670 Injectables Jobs - Page 5

Role & responsibilities APQR Preparation & Management: Collect, compile, and analyze data from various departments (Production, QC, QA, Warehouse, etc.) for APQR. Ensure timely preparation and completion of APQRs for all marketed products. Review trends in product quality, deviations, complaints, OOS/OOT results, and change controls. Compliance & Documentation: Ensure APQRs are prepared in accordance with GMP guidelines (e.g., USFDA, & EU). Maintain accurate and complete documentation of APQRs and related records. Coordinate with regulatory affairs for submission of annual reports when required. Cross-Functional Coordination: Liaise with Production, QC, QA, and other departments to gather ne...

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical a...

Walk-in drive: Senior Chemist / Junior Research Associate - HPLC Analytical Method Validations Work Location: Hyderabad Eligibility: Must have 1 to 3 Years of experience in Analytical Method Validations by using HPLC for Formulation products. M.Sc. / M-Pharmacy or Equivalent Qualification. Job Description : Analytical method validations and method transfer as per cGMP requirements for drug products. Strong experience in handling various analytical instruments like HPLC, UPLC, UV and Dissolution USP type-I and II and type-IV. Dissolution, Assay and Related Substances method validationand method development of finished products like Tablets, Capsules, Pellets, oral suspensions and Injectables ...

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...

Medcare Hospitals Medical Centres is looking for Technician - CSSD to join our dynamic team and embark on a rewarding career journey. Sterilize and maintain medical instruments and equipment. Ensure proper inventory of sterile supplies and their distribution. Monitor adherence to infection control protocols. Maintain detailed records of sterilization activities. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Medcare Hospitals Medical Centres 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 ...

Sr. Executive IPQA Location- Baddi Experience- 7+ years in injection plant Salary Package- 40-50 K Interested one share resume on 9815675900

Role & responsibilities : Ensure cGMP and GDP practices are followed in the respective facility work areas. Review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR). Conduct in-process checks and line clearance at various batch manufacturing stages (Manufacturing, Filtration, Filling, Sealing). Review executed batch records for completeness and accuracy. Collect samples at different stages of batch manufacturing, including in-process and finished product sampling. Ensure shop floor compliance by reviewing equipment usage logbooks. Oversee validation activities such as Aseptic Process Simulation (Media Fill) and Process Validation. Review Risk Assessments for equipment, inst...

Egg Handling Pre-incubation Egg Candling Allantoic Fluids/Embryo Harvesting Inactivation Aseptic Handling and Sampling cGMP Practices Documentation

JOB OVERVIEW: Identify, develop, and explore new market opportunities that are aligned with critical care products for US hospital markets. Develop a pipeline for US hospital markets to manage and maintain a portfolio of critical care products. ESSENTIAL QUALIFICATION: Masters of Business Administration or Graduate degree in life sciences preferred. RELEVANT EXPERIENCE: 12- 15 years of experience working for a pharmaceutical company (including generics) in portfolio management, marketing, business development, licensing, or strategic analysis capacities, preferably with respect to injectable, critical care or other hospital drug products. KEY ROLES/RESPONSIBILITIES: Identify and evaluate new...

Roles and Responsibilities Conduct market complaint investigations, deviation management, and OOS/OOT handling according to established procedures. Ensure compliance with regulatory requirements through vendor qualification, equipment qualification, cleaning validation, water validation, injectable processing, and process validation. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and maintain documentation related to quality control processes. Provide technical support for product testing and analysis. Desired Candidate Profile 4-8 years of experience in Quality Assurance (QA) or a related field within the pharmaceutical industry. ...

Roles and Responsibilities Ensure compliance with cGMP guidelines during batch manufacturing of eye drops, injectables, parenteral products, and injections. Monitor production processes to ensure quality standards are met. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve issues related to formulation development and process optimization. Develop and maintain documentation for batch records, SOPs, and other relevant documents. Desired Candidate Profile 8-12 years of experience in pharmaceutical industry with expertise in ophthalmic manufacturing. Bachelor's degree in Pharmacy (B.Pharma) or equivalent ...

Quality assurance, Change management, Change control, APQR's, Media fill, Microbiology Compliance and Documents handling in software

Job Purpose: To lead and execute formulation development of Novel Drug Delivery Systems (NDDS) in the injectable segment, including liposomes, microspheres, nanoparticles, depot injections, and other complex injectable formulations for regulated and semi-regulated markets. Key Responsibilities: Design and develop NDDS injectable formulations such as liposomes, emulsions, microspheres, suspensions, nanoparticles, and depot systems. Conduct pre-formulation and formulation studies, compatibility studies, and risk assessments. Execute lab-scale and scale-up batches as per QbD principles and DoE designs. Evaluate and finalize suitable processes, components, and primary packaging materials. Ensure...

Role & responsibilities Regulatory Submissions: Lead end-to-end preparation and submission of ANDA and NDA dossiers to the USFDA Manage query responses, amendments, and post-approval submissions (PAS, CBE, Annual Reports) Ensure compliance with current USFDA regulations and guidance documents FDA Interactions: Prepare and submit FDA meeting requests and meeting packages (Type B, C meetings) Participate in and support FDA meetings as the regulatory lead Handle Controlled Correspondence with the FDA for product development and regulatory strategy Product Expertise: Provide regulatory support for complex formulations , including injectables and liquid dosage forms Collaborate with R&D, QA, QC, ...

Hi, We at CIPLA Limited are hiring for Hospital Business Manager (KAM) positions across Coimbatore , Lucknow and Kanpur locations. Please find below job details : Position : Hospital Business Manager Role : Hospital Business / Key Accounts Management Location : Coimbatore , Lucknow and Kanpur Job Purpose Develop and implement a key account management capability, leveraging Cipla's relationships and strengths across therapies, to prioritize, segment, and service key corporate hospitals Key Roles and responsibilities Develop and drive implementation of Cipla India's key accounts strategy and roadmap, by segmenting, prioritizing and targeting the key corporate hospitals (long-term partnership a...

Responsibilities Global Pay Plus Testers. MT MX messaging , SWIFT payments Preferred Skills: Banking->GPP Financial Services Domain->Payments->GPP Generic Skills: Banking Roles and Responsibility Manage and process payments transactions efficiently. Collaborate with cross-functional teams to resolve payment-related issues. Develop and implement new payment systems and processes. Analyze payment trends and provide insights for improvement. Ensure compliance with regulatory requirements and industry standards. Provide excellent customer service and support to clients. Job Requirements Strong knowledge of payment processing and reconciliation. Experience with payment gateways and payment system...

To offer consultation & patient diagnosis, perform/supervise all medical procedures of Dermat Led services ensuring efficacy, safety & high professional standards of medical procedures carried out under your supervision. Required Candidate profile Consultation & Patient Diagnosis Perform doctor led services Candidate must be MD or DVD or DDV or DNB in Dermatology Lucrative incentive will also be given CONTACT-Ishan/Neetu 9910796268/7838473883 Perks and benefits Leaves & Incentives as per company policy

* Documentation & qualification of laboratory instruments. * Preparation & review of SOPs and URS Qualification * Expertise in Water System Qualification * Strong command of written English * Supporting audits and ensuring regulatory compliance.

Roles and Responsibilities Operate production equipment such as granulation, compression, coating, packaging machines to ensure efficient manufacturing processes. Monitor and control the quality of injectable products during production runs to meet regulatory requirements. Perform routine maintenance tasks on equipment and machinery to prevent breakdowns and optimize performance. Collaborate with cross-functional teams to resolve issues related to productivity, quality, or safety. Ensure compliance with Good Manufacturing Practices (GMP) guidelines in all aspects of production operations.

Consultant – FDA & Intl Pharma Compliance | 20-25 yrs exp in USFDA/MHRA/WHO GMP, audits, DMF/CTD, QMS, validation & formulation (solid, liquid, semi-solid, injectables). Mentor QA/QC/R&D, guide compliance for global markets.

Job Title: Senior Manager - Engineering Business Unit: Sun Global Operations Job Grade G9B Location : Halol At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: This role is responsible for oversee...

Excellent scope for both (Fresher & Experienced Dermatologist) to offer client consultation, supervise and execute advanced skin & hair cosmetic procedures at the clinic. Responsibilities & Duties: 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. Deliver treatments of the highest quality, following established SOPs and company guidelines. Strive for high client satisfaction in all consultations and treatments, as reflected by client feedback and evaluations ...

Role & responsibilities JOB RESPONSIBILITIES 1. Responsible to establish overall Production plan for the site. 2. Responsible for coordination with Cross function team in securing the inputs required for mapping the schedule. 3. Responsible to ensure to materials availability well before execution of the batches on line. 4. Coordination with respective stake holders in getting the inputs on the material releases. 5. Responsible to prepare production plan weekly/fortnightly/monthly plans. 6. Intimation/ submission of production plans to all cross functional teams. 7. Responsible to keep the relevant team informed on the plan changes. 8. Responsible to accommodate the priority products/adjustm...

Title: Parenteral Line Manager Job Grade: G9 Senior Manager Educational Qualification: B.Pharm / M.Pharm Location: Baska, Gujarat Experience: Knowledge of parenteral manufacturing operations Understanding regulatory guidelines Leadership & Team Management Skills Problem Solving & Decision-Making Proficiency in handling production documentation & compliance Min. 15 years of experience working in sterile manufacturing plant or Block In-charge experience Position Summary Responsible for plant operations from material procurement to product dispatch along with operational activities, manufacturing actions, lean management, training, regulatory compliance, cross functional coordination, new produ...