377 Osd Jobs - Page 5

Roles and Responsibilities ONLY FOR MALE CANDIDATES. Conduct quality control tests on OSD products to ensure compliance with regulatory requirements. Perform IPQA activities such as inspection, sampling, and testing of raw materials, intermediates, and finished goods. Ensure adherence to cGMP guidelines during formulation development and manufacturing processes.

Role & responsibilities Candidate should be handling plant maintenance & Process Maintenance with OSD machines(Granulation, compression, packing and so on.) Preferred candidate profile

Job Summary We are seeking an associate for the Quality Control team responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. Roles & Responsibilities • You will be responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. • You will ensure accuracy of the documentation before submitting it for the Group Leader’s review or uploading online. • You will adhere to safety precautions and procedures during analysis. • Lab safety, following JSA (Job Safety Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized. Qualification Educational qualification: A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field Minimum work experience : 5 to 7 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry Skills & attributes: Technical Skills • Proficient in various analytical techniques, including sampling and analysis of packaging and raw material samples. • Experience with the operation and maintenance of analytical instruments, ensuring proper use and care as per SOPs. • Competent in SAP activities related to sample tracking, documentation, and data entry. • Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications. • Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment). • Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents. Behavioural Skills • Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks. • Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates. • Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities. • Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations. • Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Responsible for formulation and process development of oral immediate-release dosage forms, including oral film and tablet formulations. Troubleshoot and problem-solve unresolved or new formula issue

Studies, and process optimization as per regulatory guidelines (USFDA, EU, WHO). Prepare and review development reports, PDRs, BMRs, MFCs, and technology transfer documents. Collaborate with cross-functional teams (QA, QC, RA, Production).

" Job Title: Head Procurement - Raw Materials (DGM/ GM) Location: Mumbai Reporting to: Commercial Head About the client: PSS has been mandated to hire the Head of Procurement - Raw Materials for a well-established and highly reputed Indian pharma company manufacturing formulations OSD and Injectables. Key Responsibilities: Department: Procurement Raw Materials Location: Mumbai HO Reporting to: Commercial Head Job Responsibilities: Overseeing the sourcing and procurement of Raw Materials for the manufacturing plants. Identifying, evaluating, and developing new vendors by inviting quotations, negotiating, and pricing. Preparing comparison statements, obtaining the necessary approvals, and processing the orders. Obtaining all supportive regulatory documents for filing drug dossiers. Follow up with vendors for dispatch details. Follow up with the Logistics team / CHA for clearance of the material. Preparing the raw material cost estimations for projects based on the requirement. You will be responsible for Vendor development, Vendor Audit, and Ongoing Vendor Management, meeting Quality, Food Safety, and other regulatory requirements of the industry. You will ensure procurement of Quality & quantity on time with a focus on Cost optimization and savings. Educational Qualifications and Experience: MBA in Operations/ Supply Chain with 15 years of work experience in the Procurement of Raw Materials in the Pharma industry. Good understanding of procurement processes in a manufacturing setup, commercial acumen, ability to negotiate, supply chain. Ability to manage internal and external stakeholders of the company. #LI-NV1 ",

Job Description Experience: 7 to 13 years Qualification: B. Pharm / M. Pharm / M. Sc Budget: 12 to 16 LPA Designation: Sr. Executive Required Key Skills: Supply & Planning, Product Management, Should have worked on Kinaxis software, Should be well versed with system, Should have process knowledge of Tablet, Capsule & Injectables. Candidate from OSD/Inject unit is preferred. Should have good interpersonal and communication skills. Job Description: Should co-ordinate with PDL, R&D and quality for integrated plan for exhibit/ Pre-validation batches for next 3M , 12M. Should co-ordinate with Prod for planning execution and updating daily status. Should maintain R Vs C Vs A metrics with actuals and Gap and shall populate the data with all CFT in weekly meet. Should be able to handle procurement plan through SAP with good knowledge to carry out MRP process in SAP, knowledge of Kinaxis will be additional advantage. Should have good knowledge of inventory analysis and management of RM/PM/SFG/FG s with good excel working. Should have basic understanding about machines used in manufacturing processes and its output rate with material and capacity view during prod plan in finalization. Should have strong analytical skill, managing large data basis, excellent problem-solving mindset and inter-personal skill with effective communication and presentation, ready to accept new challenges in defined role. Efficient coordination with procurement, artwork development, CQA, and other relevant stake holders for effective operations. Timely review of all the responsible KRA s and ensure for strong adherence Candidate from Pharma background is preferred. Work Experience 7- 13 yrs experience in Pharma Supply planning Education Graduation in Production Management Post Graduation in Science Competencies Innovation & Creativity Strategic Agility Result Orientation Collaboration Stakeholder Management Customer Centricity Developing Talent Process Excellence

Urgent hiring for Research Scientist / SRA Formulation R&D (OSD) for Roorkee & Gurgaon location Location: Roorkee Department: Formulation & Development (F&D) Industry: Pharmaceuticals OSD & Liquid Job Description: We are hiring a Research Scientist – Formulation R&D for its Roorkee facility . The candidate must have strong experience in formulation development, technology transfer , and scale-up activities for regulated and semi-regulated markets . Key Responsibilities: Execute and support formulation development and scale-up for OSD products Conduct technology transfer from R&D to production Prepare and review MFC, MFR, PDR , and tech transfer documentation Develop and optimize exhibit and validation batches Ensure compliance with regulatory standards for global markets Coordinate with cross-functional teams including QA, Production, and Regulatory Knowledge of bioequivalence/bio study is desirable (not mandatory) Requirements: M.Pharm with specialization in Pharmaceutics (mandatory) 3–6 years of experience in Formulation R&D (OSD) Must have experience working for regulated and semi-regulated markets Strong documentation and project execution Apply at: anupriya.1@walterbushnell.com WhatsApp CV to: 9650111639

Should have minimum 1-3 years of experience in Primary/Secondary/Blister Packaging department

Walk In Drive For Production OSD In Formulation Division @ Burgula Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 10 Years Skills :- Supervisor :- Granulation | Compression | Coating | Cartornator| Packing Operators :- Granulation | Compression | Coating | Cartornator| Packing Division :- Formulation Interview Date:- 10-07-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Venue Location:- Plot No- 42, Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana 502325 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Coating , Granulation , Compression, Capsule Filling , Blister Packing , Cam Cartontor, Hi Cartonator, Primary Packing , Secondary Packing, Documentation. About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries. Evaluation of regulatory authority deficiencies and preparation of action plan accordingly. Also follow up of response documents with concern stake holders. Evaluation and approval of QMS documents, wherever applicable. To update cross functional teams for different regulatory compliance & requirements. Responsible for outlining requirements for labelling, storage and packaging. Review of product development report and QBD concepts. Updating product approval package to plant team. Preferred candidate profile Should Have Formulation Regulatory Affairs Relevant Experience in US/EU/Canada Perks and benefits

1. To prepare & review SOP, BPR, BMR, Protocol. 2. To plan production schedule effectively as per export order & market requirement as per availability of RM/PM. 3. To co-ordinate with cross functional dept to achieve the goal laid down by the mgt. 4. To follow good housekeeping program & maintain proper cleaning of the dept as per cGMP. 5. To give job training to subordinates & workmen. 6. To ensure proper safety, maintenance of machinery & equipment of the dept. 7. To ensure various in-process control checks during the production of the batch as given in BMR & BPR. 8. To do reconciliation after completion of batch activity. 9. To ensure appropriate process validation, equipment qualification & calibration. 10. To identify and report operational as well as maintenance problems to avoid production delay. 11. To have effective control on manpower and machine utilization on daily basis. 12. To guide officers or workers in case of any technical problems or issues. 13. To provide technical input/suggestions towards new product development/improvement in process. 14. To ensure online documentation of BMR, BPR, logbooks, validation, protocols, reports of all production activities. 15. To prepare and send daily production report to the plant head/management. 16. To sent intimation of indent of raw material, packing material. 17. To transfer the finished goods to FG store Dept. 18. To perform various trial batches as per requirements. 19. To co-ordinate with workers, officers, plant head/management for smooth conduct of audit. Perks and benefits

1. To prepare & review SOP, BPR, BMR, Protocol 2. To plan production schedule effectively as per export order & market requirement. Also, availability of RM/PM. 3. To co-ordinate with various production dept to achieve the goal laid down by the mgt. Required Candidate profile 4. To follow good housekeeping program & maintain proper cleaning of the dept as per CGMP. 5. To give job training to subordinates & workmen. 6. Reconciliation after completion of batch activity.

We are seeking an experienced and dynamic Production Manager to lead the end-to-end lifecycle of pharmaceutical and nutraceutical formulations. Hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets, and Protein Powders.

Role & responsibilities : 1 To perform Operation activity of equipment and instruments as per SOP. 2. To affix the status label to equipments, instruments and IPC at each and every processing stage 3. To operate the equipment in safe and effective manner for production processing. 4. To follow and adhere to GDP and cGMP practices. 5.Inspect equipment to identify any replacement, and repairs. 6. Ensure that the equipment are maintained in good and safe working condition. 7. To Perform regular equipment maintenance to ensure production capacity and quality. 8. Identify and report unsafe operations and near misses to supervisor immediately. 9. Perform the activity as per SOP and instruction given in BMR and BPR. 10. To perform balance Calibration and instrument calibration as per SOP Preferred candidate profile: 1. 02- 07 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.

Role : SCCM Administrator Location : Greater Noida OSD & Imaging (SME-Level) Design, maintain, and troubleshoot SCCM OSD Task Sequences. Manage custom Windows image creation and driver injection. Automate imaging processes using MDT or native SCCM features. Handle UEFI, BitLocker integration, and post-deployment configuration. Troubleshoot PXE boot issues, WinPE, and Task Sequence failures. SCCM Administration (L2 Level) Manage SCCM site roles: MP, DP, SUP, WSUS, and fallback status points. Perform client health checks and resolve client communication issues. Monitor and resolve package distribution and application deployment errors. Maintain and configure boundaries, boundary groups, and collections. Administer Software Update Groups and schedule patch deployments. Security & Compliance Work with Endpoint Protection configurations (if applicable). Ensure compliance baselines are implemented and reported properly. Monitoring & Reporting Generate custom SCCM queries and reports (using SSRS/Power BI). Monitor logs using CMTrace and address underlying component issues.

Job Description: Regulatory Affairs Assistant Manager / Manager Injectable & OSD Facility Department: Regulatory Affairs Location: GIDC Ankleshwar Key Responsibilities: Prepare and submit dossiers (CTD/ACTD) for ROW & US markets. Ensure compliance with local regulatory guidelines and GMP standards. Liaise with regulatory agencies and respond to queries promptly. Manage product registrations, renewals, and variations. Monitor regulatory updates and ensure adherence to changes. Support quality audits and review labeling/artwork for compliance .

Preferred Candidate Profile : He should have core experience in Formulation Plant Maintenance, QMS, Instrumentation. OSD Experience is a must. Note: 1.) **Pharmaceutical experience compulsory.** 2.) API/Utility/HVAC experience candidates will not be considered.

Role & responsibilities Responsible for Pre-formulation studies for lab formulation development trials of solid orals, Oral Liquid, injectable, products, and Nutraceuticals product. To design strategy for projects through literature surveys. Respective API characterization, excipients characterization, drug and excipient study and its ratio. Worked on different manufacturing strategies for the development of products. To evaluate product for stability in manufacturing, monitor and review the stabilized batches. To study on existing formulations. Responsible for co-ordination, execution and monitoring of scale up activity, Responsible for Trial batches, Scale up batches, Optimization batches, Exhibit batches. Co- ordination with all cross-functional teams. TT sites and LL Sites To design/assist/support/ review for documents such as SOP, LNB, QQ, Risk assessment, PDR, MFR, Scale up BMR, stability protocol, qualification, validation documents, change controls, deviations, investigations and CAPAs etc. Preferred candidate profile

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

Job Title: PPIC Executive - Oral Solid Dosage (OSD) Plant Company: Aurobindo Pharma Location: Naidupeta, Tirupati District, Andhra Pradesh Employment Type: Full-time Experience Required: 2-8 Years Job Description: We are seeking a dedicated Production Planning and Inventory Control (PPIC) Executive to join our Oral Solid Dosage (OSD) Plant operations team at our Naidupeta facility in Tirupati District. The ideal candidate will be responsible for planning, coordinating, and monitoring production activities to ensure optimal inventory levels and timely delivery of products. Key Responsibilities: Develop and maintain production schedules for OSD manufacturing Coordinate with Supply Chain Management (SCM) to ensure raw material availability Monitor production progress and update schedules as needed Analyze and resolve production bottlenecks Maintain inventory control systems and ensure accurate stock levels Generate and analyze production reports for management review Collaborate with quality assurance to ensure adherence to GMP standards Participate in continuous improvement initiatives Required Qualifications: Bachelor's degree in Pharmacy, Engineering, Supply Chain Management, or related field 2-8 years of experience in PPIC, preferably in pharmaceutical OSD manufacturing Proficient in ERP systems and MS Office applications Strong analytical and problem-solving skills Knowledge of GMP regulations and pharmaceutical manufacturing processes Excellent communication and interpersonal skills

Role & responsibilities Job Summary: We are seeking a diligent and experienced QA & QC & IPQA & HPLC Production . The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance (QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range : 15,000 to 25,000 (negotiable based on experience & skills) Experience: Freshers & Experience Both Required in QA/QC/Production/ department of Tablet & Capsule or pharma manufacturing unit Role & responsibilities Quality control analyst Responsible for testing and analyzing pharmaceutical products to ensure they meet established quality standards. They work in laboratories, using analytical Techniques to test raw materials, in-process samples, and finished products. Quality assurance analyst Responsible for ensuring compliance with regulatory requirements by conducting audits, inspections, and assessments Preferred candidate profile Qualification: Relevant degree in any of the following fields, B.Pharma, M Pharma, D Pharma ,B.Sc or M.Sc, BBA, MBA, BA,ITI Any Tared Company - Top Pharmaceuticals Companies based at Baddi HP. Fresher & Experience. Job Location- Baddi Nalagarh Parwanno Solan ( Himachal Pradesh ) Functional : QC,QA & Production. Industry: Pharma manufacturing unit/ The Saksham Success Enterprises Near Sunder Ayan by pass solan 173212 Himachal Pradesh Contact us SHILPA 9129999003( 9:30 AM to 6:30 pm ) Preferred candidate profile The Saksham Success Enterprises Near Sunder Ayan by Pass Solan 173212 Himachal Pradesh Contact us SHILPA 9129999003( 9:30 am to 5:30 pm )

Job Title: Executive - Senior Officer - Quality Assurance Department: Quality Assurance Location: Vadodara Experience: 4 6 years Qualification: B.Pharm / M.Pharm Job Summary: The Executive Quality Assurance is responsible for ensuring compliance with cGMP standards through effective execution of Validation, Annual Product Quality Review (APQR), and Quality Management System (QMS) activities. The role involves coordination with cross-functional departments, documentation management, and continuous quality improvement. Key Responsibilities: 1. Validation: Prepare, review, and execute validation protocols and reports (Process, Cleaning, Equipment, HVAC, Utilities, etc.). Ensure timely qualification and requalification activities. Review and evaluate validation data and ensure compliance with regulatory and internal quality standards. Coordinate with production, engineering, and QC for smooth execution of validation activities. Maintain validation master plan and validation documentation repository. 2. Annual Product Quality Review (APQR): Coordinate collection and review of data from production, QC, and other departments for APQR. Prepare and compile APQR reports as per regulatory guidelines and internal SOPs. Identify trends, deviations, and opportunities for process improvements based on APQR findings. Ensure timely completion and approval of APQRs. 3. Quality Management System (QMS): Participate in implementation and maintenance of QMS elements (Change Control, Deviations, CAPA, Risk Management, Document Control, etc.). Ensure timely closure of QMS records and proper documentation. Support internal and external audits, including regulatory inspections. Contribute to continual improvement initiatives and ensure regulatory compliance. Key Competencies: Sound understanding of cGMP, ICH, 21CFR, WHO, and regulatory requirements. Strong analytical, documentation, and communication skills. Proficient in handling QMS software (e.g., TrackWise, Veeva, or similar tools). Ability to work independently and as part of a team. Attention to detail and quality-focused mindset. Preferred Skills: Experience in pharmaceutical manufacturing environment (oral solid dosage). Exposure to regulatory audits (USFDA, MHRA, EU, etc.). Knowledge of data integrity practices and electronic documentation systems.

Preferred candidate profile Experience: 2-6 years Role : Operator/ Technician/ Officer/ Supervisor Granulation/ Wurster Coating - Machines: RMG/ FBP/ FBD/ Wurster Coating/ Roll Compactor IPQA : Manufacturing & Packing Quality Control : Advanced Instrumentation Warehouse - RM/ PM/ FG Engineering - HVAC & Utilities ,Water System Work Location: Granules India Limited Sy No. 160/A, 161/E, 162 & 174/A, Gagillapur Village, Dundigal-Gandimaisamma Mandal, Medchal-Malkhajgiri District 500 043, Telangana, India Walk-In Interview Location: Granules India Limited Sy No. 160/A, 161/E, 162 & 174/A, Gagillapur Village, Dundigal-Gandimaisamma Mandal, Medchal-Malkhajgiri District 500 043, Telangana, India

Walk In Drive for Production OSD Department In Formulation Division @ Kothur Qualification :- BSc | B Pharmacy| M Pharmacy Experience:- Fresher Interview Date:- 05-07-2025 Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF-II, Kothur Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-02,Kothur, Nandigama. Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.