670 Injectables Jobs - Page 4

Job Summary We are seeking an individual to oversee batch manufacturing, ensuring adherence to cGMP (Current Good Manufacturing Practices), providing training, and coordinating day-to-day activities. Responsibilities include minimizing machine downtime, managing subordinate staff, assuring compliance with standards and SOPs (Standard Operating Procedure), leading regulatory audits, compiling reports, ensuring safety norms, and budget management. Roles & Responsibilities • You will be responsible for enforcing cGMP for batch manufacturing in order to obtain high-quality products and achieve targeted production within a span of control. • You will be responsible for imparting general and cGMP ...

Walk In drive for Formulation Research & Development - Department FR&D - MSN R&D Center Pashamylaram on 18.10.2025 (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 an...

Fill cart with supplies and transport cart to assigned area. Enter guest rooms following procedures for gaining access and ensuring vacancy before entering. Replace guest amenities and supplies in rooms. Replace dirty linens and terry with clean items. Make beds and fold terry. Clean bathrooms. Remove trash, dirty linen, and room service items. Check that all appliances are present in the room and in working order. Straighten desk items, furniture, and appliances. Dust, polish, and remove marks from walls and furnishings. Vacuum carpets and performs floor care duties (eg, in guest rooms and hallway). Follow all company and safety and security policies and procedures; report any maintenance p...

Role & responsibilities Leading a team of PHD & master graduates in areas of natural products identifying & executing new researching projects aligning with company goals Monitoring & maintaining lab instruments to ensure minimum down time Working with manufacturing teams for trouble shooting process related issues Working with other teams to support multi-disciplinary research projects.

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

• Communicate and collaborate with subordinates on goals. • Ensure complete strategy/system implementations as per directives • Induct new employee as per companys policy, ensuring no deviation while practicing policies and code of conduct • Guide team members to resolve issues, dealing with stockist & chemist. • Prepare and submit the tour programme for self and team as per the guidelines • Monthly analysis of Primary/ Secondary sales, customer coverage etc • Build business relationships with key customers • Brief sub-ordinates on the incentive scheme • Ensure Annual target Achievement of all HQ • Ensure achievement of all New Launches If Interested and have relevant experience, requesting ...

Role Overview: The Engineering Officer will be responsible for supporting engineering projects, supervising maintenance and technical operations, and ensuring compliance with safety and regulatory standards. Youll work closely with senior engineers, technicians, and cross-functional teams to keep operations running smoothly and efficiently. Key Responsibilities: Technical Support & Maintenance: Oversee routine and preventive maintenance of equipment, systems, or facilities Ensure operational readiness and minimize downtime through proactive planning Troubleshoot technical issues and support on-ground teams in repairs and upgrades Project Execution: Assist in planning, budgeting, and executin...

We are hiring for Plant Maintenance/ Process Maintenance Engineer at Amneal Pharmaceuticals Ahmedabad. Only for Pharma experience candidates : Job description: We are looking for passionate and skilled professionals to join our Engineering Injectable plant maintenance Department. (Instrumentation / Electrical / Mechanical). Position: Officer / Executive Qualification: Diploma / B.Tech. (Instrumentation / Electrical / /Mechanical) Experience : 4 to 9 Years Location: Amneal, SEZ Matoda, Ahmedabad What We are Looking For : Hands-on experience in Preventive & Breakdown Maintenance of injectable manufacturing lines such as : Vial Line, Microfiber line, PFS Line & Ophthalmic Line. Schedule mainten...

Knowledge of QAMS (Quality Management System). Preparation & review of MPCRs and electronic batch record in software application. Knowledge of preparation and handling of eLog book application. Preparation & review the SOP, Risk assessment and Protocol (e.g. URS/DQ) of various equipment, facility and utilities. Prepare, review the audit report as per regulatory requirements. Handling of Change Control, Deviation and Incident. Root cause analysis and effectiveness of Corrective & Preventive action for Compliance and implementation after recommendations. Preparation of Investigation and impact assessment. Preparation and review of investigation report generated by deviation. Coordination with ...

Requirement of B.com/m.com Fresher's for Accounts & Warehouse Department

Key Responsibilities : 1. Documentation & Compliance Ensure compliance with cGMP, WHO, EU GMP, USFDA, and other regulatory requirements specific to injectable formulations. Review, control, and maintain SOPs, Quality Manuals, and other QMS documents. Control issuance, retrieval, and archival of GMP documents as per SOPs. 2. Deviations & CAPA Investigation and documentation of deviations, incidents, and non-conformances. Identify root causes using tools like 5 Whys / Fishbone analysis. Initiate, track, and ensure timely closure of Corrective and Preventive Actions (CAPA). 3. Change Control Review and manage Change Control records related to injectable manufacturing. Ensure impact assessments ...

Dear Candidate, We are looking for formulation scientists for our Ophthalmic in Formulations, focusing on the formulation development of sterile ophthalmic dosage forms solutions, suspensions, and emulsions. This role involves complete ownership of formulation and process development with a strong emphasis on regulatory compliance and timely execution. Position: Assistant Manager Department: Ophthalmic team - Formulation Development Required Exp : 6-12years Role & Responsibilities: Formulation & Process Development Independently develop formulations for ophthalmic, injectables and nasal sprays Design and interpret DoE studies for optimization and robustness Technology & Excipient Evaluation ...

For Production (Injectable): Exposure pertaining to Groninger vial filling, Groninger Bottle fiiling, Fedegari Autoclave, NKP vial Filling machine, lyophilizer, Spray dryer, Aseptic process, complex manufacturing, Exposure to CIP/ SIP, SKID manufacturing, pre-fill syringe, QMS is required For Production (OSD): Exposure of granulation, compression and coating process, BMR, Change control, CAPA, For Engineering: Exposure of maintenance of Sterile Manufacturing Plant, maintenance of Autoclave, Filling machine - Vial, Ampoule, Ophthalmic, Lyophilizer, Freeze dryer machine, BFS machine is required Job Location: Sun Pharmaceutical Medicare Limited (Baska) : Nr. Hotel Sarvottam, Survey NO 22 & 24 ,...

Role & responsibilities Prepare, review and submit regulatory documents for new drug applications, product registrations, amendments and renewals to the US, Brazil, EU, India and State Level authorities. Regulatory Submissions : Prepare and submit regulatory documents, including INDs (Investigational New Drug Applications) and NDAs (New Drug Applications) to regulatory authorities. Compliance and Licensing: Ensure compliance with regulatory requirements of US, Brazil, EU & India. Liaise with regulatory authorities for drug licensing, including product registrations, renewals and manufacturing licenses for local and international markets. Ensure timely submission of import licenses and NOcs (...

Role : Executive Small Volume Parenteral Manufacturing Location: Ahmedabad Department: Injectable / Sterile Production Key Responsibilities: Production Operations: Plan, organize, and execute the manufacturing batches of small volume injectable products. Operate / supervise key equipment: vial/ampoule washing, sterilization (autoclave, filtration), filling, sealing, capping, tunnel sterilizer, lyophilizer (if applicable) etc. Ensure line readiness, material dispensing, line clearance before/after operations. Aseptic Process & Sterility Assurance: Maintain cleanroom operations, gowning, environmental monitoring, microbial monitoring. Ensure correct operation of aseptic filling / sterile filtr...

Role Description Key Accounts Manager Must have experience in private hospitals Products - Injectables, antibiotics. (Critical care) Reports To Regional Sales Manager Experience 5 - 8 yrs Location Delhi, Hyderabad, Bangalore. Responsibilities 1. Drive achievement of sales targets for the assigned Key Accounts (Monthly, Quarterly and Annually) both in Primary & Secondary, with tight control on commercial policy discipline. 2.Develop and Drive the Sales Plan based on: a) Deep understanding of each Key Account, in terms of their systems and processes, Key decision makers and influencers, antibiotic consumption patterns. b) Analysis of market trends & competitor activities c) Analysis of our own...

Responsibilities: Lead formulation development for OSD, external preparations, oral liquids, and injectables. Oversee pre-formulation studies, prototype development, and scale - up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (QA, QC, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation. Required skills: Strong knowledge of formulation science and process optimization. Experience in QbD, DoE, and stability studies. Excellent leadership and communication skills. Required Qualification: - B.Pharm/M.Pharm

Biological E. Limited invites experienced, dynamic and self-motivated candidates with 2 to 8 years of experience for the below positions at its Vaccine Business, Shamirpet, Hyderabad: Designation: Sr. Executive/Executive/Sr. Officer/Officer Qualification: M.Sc. (Lifesciences) / B. Pharmacy / Diploma / B.Sc. / ITI PRODUCTION BULK MANUFACTURING (DRUG SUBSTANCE / ANTIGENS) Desired Experience: Applicants with relevant experience in vaccine, biosimilars, or injectable manufacturing will be considered. Perform upstream and downstream activities for bacterial or viral antigens. Execution of production batches in both upstream and downstream areas. Focus on timely execution to ensure that the proces...

Biological E. Limited (BE) invites experienced professionals to join its Specialty Injectables Business located in Genome Valley, Shamirpet, Hyderabad . Available Positions listed below: 1. PRODUCTION PHARMA (Injectables) • Designation: Officer / Senior Officer / Executive / Senior Executive • Qualification: Diploma / B.Sc / B.Pharm / M.Pharm / M.Sc • Experience: 2 to 10 years • Roles: Filling / Autoclave / Compounding / Lyophilization 2. QUALITY CONTROL (Injectables) • Designation: Executive / Senior Executive • Qualification: B.Pharm / M.Sc • Experience: 2 to 6 years (Injectables) • Roles: Raw Materials / Finished Goods / Stability 3. MICROBIOLOGY (Injectables) • Designation: Executive / S...

Biological E. Limited invites experienced, dynamic and self-motivated candidates with 2 to 8 years of experience for the below positions at its Vaccine Business, Shamirpet, Hyderabad: Designation: Sr. Executive/Executive/Sr. Officer/Officer Qualification: M.Sc. (Lifesciences) / B. Pharmacy / Diploma / B.Sc. / ITI PRODUCTION BULK MANUFACTURING (DRUG SUBSTANCE / ANTIGENS) Desired Experience: Applicants with relevant experience in vaccine, biosimilars, or injectable manufacturing will be considered. Perform upstream and downstream activities for bacterial or viral antigens. Execution of production batches in both upstream and downstream areas. Focus on timely execution to ensure that the proces...

Greetings from Kashiv Biosciences!!!! We are looking for Qualification, Validation and QMS Engineer for our Engineering Team in our Biosimilar Manufacturing facility based out of Ahmedabad. Below are the roles and Responsibilities. Roles and Responsibilities: Responsible for Engineering compliance , Equipment Qualification, Validation and QMS activity. Timely escalation of any challenge bottle necks pertaining to engineering compliance to the management (site leadership team) to ensure proper planning and solutions. Representing as a Subject Matter Export of Engineering department in front of regulatory auditors. Responsible for engineering investigations pertaining to equipment failures and...

Foreman Injectables 1 Post based in Amritsar The ideal candidate brings 5-6 yrs exp 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) Operate and tro...

Job Summary We are looking for an individual to ensure strict adherence to safety protocols, SOPs, and quality standards, overseeing batch manufacturing activities, and coordinating with various departments to maintain operational efficiency. The role involves planning and executing production activities, coordinating with cross-functional teams, and ensuring compliance with regulatory requirements, critical for maintaining product quality and meeting production targets. Roles & Responsibilities • You will be responsible for adherence to company safety norms, policies, and SOPs (Standard Operating Procedures). • You will oversee batch manufacturing activities according to e-BMR instructions ...

Roles and Responsibilities Ensure compliance with regulatory requirements for equipment qualification, utility qualification, area qualification, transport validation, smoke testing, injectables, sterile, injection, vial washing, isolators, insulators, terminal sterilizer, RABS, Automatic leak testing machine chambers. Utility qualification (HVAC, WFI, PW etc), Facility and Area Qualification. Air flow visualization study (Smoke study) Develop and implement effective QA procedures to maintain high standards of production. Collaborate with cross-functional teams to resolve quality issues and improve processes. Maintain accurate records of all QA activities, Prepare and develop IQ,OQ,PQ & RQ p...

Roles and Responsibilities Conduct analytical testing using various instruments such as GC, HPLC, spectrophotometer, etc. Prepare samples for analysis and record results accurately. Maintain laboratory equipment and ensure proper functioning of instruments. Develop and validate new methods for analyzing chemicals and materials. Collaborate with cross-functional teams to resolve issues related to product quality. Should be familiar with software Caliber LIMS To analyze AMV, IP, CV, PV, FP stability products Worked in CGMP, GLP and GDP maintained environment in laboratory Who can Apply : Candidates with core Injectables experience