876 Injectables Jobs - Page 2

Key Responsibilities: Patient Consultations & Diagnosis: Conduct in-depth consultations with clients to assess their aesthetic needs and medical history. Diagnose skin conditions and develop personalized treatment plans. Advise on both clinic-based treatments and at-home care to optimize results. Performing Aesthetic Procedures: Administer non-invasive treatments such as lasers, injectables, chemical peels, microdermabrasion, and other cosmetic dermatology procedures. Maintain clinic standards and follow strict protocols for safety and efficacy during all treatments. Stay updated on the latest techniques and technological advancements in aesthetic medicine. Writing Prescriptions & AM-PM Rout...

Roles and Responsibilities Perform sterilization processes such as autoclave, vial washing, and lyophilization. Operate equipment including OT (Operation Theatre), tunnel, injectables, injection machines, USFDA compliant systems. Ensure proper cleaning and aseptic techniques are followed in ICU settings. Maintain accurate records of media fill testing results. Collaborate with team members to ensure smooth operation of CSSD department.

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

Biological E. Limited invites experienced applicants to join in the below departments for our Vaccine Facility in Hyderabad with 1- 7 years experience for Production - Blending, Filling , Manufacturing - Antigens & Engineering Departments on Friday, 12th December 2025. Educational Qualifications: M. Sc (Lifesciences), B. Tech (EIE, EEE), Diploma (Lifesciences), B. Sc (Lifesciences), ITI(with relevant experience) Roles and Responsibilities: 1. Production Bulk Manufacturing (Drug Substance / Antigens) To perform Upstream and Downstream activities of bacterial & viral antigens (Vaccines) Execution of upstream and downstream production batches. Focus on timely execution, to ensure that the proce...

Greetings from Immacule Lifesciences Pvt Ltd! We Are Hiring Packing Department Operators for Our New Injectable Manufacturing plant Location: Nalagarh We are looking for Visual Inspection Operators with the following qualifications: Education: ITI / Diploma Experience: 3 7 years in Visual Inspection machine operation & troubleshooting USFDA-approved injectable manufacturing plants (mandatory) Interested candidates with relevant experience, please share your updated resume via WhatsApp at: 9490101534 or mail ID: Eswar.reddy@immacule.in

Job Description Strong expertise in formulation development of sterile liquid injectable dosage forms, including end-to-end development and troubleshooting. Hands-on experience in drug device combination product development, with good understanding of device compatibility, functionality, and regulatory expectations. Proven experience in developing and handling lyophilized drug products (peptides, proteins, and small molecules), including cycle development and optimization.

Key Responsibilities JOB DESCRIPTION Your Responsibilities Include, But Are Not Limited To Prepare Regulatory strategies for Complex Products [like injectables that may include Peptides, Microspheres, Liposomes, Nano-suspensions etc./ Ophthalmic/ Otic/ Topical gel/ DDCP etc.] and 505(b)(2) Products for US and EU market. Draft Pre-ANDA/Pre-IND/ScA meeting packages for US and EU market. Draft controlled correspondences on complex issues. Draft Deficiency responses for Complex Products and 505(b)(2) Products. Review API and FP in-vitro characterization/sameness reports. DMF review for complex APIs as per the workflow. To collaborate and work closely with cross functional teams. Qualifications M...

Job Description: You will be working as an Assistant Manager for Injectables and Ophthalmic products in Chennai. With 7-8 years of experience, you will be responsible for leading a team of 2 individuals. Your role will involve ensuring the quality and timely production of injectables and ophthalmic products. Key Responsibilities: - Leading a team of 2 individuals in the production of injectables and ophthalmic products - Ensuring the quality standards are met for all products - Overseeing the timely production and delivery of the products - Collaborating with other departments to optimize production processes Qualifications Required: - M.Pharm in Pharmaceutics Please note that the above job ...

**Role Overview:** You will be joining Dr. Jamuna Pai's Skin Lab in Ahmedabad as a full-time Consultant Dermatologist. Your main responsibilities will include diagnosing and treating various skin conditions and diseases, performing cosmetic dermatology procedures, and providing advanced treatments for acne, pigmentation, anti-aging, and more. Your role will involve conducting consultations, creating personalized treatment plans, and staying updated with the latest advancements in dermatology and cosmetic skin care. Collaboration with other healthcare professionals to ensure comprehensive patient care will also be a key aspect of your role. **Key Responsibilities:** - Diagnose and treat a wid...

Dear Candidate, Greetings from Intas Pharmaceuticals Ltd.! Intas Pharmaceuticals is a leading, vertically integrated global pharmaceutical company headquartered in Ahmedabad, India, with a strong presence in over 85 countries. Driven by innovation and quality, Intas is committed to developing and manufacturing affordable medicines that improve lives across the world. We are pleased to announce a Walk-In Drive for our SEZ Plant for professionals experienced in Injectable/Parenteral Manufacturing operations including Sterile Aseptic Clean Area Manufacturing Experience Required: - 3 to 12 Years Qualification Required: - Diploma / ITI Walk-In Drive Details: - Date: Sunday, 7nd December 2025 Time...

1. Manufacturing- Experience Operators Any Diploma / B. Sc with 2 to 12 years of relevant Experience in manufacturing injectables Operate production equipment such as Injectable , Sterile , Parenteral machines, Vial / Ampoule filling , Capping , Compounding , Washing ,Sealing, Terminal sterilization, Stopper process. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance tasks on equipment as required. Collaborate with other team members to resolve issues and improve overall efficiency. Ensure adherence to Good Manufacturing Practices (GMP) guidelines. Must ha...

Role & responsibilities Leading a team of production QMS members Responsible for preparation & review of the master documents of sterile manufacturing department and warehouse department for Parenteral facility. Responsible for preparation and review of Protocols and reports based on the requirements. Responsible for Document management like BMRs, BPRs, Master SOPs etc.. Responsible for the handling (Preparation/Initiation/Execution and Approval) of Change Control, Deviations, CAPA, Investigation, QRM, Protocol, Purchase specification etc.. for sterile manufacturing department & warehouse department. Responsible for the Review and Approval of CFTs Change Control, Deviations, Investigation, Q...

Pfizer Healthcare India Private Limited - Visakhapatnam Hiring Diploma Pharmacy / Diploma Mechanical Freshers (2024 & 2025 Batch) Job Role - Junior Associates - Manufacturing Eligibility Criteria: Diploma Pharmacy/ Diploma Mechanical only (2024 & 2025 Pass out) & Pass Percentage 60% in Academic & No backlogs. Job Description Operate production equipment such as injectable machines, sterile machines, parenteral machines, formulation machines, filling machines, capping machines, compounding machines, washing machines, sealing machines, Visual inspection & packing machines. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain a...

Role & responsibilities 1. Responsible to review technology transfer documents received from R&D 2. Responsible to ensure completion of new product introduction at site by effective gap assessment in coordination with cross functional departments. 3. Preparation of scale up batch BPCR, protocol, reports and monitoring of scale up batches and technical support during execution of scale up batches. 4. Handling of new product change controls and knowledge in QMS activities 5. Monitoring of exhibit batches and technical support during execution of exhibit batches. 6. Responsible to conduct new product technical meetings for product process validation activities with cross functional departments ...

"• Operation, & Maintenance, of all packaging equipment & Parenteral of following block: Main Pharma Block. Cephalosporin Block, Rifampicin Block • Operation & Maintenance of associated systems • To develop Total Quality Maintenance system on all manufacturing equipment • To develop workable history card system. • To create a PPM team to ensure thorough overhauling. • To ensure Preventive maintenance of all manufacturing equipment. • To co-ordinate with various contractors & consultants in matters related to Engineering works. • Follow up for periodical Scheduled maintenance of all utility equipment. • Placement of PPM schedule near the concerned equipment. • To develop a workable History ca...

"• To ensure smooth and efficient functioning of plant machineries at main Pharma block. • To attend routine breakdown maintenance of production machinery of main pharma block. • To attend the modification and development work in machinery as per guidance of engineer. • To ensure proper shift handover charge to next shift technician. • To ensure area readiness for audit point of view."

Role & responsibilities To follow the cGMP Rules and regulation. Documentation Control: maintenance, updation and issuance of documents in compliance with regulatory requirements and implementation of Good Documentation Practices. Review and approval of all Master documents like SOP, Batch Manufacturing record, Batch packing record, Calibration schedule, Preventive maintenance Schedule and other quality related documents. Responsible for preparation and review of protocol and report for Process validation, Cleaning validation as per the schedule and validation master plan. Handling of documents like SOPs, formats / Annexures, Log Books, BMR / BPR & all other GMP Documents like Change control...

Role & responsibilities 1.Production Planning & Execution Develop and oversee monthly, weekly, and daily production schedules based on Sales or Demand forecasts and inventory levels Monthly Production plan preparation based on pending export, tender orders and sales forecast. Create Plan order in SAP. Monitor Daily production plan VS Actual, incase of any deviation then discuss with production team Optimize batch planning to minimize changeovers and maximize equipment utilization. Track and monitor production performance, identifying and resolving issues. 2. Inventory & Material Management Inventory Monitoring and Product availability Ensure the availability of raw materials, excipients, and...

Prepare marketing strategy for the assigned group of products • Develop a strategic business plan for the group of products in collaboration with marketing & sales department • Ensure that the operational marketing plan is in line with overall marketing plan and priorities to achieve the sales targets • Prepare marketing collaterals for the branding of the new product & prepare plan, budget and executing the launch of the products in coordination with internal team, sales team and marketing team. • Identify target audiences, plan marketing activities to achieve volume estimations, review products and execute promotions to ensure product movements Role & responsibilities Preferred candidate p...

Role & responsibilities Should have an experience of minimum 20 years from a reputed pharma industry and out of that at least in one organization is biologicals/Biosimilars/Monoclonal antibody Manufacturing facility . Should have experience in handling Fermenters/Bioreactors, all utilities related to Biological production, Drug Substance and Drug Product, Validations and related documentation. Should have experience in Break down maintenance and Preventive maintenance of all equipment. Should have experience in handling all Statutory audits.

Role & responsibilities Prepare marketing strategy for the assigned group of products Develop a strategic business plan for the group of products in collaboration with marketing & sales department Ensure that the operational marketing plan is in line with overall marketing plan and priorities to achieve the sales targets Prepare marketing collaterals for the branding of the new product & prepare plan, budget and executing the launch of the products in coordination with internal team, sales team and marketing team. Identify target audiences, plan marketing activities to achieve volume estimations, review products and execute promotions to ensure product movements. Liaise closely with field fo...

Role & responsibilities :- 1.Production Planning & Execution Develop and oversee monthly, weekly, and daily production schedules based on Sales or Demand forecasts and inventory levels Monthly Production plan preparation based on pending export, tender orders and sales forecast. Create Plan order in SAP. Monitor Daily production plan VS Actual, incase of any deviation then discuss with production team Optimize batch planning to minimize changeovers and maximize equipment utilization. Track and monitor production performance, identifying and resolving issues. 2. Inventory & Material Management Inventory Monitoring and Product availability Ensure the availability of raw materials, excipients, ...

Role & responsibilities To develop, execute, and monitor production planning and scheduling strategies for pharmaceutical manufacturing, ensuring smooth operations, material availability, and compliance with regulatory requirements. Reporting To Head-PPC Geographic Location Ahmedabad, Gujarat, India Education: B. Pharm / M. Pharm / B.Sc. / M.Sc. / MBA (Operations / Supply Chain) or equivalent. Experience & exposure Experience: 10-15 Years years in Production Planning & Control (PPC) in Injectable Pharmaceutical Manufacturing. Key Responsibilities 1.Production Planning & Execution Develop and oversee monthly, weekly, and daily production schedules based on Sales or Demand forecasts and invent...

Role & responsibilities Consult with and treat patients at the designated clinic, perform all dermatology-led medical procedures, and supervise non-dermatology-led procedures. Ensure the efficacy, safety, and adherence to high professional standards for all medical procedures performed under your supervision. Preferred candidate profile MBBS and Masters (MDDVL), Diploma (DDVL, DVD) or Doctorate (DNB) in Dermatology. Strong knowledge and experience in medicine and dermatology. Excellent communication skills and Energy Levels. Ability to connect well with clients.

EXP IN INTERNATIONAL MARKET Fluent in English communication Passion to promote brands scientifically Good analytical skills and good in multitasking Willing to travel abroad Should be B.Sc./B. Pharma + M.Sc/M. Pharma/MBA Location : Ahmedabad (Head Office) + Frequent travel to assigned continents