241 Solid Orals Jobs

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitization and sterilization of the items to be sent into Grade-B area Destruction of the rejected & unwanted materials and recording of the same Release of vaccine from blending to filling area To follow the usage of personnel protective equipment (PPE) during handing of corrosive liquids, WFI and steam Solution preparation Operation of Filter integrity machine Perform aseptic operations in Grade B area Any other tasks assigned by the supervisor.

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks. Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control. Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing. Familiarity with validated software systems that meet FDA electronic records and signatures requirements. Strong understanding of equipment qualification (D, I, O, P), process validation, and cleaning validation. E-BMR G E-Log: Experience with electronic Batch Manufacturing Records and Logbooks for real-time documentation and traceability. uality Management Systems (MS): Implementation and maintenance of MS aligned with regulatory standards . Risk Assessment: Ability to conduct and document risk assessments for processes, equipment, and product quality.

Were looking for a skilled Shopify Developer to create and maintain e-commerce solutions on the Shopify platform. Key Responsibilities: Develop and maintain Shopify stores with focus on front-end features Customize Shopify themes to meet client requirements Collaborate with designers and project managers Implement responsive designs for mobile and desktop Requirements: Minimum 1 year of Shopify development experience Strong knowledge of Liquid, HTML, CSS, and JavaScript Understanding of e-commerce best practices and SEO Excellent problem-solving skills and attention to detail

Walk In drive for Formulation Research & Development - Department FR&D - MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Formulation R&D Department ( Formulations R&D) in Formulation Division - R&D Center. Key Responsibilities: Formulation Development : Lead the formulation development process for new pharmaceutical products, including solid oral dosage forms, liquids, and semisolids. Experimental Design : Plan and execute formulation experiments, optimizing product composition, excipients, and processes for efficacy and stability. Documentation : Maintain comprehensive records of experimental procedures, results, and regulatory documents, ensuring compliance with industry standards and protocols. Regulatory Compliance : Collaborate with regulatory affairs to ensure that all formulations adhere to applicable regulatory guidelines and quality standards. Analytical Techniques : Employ a variety of analytical techniques, such as HPLC, dissolution testing, and spectroscopy, to evaluate formulation properties. Scale-up and Tech Transfer : Assist in the scale-up of successful formulations from laboratory to pilot plant and full-scale manufacturing, facilitating technology transfer. Team Collaboration : Work closely with cross-functional teams, including analytical, regulatory, and quality control, to drive projects to completion. Position : Executive / Senior Executive / Junior Manager Qualification : M Pharma (Pharmaceutics) Work Location : MSN R&D Center, Pashamylaram. Department : Formulation Research & Development - ( FR&D ) Experience : 2 to 10 Years Date of Interview : 20.09.2025 ( Saturday) Interview Time : 9.00 AM to 3.00 PM Note : Preferable Male Candidates only Interview Venue Details : MSN Laboratories Pvt Ltd, MSN R&D center, Pashamylaram, Isnapur,Patancheru,Sangareddy,040-30438786

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. Preparation and review of departmental SOPs 7. Reviewing of Equipment qualification protocols and Reports. 8. Review of supplier qualification documents. 9. Review of calibration documents 10. Receiving and reviewing of executed raw datas & ATRs and archiving for bio batches. 11. Reviewing of analytical method validation protocols & reports. 12. Maintenance, Retrieval and Archiving of all GMP related documents and records. 13. Preparation & review of department Schedules 14. Responsible for document distribution to the user departments. 15. Responsible for Document control activities. 16. Responsible for preparation, review and submitting License Applications. 17. Handling of Change controls (Permanent and Temporary), OOS and Incidents. 18. Responsible for approval of documents in absence of Head FDQA. 19. Responsible for performing job assigned by Head FDQA or his authorized designee. Note : Formulation R&D, API R&D Candidates also eligible for this positions Position : Executive / Senior Executive Qualification : M.Sc, M Pharma / B Pharma Only. Work Location : MSN R&D Center, Pashamylaram. Department : Development Quality Assurance - Formulation Department. Experience : 2 to 8 Years Date of Interview : 20.09.2025 (Saturday ) Interview Time : 9.00 AM to 3.00 PM Venue Details : MSN Laboratories Pvt Ltd. MSN R&D center, Pashamylaram , Isnapur, Patancheru, Sangareddy - 040-30438786

Your Day-to-Day Tasks Include: 1. Initiating first level contact with Inbound and Outreach leads. 2. Creating and executing an outreach strategy in collaboration with the PDR Managers and PDR team leads.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Capital Placement Services Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills Green Field Projects UPLC Gujarat R&D (Synthesis) PDR R&D Develo

Officer Sr. Officer - Engineering: Qualification - B. E (Mechanical/ Electrical) Experience - 03-06 years experience in pharmaceutical manufacturing machine maintenance Job Responsibility - 1. E xperience in maintenanceof semisolids (Ointment/ cream / gel manufacturing machines, Metal andlaminated tube filling machines) oral liquid manufacturing (mfg. Tanks withbottom entry agitators, volumetric filling machine, ROPP Cap sealing machine). 2. Should be able to draw & edit 2 D drawings with AutoCAD. 3. Mechanicalseal handling, assembly, dismantling and troubleshooting 4. Should haveknowledge about CLIT 5S and Kaizen 5. Maintaindocumentation related to ISO - EMS and OHS standards 6. GMPdocumentation (Preparation of qualification protocols for Productions machines, daily log books updation) 7. To scheduleand execute planned maintenance of machines. 8. Should be ableto operate and maintain utilities like compressor boilers and chillers 2.

We are seeking an experienced in Production Manager to lead the end-to-end lifecycle of pharmaceutical / Nutraceutical .The candidate should possess hands-on experience in the manufacturing of Tablets, Capsules, Softgels, Sachets & Protein Powders. Required Candidate profile 1. Production Planning & Management , Quality Assurance & Compliance, Process Improvement & Cost Control, Equipment & Facility Management, Team Leadership, Compliance with Health & Safety Regulations

Job profile Qualification : Bachelors Degree / Master Degree Industry Type : FM Services, Hotels, Projects, Overall Experience : 12 -14 years Industry Experience : 10-12 years of relevant / equivalent experience Technical Skills : Building Services Generic Skills : Leadership, Communication, Vendor/people management, Strategies Behaviors : Team work, Learning attitude, Innovation mindset Job Aim: To take complete ownership for all client deliverables for all the facilities in the city. The person will be responsible to provide comprehensive facility management services, as per the contractual terms with a focus on continuous improvement for the respective facilities. Will also be responsible to achieve financial and other Key Performance Indicators ( KPIs) established by the Client. The Regional Head must be a team player and work with other functions within JLL and also the client stakeholders to achieve outcomes. Competencies Interpersonal skills with a strong client focus. Team Leader with line management skills and the ability to delegate Client /Supplier relationship management Technical comprehension and experience with performance based service contracts and vendor management Knowledge of occupational safety requirements Strong budget management and financial analysis skills Excellent written and oral communication skills. Strong analytical skills. Responsibilities Operations delivery Overall service delivery of the region KPI / Compliance Scores and management Manage escalations with closure in a timely manner People Management Ensure right expectation setting for the team, ability to maximise performance of the team. Training for the team Growth Plan for the team Employee assessment, identify shortcomings and plan development Technology Ensure optimum utilization of all technology tools that are implemented from time to time. Innovation/ Initiative Keep a track and updates on Energy savings project for the region. Focus / Thrust on improvements/ initiatives Financial Acumen Keep a track one Office services / R&M /Capex Budgets /work closure Understanding of the facility / City spend Track FM Operational Expenses CRM / SRM Client/employee engagement, Leadership connects Service partners engagement Vendor management Vendor engagement /Identification and evaluation on larger aspects Expansion/Go live Overall planning / Cost proposal & approval Approval/transition/Go live Ensure/oversee closure on project snag BCP /Risk management Oversee, assess risk, plan and handle any BCP situation. Certification/Internal Audit Ensure/oversee preparation end to end for all audits Business Reviews Responsible for Quarterly Business Reviews Publish timely and relevant reports for client and senior management

Job profile Qualification : Bachelors Degree / Master Degree Industry Type : FM Services, Hotels, Projects, Overall Experience : 12 -14 years Industry Experience : 10-12 years of relevant / equivalent experience Technical Skills : Building Services Generic Skills : Leadership, Communication, Vendor/people management, Strategies Behaviors : Team work, Learning attitude, Innovation mindset Job Aim: To take complete ownership for all client deliverables for all the facilities in the city. The person will be responsible to provide comprehensive facility management services, as per the contractual terms with a focus on continuous improvement for the respective facilities. Will also be responsible to achieve financial and other Key Performance Indicators ( KPIs) established by the Client. The Regional Head must be a team player and work with other functions within JLL and also the client stakeholders to achieve outcomes. Competencies Interpersonal skills with a strong client focus. Team Leader with line management skills and the ability to delegate Client /Supplier relationship management Technical comprehension and experience with performance based service contracts and vendor management Knowledge of occupational safety requirements Strong budget management and financial analysis skills Excellent written and oral communication skills. Strong analytical skills. Responsibilities Operations delivery Overall service delivery of the region KPI / Compliance Scores and management Manage escalations with closure in a timely manner People Management Ensure right expectation setting for the team, ability to maximise performance of the team. Training for the team Growth Plan for the team Employee assessment, identify shortcomings and plan development Technology Ensure optimum utilization of all technology tools that are implemented from time to time. Innovation/ Initiative Keep a track and updates on Energy savings project for the region. Focus / Thrust on improvements/ initiatives Financial Acumen Keep a track one Office services / R&M /Capex Budgets /work closure Understanding of the facility / City spend Track FM Operational Expenses CRM / SRM Client/employee engagement, Leadership connects Service partners engagement Vendor management Vendor engagement /Identification and evaluation on larger aspects Expansion/Go live Overall planning / Cost proposal & approval Approval/transition/Go live Ensure/oversee closure on project snag BCP /Risk management Oversee, assess risk, plan and handle any BCP situation. Certification/Internal Audit Ensure/oversee preparation end to end for all audits Business Reviews Responsible for Quarterly Business Reviews Publish timely and relevant reports for client and senior management

Regional Head – Operations Job type : Full time Reporting Manager : India Operations Director / Account Director No of staff managed : 200 Job profile Qualification Bachelor’s Degree / Master Degree Industry Type FM Services, Hotels, Projects, Overall Experience : 12 -14 years Industry Experience 10-12 years of relevant / equivalent experience Technical Skills Building Services Generic Skills Leadership, Communication, Vendor/people management, Strategies Behaviors Team work, Learning attitude, Innovation mindset Job Aim: To take complete ownership for all client deliverables for all the facilities in the city. The person will be responsible to provide comprehensive facility management services, as per the contractual terms with a focus on continuous improvement for the respective facilities. Will also be responsible to achieve financial and other Key Performance Indicators ( KPIs) established by the Client. The Regional Head must be a team player and work with other functions within JLL and also the client stakeholders to achieve outcomes. Competencies Interpersonal skills with a strong client focus. Team Leader with line management skills and the ability to delegate Client /Supplier relationship management Technical comprehension and experience with performance based service contracts and vendor management Knowledge of occupational safety requirements Strong budget management and financial analysis skills Excellent written and oral communication skills. Strong analytical skills. Responsibilities Operations delivery Overall service delivery of the region KPI / Compliance Scores and management Manage escalations with closure in a timely manner People Management Ensure right expectation setting for the team, ability to maximise performance of the team. Training for the team Growth Plan for the team Employee assessment, identify shortcomings and plan development Technology Ensure optimum utilization of all technology tools that are implemented from time to time. Innovation/ Initiative Keep a track and updates on Energy savings project for the region. Focus / Thrust on improvements/ initiatives Financial Acumen Keep a track one Office services / R&M /Capex Budgets /work closure Understanding of the facility / City spend Track FM Operational Expenses CRM / SRM Client/employee engagement, Leadership connects Service partner’s engagement Vendor management Vendor engagement /Identification and evaluation on larger aspects Expansion/Go live Overall planning / Cost proposal & approval Approval/transition/Go live Ensure/oversee closure on project snag BCP /Risk management Oversee, assess risk, plan and handle any BCP situation. Certification/Internal Audit Ensure/oversee preparation end to end for all audits Business Reviews Responsible for Quarterly Business Reviews Publish timely and relevant reports for client and senior management Location On-site –Bengaluru, KA Scheduled Weekly Hours: 40 If this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements. We’re interested in getting to know you and what you bring to the table! JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL’s recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely. Candidate Privacy Statement . For candidates in the United States, please see a full copy of our Equal Employment Opportunity and Affirmative Action policy here. Jones Lang LaSalle (“JLL”) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process – including the online application and/or overall selection process – you may contact us at Accommodation Requests . This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page I want to work for JLL.

Regional Head – Operations Job type : Full time Reporting Manager : India Operations Director / Account Director No of staff managed : 200 Job profile Qualification Bachelor’s Degree / Master Degree Industry Type FM Services, Hotels, Projects, Overall Experience : 12 -14 years Industry Experience 10-12 years of relevant / equivalent experience Technical Skills Building Services Generic Skills Leadership, Communication, Vendor/people management, Strategies Behaviors Team work, Learning attitude, Innovation mindset Job Aim: To take complete ownership for all client deliverables for all the facilities in the city. The person will be responsible to provide comprehensive facility management services, as per the contractual terms with a focus on continuous improvement for the respective facilities. Will also be responsible to achieve financial and other Key Performance Indicators ( KPIs) established by the Client. The Regional Head must be a team player and work with other functions within JLL and also the client stakeholders to achieve outcomes. Competencies Interpersonal skills with a strong client focus. Team Leader with line management skills and the ability to delegate Client /Supplier relationship management Technical comprehension and experience with performance based service contracts and vendor management Knowledge of occupational safety requirements Strong budget management and financial analysis skills Excellent written and oral communication skills. Strong analytical skills. Responsibilities Operations delivery Overall service delivery of the region KPI / Compliance Scores and management Manage escalations with closure in a timely manner People Management Ensure right expectation setting for the team, ability to maximise performance of the team. Training for the team Growth Plan for the team Employee assessment, identify shortcomings and plan development Technology Ensure optimum utilization of all technology tools that are implemented from time to time. Innovation/ Initiative Keep a track and updates on Energy savings project for the region. Focus / Thrust on improvements/ initiatives Financial Acumen Keep a track one Office services / R&M /Capex Budgets /work closure Understanding of the facility / City spend Track FM Operational Expenses CRM / SRM Client/employee engagement, Leadership connects Service partner’s engagement Vendor management Vendor engagement /Identification and evaluation on larger aspects Expansion/Go live Overall planning / Cost proposal & approval Approval/transition/Go live Ensure/oversee closure on project snag BCP /Risk management Oversee, assess risk, plan and handle any BCP situation. Certification/Internal Audit Ensure/oversee preparation end to end for all audits Business Reviews Responsible for Quarterly Business Reviews Publish timely and relevant reports for client and senior management Location On-site –Bengaluru, KA Scheduled Weekly Hours: 40 If this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements. We’re interested in getting to know you and what you bring to the table! JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL’s recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely. Candidate Privacy Statement . For candidates in the United States, please see a full copy of our Equal Employment Opportunity and Affirmative Action policy here. Jones Lang LaSalle (“JLL”) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process – including the online application and/or overall selection process – you may contact us at Accommodation Requests . This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page I want to work for JLL.

Greetings!!!! We are looking for a QA - Manger - OSD _Chennai Location Job Description: Responsible for BMR, batch release, validations, qualifications, SOPs, GMP compliance. Handle audits, QMS (Deviation, OOS, OOT, CAPA), and technology transfer. Exposure to analytical operations will be an added advantage. Strong experience in OSD / Liquid formulation QA required. Key Skills: QA, Quality Assurance, BMR, Batch Release, Validation, GMP, SOP, QMS, Audit, Deviation, OOS, OOT, CAPA, Pharma QA. Salary: As per market standards Note: Immediate joiners preferred. Interested Candidates Kindly share your updated cv to uma@bvrpc.com

Job Description Responsible for submissions of Response to Deficiencies to Health Agencies of Europe, Australia, New Zealand and Canada market and Customers. Responsible for post approval submissions to Europe, Australia, New Zealand and Canada market. To provide Regulatory inputs during inspections by Regulatory authorities and Customer as and when required. To provide Regulatory inputs during product development, manufacturing and testing and to evaluate all types of change proposals during product life cycle Work Experiance Should have worked in Regulatory Affairs Dept for regulated markets like EU/UK, Australia, Canada, US etc (minimum 1-2 years). Submission of new submissions, deficiency responses and/or post-approval submissions for above markets. Worked on various dosage forms including complex generics. Compilation of Module 2 and 3 CTD sections for above submissions. Review of documents for all these sections. Knowleage of ICH as well as country specific guidance for documents to be submitted in all above sections. Hands on experiance for ECTD compilation. Competencies Strategic Agility Process Excellence Collaboration Innovation & Creativity Result Orientation Stakeholder Management Customer Centricity Developing Talent Education Masters Graduation in Pharmacy or Science

Job Title: HVAC Executive (MNC) Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: Minimum 5 Years Salary: Up to 7 LPA 9796871050 Job Description: We are looking for an experienced HVAC Executive to join our team in the pharmaceutical industry. The ideal candidate should have hands-on experience in HVAC system validation, operation, and maintenance along with a strong understanding of Quality Management Systems (QMS). Key Responsibilities: Ensure smooth operation, preventive maintenance, and breakdown maintenance of HVAC systems. Execute and monitor validation activities for HVAC systems as per regulatory guidelines. Maintain proper documentation in compliance with cGMP, regulatory, and company requirements. Prepare and review SOPs related to HVAC operations and maintenance. Coordinate with cross-functional teams to ensure uninterrupted facility operations. Support quality audits and inspections by providing HVAC-related documents and compliance reports. Monitor and control environmental conditions (temperature, humidity, differential pressure, etc.). Implement energy efficiency and cost optimization measures in HVAC operations. Ensure adherence to QMS standards including deviation handling, CAPA, and change control. Desired Candidate Profile: B.Tech in Mechanical related engineering discipline. Minimum 5 years of experience in HVAC operations and maintenance in a pharmaceutical manufacturing environment. Strong knowledge of HVAC validation, QMS practices, and regulatory compliance. Ability to troubleshoot HVAC equipment and systems. Excellent documentation, analytical, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Facility Management & Administration Executive / Sr. Executive Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (in Pharma Industry) Salary: Up to 7 LPA (Negotiable) 9796871050 Job Description: We are looking for an experienced Facility Management & Administration Executive/Sr. Executive with strong exposure to pharmaceutical industry facility operations. The candidate will be responsible for managing housekeeping, pest control, laundry, security, canteen services, contract labour management, and ensuring compliance with QMS and cGMP requirements. Key Responsibilities: Oversee facility management services including housekeeping, pest control, laundry, security, and canteen operations. Manage and monitor contract labour workforce ensuring compliance with labour laws and company policies. Implement and monitor QMS practices in facility operations with adherence to pharma industry standards. Coordinate with internal departments to ensure seamless support for production and administrative functions. Ensure compliance with cGMP, safety standards, and regulatory requirements in all facility-related operations. Prepare and maintain records, SOPs, and documentation related to facility management. Handle vendor management, service contracts, and negotiations. Support audits and inspections by providing facility and administration compliance documents. Drive continuous improvement initiatives in facility management and cost optimization. Desired Candidate Profile: Graduate / Diploma / MBA preferred with relevant specialization. 5+ years of experience in facility management & administration in a pharmaceutical industry. Strong knowledge of QMS, cGMP, and pharma compliance requirements. Experience in managing contract labour and third-party vendors. Excellent organizational, leadership, and communication skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: QMS Production Executive Industry: Pharmaceutical (OSD Plant) Location: Bari Brahmana (Jammu) Experience Required: 5+ Years (OSD Pharma Plant) Salary: Around 6 LPA 9796871050 Job Description: We are seeking an experienced QMS Production Executive to join our Oral Solid Dosage (OSD) pharmaceutical manufacturing plant. The ideal candidate should have in-depth knowledge of Quality Management Systems (QMS) and hands-on experience in managing production activities in compliance with cGMP and regulatory requirements. Key Responsibilities: Ensure compliance with QMS requirements in production operations. Manage and maintain production documentation including BMR, SOPs, deviations, and change controls. Monitor and review CAPA, deviations, OOS, and audit observations related to production. Coordinate with QA, QC, and regulatory teams to ensure smooth operations. Support qualification and validation activities for equipment and processes. Implement best practices to ensure adherence to GMP, safety, and regulatory guidelines. Train production staff on QMS and compliance requirements. Support internal and external audits and regulatory inspections. Desired Candidate Profile: B.Pharm / M.Pharm or equivalent qualification. 5+ years of experience in OSD pharma production with strong QMS exposure. Strong understanding of cGMP, QMS, and regulatory compliance. Good documentation, analytical, and problem-solving skills. Ability to work independently and lead a team effectively. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Production Supervisor Industry: Pharma (MNC) Location: Bari Brahmana, Jammu Qualification: M.Sc. Chemistry / B.Pharm Experience: 3 to 6 years Salary: Up to 5 LPA Contact: 9796871050 Job Responsibilities Supervise day-to-day production activities in OSD, Capsule, and Tablet manufacturing plant . Ensure adherence to cGMP, SOPs, and regulatory guidelines during production. Monitor production processes to meet daily, weekly, and monthly targets. Maintain accurate documentation and batch records as per pharma compliance. Coordinate with QA, QC, Engineering, and Warehouse teams for smooth operations. Implement continuous improvement practices to enhance productivity and reduce wastage. Ensure proper training and guidance to operators and shop floor staff. Maintain strict compliance with EHS (Environment, Health & Safety) standards. Key Skills & Competencies Strong knowledge of pharma production processes (OSD, Tablets, Capsules). Familiarity with regulatory audits (USFDA, MHRA, WHO, etc.) . Excellent leadership, team handling, and communication skills. Ability to handle deviations, change control, and CAPA. Good problem-solving and decision-making abilities. Desired Candidate Profile 36 years of relevant experience in a reputed Pharmaceutical OSD plant . Hands-on experience in tablet/capsule manufacturing processes. Strong understanding of GMP compliance and documentation practices . Candidates with exposure to multinational pharma setups will be preferred. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: OSD Packaging Supervisor Industry: Pharmaceutical Qualification: B. Pharma Location: Bari Brahmana (Jammu) Experience Required: 2 to 5 Years Salary: Up to 5 LPA (Negotiable) 9796871050 Job Description: We are seeking a skilled and detail-oriented OSD Packaging Supervisor to join our pharmaceutical team. The candidate should have experience in Oral Solid Dosage (OSD) packaging operations, ensuring compliance with GMP standards and regulatory requirements. Key Responsibilities: Supervise daily packaging activities of OSD products as per production schedules. Ensure compliance with cGMP, SOPs, and regulatory guidelines during all packaging operations. Monitor line clearance, in-process checks, and reconciliation of packaging material. Handle and train packaging staff to maintain efficiency and quality standards. Maintain documentation including batch packaging records, deviation reports, and logbooks. Coordinate with quality assurance and production teams for smooth operations. Implement safety measures and maintain housekeeping standards in packaging areas. Support regulatory audits and inspections with packaging-related documentation. Desired Candidate Profile: B. Pharma degree is mandatory. 2 to 5 years of experience in OSD packaging operations in a pharma manufacturing setup. Knowledge of blister, strip, and bottle packaging lines. Familiarity with cGMP, QMS, and documentation practices. Strong leadership, communication, and team management skills. https://www.linkedin.com/in/satnam-singh-37b9b518/ Job Title: Granulation Operator Industry: Pharmaceutical Location: Bari Brahmana (Jammu) Qualification: ITI / Diploma Experience Required: 3 to 6 Years Salary: Up to 4 LPA 9796871050 Job Description: We are looking for an experienced Granulation Operator to join our pharmaceutical manufacturing unit. The candidate will be responsible for operating and monitoring granulation equipment and processes while ensuring compliance with cGMP and safety standards. Key Responsibilities: Operate and monitor granulation machines (RMG, FBD, multi-mill, sifter, etc.). Perform granulation activities as per SOPs, BMR, and regulatory requirements. Ensure proper cleaning, calibration, and maintenance of equipment. Monitor critical process parameters (temperature, pressure, RPM, etc.). Maintain accurate documentation of production processes and equipment logs. Support in process validation and qualification activities. Adhere to safety protocols, GMP standards, and quality guidelines. Coordinate with production, maintenance, and QA teams for smooth operations. Desired Candidate Profile: ITI / Diploma in relevant discipline. 3 to 6 years of experience as a Granulation Operator in the pharmaceutical industry. Hands-on experience in handling RMG, FBD, sifter, multi-mill, and related granulation equipment. Knowledge of cGMP, documentation, and safety compliance. Team player with good communication and problem-solving skills. https://www.linkedin.com/in/satnam-singh-37b9b518/

Formulation Development (OSD) 1 to 5 Years Experience Company Overview Jodas Expoim Pvt. Ltd. JODAS Expoim is a research-driven, specialty biopharmaceutical company based in Hyderabad, Telangana, with EUGMP–certified facilities focused on oncology, contrast media, and cephalosporin injectables Position Summary We’re seeking a motivated Formulation Development Scientist with 1 to 5 years of experience in Injectables or OSD formulations. You'll contribute to pre-formulation, prototype development, stability studies, and support scale-up activities within a cGMP environment. Key Responsibilities Conduct literature and patent reviews to inform formulation strategy . Execute pre-formulation studies, characterize APIs and excipients, and assess compatibility . Develop and refine prototype formulations to match innovator quality profiles Perform lab-scale trials and support stability testing protocols. Assist in scale-up/tech-transfer and oversee pilot manufacturing batches and PDRs Prepare documentation for regulatory and manufacturing use, including pre-product development strategies and specifications Maintain detailed lab records and communicate findings in clear, data-driven reports Required Qualifications Bachelor’s or Master’s in B.Pharm, M.Pharm, 1–5 years of experience in formulation R&D, particularly in OSD . Hands-on experience with pre-formulation characterization, prototype work, stability studies, and lab documentation. Familiarity with cGMP, lab safety, and regulatory documentation standards. Best Regards Team Jodas Expoim

Roles and Responsibilities Conduct formulation development activities for solid oral products, including granulation, compression, coating, and packaging. Develop new product formulations that meet customer requirements and company standards. Collaborate with cross-functional teams to ensure successful project execution. Maintain accurate records of experiments, results, and observations.

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Assist in formulation development of Solid Oral Dosage form. Perform literature & patent search, pre-formulation studies, documentation, data compilation & ensure SOP/GMP compliance for global market products. Required Candidate profile Execution of process evaluation, optimization,scale-up and exhibit batches/Meeting product development timelines/literature survey/ICH guidelines/Solid Oral- Share CV- stuti.naik@enaltec.com

Responsible for managing formulation development of Solid Oral dosage forms for global markets. Oversees pre-formulation, patent search, documentation, compliance, and team guidance as per regulatory standards. Required Candidate profile Pharma professional with 7–10 years in formulation development, strong regulatory knowledge, documentation, data analysis & proven team leadership skills. Share CV- stuti.naik@enaltec.com

Walk-in interview For Sun Pharmaceutical Industries Limited, Dadra Date: 14th Sept 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: Operator / Sr. Officer / Executive / Sr. Executive Engineering Education: ITI / Diploma / B. E (Elect. / E.C /Inst./ Mech) Department: Engineering Experience : 6 8 years of Experience of handling Engineering QMS, OSD Process Maintenance, Engineering Projects, Utility and Water System in OSD manufacturing plant. 2) Designation Operator / Officer / Executive Manufacturing & Packing Education: ITI / Diploma/ B. Sc/ B. Pharm / M. Pharm Department: OSD Manufacturing & Packing Experience: 6 - 8 years of work experience in pharmaceutical company, handling Granulation, and Primary & Secondary Bottle Packing activities in a regulated OSD manufacturing plant. 3) Designation: Technician Warehouse Education: ITI / Diploma Department: OSD Warehouse Experience: 4 - 8 years of work experience in pharmaceutical company handling Raw Material & Packing Material Dispensing in Warehouse in a regulated OSD 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.

Role & responsibilities Solid Oral - Production & Packing Officer - Executive and Plant Operator - Technical Assistant : Tablet/ Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. Tablet/ Capsule - Blister Line (BQS), CVC Bottle Line Warehouse (Supervisor / Machine Operator): Officer Senior Executive and Plant Operator - Technical Assistant: RM, PM, FG, Dispensing, Dispatch , Documentation Engineering Executive/Sr. Executive: Process Equipment (Mechanical/Electrical/Instrumentation) of OSD Plant like preventive maintenance and breakdown related activities of equipment of OSD plant such as FBD, FBP, RMG, coating, compression, capsule, Packing machine etc. Technician: Process equipment's- Fitter/Electrician/ Instrumentation: Handling preventive maintenance and breakdown of equipment of OSD Plant such as FBD, FBP, RMG, coating, compression, capsule, sifter, stirrer, Wurster coater, packing machine etc. HVAC Operator - Operation and maintenance of AHU, Cooling tower, BMS, Chiller Quality Assurance (IPQA) Officer / Senior Executive: IPQA in process (Mfg. and Pkg.) Quality Control (Analyst) Officer / Sr. Executive: HPLC / GC / IR / UV / Dissolution and other QC Equipment/ QC Method Validation and Transfer.

Coordinate technology transfer activities for (OSD) formulations from R&D to manufacturing sites, Support scale-up, exhibit, and validation batches, participate in investigations, deviation handling, and change control activities.