261 Finished Products Jobs - Page 4

Role & responsibilities Responsibilities Preparation of SOPs, Protocols, Quality Documents Etc. Document Quality Assurance activities and create Audit reports Artwork checking & Approval Preparation of regulatory documents Draft preparation for product permission COA preparation Raw material, finish TR preparation All validation document prepn. All calibration documents prepn. AMV prepn. Specification & STP Prepn. As per Pharmacopoeia . Address and discuss issues and proposed solutions with superiors. Requirements and skills Proven work experience as a Quality Assurance officer or similar role Working knowledge of tools, methods and concepts of quality assurance Solid knowledge of relevant regulatory standards Good communication skills, both verbal and written Excellent data collection and analysis skills Strong attention to detail Computer Savy, knowledge of Ms OFFICE, EXCEL, PowerPoint etc. Working experience in Software like Pharma suit, Pharma cloud, ERP etc. Preferred candidate profile

Job Summary: We are seeking a dedicated and detail-oriented Quality Control professional to perform wet lab testing, maintain lab compliance, and ensure the accuracy and integrity of analytical data. The role involves hands-on testing, documentation, and adherence to GLP, cGMP, and internal quality standards under the supervision of senior QC personnel. Key Responsibilities: Implement SOPs, STPs, and follow department procedures accurately Analyze samples assigned by HOD/seniors and record results in prescribed formats Prepare and maintain reagents, working standards, and reference standards Store and manage control samples with proper documentation Maintain testing documentation and ensure adherence to GLP in the QC lab Calibrate laboratory instruments as per schedule and maintain records Operate and maintain wet lab instruments (e.g., pH meter, Fluoride meter, Polarimeter, IR, UV, etc.) Assist in the investigation of deviations, OOS, complaints, and CAPA Supervise cleaning and upkeep of glassware and ensure lab hygiene Perform product sampling and analysis for intermediates, semi-finished, and finished products Support in the preparation of specifications and STPs under senior guidance Review QC documents and records for completeness and accuracy Execute all other tasks assigned by seniors or departmental heads Qualification : MSc Chemistry Experience : 1-4 Years

Job Summary - Assistant Manager - Quality Control The Assistant/Deputy Manager - Quality Control is responsible for overseeing and managing all QC operations to ensure timely, accurate, and compliant testing of raw materials, intermediates, finished products, and stability samples. This role supports the HOD in planning, executing, and supervising laboratory functions and ensures adherence to cGMP, GLP, and applicable regulatory standards. Key Responsibilities: Supervision of day-to-day QC lab operations Acting as HOD designee in their absence Timely testing and release of raw materials, intermediates, and finished products Implementation of QMS and handling of deviations, OOS, OOT, and complaints Compliance with ISO 9001, FSSC, Halal, Kosher & cGMP standards Review and update of product and material specifications Validation and revalidation of analytical methods Training of analysts on SOPs, GLP, GDP, and lab techniques Execution and monitoring of stability studies Instrument qualification, calibration, and maintenance Review and approval of analytical reports and lab documentation Leading and supporting internal/external audits Coordination with QA and Regulatory Affairs departments Implementation of pharmacopeia updates and regulatory requirements Driving continuous improvement and supporting special projects Qualification : B Pharma / MSc Chemistry Experience : 7-12 Years

Job Description :- QC Executive Scicore Nutra Private Limited is a state-of-the-art facility, located in Sanand Gujarat, is dedicated to producing high-quality nutrition products that are safe, effective, and meet the highest standards of quality. Our team of experts is committed to ensuring that every product we manufacture is produced with the utmost care and attention to detail. At our manufacturing unit, we use only the best raw materials and employ advanced manufacturing processes to ensure that our products are of the highest quality. We also adhere to strict quality control measures to ensure that every product meets our rigorous standards. This starts with doing a rigorous vendor qualification as well as testing of all raw materials supplied by these vendors for every batch. We do in-house stability studies to make sure our products last the full shelf life and give the best results to our customers. Our goal is to provide our customers with nutraceutical products that promote health and wellness, and we are committed to using science-backed ingredients and formulations to achieve this goal. We are also committed to continuous innovation and improvement and are always looking for new ways to enhance our products and processes. Benefits Provided: 1 Free Air-Conditioned Transportation to the Factory 2 Paid Leave 3 Tea/Coffee & Canteen Facility 4 Accident Insurance 5 Provision for Bonus & Gratuity 6 Training programs for professional advancement 7 Progressive work environment conducive to personal and professional growth Job Title - QC Executive Role & Responsibility: 1.To follow and ensure Good Laboratory Practices. 2.To perform the work according to work allotment. 3.To follow good documentation practices while making entries in Documents and records. 4.Make sure that materials are appropriately tested and results are reported. 5.To perform the Initiation and review of any change related to the department. 6.Make sure that deviations and Out of Specification Investigation are investigated and solved it with CAPA. 7.To perform the Preparation and review of all SOPs related to department, Specification and test procedures. 8.Preparation and execution of validation protocol for method validation and Analyst validation. 9.SOP Review, revision and Harmonization. 10.To perform the new products analysis method, review and arrange for necessary Corrections in test procedures. 11.To perform the Analytical method, transfer activity and report protocol review. 12.Arranging AMC of Instrument and servicing. 13.To perform the Instrument spare procurement and maintenance. 14.To Review of periodic calibration of Instruments. 15.Reference Standard procurement and management. 16.Monitoring the activity of working standard preparation and managements. 17.In- house training of Analysis and training of corporate training modules. 18.Review Analyst Qualification/ certification. 19.Departmental correspondence, Internal and external Audit compliance action. 20.Co-ordination with maintenance Dept. for QC Dept. utilities and its Maintenance. 21.To Review Qualification of Laboratory Instruments Equipment. 22.Handling Change control, OOS, OOT, Incident and deviation & CAPA. 23.Monitoring stability sample analysis, Microbiology Lab record review. 24.To check pharmaceutical addendum & supplement to make necessary amendment in the specification, whenever change in the Pharmacopoeia is observed. 25.Co-ordination for SCM related activity with IT and QA. 26.Storage of Laboratory data & records. 27.Instrument Data back up, and software users rights. 28.Arranging for outside testing and calibrations and its report Review. 29.To ensure the Approval and Rejection of Raw Material, Packing Material & Intermediates products. 30.Review of analytical results/data of in-process. Intermediate, water analysis finished API and issue COA for each batch of API. 31.Trouble shooting of the QC Instruments 32.If any additional responsibility assigned by senior. 33.To ensure all QC staff do the performance under GLP 34.Any additional job responsibilities as assigned by HOD. Department :- Quality Control Number Of Positions :- 01 Experience :- 2 to 5yrs Employment Type :- Full Time, Permanent Education UG :- B.SC in Any Specialization PG :- M.SC in Any Specialization Compensation :- As per Industry norms & experience Key Skills :- QC, UV, HPLC, Analytical, Method Development, Wet Analysis, PH Meter, GLP, Stability Analysis, SOP Review

The ideal candidate should have strong knowledge of sportswear products and demonstrate His passion to achieve maintain the quality of products as per brand standards. Job Responsibilities Ensure raw materials and finished products meet specifications through meticulous examination and precise measurement tools. Perform durability, functionality, and safety tests to validate product quality and performance using standardized methods. Maintain detailed records of inspections, noting deviations or defects found to ensure traceability and quality control. Communicate identified defects promptly to supervisors and collaborate on corrective actions for timely resolution. Verify products meet industry standards, company policies, and regulatory requirements by staying updated on quality regulations. Oversee production stages to uphold consistent quality standards and identify areas for improvement in machinery and workflows. Develop and enforce effective protocols to optimize inspection processes and enhance product quality assurance Analyze quality-related customer concerns, identify root causes, and collaborate on solutions to prevent recurrence Ensure adherence to safety protocols during inspections and production activities to promote a secure workplace for all personnel. Requirements Candidate must have a graduation or any equivalent education. Having a bachelors degree can expand your job horizons and earning potential as well Real-time experience in the same domain is preferred Excellent documentation and presentation skills Excellent knowledge of Microsoft Excel, PowerPoint etc. Profound knowledge of quality control standards.

Overall responsibility of Quality Control department (Finished product, in-process, Raw Material, Packaging Material, stability etc. )and Microbiology department. Daily review /Monitoring of Quality Control activities Handling of all Quality Control related matters. In Process Control during batch manufacturing. Overall QC Data management and coordination with corporate team. Handling of Change Control Proposal, Out of Specification, Incidents and Planned Deviations etc. through CAPA track wise software. Well versed with Handling of HPLC, UV and Dissolution Apparatus etc. Preparation & Review of Analytical Method Validation/verification/CMV Protocols & Reports. In depth knowledge of ICH, PIC/S guidelines on AMV. Monitoring implementation of Good Laboratory Practices and ensuring laboratory compliance as per requirements of regulatory guidelines. Coordinate with Manufacturing/Ware house PPIC for planning of testing of required materials. Exposure of Regulatory Audits Review of QC and Microbiology Specifications, Standard testing Procure(STP) and Standard Operating Procedure Investigation of Laboratory events/OOS/OOT/Deviation. Monitoring of Stability studies for the products manufactured at the site as per respective protocols/procedure Review and approval of analytical testing/Microbiology testing reports

Manage the implementation of Hikal policies and maintain the discipline standards with the organization as desired / acceptable by the stakeholders. Shall remain prepared for all possible emergency situations and responding to them as per the Emergency Management Plan. No avoidable EHS incidents. Shall be responsible to maintain the high discipline standards within the team members as desired by the organization. Achieve the departmental objectives / targets and Environment Management Plan set by the management. Receipt and verification of all raw materials and packing materials for daily shift production. Shifting and storage of Raw Material, Packing Material and Finished Goods to pre-designated areas at defined storage condition as per specification. Raw materials, packing materials, Intermediates and Finished products reconciliation records updation. Online Batch production and control records and logs updation related to daily shift production activities. All types of work permit and job card management/supervision during the shift hours. Maintaining the equipment and area clean and operate the process in hygienic manner, shop floor housekeeping as per predefined standard operating procedure (SOP). Immediate recording and reporting of any deviations or violation of standard parameters. Work allotment to subordinates and supervisors involved in shift production activities.

Role and Responsibilities: (will include but not be limited to the following) Follow SOP of Packing Ensure All Packing activity must comply with Quality Policy Ensure Packing Material Availability as per Production Plan Scheduling of Manpower Production Plan completion above Target To Sort & Repack market return Goods in time Optimum Utilization Primary Packing Material (Poly Bag) Ensure all SFG to be converted in to FG Ensure Consumption Variance Must be below Target for PPM & SPM No m/c Downtime due to Polybag Sealing, Availability of Printed Polybag. Accurate FG transfer from Packing Dept to Dispatch Line Clearance SOP Strictly to be followed Accurate FG transfer from Packing Dept to Dispatch Training Manpower whenever required ISO Audit & Documentation Follow GMP standards set by company, maintaining 5S and Cleanliness at Online and Offline Packing area and at shop floor Process Improvement To Control the Cost of Overtime Qualifications, Education & Work Experience Requirements Graduate/ Diploma with 3 to 5 years work experience of manpower handling in Packing area Preferred Skills Manpower Handling Data collection and analysis Problem Solving Attention to detail

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control (GMP / GC / LCMS / HPLC) Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits Common Requirements: Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry or related) Sound knowledge of current GMP guidelines (US-FDA, MHRA, EU, WHO) Good documentation, investigation and communication skills Willingness to work in shifts and collaborate with cross-functional teams How to Apply Subject Line: Immediate Joiner Send you updated resume : naidupetahr@aurobindo.com

A dynamic Sr. Purchase Manager with B.E.Civil & with strong experience in Procurement field from Civil Constructions. Should be well worse in leading the department & able to acquire desired out put. Projects purchases etc.etc.

UPLC Knowledge must Pharma Company Exp Required Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials Required Candidate profile Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.

QC chemist For Agro chemical Industry In Saykha, Bharuch, Gujarat Job Title : Chemist Department : Quality Assurance & Quality Control Experience Required : 06-08 years (Agrochemical or Chemical Industry Experience Must) JOB DUTIES AND RESPONSIBILITIES (Please mention in below table) 1 Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples) 2 Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. 3 Using chromatography, spectroscopy, and spectrometer techniques. 4 Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. 5 Conferring with scientists and engineers to analyze, interpret, and develop tests. 6 Writing and preparing standards and specifications for processes, tests, and products. 7 Maintaining laboratory instruments, troubleshooting malfunctions. 8 ensuring compliance with laboratory safety procedures and standards. 9 Strong problem-solving, critical thinking, and analytical skills. 10 Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC. Experience 3 - 8 Years Industry Manufacturing Production Quality Qualification B.Sc, M.Sc Key Skills Pharmaceutical QC Chemist Bharuch Agro Chemical MSC Chemistry GC-MS Agrochemical Chemical Test Procedures UPLC Chromatography Finished Products LCMS Quality Control

Role & responsibilities: 1 Preparation of standard operating procedure with its annexure. 2 Preparation of Specification, standard test procedure of Raw Material, Packing Material, Finished product as per pharmacopeia and in-house methods. 3 Performing instrument qualification and calibration as per schedule. 4Sampling , analysis and review of raw water, purified water, raw material, packing material, finished product and in process sample, stability sample as per Specification with ERP entries 5 Preparation of COA of raw material, packing material, finished product and in process sample and stability study summary sheet ,trend analysis. 6 Maintenance of reference standard, primary standard and Preparation and maintenance of Working Standard. 7 Preparation and standardisation of Volumetric Solution and preparation of reagents. 8 Handling of all instruments and equipments in quality control. 9 Analysis of samples on HPLC,GC,IR and UV 10 Arrangement and maintenance of control sample and stability study sample 11 Sample send to public testing laboratory for analysis and coordination with laboratory for the same. 12 Monitoring the of chemicals and glassware received. 14 Monitoring the disposal of scrap, chemical and reagent waste and left over sample. 15 Calibration of Glassware 16 To follow the Good Documentation Practice and Good Laboratory Practice in the Laboratory. 17 To perform the analysis and Reporting of Water Validation, Method validation, Cleaning Validation and process validation 18 Any other task which is given to you by your senior in case of emergency. Knowledge Require 1. 2-5 years of experience in Formulation Pharmaceutical Plant. 2. Relevant Experience in Pharma formulation plant. 3. Computer proficiency in MS Office, Excel, e-mail and internet function

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials Required Candidate profile Experience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.

Quality Control Chemist / Officer / Manager Candidate Profile: Post Graduate / Graduate in Science Minimum 2 years of experience in relevant field & designation Post Graduate / Graduate in Science Minimum 2 years of experience in relevant field & designation Joining Form Select Applied For Select Applied For Production Chemist / Officer / Manager Marketing Manager Accounts Manager Quality Control Chemist / Officer / Manager

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / B.E. Mechanical / Diploma Printing Packaging Technology with 0 to 2 Years of experience in Production Planning Printing & Packaging Industry. Co-ordinate with Marketing Team regarding orders. Prepare production schedule. Client Communication. Required Candidate profile Create product masters in the software. Co-ordinate with clients regarding orders. Check current inventory. Prepare requisition for raw material. Update production schedule depending upon the output. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 3 to 5 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / B.E. Mechanical / Diploma Printing Packaging Technology with 0 to 2 Years of experience in Production Planning Printing & Packaging Industry. Co-ordinate with Marketing Team regarding orders. Prepare production schedule. Client Communication. Required Candidate profile Create product masters in the software. Co-ordinate with clients regarding orders. Check current inventory. Prepare requisition for raw material. Update production schedule depending upon the output. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 3 to 5 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.Sc. / B.E. Mechanical / Diploma Printing Packaging Technology with 0 to 2 Years of experience in Production Planning Printing & Packaging Industry. Co-ordinate with Marketing Team regarding orders. Prepare production schedule. Client Communication. Required Candidate profile Create product masters in the software. Co-ordinate with clients regarding orders. Check current inventory. Prepare requisition for raw material. Update production schedule depending upon the output. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 3 to 5 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 1 to 3 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Incoming R M Inspection / In process Inspection / Final QC Inspection. Proper record keeping. Required Candidate profile To check the material as per the standard procedure and as per the time frequency. Detect non-conformities. Check the root cause of the non-conformity and take corrective and preventive action. Perks and benefits Negotiable - Depending Upon Candidate & Experience