377 Osd Jobs - Page 4

Walk In Drive For Production OSD In Formulation Division @ Bollaram Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | B Tech Experience :- 2 To 4 Years Skills :- Operators :- Granulation | Compression | Coating | Cartornator| Packing Division :- Formulation Interview Date:- 19-07-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF UNIT-I, Bollaram 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 Should have knowledge of SLD drawing Should be able to read the Electrical and Mechanical Drawing. Should be able to understand of P&ID and isometric Drawing. Basic knowledge of AutoCAD Hands on experience of Budget preparation of project work. Hands on experience on Project planning, handling and management. Should have able to manage material stock and record for consumption sheet preparation. Understand Companys Health & Safety Policy and follow all company HSE procedures. Should able to deliver the assigned task on time. Finalization of technical specification of machine Hands on experience on documentation like OQ,IQ,URS etc. Hands on experience of execution and commissioning of pharma machineries and utility Equipments Should have knowledge of HVAC system and clean room applications Should have knowledge of CGMP and revised schedule M Hand on experience of solid oral facility (Nutraceutical experience also be considered)Hands on Experience of WTP/utilities (Boiler, Chiller, WTP, Compressor, ETP, STP) piping, installation and commissioning. Hands on experience of vendor co ordination Should be able to present Project status/ reports and Daily work status/report. Manpower handling Hands on experience on Facility qualification, HVAC and Compressed Air Validation Provide technical input as required to ensure projects progress in line with their scope requirements. Support the development and completion of documentation in relation to purchasing, planning, implementation, commissioning and validation activities in relation to the above. Be responsible for Supervision of 3rd party contractors and internal service providers Be responsible for tracking and reporting project delivery, ensuring projects are delivered on time and within budget. Ensure training has been Given before undertaking specific duties and that all training is recorded in training records. Preferred candidate profile 5-7 years of hands-on experience in project engineering or project management roles within OSD pharmaceutical manufacturing . In-depth knowledge of OSD manufacturing processes , equipment, utilities, and facility layouts. Hands on Experience of HVAC system, cleanroom classification, and GMP /cGMP requirements. Hands-on experience with equipment installation, commissioning, and qualification (IQ/OQ/PQ).

(We are looking fo the Immediate joining candidates or willing to leave early for their current company) Role & responsibilities HPLC Analysis of Solid Orals/Nasal hands on experience on QC activities, RM, Packing, In Process and Finished Products Compliance with GMP/GLP Practices Preferred candidate profile 2-7 years of experience Prior experience of working in Regulated plants (USFDA/MHRA Approved) Perks and benefits Working in a state-of-the-art fully automated world class manufacturing. Opportunity to work on diverse dosage forms in a multi-product facility. Attractive attendance bonus & Special Allowances Unmatched opportunities to learn and grow Thanks & Regards Dhivakar D BVR People Consulting dhivakar@bvrpc.com

Walk In Drive for Engineering Services Department In Formulation Division @ RK Puram Department:- Engineering Services OSD Skills- Instrumentation | Utility | Process Maintenance | HVAC | Electrical | Water System Qualification :- Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulation Work location :-MSNF-V, RK Puram Interview Date-16-07-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- MSN Formulation Unit-V RK Puram, 25GX+XHX, Solipur, RK Puram,Telangana 509216 Contact No:- 040-304338701 | 8787 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, 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.

Walk In Drive For Production OSD In Formulation Division @ Kothur Department:- Production OSD Qualification :-ITI | Diploma | BSC | B Pharmacy | M Sc | M Pharmacy Experience :- 2 To 8 Years Skills :- Packing Operators :- Blister Primary & Secondary | Capsule Filling | Oral Liquid | Cartornator | CVC | Production Documentation | Granulation Executive | Executive Manufacturing | Executive Packing Operators :- Coating Operator | Granulation Operator | B Max Operator Division :- Formulation Interview Date:- 17-07-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur Venue Location:- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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.

Position : Block Head Production (OSD) Location : Sikkim Grade - Senior Manager-2 Position Summary This role is responsible for overseeing the operations of a specific c block within the manufacturing facility, ensuring efficient production processes, compliance with quality and safety standards, and meeting production targets. To meet the production targets To ensure the implementation of current Good Manufacturing Practices and SOPs at work place To maintain and improve the product quality as per standard To ensure Accuracy, Reliability, validity, integrity and completeness of the cGxP data/records To plan the department activities as per weekly delivery schedule for OSD and Liquid orals To ensure the eff ective control on man, machine and material in the department To participate and coordinate various on-going qualifi cation and validation activities Collaborate with the site quality head, QA & QC head in ensuring that the production is aligned to the qualitystandards and regulatory requirements To ensure the completeness of all the trainings (Sops, Technical, Developmental and Regulatory etc.) assigned toblock personnels To organize and implement the on-job training activities in the department To ensure the implementation of EHS practices during work To ensure the maintenance of equipment and upkeep of department constantly To control the rejection during manufacturing and packing operations To do counseling and grievance handling of the subordinates To prepare, review and approve the Standard Operating Procedures To evaluate deviations, change controls and other quality documents for appropriate conclusion To ensure the market compliant investigations as per the track wise module and its timely closure and awarenesstraining to all the concerned persons Handling of QMS related activities of Block To carry out the batch failure investigation for root cause identification and accordingly appropriate corrective action and preventive action taken To review and approve the equipment qualification protocols, process validation protocols, reports, specifications etc.

Job Description: Blister Packing Machine Operator ( BQS- Primary & Secondary) ( No. of positions- 02 nos.) To perform daily activities of Blister Packing area. Well versed with the BQS Primary or Secondary machine handling. (Make BQS Primary- ACG Pam pack, BQS Secondary- ANTRAS). To perform weighing balance calibration & verification activities. To record and maintain proper documentation of production area along with area log books. 2. Coating Operator (No. of positions - 01 nos.) To perform daily activities of Coating area. Well versed with the Coating machine handling. (Make Kevin Autocoater). To perform weighing balance calibration & verification activities. To record and maintain proper documentation of production area along with area log books. Interested candidates can share their resumes on below mentioned E-Mail ID's: n32admin@v-ensure.com career@v-ensure.com a.salunkhe@v-ensure.com Interested candidates can also reach on 8356911996 for further details. While sending the resume mention your expertise area in the subject line & mention below details in the mail body: Current CTC Expected CTC Notice period Total Experience Reason for change

Overview We Have following Job Opportunities 1. OSD Officer / Executive (Tablets, Capsules) 4Nos (0 to 3 years Experience with B,Pharma) 2. Liquid Orals Officer / Executive (Tablets, Capsules) 2Nos (0 to 3 years Experience B,Pharma) 3. Granulation and Blending Operator / Technicians 02 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 4. Tablet Press Operator (Cadmech ) 04 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 5. Coating Operator / Technicians -01 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 6. Blister Machine (PVC & ALU-ALU) Operator / Technicians -04 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 7. Liquid Filling Machine Operator / Technicians -03 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 8. Capsule Filling Machine Operators -02 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 9. B.Pharmacy / M.Pharmacy freshers 06 Nos (For QA and Production) 10. Electrician -02 ( 5 to 10 years Experience with 12th Pass / ITI/ Diploma) Job Location : Africa Company will provide Visa, Tickets, Accommodation, Medical and Food. Apply for job only who have Passport Joining Date: Should join with in 2 months Inventis Pharm LDA Send your CV and Passport copy to inventis.ao@gmail.com or whatsapp +918885700578 Before applying for this position you need to submit your online resume . Click the button below to continue. About Inventis Pharma LDA We Have following Job Opportunities 1. OSD Officer / Executive (Tablets, Capsules) - 4Nos (0 to 3 years Experience with B,Pharma) 2. Liquid Orals Officer / Executive (Tablets, Capsules) - 2Nos (0 to 3 years Experience B,Pharma) 3. Granulation and Blending Operator / Technicians - 02 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 4. Tablet Press Operator (Cadmech ) - 04 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 5. Coating Operator / Technicians -01 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 6. Blister Machine (PVC & ALU-ALU) Operator / Technicians -04 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 7. Liquid Filling Machine Operator / Technicians -03 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 8. Capsule Filling Machine Operators -02 ( 2 to 5 years Experience with 12th Pass / ITI/ Diploma) 9. B.Pharmacy / M.Pharmacy freshers - 06 Nos (For QA and Production) 10. Electrician -02 ( 5 to 10 years Experience with 12th Pass / ITI/ Diploma) Job Location : Africa Company will provide Visa, Tickets, Accommodation, Medical and Food. Apply for job only who have Passport Joining Date: Should join with in 2 months Inventis Pharm LDA Send your CV and Passport copy to inventis.ao@gmail.com or whatsapp - +918885700578

Interview on 26 July, Saturday for BSC Chemistry Fresher for Production Department for Large Formulation Pharma Company in Ankleshwar Call / WhatsApp on 7600033423 for More Details Send CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp INTERVIEW VENUE: SDP HR SOLUTION, 610, GOLDEN SQUARE, OPPOSITE HOTEL REGENTA, NEAR ABC CIRCLE, BHOLAV, BHARUCH We Provide Best Jobs in Gujarat

Interview on 26 July, Saturday for BSC Chemistry Fresher for Production Department for Large Formulation Pharma Company in Ankleshwar Call / WhatsApp on 7600033423 for More Details Send CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar Required Candidate profile Join My LinkedIN: https://www.linkedin.com/in/urvisdp INTERVIEW VENUE: SDP HR SOLUTION, 610, GOLDEN SQUARE, OPPOSITE HOTEL REGENTA, NEAR ABC CIRCLE, BHOLAV, BHARUCH We Provide Best Jobs in Gujarat

Walk-in interview For Sun Pharmaceutical Industries Limited, Dadra Date: 20th July 25 (Sunday) We are recruiting for our OSD manufacturing facility located at Dadra Time: 10 AM to 4 PM Interview Venue: Sun Pharmaceutical Industries Ltd, Survey No. 694, Dadra - 396193, (U.T. of D & N. H.), India, Following are the requirements for our manufacturing facility at Dadra Location. 1) Designation: Officer / Sr. Officer / Executive Granulation & Packing Education: B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 2- 6 years of experience in OSD manufacturing handling Granulation, Compression, Tablet Coating, Tablet Inspection, and Bottle Packing activities in an OSD manufacturing plant, should have knowledge of cGMP. 2) Designation: Technician Manufacturing & Packing Education: ITI / Diploma/ B. Sc Department: OSD Manufacturing & Packing Experience: 3 - 7 years of work experience in pharmaceutical company, handling Granulation, Compression, Tablet Coating, Tablet Inspection and Bottle Packing activities in a regulated manufacturing plant. For all the positions, we are looking for candidates with experience in regulated plants like USFDA, MHRA, ANVISA, TGA etc. Interested candidates meeting with criteria should carry their updated resume along with photograph, Photocopy of Salary Supporting/Appointment/latest Increment letters giving salary breakups of Monthly & Annual Salary is must. Those who are unable to attend the personal interview may send their resume by e-mail to rupeshkumar.upadhyay@sunpharma.com

Dear All, We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 13th May 2025 (Sunday) Interview Location: Indore Timings: 9:00 am 5:00 pm Interview Venue: Enrise By Sayaji Rau, Survey No. 27/1 27/2, Village Pigdambar Rau Tehsil Mhow Ab Road Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ B.E/B.Tech/B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Sr. Executive/ Assistant Manager: B.E/ B.Tech with 5-10 Years Process Equipment( Electrical / Instrumentation), Instrumentation, Water System and Utility . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment and Utility. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration . QMS documentation exposure is required. Quality Assurance (Qualification) Assistant Manager / Deputy Manager / Associate Manager: B.Pharm with 10-20 years QA & MFG Qualification. Candidates should have experience in Qualification, Validation. They would have to prepare, execute and review of equipment/ instrument/ system /utility /area qualification program. Review of data backup activity, data restoration and its compliance. QMS documentation exposure is required. completion of CAPAs and to perform change control/CAPA effectiveness. Associate Manager: CSV B.Pharm with 15-20 years with experience in Issuance and retrieval of documents. Candidate should have experience in Review of various Qualification and CSV Documents. Review of system audit trail, system security user privileges and ensure the compliance. Review of data backup activity, data restoration and its compliance. To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness. Quality Control: Assistant Manager & Deputy Manager: Planning & review of reports in Raw Material & Packing material section Executive / Sr. Executive : Analyst - Expertise in analysis of In-process, process validation, FP and method transfer of solid dosage forms (Tablets / capsules) and Raw material with hands on experience in HPLC, UV, Dissolution, GC, IR, Polarimeter, Malvern 3000 etc For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

Position Title: Team Member Formulation & Development – Tech Transfer ( Officer / Executive ) - OSD Department: Formulation & Development - Tech Transfer Location: Vadodara Reports To: Manager – Formulation & Development – Tech Transfer Job Overview: The Team Member will support the successful transfer of products from development to manufacturing by ensuring process accuracy, documentation integrity, and adherence to quality standards. This role involves close collaboration with cross-functional teams, participation in validation processes, and troubleshooting to optimize manufacturing efficiency. Key Responsibilities: Process & Documentation: Prepare Technology Transfer Dossiers (TTD) and ensure the accuracy and completeness of all transfer documents, including SOPs and batch records. Validation Support: Assist in process and equipment validation activities, ensuring alignment with manufacturing and regulatory requirements. Risk Management: Identify potential risks during technology transfer and collaborate with relevant teams to implement mitigation strategies. Collaboration: Work closely with cross-functional teams, including R&D, Quality Assurance, and Production, to ensure a seamless transfer process. Troubleshooting: Resolve issues encountered during the transfer process and manufacturing runs, and implement practical solutions. Training: Support and participate in training programs for team members to ensure understanding of processes and compliance requirements. Compliance: Ensure adherence to all regulatory and quality standards throughout the transfer process and during manufacturing. Reporting: Maintain accurate and comprehensive project documentation to support future references and regulatory inspections. Key Skills: Technical Skills: Knowledge of GMP, process validation, and regulatory standards. Familiarity with product development, manufacturing, and technology transfer processes. Soft Skills: Strong communication and collaboration abilities for effective teamwork. Analytical thinking and problem-solving skills to address challenges. Attention to detail to ensure accuracy and compliance. Qualifications & Experience: Education: B. Pharm or Master of Science (M. Sc). Experience: 4-7 years of experience in product development, manufacturing, and technology transfer. Skills: Hands-on expertise in GMP, validation processes, and adherence to regulatory guidelines.

Looking candidates for PDR (Formulation & Development ) Dept. 5-10 years of relevant experience in solid oral dosage (Regulated Market US & Europe) Roles and Responsibilities 1.Candidate should perform literature search 2.Pre formulation development Required Candidate profile 1.knowledge of documents – Master formula card, Bill of Material, stability protocol 2.Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR

Roles and Responsibilities Operate granulation equipment such as roller compactor, fluid bed dryer, etc. to produce high-quality granules. Monitor and control process parameters to ensure product quality and consistency. Perform routine maintenance tasks on equipment to prevent breakdowns and optimize performance. Collaborate with other departments (e.g., formulation, packaging) to ensure smooth production operations. Ensure compliance with cGMP regulations and company policies. Desired Candidate Profile 2-7 years of experience in OSD (Oral Solid Dose) manufacturing or related field. B.Pharma degree from a recognized institution. Strong understanding of FBD (Formulation & Bulk Drugs), USFDA guidelines, RMG (Revised Manufacturing Guidelines). Proficiency in operating various types of granulation equipment.

Walk-in @ Indore We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume. *Job Location: Matoda, Ahmedabad, Gujarat. Engineering (Instrumentation / QMS / Process Equipment maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech with relevant functional experience in Calibration / Instrumentation / QMS activities QUALITY ASSURANCE QMS / Documentation / Validation and Qualification / IPQA (OSD) (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. QUALITY CONTROL (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M.Sc. (Organic Chemistry / Analytical Chemistry) B. Pharmacy / M Pharmacy MICROBIOLOGY (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M. Sc (Microbiology) Injectable Manufacturing (Executive/Senior Officer / Officer / Associate) Experience - 01 to 06 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations / Visual inspection / QMS activities OSD Manufacturing (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing operations / QMS activities Time and Venue : 20th July 2025 09:30 Hrs to 18:00 Hrs ______________________________________________________ PAPAYA TREE Group of Hotels - Indore, Address: AB Road , Near Dr. Hardia Eye Clinic, Rau, Indore, MP ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. Note: Having relevant qualification only can attend the scheduled walk-in.

SCCM L2 Job Title: Software Distribution Engineer Proposed Grade: Band B3 & B2 Primary Skill: Software Distribution & Patch Management, Windows, MECM, Intune Location: Bengaluru / Chenna Experince - 7- 10 years Rates including mark up - 130K/M - 140 K/M Experience: Proven experience in software distribution and patch management, particularly in Oracle JRE to Microsoft SDK migration. Strong knowledge of Windows operating systems and related technologies. Responsibilities: Perform software distribution and patch management tasks for Oracle JRE to Microsoft SDK migration. Ensure compatibility and functionality of distributed software on target systems. Collaborate with cross-functional teams to gather requirements and provide technical solutions. Troubleshoot and resolve issues related to software distribution and patch management. Maintain documentation and provide training to end-users as needed. Mandatory Skills: Software Distribution & Patch management.Experience3-5 Years.

Role & responsibilities Prepare document as when required like SOP, BMR/BPR/Process validation Protocol/Report in Production Department Handling of QMSs (Change control, Deviation and CAPA) Maintain cGMP requirements. Execution of batches and maintain BMRs. Perform SAP related activities Execute trainings Regulatory audit exposure

Regulatory Affairs Executive ( for Cosmetic Industry ) Kheda, Gujarat 3–5 Years Experience CTC up to 6 LPA Strong knowledge of global cosmetic regulations (EU/USA/ASEAN/Gulf) Expertise in labeling, claims review, and documentation

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:- MSNF Unit-VI Burgula X5R8+CXH, Mothighanapur, Burgul, Telangana 509202 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.

Opportunity to work with one of the fastest growing Pharmaceuticals in India!! About us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality and affordable medicines across the nation. With more than 4 decades of medical service to society, Unison is today one of the fastest-growing companies in Gujarat State. In addition to this, the company is ranked 82 among the top companies of India (Rupee wise sales) MAT March 2020. This makes Unison a distinguished company across the pharma industry. We are expanding our team!! Looking for passionate Formulation Scientists for DOM/EMB market at our dedicated R&D center. Department : Formulation Development Formulation : Solid Orals Market : Domestic / Emerging Experience Required : 4-7 years Designation : Sr. Officer / Executive Location: R&D Center, Moraiya, Ahmedabad. Roles & responsibilities (Not Limited to): To perform detailed Literature and Patent Search, preparation of Summary and Product Development. Strategy documentation. API Characterization and Reference Product Evaluation. Formulation development of Oral solid Product (planning, execution, scale-up and exhibit batch). Execution of scale-up and exhibit batches for developed dosage form. Coordination with cross functional departments like DQA, IPR, RA, ADL,TT, Packaging Development, Production, QA and QC for product development related activities. Perks & Benefits: Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills & experience, we encourage you to apply for this position. Interested candidate can revert with their resume on career@unisonpharmaceuticals.com Regards, Team HR Unison Pharmaceuticals Pvt Ltd

Role & responsibilities We are seeking a diligent and experienced QA & QC & 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: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile 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 B.Pharma , B.Sc or B.Tech Biotech D.Pharma Divya ( 9736044662 ) (9:30 AM to 7:30 PM ) Preferred candidate profile Company - Top Pharmaceuticals Companies based at Baddi HP. Fresher & Experience. Job Location- Chanigarh,Panchkula, Paonta Sahib ,BADDI ( Himachal Pradesh ) Functional : QC,QA & Production.Industry: Pharma manufacturing unit/ Food Technology The Saksham Success Enterprises Near Sunder Ayan by pass solan 173212 Himachal Pradesh Contact us Divya ( 9736044662 ) (9:30 AM to 7:30 PM )

Project Role : Business and Integration Architect Project Role Description : Designs the integration strategy endpoints and data flow to align technology with business strategy and goals. Understands the entire project life-cycle, including requirements analysis, coding, testing, deployment, and operations to ensure successful integration. Must have skills : Oil and Gas Upstream Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business and Integration Architect, you will design the integration strategy endpoints and data flow to align technology with business strategy and goals. You will understand the entire project life-cycle, including requirements analysis, coding, testing, deployment, and operations to ensure successful integration. Roles & Responsibilities:Candidate will need to lead from front and independently work with a team of developers for end-to-end integration with applications and work on development of upstream solutions across the business value chainWork with global Oil & Gas leaders and internal consulting teams with high-intensity collaboration. Track and develop deep knowledge on the Oil and Gas and Energy market and trends Develop capabilities/offerings that are relevant to the firms initiatives and client needs, running campaigns with global leaders to expand teams services and offerings Author regular and differentiated points of view on hot topics that demonstrate our capabilities Collaborate with cross-functional teams to implement and maintain business process management (BPM) tools.Support the implementation of data integration projects and troubleshoot technical challenges in process workflows.Document process designs, technical workflows, and business requirements effectively.Drive continuous improvement initiatives by identifying bottlenecks and implementing solutions using data-driven insights.Stay updated on industry trends, best practices, and emerging technologies to enhance business processes. Drive growth of individual Oil & Gas accounts and identifying and driving proactive opportunities Work with leaders on strategic planning, periodic reviews and creating/executing a roadmap Have a sharp sector and account focus keeping a close watch on the sector engagements Get involved in and drive business development activities (RFPs / RFIs / Proposals, etc.) Professional & Technical Skills: Application & Business Process UnderstandingThe candidate must have deep domain expertise on Oil and Gas and Upstream, either through working with relevant companies or via services companies.Must have experience in data analysis and interpretation. It will be an advantage to have experience on tools such as Power BI, Petrel, Tableau, etc.Must understand Subsurface / Wells / Seismic Data and solutions/practices/software to manage it. Good understanding of data acquisition and handling in their relevant field of work and business process workflowsGood understanding of oProduction Surveillance, Production optimization, Concepts of Digital Oil Field, Process Engineering and field Operations, OR oStrong practical knowledge and hands-on experience with the Halliburton EDM software platform, with strong Drilling experience, OR oWorked with Wells & Reservoir Modeling, Monitoring and Support and Formation Evaluation process with good understanding of Economic Evaluation & Analysis for full field Development, ORoG&G data handling, hands on application knowledge (e.g. Petrel / Eclipse / CMG / DSG / EDM / SeisWorks / IHS Kingdom / Geographix / Techlog / Delfi / Neuralog etc. as applicable) and Application configuration experienceUnderstanding the data objects generated by and associated with well planning and well operations activitiesStrong understanding of the business value-chain, operations and processes involved in renewables. Must know the business challenges and trends and should be able to translate them into implications / opportunities for a consulting / services company.Experienced in client interaction and stakeholder / people management.Business / Technology Consulting experience, preferably with a leading consulting firm.Excellent business communication and presentation skills. Brings an innovation mind-set to think of new solutions and ideas of engagement and collaboration.Hands-on experience with modern, large-scale databases and IT systems.Understanding the data objects generated by and associated with well planning and well operations activitiesHands-on manage corporate data, including data modeling, data cataloging, data governance, quality control and risk control.Develop and apply procedures, standards and guidelines to collect, secure, handle and share data across the organization.Align, integrate and consolidate data assets across organizations for better consistency, reliability and efficiency of data operation.Triage, troubleshoot and authorize the maintenance of data-related problems.Leverage domain knowledge to partner with business entities to identify patterns, relationships, opportunities and problems in business data. Drive business data requirements.Develop functional data design based on the business data requirementsHelp Data Engineers understand the functions that they need to provide technical design and implementation. Additional Information:- The candidate should have a minimum of 5 years of experience in Oil and Gas Upstream- This position is based at our Bengaluru office- A 15 years full time education is required Qualification 15 years full time education

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. Company Benefits: 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 Progressive work environment conducive to personal and professional growth. Role & responsibilities 1. Assist in performing in-process quality checks during the production of nutritional food products. 2. Conduct sampling and testing of raw materials, in-process products, and finished goods such as moisture content, pH levels, or texture. 3. Review and verify batch records, ensuring that they are complete, accurate, and compliant. 4. Assist in the preparation and documentation of IPQA-related reports and records. 5. Monitor cleanliness and hygiene standards in the production area. 6. Participate in internal audits and inspections as per company requirements. 7. Collaborate with production teams to resolve quality-related issues promptly. 8. Support the quality control team in investigating and resolving any quality-related issues or deviations. 9. Ensure adherence to Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), GDP, and other regulatory guidelines. 10. To follow the procedure for In process Checks in Production & Packing area 11. Review of all documents relating to the Manufacturing & Packing. 12. IPQA of Dispensing, Manufacturing, Packaging and Dispatch activities. 13. Preparation & Review of PROCESS VALIDATION and CLEANING VALIDATION protocols and records. 14. Preparation, Review and Issuing control of BMR & BPR. 15. To follow the Sampling procedure. 16. Provide LINE CLEARANCE in MIXING AREA, FILLING AREA, DISPENSING and PACKING AREA. 17. Knowledge of APQR Data Collection. 18. Calibration and Verification of Instrument (Leak Test & Weighing Balance) 19. Overall Responsibility to Review Logbooks, In-process formats and other online records.

Role & responsibilities :- Hands on experience for BMR, Process validation report, Stability Protocol, Sampling Plan, Knowledge about GDP initiation and closure of Change control, deviation in GMP. Having good knowledge of guidelines SUPAC, cGMP, Compliance, ICH Q1A,Q2,Q7, Q8,Q9, A10, Q13. Knowledge about GAP assessment between sending unit and receiving unit equipment / instrument / documents. Hands on experience with Advanced Microsoft Word, Power point and excel Effective communication and Co-ordination with CFT. Sound Scale up/down knowledge Calculation, forecasting, Risk assessment etc. Plan Lab scale experiments and perform. Preferred candidate profile :- Must Have Experience in Tech Transfer Department Documentation. M. Pharma in Pharmaceutics Proficiency in MS- Word, Excel, PowerPoint Perks and benefits :- As per Company Standard