.

QA manager ,QA validation, Qms , Injection and osd both

The QC manager must have a minimum of 12 years of experience in a pharma QC lab.He/she must have hands-on experience in operation of HPLC, GC, IR, UV and other instruments used in pharmaceutical analysisResponsible for managing the QC laboratory in accordance with cGMPand GLP requirements. The Manager must be able to manage and lead a team of QC analysts in order to maintain smooth running of the laboratory. He will have to supervise regular testing on the incoming raw material, bulk and semi-finished product and finished product.Maintain regularity of testing and timely release of test reports.

Skill Set for QA Manager (Pharmaceutical Company)1. Technical Knowledge: Good Manufacturing Practices (GMP): Comprehensive understanding of GMP regulations and guidelines. Regulatory Compliance: Knowledge of regulatory requirements and standards (e.g., FDA, EMA). Quality Control (QC) Processes: Proficiency in developing and implementing QC tests and procedures. Validation and Qualification: Expertise in validation processes (e.g., equipment, process, cleaning validation). Documentation: Ability to maintain accurate and thorough QA documentation, including SOPs and batch records.2. Analytical and Problem-Solving Skills: Root Cause Analysis: Ability to conduct thorough investigations to identify the root cause of quality issues. Risk Management: Proficiency in risk assessment and management techniques. Data Analysis: Strong skills in analyzing QC test results and other data to make informed decisions.3. Leadership and Management: Team Leadership: Ability to lead, mentor, and develop a QA team effectively. Project Management: Skills in managing projects, timelines, and resources efficiently. Decision-Making: Capable of making sound decisions under pressure and in a timely manner.4. Communication and Interpersonal Skills: Written Communication: Strong skills in writing reports, SOPs, and other QA documentation. Verbal Communication: Effective communication skills for presentations and interactions with regulatory bodies, management, and cross-functional teams. Interpersonal Skills: Ability to build and maintain positive relationships with colleagues, regulatory authorities, and other stakeholders.5. Attention to Detail: Accuracy: Ensuring all QA activities and documentation are accurate and precise. Thoroughness: A meticulous approach to quality checks, audits, and compliance activities.6. Continuous Improvement: Innovation: Ability to identify areas for improvement and implement innovative solutions. Best Practices: Keeping

Hiring for 842 Urgent opening For Quality Control Engineer Jobs in Bhiwadi, Greater Noida, Haridwar, with minimum 3 Years Experience,Required Educational Qualification is : Higher Secondary,Secondary School,Diploma with Good knowledge in Quality Check, wire and cable etc.

We are looking for 2 Quality Assurance Inspector Posts in Haridwar Road, Dehradun,Quality Assurance Incharge,Quality Analyst, with deep knowledge in Quality Control, Quality Assurance Incharge,Quality Analyst and Required Educational Qualification is : Higher Secondary, Secondary School, Diploma

Systematic planning and preparation of product labels, handling and distribution of product BOMs SOP and specification sheets.Process control to eliminate deviation in FGs.Knowledge of QMS principles / GMP requirements in a Pharma industryKnowledge of shop floor activities and man managementShould have robust knowledge of FSSC 22000 & FSSAI regulationsKnowledge of analytical techniques and operation of basic instruments used in quality function of a Pharma process industryPersonal Attributes:Able to communicate and motivate coherently (both written & verbally)Using problem solving skills and root cause analysis to resolve and/or mitigate operational issuesGood supervisory, planning & training skillsHigh level of integrity and characterReady to work in rotational shiftSelf-starter and able to anticipate work requirementsFlexible to change schedule and hours of work to meet the needs of the plantAbility to undertake and perform duties to a satisfactory level in a busy work environment

Testing and InspectionDefect IdentificationData Analysis

We have vacancy for 6 Quality Control Analysts in Rudrapur, Uttarakhand, Freshers can also apply. Educational Qualification : B.Sc, B.Pharma, M.Pharma, M.Sc Skill Chemical analysis, Instrumental analysis, Sample preparation. Equipment maintenance. etc.HPLC: 2 analystsGC: 2 analystsIR: analystsCandidates with prior experience in pharmaceutical quality control environment will be preferred.Send Resume @7861999933Email At toscrecruitments@gmail.com

Job Openings for 1 Pharma Quality Assurance Head Job with minimum 8 Years Experience in Rudrapur Pantnagar, Udham Singh Nagar Educational qualification of : B.Pharma/ M.Pharma/ M.Sc Must Have Experience of Tablet / Capsules / Liquid Orals / Ointments / Dry Powder Injections. etc.1. Developing and Implementing Quality Systems.2. Ensuring Regulatory Compliance as per CDSCO norms.3. Quality Control Management.Send Resume @7861999933Email id: toscrecruitments@gmail.com

Systematic planning and preparation of product labels, handling and distribution of product BOMs SOP and specification sheets.Process control to eliminate deviation in FGs.Knowledge of QMS principles / GMP requirements in a food industryKnowledge of shop floor activities and man managementShould have robust knowledge of FSSC 22000 & FSSAI regulationsKnowledge of analytical techniques and operation of basic instruments used in quality function of a food process industryPersonal Attributes:Able to communicate and motivate coherently (both written & verbally)Using problem solving skills and root cause analysis to resolve and/or mitigate operational issuesGood supervisory, planning & training skillsHigh level of integrity and character Ready to work in rotational shiftSelf-starter and able to anticipate work requirementsFlexible to change schedule and hours of work to meet the needs of the plantAbility to undertake and perform duties to a satisfactory level in a busy work environment

Essential Duties & Responsibilities:Overall supervision of performance of QC officers, QC supervisors & Hygiene supervisors.Monitoring the CCPs and OPRPs and documentation of the same.Ensuring plant sanitation and pest control programs.Training to different level of employees on HACCP, GMP, GHP.Preparation of Weekly Shift schedule of QC officers, QC supervisors & Hygiene supervisors.Assisting in Vendor audit.Assuring RM & PM inspection before unloading.Timely procurement of hygiene chemicals, protective gears and cleaning accessories for the plantcleaning.Maintaining Data log of customer complain.JD inclusions :-FSMS and has Lead auditor certificate along with experience in FSMS implementation,-Candidate from Beverages /Dairy and other streams can be considered provided they aware ofFSMS( Food Safety Management System)Key Result Areas:Statistical process control of FGs.100 % compliance of CCPs and OPRPs.Zero pest incidence in the plant.Personal Attributes:Good presentation skills & written and oral communication skillsStrong Leadership skillsHigh level of integrity and characterDesire to succeed in a competitive environmentStrong customer service focusTeam builder installing trust and respectSolid interpersonal skills and ability to build long term relationships and trust

Systematic planning and preparation of product labels, handling and distribution of product BOMs SOP and specification sheets.Process control to eliminate deviation in FGs.Knowledge of QMS principles / GMP requirements in a food industryKnowledge of shop floor activities and man managementShould have robust knowledge of FSSC 22000 & FSSAI regulationsKnowledge of analytical techniques and operation of basic instruments used in quality function of a food process industryPersonal Attributes:Able to communicate and motivate coherently (both written & verbally)Using problem solving skills and root cause analysis to resolve and/or mitigate operational issuesGood supervisory, planning & training skillsHigh level of integrity and characterReady to work in rotational shiftSelf-starter and able to anticipate work requirementsFlexible to change schedule and hours of work to meet the needs of the plantAbility to undertake and perform duties to a satisfactory level in a busy work environment

Core ResponsibilitiesSafety & Compliance Testing: Oversees destructive and non-destructive testing (impact absorption, penetration, and chin strap retention) to verify compliance with standards like DOT, ECE, SNELL, or ISI.Material & Component Qualification: Inspects incoming raw materials like polycarbonate, fiberglass, EPS (expanded polystyrene), and visor plastics for durability and defect prevention.Process & Quality Control: Monitors production lines (molding, painting, assembly) using Statistical Process Control (SPC) to ensure consistency and prevent manufacturing flaws.Failure Analysis: Performs Root Cause Analysis (RCA) and uses methodologies like (8D) (Eight Disciplines) or FMEA (Failure Mode and Effects Analysis) when a batch fails testing or a safety flaw is identified.Defect Documentation & Traceability: Maintains exhaustive documentation for inspection, testing, and supplier audits to ensure complete product traceability.Continuous Improvement: Works alongside design and production teams to enhance aerodynamics, ventilation, and comfort while optimizing manufacturing efficiency and minimizing waste.Key Skills RequiredDeep understanding of ballistic, impact, and mechanical physics.Knowledge of Quality Management Systems (QMS), such as ISO 9001 and IATF 16949.Proficiency in data analysis, statistical methods, and Quality Control software.Strong communication and problem-solving skills for cross-functional collaboration.

Tablets, capsules, ointments, oral liquids, dry powder injections and cosmetics. Manufacturing Exp.