233 Sterile Jobs

We are seeking an experienced Plant/Site Head with expertise in Injectable manufacturing at the leading pharma formulation facility in Tada, Andhra Pradesh. The successful candidate will be responsible for overseeing the entire plant operation, ensuring adherence to industry standards, and driving operational excellence within a fast-paced environment. Key Responsibilities: Oversee daily plant operations, ensuring smooth functioning across production, quality, and supply chain. Manage and lead a multidisciplinary team, including production, quality control, maintenance, and other support functions. Ensure compliance with Good Manufacturing Practices (GMP), regulatory standards, and safety regulations. Drive process improvements to enhance efficiency, reduce costs, and improve product quality. Lead the implementation of strategic initiatives to meet production targets and ensure timely delivery. Collaborate with cross-functional teams, including R&D, to improve product formulations and production processes. Report and liaise with senior management regarding plant performance, operational challenges, and opportunities for growth. Manage budgets, resources, and facilities to ensure operational efficiency and cost-effectiveness. Qualifications: Educational Requirements: B.Pharm or M.Pharm Experience: Minimum 19 years of experience in the pharmaceutical industry , with Injectable manufacturing experience Skills and Competencies: In-depth knowledge of Injectable formulations and manufacturing processes. Strong leadership and team management skills, with the ability to inspire and develop teams. Experience in handling plant operations, including production, quality assurance, and compliance. Strong problem-solving and decision-making skills with a focus on continuous improvement. Excellent communication skills for effective interaction with internal and external stakeholders. Familiarity with industry standards and regulatory requirements in the pharmaceutical sector. Regards, Ila Rajput Utkarsh Placement Pvt. Ltd. Baroda Mob-9824059611 Phone: 0265 - 2601938 ila@uppl.in

Walk In Drive for Engineering Services Department In Formulation Division @ Kothur Department:- Engineering Services OSD Skills- OSD ( Electrical | Mechanical) | Sterile Mechanical | HVAC | Water System Qualification :- ITI | Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulations Work location :-MSNF-II, Kothur Interview Date- 13-09-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- Unit-II Kothur, Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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 Injectables In Formulation Division @ RK Puram Department:- Production Injectables Qualification :- ITI | Diploma | B Sc | B. Tech | B Pharmacy | M Sc | M Pharmacy Experience :- 2 to 8 Years Skills :- Operators :- Filling | Production Injectables Packing / Blister | Lyo | PFS Operators | QMS | ALUS | Vial filling | Stoppering | Sealing Machine | Autoclave Division :- Formulation Interview Date: 13-09-2025 (Saturday) Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur| MSNF-V, RK Puram Venue Location :- Unit-5, RK Puram, 25GX+XHX, Solipur, RK Puram,Telangana 509216 Contact No:- 040-304338701 | 8954 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.

Job Purpose: To operate, monitor, and maintain filling machines and related equipment in compliance with cGMP, safety, and quality standards, ensuring smooth and efficient production of sterile / non-sterile products.

Role & responsibilities To perform operation and changeover of the equipments like Vial Filling & Stoppering Machine, Vial Cap Sealing Machine, Vial Washing Machine, Sterilizing and Depyrogenation tunnel, Lyophilizer, Autoclave, Pasteurizer, Incubator, Fogger and Filter integrity tester. Actively involve in fill finish operation and media fills. Preparation and review of general and equipment operation SOP’s. Involve in preparation and reviewing of BMR, MFR & Validation protocol etc. Compilation of all critical process attribute to analyze yield variation and investigation of low yield batches or OOS routed through change control or deviation. To get involve in external and internal regulatory audits and ensuring audit compliances.

Role & responsibilities Sr. Executive Visual Inspection (and Packing) : JD : Preferably with 5 to 10 Years of experience in handling visual inspection activities @ reputed Pharma / Biotech companies ( preferably in Small volume injectables ) Should be expert in KIT preparation and Qualification of Visual inspector. Should be ready to work in A/B shifts regularly. Should have GMP Audit Exposures. Handling of Packing activities and will be an advantage.

Role & responsibilities Coordinate with formulation scientists for day-to-day activities, designing formulation strategies, execution of laboratory trials and preparation of technical documents for sterile dosage forms Coordinate with other technical staff responsible for testing new drug substances, excipients, pre-formulation samples, and formulation development samples. Ensure the timely completion of new product development of sterile dosage form. Interact with Manufacturing, Validation, and Materials Management teams to ensure smooth drug product development and transition to commercial-scale manufacturing. Manage all activities associated with registration batch manufacturing, including authoring, reviewing, and approving technical documents. To perform, review and interpret literature related to drug products, including patents, research articles, reference product details, drug substance information, and excipient details Provide support in troubleshooting formulation and process-related issues for both sterile and sterile dosage forms. 6. To perform all required activities, i.e., procurement of raw materials, packaging materials, and processing aids etc. for the initiation and execution of development batches, process validation/ exhibit batches and commercial batches of the drug product. 7. To prepare and review product-specific risk assessments, QQ, Master Formulation Records (MFR), development batch Stability Protocols, Scale-up BMRs, Scale-up reports, Product Development Reports (PDR), etc. 8. To propose and review finished product specifications to the Analytical Development Laboratory (ADL) based on dosage form requirements. 9. To prepare and review of technical documents based on CTD required for dossier submission and handling all technical queries raised by all respected regulatory authority. Percolate the instruction and work assigned by Head R & D to Team members for timely completion of activities. 10. To prepare and review Standard Operating Procedures SOPs) and related documents, ensuring work is performed according to SOPs, Good Manufacturing Practices (GMP), and safety guidelines in the R&D department. 11.To assist and support in the preparation and review of qualification and validation documents, change controls, deviations, investigations, and CAPAs. 12. To visit LL sites and third-party sites for development batch trials or batch execution as required. 13. To be responsible for coordination, execution, monitoring, and troubleshooting of scale-up batches, exhibit batches, process validation batches, and commercial batches at in-house manufacturing sites, CMO sites, TT sites, and LL sites. 14. To co-ordination with Cross Functional Team to ensure timely completion of assigned activities. 15. To perform any other task assigned by HOD / Management. Preferred candidate profile

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 13 Sep 2025, Saturday TIME: 09:00 AM to 2:00 PM Fresher's & Experienced (0 6 Years) Production: Drug substance (* Shift applicable) Sterile aseptic operation Autoclave /DHS operation Automated CIP/SIP operation Cell culture Aseptic operation Zonal Centrifuge operation Facility commissioning QMS/ Deviation/ Change control/ CAPA/ Investigation of deviation Qualification requirement: M.Sc/B.Sc (Life Science) , B.Pharm/M.Pharm , Diploma / ITI Benefits PF, ESIC, Transportation/Local Allowance, Canteen Facility, GMC Venue CHIRON BEHRING: Plot No. 3502, GIDC Estate, Ankleshwar, Gujarat 393002

Walk In Drive for Engineering Services Department In Formulation Division @ RK Puram Department:- Engineering Services Sterile Formulations Skills- Sterile Process Maintenance | Instrumentation | Utility | HVAC | Electrical | Water System Qualification :- ITI | Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulations Work location :-MSNF-V, RK Puram Interview Date-11-09-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- Unit-5 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.

Role & responsibilities 1. Maintain the equipment's and responsible for machines like ultrasonic cleaner & washer disinfector steam, ETO & Plasma sterilizer 2. Responsible for machine working condition , stock of instruments, dressing materials 3. Working knowledge in receive ,clean ,assemble ,pack, sterilize ,store and distributions 4. Washing unsterile instruments both manual and ultrasonic & washer disinfector 5. Arranging the unsterile materials with label and send for sterilization 6. Storage sterile items in proper area. Preferred candidate profile Candidates should be willing to do rotational shifts

Role & responsibilities Production: Having Injectable Experience of Shop floor activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions, filtration, Lyophilizes. Having Injectable Experience of Shop floor supervising activities like Filling, Sealing, Stoppering, Garment Washing Machine, Vial Washing, Autoclave, Ophthalmic, Suspensions, filtration, Lyophilizes. Operations and Training and QMS. Engineering: Having Injectable Experience of Instrumentation and Process Mechanical (Hands on Experience on Filling Lines, Lyophilizers, Track and Trace System) and HVAC, Utilities.

Job Overview: The PDL Scientist - Injectable will be responsible for the development, optimization, and scale-up of sterile injectable formulations and manufacturing processes. The role demands expertise in injectable formulation science, process engineering, and compliance with regulatory and quality standards. Role & responsibilities Formulation Development: Design and optimize sterile injectable formulations, including solutions, emulsions, and suspensions. Perform compatibility and stability studies of active pharmaceutical ingredients (APIs) with excipients. Process Optimization: Develop robust, scalable manufacturing processes for injectable formulations. Define and optimize critical process parameters (CPP) and quality attributes (CQA). Sterility Assurance: Establish aseptic processes and ensure compliance with sterility requirements. Perform filtration studies, autoclave cycle development, and validation. Analytical Support: Collaborate with the analytical team for the development and validation of testing methods. Conduct particle size analysis, pH, and osmolarity evaluations, and other critical tests. Regulatory Compliance and Documentation: Prepare technical reports, batch records, and regulatory submissions in compliance with GMP, ICH, and FDA guidelines. Support regulatory inspections and audits with comprehensive process documentation. Technology Transfer: Facilitate the transfer of processes from lab-scale to manufacturing-scale environments. Work closely with cross-functional teams, including production, quality assurance, and regulatory affairs. Preferred candidate profile 3 - 5 years of experience in injectable formulation and process development. Hands-on experience with lyophilization, sterilization techniques, and aseptic manufacturing processes. Strong knowledge of GMP, ICH, and regulatory guidelines. Proficiency in using laboratory equipment such as autoclaves, lyophilizes, and HPLC systems. Excellent technical writing and documentation skills.

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 :- ITI | Diploma | B Tech Mechanical & Electrical Experience :- 2-8 Years Division :- Formulations Work location :-MSNF-V, RK Puram Interview Date-06-09-2025 Interview Time:- 9.00AM To 2.00PM Venue Location:- Unit-II Kothur, Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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 Injectables In Formulation Division @ Kothur Department:- Production Injectables Qualification :- ITI | Diploma | B Sc | B. Tech | B Pharmacy Experience :- 2 to 10 Years Skills :- Senior Operator & Operators :- Filling | Production Injectables Packing / Blister | Lyo | PFS Operators | QMS | ALUS | Vial filling | Stoppering | Sealing Machine | Autoclave Division :- Formulation Interview Date: 06-09-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur| MSNF-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 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 in Chandigarh for the Quality department for Baxter Ahmedabad (Injectable) plant. We are a team of motivated employees who value the importance of our mission. No matter our role, each of us understands and connects deeply to this commitment. #nowhiring experienced Quality professionals (Quality control, Microbiology, IPQA, Validation) with expertise in the injectable manufacturing facility. Department: Quality control lab Experience: 2 to 7 years Qualification: M.Sc or B.Pharm or M.Pharm Role: QC Analyst Analysis RM, PM, FP, IP, GLP and stability QMS investigation, OOS, OOT, Incident, deviation, CAPA, deviation, etc., Instruments HPLC, GC, KF, UV, IR, etc., Department: QA QMS (Injectables) Experience: 6 to 12 years Qualification: M.Sc or B.Pharm or M.Pharm QMS elements NCR, Change management, Laboratory investigations Robust exposure regulatory environment Technical writing skill Risk management Cross-function team coordination Department: QA IPQA Experience: 3 to 8 Years Key skills: IPQA, line clearance, batch record review, in-process quality check, sampling, etc., Dept - Microbiology Exp - 3-6 Yrs Key Skills: closure of CAPA/NCR/LIR and quality documents , document change control (DCR) or change control management (CCM). Register yourself to attend the walk-in drive: https://talentcommunity.baxter.com/flows/quality-careers-hiring-event-a1gdwphqt Candidates are requested to bring their resume, Aadhar card, PAN card, last 3 month's Salary slips and CTC structure

Walk-in at Matoda 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 requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech Time and Venue : 06/09/25, Saturday 09:30 Hrs to 18:00 Hrs ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. *Having relevant qualification only can attend the scheduled walk-in.

Job Role : Sr. General Manager (Engineering) / Cluster Engineering Head role Education: BE Electrical & Electronics Experience : 22 to 24 Yrs (with experience in Regulated markets and Sterile background) Responsibilities : 1. He is authorize to sign (as a doer / reviewer / verifier) A. Engineering GMP Documents B. Break Down / Preventive Maintenance Report C. Qualification Documents. D. QMS document review and closing. E. Any other documents related to QMS. Handling of Halol-1 (NOSD) Engineering Operation, HVAC, Electrical and Facility Management related activity. Preventive Maintenance approval, Instrument / Equipment inward approval, Qualification protocol and SOP review and approval. Improvements to reduce the Break down time of Production Equipments. To ensure all critical utilities as HVAC and Water systems are available round the clock as per requirement. Conceptualize and Implement Energy Conservation measures for Energy & water. Preparation of annual Revenue budget and ensure expenses are within budget. Propose annual Capital budget for finalization & implement the sanctioned Capex. Handling of Engineering & Facility modification related activity. Rolling out the Good Engineering Practices and standards in various functions of Engineering. To ensure availability of the spares and maintain inventory of critical spares having long delivery time. Standardization and Harmonization of documentation and procedure in engineering department. Ensure continuous improvement in engineering operating system in coordination with plant maintenance leaders & production team leaders to avoid breakdowns and repeated failures. Tracking of Capex and Modification related activity. Ensuring delivery of the activity in terms of safety, quality, timelines and budget. To ensure all engineering SOP, records and schedule are updated as per QMS. Participate in Technical Investigations. Participate in monthly Quality council meetings and update status of QMS documents. Ensure that QMS documents are closed as per time line. Compliance of internal and external observation points. To ensure timely completion of training related activity. Handling the Facility Management team operations for the site. To evaluate change control related to global IT division.

Walk In Drive For Production Injectable In FML @ Bollaram Department:- Production Injectables Experience :- 2-6 Years Skills :- Operators:-Lyophilization, Vial Washing, Filling Qualification :- ITI | Diploma | B SC |B Tech | B Pharmacy Division :- Formulation Interview Location:-Bollaram Plot No- 42, Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana 502325 Work Location:-Bollaram Plot No- 42, Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana 502325 Note:- We Are Hiring: Production Injectable Department We are looking for those who have experienced in Production Injectables Department as Lyophilization ,Vial Washing, Filling Operators.. 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.

Interested candidates are requested to share their resumes at dipika.parmar@milanlabs.com for interview scheduling on 7th September 2025 at Hotel Ginger, Bharuch. Please note that it is mandatory to pre-schedule the interview before reporting at the venue. Responsibilities: Carry out routine production activities for Small Volume Parenterals (SVP) in compliance with cGMP and SOPs. Operate and monitor aseptic filling, sterilization, and packaging equipment. Ensure accuracy and completeness of Batch Manufacturing Records (BMR) and other production documentation. Adhere to cleanroom and aseptic practices during SVP manufacturing. Coordinate with QA, QC, and Engineering for smooth batch execution. Support in deviation handling, investigations, and CAPA. Maintain EHS and data integrity standards in day-to-day operations. Requirements: B.Pharm / M.Pharm / B.Sc. with 2 to 5 years of experience in SVP production . Hands-on experience in aseptic filling, sterilization, and cleanroom operations. Knowledge of regulatory guidelines (USFDA, MHRA, WHO, etc.). Strong compliance and documentation skills. Key Skills: SVP Manufacturing, Aseptic Processing, Sterile Operations, cGMP Compliance, Documentation.

Key Responsibilities for Microbiologist role Ensuring Product Safety and Quality: Microbiologists play a crucial role in ensuring that pharmaceutical products are free from harmful microorganisms, which is vital for patient safety. Microbial Testing and Identification: They conduct various microbiological tests, including environmental monitoring, to identify and analyze microorganisms that may be present in raw materials, in-process products, and finished products. *Quality Control: Microbiologists are involved in quality control processes, ensuring that products meet regulatory standards and specifications. *Environmental Monitoring: They monitor the microbiological quality of the environment and water within the pharmaceutical facility to prevent contamination. *Method Validation: Microbiologists validate test methods and procedures used in the laboratory to ensure their accuracy and reliability. *Research and Development:* They may also be involved in research and development activities, such as developing new pharmaceutical products, vaccines, and medicines. *Data Management:* They document and interpret test results accurately and timely, maintaining accurate records of laboratory activities.

The ideal candidate brings 1-7 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assurance, water/air monitoring, microbial ID/trending, and method validation; establish contamination control strategy and support media fills and aseptic behaviors Manage QC lab workflows: RM/PM/FG testing, HPLC/GC operations, stability studies, instrument calibration/qualification (IQ/OQ/PQ), and review of analytical reports and CoAs Additional info: Education: B.Sc./M.Sc. in Microbiology/Biotech with sterile USFDA experience Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment. Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus.

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities.

Role & responsibilities Manufacturing of cell line/cell culture based AG for FG Cell culture operations, including inoculation and observatory monolayer work Compilation of all commercial batch data and BMR filling RM/PM issuance, sterilization, and monitoring of all supportive data Maintaining procell-related modules, areas, and utility fixed assets Receiving NPD from R&D and scaling up for commercialization Areas, equipment validation, and maintenance Cell bank passage history maintenance and reconciliation Preferred candidate profile Throughout knowledge of cell line/primary culture Propagation of cell line & maintenance Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Role Description: Quality control executive Location: Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 Experience: 5 to 6 years Roles Responsibilities:- To perform all the testing related to RM, bulk, FP and stability samples To perform all the testing of packaging materials Handling of QMS documents like SOP, CAPA, repeat analysis, Deviation etc. To manage and lead the team To perform analytical method validation To prepare specifications for different materials New vendor approval Should have working experience of HPLC, GC, UV spectrophotometer, centrifuge etc. What will you need to be successful Preferred experience in sterile pharma plant. Extensive understanding of sterile and disinfectant products, GMP and GLP Should have faced and experienced regulatory audits Positive attitude, problem solving and time management hould have a knowledge of ICH guidelines and other standards Interested Relevant can share profiles to

Pfizer Healthcare India Private Limited - Visakhapatnam Walk - in interviews for Diploma Pharmacy Freshers Junior Associates - Manufacturing Dates & Venue: Written Assessment & Personal interview on Wednesday, 3rd Sep 2025 at 9:00 AM Interview address : Government Polytechnic College, Pharmacy Block, Kancharapalem, Visakhapatnam - 530007 Eligibility Criteria: Diploma Pharmacy only (2025 Pass out) & Pass Percentage 60% in Academic & No backlogs. Job Description Operate production equipment such as injectable machines, sterile machines, parenteral machines, formulation machines, filling machines, capping machines, compounding machines, washing machines, sealing machines, Visual inspection & packing machines. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance tasks on equipment as required. Collaborate with other team members to resolve issues and improve overall efficiency. Ensure adherence to Good Manufacturing Practices (GMP) guidelines.