670 Injectables Jobs - Page 3

Job Description Perform protocol for drug excipient compatibility studies and submit the protocol for review and approval Complete lab. experiment hands-on independently (Lab scale to exhibit batch and query handling). Dosage forms experience: Solid Orals Predominantly more than 90% in career. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development. Carry out /Support Scientific literature search (CVM/USFDA/Daily-med/publications). Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments. Compilation, interpretation and review o...

Supervise daily production activities of injectable formulations. Ensure compliance with cGMP, safety, and quality standards. Plan and execute production schedules to meet targets Coordinate with QA, QC, Maintenance, and Warehouse teams. Required Candidate profile Lead and train production staff for operational efficiency. Handle documentation: BMRs, SOPs, deviations, and change controls. Support audits – internal & External, regulatory schedule M compliance.

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...

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...

Aster Medcity is looking for Junior Technician - CSSD to join our dynamic team and embark on a rewarding career journey. A Junior Technician - CSSD (Central Sterile Supply Department) is responsible for assisting with the cleaning, sterilization, and distribution of medical equipment and supplies used in healthcare facilities. Their tasks may include inspecting and assembling surgical instrument sets, operating sterilization equipment, maintaining accurate records of inventory and usage, and ensuring compliance with infection control protocols. They should have knowledge of sterilization techniques and equipment. Loading the materials for sterilizationReceiving, checking and segregating the ...

Role Overview: As a Regulatory Affairs Specialist at Amneal, your primary responsibility will be to prepare regulatory strategies for complex products such as injectables, ophthalmic, otic, topical gel, and 505(b)(2) products for both the US and EU markets. You will be drafting Pre-ANDA/Pre-IND/ScA meeting packages, controlled correspondences, and deficiency responses for complex products. Additionally, you will review API and finished product in-vitro characterization reports, collaborate with cross-functional teams, and ensure compliance with regulatory standards. Key Responsibilities: - Prepare Regulatory strategies for Complex Products including injectables, peptides, microspheres, lipos...

Role & responsibilities 1. Candidate will be based at Pharma R&D Center at Thane and will Analytical Research and Development for Regulated & Row Market with focus on Injectable Dosage. 2. Candidate should have expertise in Analytical Method Validation and Method Development, Routine, Stability for Injectables for Regulated/ROW Market. 3. Experienced and responsible analytical development to develop and Validate new analytical methods for analysis of formulations Injectable dosage forms as per ICH guidelines. 4. Candidate have to support and troubleshooting in the development and validation of analytical methods working across the technical teams. (Routine, Stability, Method Development and ...

Role & responsibilities An IPQA (In-Process Quality Assurance) Lead is responsible for overseeing and guiding the IPQA team to ensure all manufacturing and packaging operations comply with cGMP and regulatory standards. Preferred candidate profile Core responsibilities Supervision and leadership: Lead and guide the IPQA team to ensure all in-process quality activities are performed correctly and efficiently. Process monitoring: Conduct real-time monitoring of manufacturing and packaging processes to ensure compliance with standard operating procedures (SOPs) and Good Manufacturing Practices (GMP). Documentation and review: Review and approve batch manufacturing and packing records, logbooks,...

Key Responsibilities: Develop and implement sales strategies to achieve targets for the Critical Care product portfolio. Identify and manage key hospital accounts Promote and detail critical care brands (e.g., antibiotics, anti-infectives, and injectables) in assigned territory. Execute brand promotion activities, CMEs, and scientific discussions with key stakeholders. Handle hospital tendering, rate contracts, and institutional business processes. Ensure effective demand generation and timely supply through coordination with distributors and supply chain. Monitor competitor activities and market trends to identify opportunities for business growth. Prepare sales reports, forecast requiremen...

Job Description As an Area Business Manager (Individual Contributor) you will handle Sales & Business Development of the Critical Care and Nephro Segment based at Kolkata HQ. You will ensure achievement of budget, new product launches. You will handle scientific / medical promotions and effective implementation of strategies. This will be Individual Role. Candidate Profile You should be Graduate or B.Sc 6-8 years in Pharma Sales out of which 2-3 years as As an Area Business Manager (Individual Contributor) promoting Critical Care products. You should be good in Man Management & Business Development. You should have good experience in scientific/ medical promotions, launching new products and...

We are looking for a highly skilled and dedicated Room Attendant to join our team in the hospitality industry. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Maintain high standards of cleanliness and hygiene in guest rooms. Provide exceptional customer service to ensure guests have a comfortable stay. Make beds, change linens, and restock amenities as needed. Handle guest requests and complaints professionally and courteously. Collaborate with other departments to ensure seamless operations. Ensure all rooms meet safety and quality standards before check-in. Job Requirements Ability to work well under pressure and manage multiple tasks simultaneously. Exce...

Looking for a motivated and detail-oriented individual to join our team as a Room Attendant in the hospitality industry. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Maintain high standards of cleanliness and hygiene in guest rooms. Provide exceptional customer service to ensure guests have a comfortable stay. Make beds, change linens, and restock amenities as needed. Handle guest requests and complaints professionally and courteously. Collaborate with other departments to ensure seamless operations. Ensure all rooms meet safety and quality standards before check-in. Job Requirements Ability to work well under pressure and manage multiple tasks simultaneo...

We are looking for a highly skilled and dedicated Room Attendant to join our team in the hospitality industry. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Maintain high standards of cleanliness and hygiene in guest rooms. Provide exceptional customer service to ensure guests have a comfortable stay. Make beds, change linens, and restock amenities as needed. Handle guest requests and complaints professionally and courteously. Collaborate with other departments to ensure seamless operations. Ensure all rooms meet safety and quality standards before check-in. Job Requirements Ability to work well under pressure and manage multiple tasks simultaneously. Exce...

We are looking for a highly skilled and dedicated Room Attendant to join our team in the hospitality industry. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Maintain high standards of cleanliness and hygiene in guest rooms. Provide exceptional customer service to ensure guests have a comfortable stay. Make beds, change linens, and restock amenities as needed. Handle guest requests and complaints professionally and courteously. Collaborate with other departments to ensure seamless operations. Ensure all rooms meet safety and quality standards before check-in. Job Requirements Ability to work well under pressure and manage multiple tasks simultaneously. Exce...

We are looking for a highly skilled and dedicated Room Attendant to join our team in the hospitality industry. The ideal candidate should have 0-2 years of experience. Roles and Responsibility Maintain high standards of cleanliness and hygiene in guest rooms. Provide exceptional customer service to ensure guests have a comfortable stay. Make beds, change linens, and restock amenities as needed. Handle guest requests and complaints professionally and courteously. Collaborate with other departments to ensure seamless operations. Ensure all rooms meet safety and quality standards before check-in. Job Requirements Ability to work well under pressure and manage multiple tasks simultaneously. Exce...

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 ...

Hiring for PPIC officer in MNC formulation pharma company in vadodara location. BSC/MSC/B.pharm/M.Pharm 2 to 6 yr CTC-Up to 5 LPA Apply on : sdpbharuch@gmail.com Sub : PPIC vadodara Free job Share with your friends Required Candidate profile SDP HR Solution 6th Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch

Role & responsibilities To achieve the targets set by the management. Build up a motivated team. To ensure total market coverage, target achievement and information flow from the team to management. Continuously handle the challenges of the market keeping the HO/ ZH/ Client informed. Data / knowledge management. Create + implement a strategy to grow the region. Vacancy management and attrition control. Team performance monitoring, review & management. Compilation of stock and sales statements. Succession Planning. Preferred candidate profile Lead generation to conversion through account management / hospital business. Ensure sales effectiveness by delivering call average and coverage. Mainta...

Job Requirements:- Hands-on experience in injectable manufacturing operations (Compounding, Vial Washing, Filling, Lyophilization, Autoclave, Visual Inspection, etc.) Knowledge of aseptic techniques and GMP compliance Experience working in a regulated pharmaceutical environment preferred

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 ...

Medicamen Biotech - SRL Pharma R&D Centre Required Formulations Profile Designation: Executive/ Scientist Qualifications: M. Pharma - Pharmaceutics Vacant Post: 6 Nos. Experience: 4 to 8 Years Please share profile on uday@shivalikrasayan.com Required Candidate profile Pharma R&D experience must in Formulation USFDA exposer prefer Preparation of Pharmaceutical Development Report Ready to relocate Bhiwadi, Rajasthan Ready to join Immediately Prefer Team Player Perks and benefits Best of Industries Salary based on Experience

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Open Positions: Operators & Supervisors OSD Production & Packing (Onco & Non-Onco) Experience: 0 to 8 Years (Freshers graduated in 2024/25 are eligible) Qualifications: I.T.I / Diploma / B. Pharmacy Key Responsibilities: Operate equipment's in Granulation (RMG, FBD, ACG, GEA), Compression (GEA, Sejong), Coating (NEOCOTA), Capsule Filling (Bosch, MG02), Blister Packing (CAM NMX, HV1, BQS, IMA/ACG), and Bottle Packing (CVC, Optel) lines. Supervise production lines, including Granulation, Compression, Coating, and Packing (Blister/Bottle). Good verbal and written English communication skills 2. Operators & Supe...

As a skilled and compassionate Aesthetic Dermatologist, you are sought after to join our practice. Your expertise in diagnosing and treating various cosmetological procedures will help enhance the appearance and health of our patients. Your responsibilities include: - Performing comprehensive skin assessments and diagnostics - Treating dermatological conditions - Conducting aesthetic procedures such as injectables, laser treatments, chemical peels, and Slimming - Developing individualized treatment plans - Educating patients about skincare - Ensuring patient satisfaction through compassionate care Staying updated with the latest advancements in dermatology, maintaining accurate patient recor...

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...

Use Your Power for Purpose As a Senior Associate, you will play a crucial role in improving patients' lives while working at Pfizer. Your contributions will directly impact the development and delivery of innovative solutions that enhance the quality of life for patients worldwide. Join us in our mission to bring breakthroughs that change patients' lives. What You Will Achieve In this role, you will: Handle Technology Transfer activities & New Product Introduction process Knowledge of validation and practices related to the manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems. Conversant with design & working principles ...