261 Finished Products Jobs - Page 8

BAPS SWAMINARAYAN HERBAL CARE is looking for QC/QA Executive to join our dynamic team and embark on a rewarding career journey You will also be responsible for identifying and resolving quality-related issues and ensuring that the company's products and services meet the requirements of customers Conduct regular quality audits to identify and resolve quality-related issues Develop and maintain quality metrics to track performance and identify areas for improvement Manage the documentation process for quality assurance procedures, including the creation and maintenance of standard operating procedures (SOPs)

Appidi Technologies Pvt Ltd is looking for QC Engineer to join our dynamic team and embark on a rewarding career journey Develop and implement quality control plans, procedures, and documentation based on industry standards and customer requirements Perform inspections and tests on raw materials, components, and finished products to ensure compliance with quality standards Conduct root cause analysis to identify and resolve quality issues, and implement corrective and preventive actions Collect and analyze quality data, generate reports, and provide recommendations for process improvements Collaborate with production, engineering, and other departments to resolve quality-related problems and implement quality improvement initiatives Train and educate staff on quality control procedures and best practices Monitor and audit production processes to ensure adherence to quality standards and specifications Participate in supplier evaluations and audits to ensure the quality of purchased materials and components Stay updated with industry standards, regulations, and advancements in quality control practices Participate in quality management system (QMS) activities, including internal audits and compliance assessments

Experience: 2-3 years in Color Cosmetics Production Job Description: Cherry Cosmo, a leading cosmetics manufacturer, is seeking a talented Production Chemist specializing in Color Cosmetics to join our dynamic team. The ideal candidate will have 2-3 years of hands-on experience in color cosmetics production, with a passion for innovation and quality. Responsibilities: Formulation and development of color cosmetics products, including but not limited to lipsticks, eyeshadows, and blushes. Conducting stability tests, compatibility tests, and quality control assessments on raw materials and finished products. Collaborating with cross-functional teams including RD, production, and quality assurance to ensure product integrity and compliance with regulatory standards. Troubleshooting production issues and recommending process improvements to enhance efficiency and product quality. Maintaining accurate records of formulation data, batch records, and regulatory documentation. Requirements: Bachelor's degree in Chemistry, Cosmetic Science, or related field. Proven experience (2-3 years) in color cosmetics production within a manufacturing environment. In-depth knowledge of cosmetic raw materials, formulation techniques, and manufacturing processes. Familiarity with regulatory requirements (FDA, EU, etc.) for cosmetics manufacturing preferred. Strong attention to detail and ability to multitask in a fast-paced environment. Excellent communication skills and ability to collaborate effectively with cross-functional teams. Self-motivated with a proactive approach to problem-solving.

We are seeking a skilled CNC Operator to join our team and contribute to the precision machining of components and parts. The ideal candidate should have experience in operating computer numerical control (CNC) machines and be familiar with machining processes. As a CNC Operator, you will play a vital role in ensuring the production of high-quality components that meet our company s standards of accuracy and efficiency. Responsibilities: Set up and prepare CNC machines for operation, including loading materials and tooling. Program CNC machines by entering the required codes and specifications. Perform routine maintenance on CNC machines to ensure their optimal performance. Monitor the machining process, making adjustments as necessary to maintain product quality. Inspect finished products to ensure they meet design specifications and quality standards. Troubleshoot and address issues with CNC machines, tools, or materials. Maintain a clean and organized work area, following safety guidelines and protocols. Document production data and maintain records of machining operations. Collaborate with team members to optimize production processes and meet production goals. Adhere to all safety regulations and company policies to ensure a safe and efficient work environment.

Role & responsibilities 1. Raw material sampling 2. Testing of: a. Raw Materials, b. Packing Materials, c. In-Process, Finished Product and d. stability samples 3. Analytical Method transfers (Including API and FP) 4. Calibration of QC instruments 5. Documentation (Preparation od Specifications and MOA etc.,) Preferred candidate profile Candidate should be from OSD manufacturing with 4 to 6 years of experience Should be good in communcation including Kannada Early joiner will have more preference

Role & responsibilities Responsibilities: - Oversee and manage quality control processes and procedures within the organization - Develop and implement quality control standards and guidelines - Conduct regular inspections and audits to ensure compliance with quality standards - Analyze data and trends to identify areas for improvement and implement corrective actions - Collaborate with cross-functional teams to address quality issues and drive continuous improvement - Train and mentor QC staff to ensure adherence to quality control protocols - Prepare and maintain documentation related to quality control activities - Participate in regulatory inspections and audits as needed

As an Associate Video Editor in the Creative Department at INTERVAL, your role is vital in craftingfinished products that align with the companys creative vision and brand guidelines This involvesassembling recorded raw material into high-quality videos for various purposes, collaborating withthe creative team, and ensuring the final output meets the desired style and tone q

Job Description Summary Manage manufacturing activities and functional sections of the manufacturing department according to the assigned mission and production plans. Organize work assignments, guide, and oversee the staff in the manufacturing department to ensure quality and timely production. Manage all people, machinery, equipment, finished products, unfinished products, and materials in the factory. Roles and responsibilities Implement and control the manufacturing schedule of the projects Review and adjust the schedule where needed. Determine the human resources required and submit the hiring request. Manage human and material resources to meet production targets. Make decisions about equipment use, maintenance, modification and procurement. Develop and implement standard operating procedures for production operations. Ensure that standard operating procedures are adhered to. Ensure implementation and adherence to health and safety procedures. Monitor quality standards of products. Implement and enforce quality control and tracking programs to meet quality objectives. Analyze production and quality control to detect and correct problems. Determine and implement improvements to the production process. Prepare and maintain production reports. Monitor and review the performance of staff and organize necessary interventions for improvement. Estimate production building costs. Train and coach manufacturing members. Plan and layout manufacturing floors. Coordinate with relevant departments to maintain production operations or adjust manufacturing plans. Manage all machinery, equipment, materials, finished products, and semi-finished products in the manufacturing department. Select and train key department members. Periodically review and evaluate the quality of employees in the department. Implement 5S activities, safety measures, and fire/explosion prevention strategies to ensure workplace safety. Develop and implement relevant ISO processes. Manage the OHSMS ISO 45001. Communicate and guide manufacturing staff on company policies and regulations. Qualifications Qualifications Education : Bachelors degree, management, engineering, industrial technology. Experience : 10 years of experience in hi-tech production and semiconductor equipment manufacturing processes and techniques. Proven work experience as a Manufacturing Manager.

Participate in client calls and understand the quality requirements both from process perspective and for targets Identify a method to achieve the quality targets and implement the same in consultation with operations manager / Team Manager Identify errors with high Inspection efficiency Provide face to face feedback and also send emails with the type of errors etc. on daily basis as per protocol Ensure correction of the error by the respective Operations associate Coach employees to minimize errors and improve performance Provide inputs to the training team on common mistakes made to enhance training curriculum Test files/batches for new clients/processes to be processed as part of familiarization Generation of QA reports on a daily basis Attainment of Internal & External SLA as per Process Defined. Meet and exceed inspection efficiency score, calibration score, knowledge and skills score, inspection productivity rate and any other appropriate metrics Record identified errors. This is an organizational record & can be used by the organization as it deems fit Strict adherence to the company policies and procedures. Extensive Quality experience Audits, Coaching & training as per process defined. Min of 1.5 Yrs of Professional and Relevant Experience Sound knowledge in Healthcare concept. Critical problem solving and issue resolution Must have Good Product and Process Knowledge Must have good analytical and judgmental skills Quality Feedback/Refresher sessions Prepare and Maintain Quality status reports

The Quality Control Inspector is responsible for ensuring that all products and services meet the companys quality standards. This includes inspecting incoming materials, finished products, and production processes to identify and prevent defects. The Quality Control Inspector also works with other departments to identify and implement quality improvement initiatives. Responsibilities Inspect incoming materials, finished products, and production processes to ensure compliance with quality standards Identify and report defects to the appropriate personnel Investigate and resolve quality-related problems Develop and implement quality improvement initiatives Collaborate with other departments to ensure the quality of products and services Maintain quality control records and documentation Qualifications Freshers or Experience who willing to work in quality control Knowledge of quality control principles and practices Experience with inspection equipment and procedures Ability to read and interpret engineering drawings and specifications Strong analytical and problem-solving skills Excellent communication and interpersonal skills Note Willing to work in a manufacturing environment

Inspect raw materials and finished products to ensure they meet quality standards. Conduct tests and analyses on resin formulations. Document and report quality issues and implement corrective actions. Collaborate with production teams to ensure consistency and quality in manufacturing. Develop and maintain quality control processes in compliance with industry standards. Eligibility criterion : bachelors degree in chemistry or related field, with relevant experience

Candidate must have experience from chemical manufactiring industry.

Urgent openings for Helpers Location : Nalasopara E, Highway Job Details : Finishing, Fitting, Box Packing, Soldering , Material Movement Job timings : 8am -8pm ( 12hr duty) Salary 13-15k per month

Testing and release of Raw material, packing material and miscellaneous material samples. To maintain reserve sample as per SOP. Preparation of specifications of raw materials, packing material, in process and finished products and stability protocol as per requirement. Preparation of study protocols with respect to laboratory. Sampling of Raw material, packing material and miscellaneous material samples and maintain reserve sample as per SOP. Preparation of volumetric solutions, reagent solution, working standards and maintain records. To perform water analysis as per specification, SOP and GTP. To maintain daily water analysis trend record. To prepare and maintain Laboratory reagent and volumetric solution as per SOP. To keep neat and cleanliness at workplace and follow the good laboratory practices in the laboratory. Testing and release of in process, finished product, standards, and stability samples. To keep update of instruments logbooks and to record the data in Laboratory Notebook during testing. To perform the calibration, Maintenance of all instruments/equipment s as per respective schedule. To attain and complete self- training record. Preparation of indents as per the materials/product requirements. To prepare COA of various product/material as per requirement whenever required. Responsible to share the login credentials with new joiners. To ensure that employees in the department are trained as per the function mapping before work. To upload training copy of new/ revised SOP To ensure training and training related activities for the Department. To ensure the regular updating of Ad hoc/Classroom training details in training software. To generate re-training of any SOP for an employee/s as and when required Submit the employee training files to training cell in case any employee left or no longer with the organization. Responsible as a Department training coordinator (DTC) for the QCC Department Initiate AIMS Requisition for creation, modification, removal, addition, or employee inactivation in AIMS Software. Preparation and review of QC related SOPS. Preparation of general test procedures, method of analysis, specification as per requirement of raw material and packaging material. To initiate and review of A) Change controls B) Out of specifications C) Deviations

Long Description 1 Exposure to perform the testing of Inprocess, Finished product, Stability and Cleaning validation samples etc. 2 Having knowledge of Analytical Instruments to perform the testing by HPLC, GC, UV, IR, KARL FISCHER etc. 3 Having Analytical testing skills to perform the MDI/DPI Products test like Assay, APSD, DDU, RS, Spray Pattern, FPM and physical testing etc. 4 Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation. 5 Exposure of Stability sample management & Regulatory Audits. 6 Exposure of Analytical method transfer, Analytical method validation / Verification activity. 7 Knowledge of GLP and Good documentation Practices. Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence Education Graduation in Pharmacy Work Experience 5 to 8 years

Responsible for overall functioning of stores. responsibility will involve Material Receipt, Storage & Issue, Inventory Management, Service PO's, AMC's, Documentation, Scrap Disposal & MIS.raw materials.daily basis for the receipt of chemicals. Required Candidate profile Liaise with Accounts Payable Department to ensure accurate and timely payment of invoices, as necessary for the business with the supplier.Knowledge of ERP system, making all entries in ERP system.

Job Responsibilities are not limited: Overall responsibility of raw material, finished goods & engineering stores. To ensure the receipt and proper storage of material. The safe practices in Stores. Must have the knowledge of MSDS & other EHS. Required Candidate profile Knowledge of NDPS Act, GST and Excise is must. Develop the talent of self & team in the WH related activities primarily. To maintain practices, records & systems as per cGMP.

- Make amendments in specifications & work instructions as per QMS (Quality Management System) - Ensure testing of materials are carried out as per quality plan and SOP - Manage the non-conformity of products with proper resolutions and put forward the deviations of results to immediate superiors - Ensure timely calibration, repair & preventive maintenance of all the LAB equipment - Provide (OJT-On job training) to the team - Ensure good housekeeping standards are met in the laboratory - Follow BBS (Behaviour based safety) to maintain safety culture at workplace - Maintain "control samples" for as a part of material verification if required by the concerned customer/party after the delivery and handle complaints regarding quality deviation in material - Arrange, handle vendor audits and comply with the requirements & findings - Facilitate/verify SAP entries of COA (certificate of analysis) for exports - Manage AMCs (annual maintenance contract) for all LAB wares - Coordinate with external vendors to carry out analysis of various samples as and when required as a part of cross verification of the quality Turn on screen reader support

Role & responsibilities You will be working as Head QC for USFDA approved Formulation Plant at Baddi and will be responsible for: 1. You will be responsible for Establish the project goals and priorities. 2. You will be responsible for team management and leadership. 3. You will be handle 50 Plus Products and handle business turnover. 4. You will be reporting to Head Quality at Plant level at Baddi. 5. You will be good in handling regulatory audits starts to end. 6. You will be good in team leader to guide and trained and developed team members. 7. You will be good in team management and monitoring team Desired Candidate Profile 1. Candidate should be B.Pharm/M.Sc. Organic Chemistry or Ph.D in Organic chemistry. 2. Candidate should be 20-25 years of experience in Pharma Formulation industry with USFDA Approved Company in Quality Control department . 3. Candidate should be handle a team size of persons in pharma companies. 4. Candidate should be good in Management and improving production and quality and quantity of company. Preferred candidate profile

Job Role: QC Assistant Job Location: Jaipur Education: BSC / MSC Experience: 1-2 Years About Brand: Minimalist (https://www.beminimalist.co) is a science-backed Indian skincare brand built on the core values of efficacy, transparency, and comprehensiveness. Known for its ingredient-first approach, the brand formulates high-performance skincare products using proven activities and clean formulations. The company believes in creating high-quality products using best-in-class ingredients at its own manufacturing facility. Minimalist empowers consumers with knowledgeclearly stating what goes into each product and whyso they can make informed choices. With a commitment to 'Hide Nothing,' the brand champions authenticity and honesty in skincare, creating solutions that work, without the fluff. With a robust portfolio of 60+ SKUs spanning Skincare, Haircare, and Bodycare, the brand is rapidly expanding its footprint. Focused on enhancing product availability, it is strategically deepening its penetration while strengthening both Modern Trade (MT) and General Trade (GT) channels in India. The brands global presence now extends across 15+ countries, including key markets such as the UK, USA, UAE, Malaysia, Indonesia, Germany, France & Italy. Roles and Responsibilities: Assist in the collection, labeling, and preparation of samples for analysis. Ensure proper storage and documentation of samples to maintain traceability. Perform regular cleaning and sterilization of laboratory equipment and workspaces. Dispose of waste materials following established safety protocols. Prepare reagents and solutions as per standard operating procedures (SOPs). Monitor inventory levels and assist in ordering laboratory supplies. Calibrate and maintain laboratory instruments to ensure accurate results. Maintain accurate records of all QC activities, including test results and equipment maintenance logs. Adhere to all laboratory safety guidelines and regulatory requirements. Qualifications: Bachelors degree in Microbiology, Chemistry, Biotechnology, or a related field. Minimum of 1-2 years of experience in a laboratory setting, preferably in quality control. Familiarity with laboratory equipment and basic analytical techniques. Strong organizational skills and attention to detail. Proficiency in using laboratory information management systems (LIMS) is a plus. Excellent communication skills and the ability to work collaboratively in a team environment.

Key Responsibilities Lead on-site Quality Control activities for agrochemical production at the plant. Ensure in-process and finished product quality meets regulatory and internal standards. Oversee sampling, testing, and analysis of raw materials, intermediates, and final products. Maintain calibration and performance of lab equipment (HPLC, GC, etc.). Prepare and manage documentation for audits, compliance, and certifications (ISO/GLP). Drive continuous improvements in plant QC practices and team efficiency. Qualifications 5-7 years of QC experience in a plant/factory setup within the agrochemical industry. Strong knowledge of analytical methods and safety protocols.

Job Title: Technical Manager – Manufacturing (Beverages) 1. Job Purpose: To oversee and manage the day-to-day operations of the manufacturing plant, ensuring alignment with long-term strategic goals. The role involves driving operational efficiency, leading cross-functional improvements, and optimizing budgets to control costs while maintaining quality and delivery standards. 2. Key Responsibilities: 2.1. Plan, organize, and manage daily plant operations to meet production targets and business objectives effectively. 2.2. Monitor and improve overall equipment and plant capacity effectiveness by optimizing volume output, enhancing asset flexibility, controlling operational costs, and maintaining quality benchmarks. 2.3. Maintain and manage production schedules, ensuring teams are empowered and held accountable for execution under your direction. 2.4. Proactively manage factory capacity, taking into account workforce availability due to holidays, leave, and other absences to avoid production disruptions. 2.5. Champion all Health & Safety initiatives, ensuring full compliance with company standards and promoting a culture of zero harm. 2.6. Ensure the consistent implementation of company policies, procedures, and operational goals across the plant, fostering a culture of accountability and continuous improvement. 2.7. Collaborate with Quality Assurance and Compliance teams to ensure all finished products meet customer expectations and regulatory standards. 2.8. Oversee the timely and accurate manufacturing and delivery of products, ensuring adherence to customer order requirements in both volume and timing. 2.9. Lead daily production meetings to review performance, align team expectations, and address any operational issues or staff concerns. 2.10. Support and develop team members through regular Performance Development Reviews (PDRs) and performance management tools, fostering a culture of professional growth and capability enhancement.

: 1. To make strategy and planning for Quality Assurance and Quality Control for smooth and effective functioning for ODF, LVP Hormone block. 2. To strategize and plan for continual improvement of GMP aspects in the facility, systems, and procedures. 3. Budgeting for Capital expenses and Operating expenses. Plan and manage departmental activities in accordance with agreed budgets and time scale. To manage department performance against agreed targets and budgets within policies and standards. 4. Setting Goals for QA and QC, monitoring and guiding them to complete the KRA. Leading and monitor performance (in relevant area) according to agreed standards and take necessary action to communicate/ advise / assist according to performance level. 5. Work across all disciplines (e.g., Manufacturing, Warehouse, Engineering, etc.) to ensure that the Company maintains a state of readiness for inspection by regulatory agencies / internal/ external. 6. To ensure timely response against observation of Corporate Internal audits, Customer audits Regulatory audits, and ensure implementation of corrective preventive action on observations. 7. To ensure implementation and execution of Abbott Policies and Procedures at site. 8 . To ensure continuous improvement at site with respect to Quality systems and processes. 9. To ensure self-inspection/internal audit and external audit as per schedule/ Plan and regularly appraise the effectiveness/ applicability of the Pharmaceutical Quality System. 10 . To ensure timely submission of Regulatory Documents and filing and their compliance. 11. To ensure Cyber Security aspects are implemented at site. 12 . To develop, ensure, implement, and maintain a GXP compliant document control system. 13. To ensure that Batch Release is done as per in-house policies and procedures as well as the other other applicable regulations and guidelines. 14. To establish ensure approval / rejection of starting materials, packaging materials, intermediate, bulk finished products as per validated methods / Pharmacopeia methods / In-house Method for the site. 15 . To ensure Product recall is do ne as site procedure and further coordination with Regional Quality for recall authorization. 16 . To ensure that Review Meet is done with the involvement of senior management, to identify the opportunities for continual improvement of products, process, and system. 17 . To ensure Quality Risks Management i.e., risks to the quality of the product based on scientific knowledge, experience with the process are mitigated and communicated to senior management as well as linked with the protection of the patient. 18 . To approve documentation, as applicable, at site. 19 . To approve / reject/extension of Exception/ Deviations and Change Controls activities. 20 . To ensure training and effective implementation of current Good Manufacturing Practices. 21 . To ensure Good Documentation Practices and Good Laboratory Practices at the site. 22. To ensure that documents are updated and amended as per new pharmacopoeias and regulatory guidelines.

Job Summary : Experienced QC professional with 8-10 years in pharmaceutical quality control and compliance. Responsible for preparing specifications, test methods, and maintaining GMP, GDP, and GLP standards. Supports regulatory affairs, handles deviations, OOS, and change controls, and reviews analytical reports. Proficient in SOP creation, method updates, and team training as per cGxP and regulatory guidelines. Responsibilities: Preparation and updating specifications and test methods to ensure compliance with statutory and company standards Preparation of specification for input materials, intermediates, active pharmaceutical ingredients, finished products and stability products to ensure compliance with company standards. Maintenance of GMP, GDP & GLP in work To maintain Quality Control documents as per statutory requirements Updation and analysis of methods and analysis as per current cGCPL guidelines and regulatory requirements. Support to Regulatory affairs departments, as required Adherence to cGMP, ISO 14001, FSSC 2200 and HACCP norms and guidelines as required Preparation of SOP and related documents Initiating and involving in the incident, deviation and OOS. Initiating change control and edit form to make any changes required in the specifications, standard testing procedures, raw data sheets and SOP and closing the same Review and approval of analytical reports as required Training of concern persons related to quality documents as required Education Qualification: MSc Chemistry Years of Experience : 8 to 10 Years

Oversee and execute analytical testing of raw materials, in-process samples, and finished products. Ensure compliance with cGMP, GLP, and regulatory guidelines. Review and approve analytical data, test results, and documentation. Troubleshoot analytical instruments like HPLC, GC, UV, and FTIR. Support method validation, stability studies, and regulatory audits. Implement quality improvement initiatives and ensure data integrity