8 Bioburden Jobs

Dear Candidate , we are hiring for Fresher for the position Microbiologist . Job Description: Department:- Microbiology Exp: 2.0 yrs to 3.0 yrs Des:- Jr Executive-Executive Qua:-MSc Microbiology Only Male Candidates Preferable Bio burden testing of in process samples as per the specification. BET testing of water samples, in-process samples, semi-finished and finished samples as per the specification. Sterility testing of finished product. Responsible to perform the MLT testing for raw materials and water samples. Maintenance and handling of Endotoxin indicators and biological indicators. Experience on culture maintenance and VITEK2 compact system To perform the method validations for MLT, BET, Bio burden and Sterility. Injectables or biologics experience is mandatory. Male candidates are preferable. Regulatory audits exposure is mandatory. IMMEDIATE JOINERS ARE PREFERABLE"

Dear Candidate , we are hiring for QC Jr Executive ,Down stream process executives & Operators. Open Positions-50 Down Stream Process Executives & Operators Required • Qualification: Bsc/Msc/ITI/B Pharmacy Experience in handling the following Equipment 1 Chromatography column and system handling. 2 Column Packing (BPG And Chromoflow) 3 TFF System 4 Centrifuge system 5 Filtration, Filter Integrity,Buffer Preparation,CIP_SIP PRODUCTION-DS M Pharmacy/Diploma/B tech/Any Degree 6 Expertise in documentation QMS/GMP Compliance / Process Awareness Biologics Company's only Preferable. • Experience: 2 to 6 years in Total Downstream CTC :up to 5.0 LPA. IMMEDIATE JOINERS ARE PREFERABLE" Interested candidates please reach out Manasa - 9502434725

Job Responsibilities: 1. Document analysis procedures and the test results mainly bioburden testing, spectrophotometric testing and mechanical studies using UTM machines 2. Document product stability studies are completed satisfactorily and supported by correct product sample analysis 3. Establish a tracking mechanism for customer & field complaints and suggest corrective actions Profile: 1. You have experience of around 3 or more years in pharmaceutical industry 2. Educational Qualification - M.Sc./M.Pharm degree with strong interest in quality control documentation 3. You work accurately, technically minded and able to work independently after training in the matter entrusted to you. Experience in a formulations/ API industry is an asset

Walk In Drive For Microbiology Department In Formulation Division @ Corporate Office Department:- Microbiology Qualification :- B Sc | M Sc (Microbiology | Bio-Technology | Biochemistry) Division :- Formulation Fresher's :- 2023 | 2024 | 2025 Passed outs only. Interview Date:- 28-06-2025 Work Location :- MSNF Unit-II, Kothur & MSNF Unit-V, RK Puram Interview Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-30438701 | 8785 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter, CTC, Pay slips ,Bank Statement, Certificates, Aadhaar Card & Pan Card We are looking for candidates those who have experience in Production OSD Department.(Coating Operator & Compression Operator) 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.

BUILD CAREER WITH CHIRON ! WALK IN INTERVIEW On 20 June 2025, Friday TIME: 10:00 AM to 2:00 PM Quality Assurance / Quality Control Experience 2 5 Years 1. Quality Assurance Qualification: M. Pharm / B.Pharm / B.Tech (Micro/Biotech/ Botany) IPQA/ Change Control/ DR/ CAPA /BMR/SOP Process & Cleaning Validation APQR / QMS Sterile aseptic operation Good Subject Knowledge Legible Handwriting. 2. Quality Control Qualification: M.Sc/ B.Sc Microbiology Environmental Monitoring Media Preparation Bioburden testing Positive Mindset Good Subject Knowledge Legible Handwriting Documents need to Carry Updated Resume ID Proof (Aadhaar & Pan card) Passport Size Photo Copies of Highest Educational Qualification Current company Appointment letter/ Increment letter Last 3 month Pay slips & Bank statement Previous company experience & relieving letter

* For Quality Control (IPPT/FP, RM/PM):- To perform all test for in process product & finish product as per the specification and schedule. To investigate failure of FP / Out of specifications (OOS) and take the corrective and preventive actions (CAPA). To perform and ensure the calibration of instruments as per the schedule. To perform and ensure preparation of reagent / volumetric solution as per schedule. To perform and ensure observation of FP retained samples. To ensure that all documents related to the testing data and related papers are maintained properly. To implement Corrective and Preventive Action (CAPA). To carry out the sampling of all the materials according to Standard Operating Procedure (SOP). To carry out the testing of Raw Material and Packing Material according to approved procedure. To release Raw Material and Packing Material. To carry out the calibration of instruments as per the schedule. To prepare the working standards as per the guidelines and various pharmacopoeias. To ensure the status tag on the released material and transfer such material in the released area. To follow the Good Laboratory practices and Good Manufacturing practices (GMP). To prepare requirement list of chemical & reagent for procurement. To perform the analysis of stability sample as per current specification. To compile the data required for internal quality audit in the plant, as and when required. * For Quality Control (Stability):- To implement the change in procedure as per change control note. To check and verify the sampling of respective samples as per defined intervals for testing. To check and verify that the samples are kept at appropriate temperature and humidity as per defined procedure, which is as per the Standard Operating Procedure. To verify results of analysis conducted in respective period, and to carry out trend analysis. To coordinate with Purchase department for routine requirement and follow up for the procurement. To sign the documents related to stability studies data. To select product batches for the stability studies. In the absence of Officer, Executive will ensure his roles and responsibilities. In the absence of Executive, Sub-department Manager will ensure these roles and responsibilities. To file deviation in case of non-compliance * For Quality Control (Micro):- To ensure the clean environment for sterile preparation by implementing the Good Manufacturing Practice (GMP) norms as per the international standards and guidelines. To do sampling of Water for Injection (WFI), Double Reverse Osmosis (DRO), Single Reverse Osmosis (SRO), Raw water and pure steam. To analyze water samples for pH, conductivity, Bacterial Endotoxin Test (BET), bioburden, Total Organic Carbon (TOC), pathogens, chlorides, hardness, silt density index and other testing as per the requirements. To analyze the samples of water system after maintenance work . To observe and record the results the microbiological plates and test tubes after analysis as well as supervise discarding method of same. To perform the timely microbiological testing of finished product samples, pre-sterile samples, Raw material as well as Packing material sample as per the requirements and SOPs and record the results for the same. Candidate Profile:- Ready to work in Rotational shifts. Excellent understanding about working area. Initiator and Learner. Decision making ability. Team player and if required, can provide training to other team members. Good communication. The above mentioned requirement is for Male Candidate Only. Hence can be ready to work in rotational Shift. Candidate having Parenteral /Injectable exposure would be preferable . Candidates having Pharma exposure will only be considered for interview process. Fresher can also email their CV on Anee.Silas@otsukapharma.in

JOB RESPONSIBILITIES QC Executive ( Microbiology )Quality Control Head Quarter : Faridabad Purpose of the position : - To ensure that water sampling, media preparation and used media destruction is done as per approved procedure. Job Responsibilities :- 1. Responsible for all type of water sampling & analysis. 2. Responsible for operation and calibration of pH meter and weighing balance. 3. Responsible for destruction of used media/used plates and used cultures. 4. Responsible to verify logbook of autoclave, water sample inward, media management, pH meter, Laminar Air Flow and weighing balance etc. 5. Responsible for media preparation in absence of other team member. 6. Responsible for Analysis of Bioburden Sample testing of in-process, finished product & raw materials samples as per approved standard operating procedure. 7. Responsible for timely submission, review, approved and release of reports related to microbiology section. 8. Responsible for culture management as per approved protocol. 9. Responsible for Preparation of culture Suspension. 10. Responsible for Growth Promotion Test for all the dehydrated media as per standard operating procedure. 11. Responsible for Revival and Sub culturing of Microorganisms. 12. Responsible for Environmental Monitoring by Settle Plate Method & Surface swab method. 13. Responsible for performing Preservative Efficacy Test. 14. Responsible for all admin related work. 15. Responsible for reporting any Non conformity/OOS/Deviation related to water and bio burden samples. 16. Responsible for reporting of DCR for any changes related to microbiology section. . 17. To provide practical training to newcomer of QC-Microbiology Section. 18. Responsible for maintaining stock of media & materials needed for analysis. 19. Functional reporting shall be as per departmental organogram. 20. Responsible to ensure the compliance of the SOP’s applicable to QC-Microbiology. 21. Any other task assigned by your Reporting Manager. The Job Responsibilities may be reviewed / added as per company requirements from time to time.

Walk In Drive For Microbiology Department In Formulation Division @ Corporate Office Department:- Microbiology Qualification :- B Sc | M Sc (Microbiology | Bio-Technology | Biochemistry) Division :- Formulation Fresher's :- 2023 & 2024 Passed outs only. Interview Date:- 10-05-2025 Division :- Formulation's Work Location :- MSNF Unit-II, Kothur & MSNF Unit-V, RK Puram Interview Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-30438701 | 8785 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter, CTC, Pay slips ,Bank Statement, Certificates, Aadhaar Card & Pan Card We are looking for candidates those who have experience in Production OSD Department.(Coating Operator & Compression Operator) 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.