876 Injectables Jobs - Page 3

Job Summary: Accountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products including technical and Regulatory aspects. Responsible for: • Development and Implementation of regulatory strategies for global registrations for products within the biosimilars portfolio • Coordination of activities and deliverables provided by other cross-functional teams to support the development, approval, and long-term planning of biosimilar products • Collaboration with partners to develop and execute global regulatory activities • DMF preparations, review of changes and routine updates to Global Regulatory Agencies • Dossier p...

Quality management System, Injectables ; Production QMS

To design, establish and maintain appropriate Quality Management Systems to meet the dynamic regulatory demands, customer specific requirements, and local statutory requirements and ensure continued compliance to the same. Direct responsibilities include but not limited to the following: Overall compliance status of the Plant across all functions. Implementation of Quality Management System. Overall qualifications (facility, equipment etc). Overall validations at Plant (process, cleaning, etc) Overall audits at Plant (regulatory and customer). Development of quality systems and training of people. Creation and execution of SOPs across all functions in conjunction with department Head’s. Manp...

Key Responsibilities 1. Business Development Identify, target, and acquire new investors for mutual fund products. Build and maintain relationships with retail, HNI, and corporate clients. Conduct investor meetings, Required Candidate profile Relationship building Sales negotiation Product knowledge (Equity funds, Debt funds, Hybrid funds, SIPs) If you interested, share me your CV at. hrcps9@gmail.com 8370014003

Role & responsibilities Job Responsibilities: 1. Handling of stability section independently. 2. Handling of additional stability studies, such as, Photo stability, In-use studies, freeze thaw studies. Split studies etc. 3. Preparation of stability protocols, reports and stability compilation. 4. Responsible for timely initiation, closure of QMS documents related Quality Control and implementation respective corrective and preventive action. (i.e. Change controls, Laboratory Incidents, OOS, OOT & CAPA) 5. Responsible to follow ALCOA + principle while doing the data recording. 6. Review of In-process, finished, stability, process validation, in-process, Raw material, Excipients, packing mater...

Primary title: Consultant Dermatologist About The Opportunity We operate in the private healthcare sector specializing in clinical dermatology and aesthetic skin services across India. Our clinic network delivers evidence-based medical dermatology, minor surgical procedures, and advanced cosmetic treatments to a diverse patient population in an on-site clinical setting. Role & Responsibilities Provide outpatient clinical assessment, diagnosis, and management for a broad range of dermatologic conditions, including inflammatory, infectious, and chronic skin diseases. Perform office-based procedures such as skin biopsies, excisions, cryotherapy, minor dermatologic surgery, and basic reconstruct...

Role & responsibilities: Prepare BMR for new products to be processed on the lines. Online BMR, BPR entries to be updated and all formats of relevant SOPs to be completed. Raise material requisition and receive the materials from stores. Preparation of SOPs for the vials and cartridge processing area and ensure training of it for the line operators. To improve the yield of the lines and to reduce the rejections. To prepare the samples as per the customer requirements and complete the entries in BMR and logbooks. To complete the SAP entries for the line activities online. To ensure that the completed batch pallets are transferred to ready to ETO area/ nonsterile FG area and line is ready for ...

Overview We are seeking a highly organized, proactive, and detail-oriented Executive Assistant to support our Senior Vice President (SVP)/ Vice President (VP). This role requires a high level of professionalism, discretion, and the ability to anticipate needs while managing a wide range of administrative and executive support tasks in a fast-paced environment. Responsibilities Manage and optimize the SVP/VPs calendar, scheduling meetings, appointments, and travel arrangements. Prepare, review, and organize correspondence and other confidential documents. Coordinate internal and external meetings, including logistics, agendas, and follow-ups. Serve as a liaison between the SVP and internal/ex...

Biological E. Limited invites experienced applicants to join in the below departments for our Vaccine Facility in Hyderabad with 2- 10 years experience for Manufacturing - Antigens Department. Educational Qualifications: M. Sc, Diploma (Lifesciences), B. Sc (Lifesciences), ITI(with relevant experience) Roles and Responsibilities: 1. Production Bulk Manufacturing (Drug Substance / Antigens) To perform cell culture and virus culture activities. Handling of anchorage dependent mammalian cell cultures Preparation and maintenance of cell banks (Master and Working seed banks) Revival of cell banks in TC flasks Handling of cell growth in TC flasks from T525 to CS40 Preparation of Bioreactors and ce...

We are hiring for the Injectable manufacturing Unit Location - Pune Experience - 1 to 1 0 Yrs Number of position - 10 Autoclave Operator - 5 Filling operator - 5 Aseptic are experience mandatory. Kindly share your CV with the mention of current CTC, ECTC and NP.

Role & responsibilities Perform validation activities: Equipment validation, process validation. Develop and execute protocols: Create and perform validation protocols and test plans for equipment, processes, and systems. Ensure compliance: Ensure all activities and documentation adhere to company SOPs and external regulatory requirements, such as GAMP and GMP. Document and review: Prepare & review documentation, including reports, batch production records (BPRs), and change controls. Collaborate with teams: Work with cross-functional teams. Analyze data: Analyze validation data to identify trends, resolve issues, and confirm that systems meet their intended specifications. Support audits: S...

Walk In Drive For Production Injectables In Formulation Division @ Jadcherla Department:- Production Injectables Qualification :-ITI| BA | Diploma |B Com | BSC | B Pharmacy Experience :- 2 To 8 Years Division :- Formulation Work Location :- MSNF-II,Kothur, MSNF-V, RK Puram Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Lyo, Compounding, Autoclave,Vial Filling, Vial ...

Walk In Drive Quality Assurance Sterile Department In Formulation Division @ Elite Hotel ( MANJEERA HOTELS AND RESORTS) Department :- Quality Assurance Sterile Qualification :- B Pharmacy | M Pharmacy | MSC Chemistry Experience :- 2 to 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location:- Elite Hotel ( MANJEERA HOTELS AND RESORTS) NH 44, Hyderabad - Bangalore Highway, Jadcherla, Macharam, Telangana 509301 Contact No:- 040-30438701 | 070970 92829 | Note:- Candidate should bring Update Resume ,Increment Letter,Payslips, Bank Statement, Certificates,Aadhar Card & Pan Card We are looking for candidates those w...

Role & responsibilities Production - Autoclave, Compounding, filling, QMS, Vial Washing, Lyophilizer QC- Instrument Analysis, Finished Products & Stability EHS

Company Description SKIN COSMO combines luxury skincare with cutting-edge scientific innovation to offer premier treatments that enhance and rejuvenate natural beauty. We focus on using advanced dermatological solutions to provide personalized care, ensuring every client enjoys a radiant complexion and a boost in confidence. Known for our state-of-the-art technologies and tailored approaches, SKIN COSMO stands out as a leader in the cosmetology industry. Our mission is to deliver transformative skin treatments while prioritizing client satisfaction and well-being. Role Description This part-time Aesthetic Physician role is an on-site position located in Bengaluru. The Aesthetic Physician wil...

Job Description: Qualification: B.Pharm / M.Pharm / M.Sc (Chem) / M.Sc (Microbiology) With Production experience of 510 years Experience required in sterile / Injectable / OSD / USFDA / EUGMP / PICS approved facilities API is not preferable Disclaimer: The job location mentioned in this description is based on publicly available information or company headquarters. Candidates are advised to verify the exact job location directly with the employer before applying

Consult and diagnose skin concerns, provide treatments and cosmetic procedures, ensure follow-ups and patient satisfaction. Supervise dermat services, ensure safety, quality process adherence, and handle emergencies at clinic level. Required Candidate profile MBBS with a post graduate qualification in dermatology (MD, DNB, DVD, DDV) from recognized and reputed medical colleges. Perks and benefits Highly competitive incentives

Job Title : Consultant Dermatologist Aesthetic & Clinical (Full-time/ Part-time/ Contract) Location Dermis 365 Advanced Skin, Hair, Body & Laser Clinic Kanakapura Road, Bengaluru https://maps.app.goo.gl/qBXwWBXJum4xW31e8 About Dermis 365 Dermis 365 is a doctor-led, protocol-driven advanced aesthetic clinic offering skin, hair, body contouring, lasers and IV therapy . Our focus is on safe, ethical, evidence-based treatments with strong clinical protocols and a premium patient experience. Role Overview We are looking for an experienced Consultant Dermatologist who is passionate about aesthetics and results-driven treatments. You will lead clinical decision-making, consultations and advanced pr...

Position : AGM - Production Injectables. Experience : 14 to 18 years. Designation : Assistant General Manager Qualification : M. Pharmacy/Pharmacy Experience from sterile formulation industry (Injectable) No.of Vacancies : 1 Job Description Responsible to ensure all the activity in manufacturing area of lines. Approval of Indented Raw Materials, Primary Packaging Materials as per the production plan. Coordination with cross functional team in the batch planning and ensure the Process flow, Personnel flow; Material flow shall be done as per the procedures. To ensure compliance to the validation schedules - qualification, requalification of area, equipment, and facility. To Ensure Prior intima...

Role & responsibilities At least 8 years experience in formulation and development for oral liquid dosage and Injectable device dosage form for with US & EU Should have done active contribution in liquid products development which includes identification of excipients, prototype formulation based in innovator product characterization Identification of right primary packaging components. Initiate stability batches with generating required GxP documents Candidate should have detailed understanding of scale up and EB manufacturing Should independently monitor and prepare formulation development documents like development report, MFC, specifications, tech transfer documents. Candidate should sup...

Job Description Sr. Executive, Regulatory Affairs (ROW Markets) Department: Regulatory Affairs (RA ROW) Experience: 4–8 Years Location: Hyderabad Company: Jodas Expoim Pvt. Ltd. Role Summary The RA-ROW Sr. Executive will be responsible for preparing, reviewing, and submitting regulatory dossiers for Rest of World (ROW) markets, ensuring compliance with country-specific regulatory requirements. The role requires strong coordination with cross-functional teams in Manufacturing, QA, QC, R&D, Packaging Development, and SCM to support product registrations, renewals, and post-approval lifecycle management. Key Responsibilities 1. Dossier Preparation & Submission Prepare, compile, and review regul...

Amneal Pharma Walk-in Drive @ Pharma-SEZ, Matoda, Ahmedabad, (Gujarat) for Quality Assurance (Injectable/ Sterile) on 30th November 2025 (Sunday) We are looking for suitable candidates for Quality Assurance (IPQA-EM) for Injectable Manufacturing, SEZ Matoda, Ahmedabad Interview Details: Date: 30th November, 2025 (Sunday), Time: 09:00 AM to 03:00 PM Interview Venue : Amneal Pharmaceuticals Pvt Ltd Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad | Gujrat Job Location: Ahmedabad (SEZ Matoda) Department : Quality Assurance Designation : Apprentice - IPQA EM Total Experience: Fresher Qualification: M.Sc (Microbilogy) Required Skills: -Basic knowledge of microbiology ...

Key Responsibility: Quality Management System (QMS) Activities: Oversee and perform all Quality Management System (QMS) activities for the Quality Control Microbiology department. Conduct and review investigations related to microbiological laboratory OOS/OOT, environmental monitoring deviations, and sterility failures. Identify root causes and recommend corrective and preventive actions (CAPAs). Ensure timely closure of laboratory deviations and maintain thorough documentation. Lead the preparation, review, and approval of QMS documentation, including change controls, risk assessments, and quality records. Perform and oversee the preparation and review of documentation related to microbiolo...

Amneal Pharma Walk-in Drive @ Pharma-SEZ, Matoda, Ahmedabad, (Gujrat) for Quality Assurance (Injectable/ Sterile) on 30th November 2025 (Sunday) We are looking for suitable candidates for Quality Assurance (IPQA / IPQA-EM) for Injectable Manufacturing, SEZ Matoda, Ahmedabad Interview Details: Date: 30th November, 2025 (Sunday), Time: 09:00 AM to 03:00 PM Interview Venue : Amneal Pharmaceuticals Pvt Ltd Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad | Gujrat Job Location: Ahmedabad (SEZ Matoda) Department : Quality Assurance Requirement 1: IPQA Designation : Officer/ Sr. Officer /Executive/ Sr. Executive Total Experience: 02 to 08 years Key Responsibilities: Mon...

Role & responsibilities Sacleup Formulation Study Preferred candidate profile Fresh Mpharm Graduate