MJ Biopharm has two manufacturing locations . Our Facility located in Taloja, near Mumbai, is WHO GMP Certified, state-of-the-art facility . Other facility Facility is in Pune

Role & responsibilities We are hiring for the Apprentice role. Engineering - Mechanical / Electrical / Instrumentation & Automation Number of position - 5 Flexible to work in Shifts Only male candidate can apply

Job description Role & responsibilities We are hiring for the Apprentice role. Engineering - Mechanical / Electrical / Instrumentation & Automation Number of position - 5

We are seeking an experienced Automation Engineer to join our pharmaceutical manufacturing team. The ideal candidate will have expertise in Rockwell and Siemens PLC/SCADA & HMI systems. You will be responsible for designing, implementing, and maintaining automation systems to ensure efficient and compliant production processes. Key Responsibilities: Automation Projects Design, program, and test automation systems using Rockwell and Siemens PLC/SCADA/DCS & HMI. Integrate automation systems with existing manufacturing equipment for i.e. Fermenter, Centrifuges, Chromatography columns, Autoclaves, DHS, Lyophilizer, Utility equipments ( Compressor, Chiller, Boiler, CSRO,HSRO,PUWG,PSG,WFIG, AHU’s, EMS system. Troubleshoot and resolve issues with automation systems to minimize downtime. Ensure compliance with GMP, GAMP and 21 CFR part 11 guidelines. Develop and maintain system documentation and provide training to staff. Collaborate with cross-functional teams to optimize production processes. Attend the preventive & breakdown maintenance of Rockwell and Siemens PLC/SCADA/DCS & HMI. Maintain the SCADA/DCS & HMI system application and database backup regularly. SCADA/DCS/HMI & PLC systems qualification & validation as per life cycle management requirements. Automation Systems like PLC/SCADA/DCS/HMI & I/O modules spare management & procurement. Being part of Project team involvement for Equipment’s URS/DQ/SAT/FAT/IQ/OQ & PQ.

Role & responsibilities To Lead QC Function (QC chemical & Micro) of both main QC and DPI QC lab Handle Audit Readiness, Investigation, documents review. Day to day Work allocation and meeting timeline of RM, PM, FG, stability Studies Team Management (QC, Micro) Coordinate with such as WH, Production, QA, PPIC, etc

Role & responsibilities To manage the overall work of the reception and administration ensuring that all functions are carried out in an orderly and timely manner. To provide a comprehensive first point of contact service for any incoming calls and visitor enquiries. EPABX machine operation. Supervision on trouble shooting of telephone service and EPABX. To indent and maintain inventory of hygiene, cleaning, utensils, crockery, linen, shoe covers, disposable caps etc. To supervise canteen and garden services Preferred candidate profile

Sr. Officer Accounts | Role & responsibilities Data entry in SAP BI e.g A/P, A/R Invoices Basic GST/ TDS Data preparation Communication with Depts./ Vendor for bills/ Ledgers etc. Documentation Related to A/C Entries Basic MIS Reports in excel. Interested Applicant can send CV on " janhavi.shedekar@mjbiopharm.com or contact on "9867700982"

Role & responsibilities - Assistant Manager- Purchase *Procurement of API/RM * Negotiation and Finalization of rate contact and other commerical terms. *Sourcing New and Alternate Vendor. *Coordinate with Vendor , R&D and RA team for technical Support. *Vendor Qualification and audits as per the internal policy. Interested applicant can send CV on shital@mjbiopharm.com/janhavi.shedekar@mjbiopharm.com or contact on 9619744167.

Quality Management System: Oversight/Handling of Handling of Change Control, Incident / Deviation and CAPA. Following and tracking of Change Control, Incident /Deviation and CAPA. Involved in the investigation activity whenever required. Ensure that products are manufactured in compliance to Regulatory requirements and as per Good Manufacturing Practices. Ensure that production and manufacturing activities are undertaken in compliance to SOPs, systems, procedure and GMP/GLP requirements. Maintain GMP compliance in various departments to manage the production in line with the current GMP requirement. Handling of Change Control, Deviation, risk assessment and CAPA as per company procedure Verification & Follow-up of CAPA implementation as per provided target completion date. Involved in the handling of Market Complaints. Review of QMS documents. Vendor Qualification Activity: Oversight of Vendor Qualification related documentation. Planning and execution of the vendor Qualification activity with co-ordination with user department. Preparation and review of document related to Vendor Qualification. Execution of schedule / planned Vendor/Supplier Qualification as per the Protocol. Qualification/ Validation - Data compilation and Report preparation. Review and compilation of data generated in validation and qualification of vendors. Coordination with external agency for Qualification, validation, calibration and outside services related to Vendor Qualification. Qualification of External agency for Qualification, Validation and Calibration agency as per the SOP. Planning of the vendor audit as per requirement. Self-Inspection: Oversight of Self-Inspection program 4. Management and overall tracking of audit observation- Audit & Compliance (Internal and External audit). Oversight of IPQC & Microbiology Section: - Ensure in-process product and process related quality assurance activities (IPQA) are undertaken by IPQC team. Validation and Qualification Activity: Review of Validation and qualification related activities as and when required. Planning of the validation activity with co-ordination with user department.

Position - Front Desk Apprentice Experience - 0 to 1 year Location - Pune (Hinjewadi Phase 2) Role & responsibilities To manage the overall work of the reception and administration ensuring that all functions are carried out in an orderly and timely manner. To provide a comprehensive first point of contact service for any incoming calls and visitor enquiries. EPABX machine operation. Supervision on trouble shooting of telephone service and EPABX. To indent and maintain inventory of hygiene, cleaning, utensils, crockery, linen, shoe covers, disposable caps etc. To supervise canteen and garden services If interested please share your CV on nikita.bhugul@mjbiopharm.com

1. Calibration of Instrument and equipment 2. Media preparation room MLT/BET area, 3. Recording Daily and weekly cleaning activities of microbiology department. 4.Ensure good Laboratory practices in Micro department.

Key Responsibilities: Design, install, calibrate, and maintain instrumentation systems (e.g., sensors, transmitters, analyzers) used in pharmaceutical manufacturing. Develop and implement automation solutions using PLCs, SCADA, DCS, HMI, and MES systems. Troubleshoot and resolve instrumentation and control system issues to minimize downtime and maintain product quality. Collaborate with cross-functional teams including production, quality assurance, and IT to support technology integration. Ensure all systems comply with regulatory standards such as FDA 21 CFR Part 11, GAMP 5, and cGMP. Support validation activities, including writing protocols and executing IQ/OQ/PQ of automated systems. Monitor system performance and generate reports on KPIs and reliability metrics. Lead or assist in automation-related projects and continuous improvement initiatives. --- Required Qualifications: Bachelors degree in Instrumentation Engineering, Automation, Electrical Engineering, or related field. 35+ years of experience in instrumentation and automation within a pharmaceutical or biotech manufacturing environment. Hands-on experience with PLC platforms (Siemens, Allen-Bradley, etc.), SCADA, DCS, and industrial communication protocols. Strong understanding of pharmaceutical manufacturing processes (e.g., sterile filling, granulation, packaging). Knowledge of validation, documentation, and regulatory compliance standards.

Position - Front Desk Apprentice Experience - 0 to 1 year Location - Pune (Hinjewadi Phase 2) Salary - 1.8 Lacs Role & responsibilities To manage the overall work of the reception and administration ensuring that all functions are carried out in an orderly and timely manner. To provide a comprehensive first point of contact service for any incoming calls and visitor enquiries. EPABX machine operation. Supervision on trouble shooting of telephone service and EPABX. To indent and maintain inventory of hygiene, cleaning, utensils, crockery, linen, shoe covers, disposable caps etc. To supervise canteen and garden services If interested please share your CV on nikita.bhugul@mjbiopharm.com

Roles and Responsibilities Conduct equipment qualification, validation, and vendor qualification activities according to established procedures. Perform process validation protocols, reports preparation, and CAPA implementation as required. Ensure compliance with regulatory requirements by maintaining accurate records of documentation and data analysis. Collaborate with cross-functional teams to identify areas for improvement in validation processes. Develop and execute test plans for new equipment installations or modifications.

Role & responsibilities Contractual Role for 6 Months. Exploration of updated guidelines needed for dossier compilation for ROW market/ Regulated Market. Preparation, compilation, review, and submission of Pharmaceutical Dossiers to emerging market as per International Conference on Harmonization (ICH) and country specific guidelines in Common Technical Document (CTD), Asian Common Technical Document (ACTD) and regional format. Internal communication & follow-ups with various departments for various documents. To arrange and send samples for registration purpose to various countries. Review at all quality data received from various departments before using in dossiers and technical packages. Preparation and submission of Query response raised by the Health Authority. To undertake any other assignment given by superior of the department / management from time to time. To support in documentation in national and international tenders. Management of Product Database. Archival of dossier. For COPP Application- Support with documents. Preferred candidate profile Must be from Formulation background interested applicant can send CV on shital@mjbiopharm.com , janhavi.shedekar@mjbiopharm.com or contact on 9619744167. Perks and benefits

Roles and Responsibilities - Vial Operator 1. Operate the Vail/ Cartridge filling Machine. 2. Operate the Vail/Cartridge Washing and Tunnel 3. Having Knowledge in Aseptic Operation 4. Operate the Autoclave 5. Knowledge in Equipment preparation. Desired Candidate Profile Must have worked in Sterile injectable Plant. Interested Applicant can send their CV on janhavi.shedekar@mjbiopharm.com or contact on 9619744167.