321 Injectables Jobs - Page 11

Key Responsibilities: Execute routine downstream operations including chromatography (affinity, ion exchange, HIC), filtration techniques (TFF, UF, DF, NF), buffer preparation, and formulation of mammalian cell culture-derived products. Maintain accurate documentation including batch records, deviation reports, SOPs & other QMS elements. Support scale-up and tech transfer from lab to pilot/production scale. Ensure strict compliance with cGMP and safety protocols. Collaborate with QA/QC, maintenance, and engineering teams for smooth operations. Troubleshoot process deviations and contribute to root cause analysis and CAPA implementation.

To provide effective disinfection and sterilization services. Assist in performing sterilization activities, such as reprocessing, segregation, decontamination and packing under supervision of medical and surgical equipment/instruments. Assist in performing sterilization activities, ensures all surgical items and instruments are sterilized as per the rules and with the required procedure. Essential duties and responsibilities Responsible for receipt of different un-sterile instrument packs with a checklist and record in appropriate register. Disassembling, decontaminating, inspecting and reassembling surgical/medical instruments in accordance with established procedures. Responsible for cleaning setting up the sets as per the protocol. Autoclave according to laid down protocol and dispatch to respective departments/sections. Ensure that each autoclave cycle is recorded. Packing and wrapping, sealing and labelling instruments and sets. Contributes to effective communication, facilitating teamwork and co-operation within the Department and with other Departments. Responsible for the care and handling of all surgical instruments, sterile stock, linen, supplies and equipment in line with competencies. Performs all duties in accordance with position description & CSSD Technician Competencies Initiates and maintains effective communication lines and teamwork/collaboration within the Operating Theatre & CSSD Maintains a safe clean environment using only authorized cleaning products and adheres to the principles of infection control Promotes & adheres to Occupational Health & Safety Policies & Procedures Any other tasks assigned by supervisor that you are capable to perform. Participates as a team member promoting and contributing to a supportive team environment Attends all compulsory core education and teamwork within the facility Set up instrument wash room with distinct areas for clean and dirty. Set up of all Sterilizers Apply the principles of microbiology & infection control to all activities in restricted and semi-restricted areas. To maintain Quality Control parameters for all methods of sterilization and to document the effectiveness of each method. Working conditions Will work in Shifts (Morning, Evening & Night) of 8.5 hours a day. Will remain on call for emergencies. Stretched working hours Skills & Abilities Should have very good assisting skill. Should have basic knowledge of computers. Should be polite & good in communication while handling patient. Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities: Perform sterilization of surgical instruments and medical equipment. Operate autoclaves and other sterilization equipment. Ensure compliance with infection control protocols. Maintain and monitor sterilization records and inventory. Assist in the preparation and packing of instruments for surgeries. Preferred candidate profile : Diploma with Minimum 2+ Years experience as CSSD Technician in Hospital For inquiries, kindly reach out to - Mr. Hament, at 7011324972 or via email at hament.gautam@fortishealthcare.com

Job Description Roles & Responsibilities You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. You will be responsible to support in scale-up to pilot/plant scales for Injectable Products. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible for technology transfer and execution of the batches. You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up). You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development. You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements. You will be responsible for designing and implementing stability studies for injectable formulations to ensure product quality and shelf life. You will be accountable for troubleshooting formulation and process-related issues during development and manufacturing stages. You will collaborate with cross-functional teams to ensure alignment of formulation development with regulatory requirements and commercial objectives. You will be responsible for staying current with emerging technologies and regulatory guidelines in injectable drug development and incorporating them into your work. You will mentor junior scientists and contribute to the continuous improvement of the formulation development process. Qualifications Educational qualification: Masters in Pharmaceutical/M.Tech in Chemical Engineering Minimum work experience: 5 to 8 years of experience in pharmaceutical company in Injectable products. Skills & attributes: Technical Skills Have work experience on Formulation Development and expertise in inhalation/injectable dosage form. Experience in areas of product development for Generic Injectable Experience in Quality by Design (QbD). Experience in Process Optimization and scale up. Experience in Operational Excellence. Knowledge on Good Manufacturing Practice and Good Laboratory Practice. Experience in Technology Transfer. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams.

To Maintain the machine and work place clean in all respect. Carry out all activities in area with required status labelling procedure as per SOP. To maintain overall cGMP and GDP in department. To impart training and evaluation of company employees. Preparation of SOP, BPR and Validation Protocol. Handling of deviation, incident, change control and CAPA. Responsible for all activities carried out in shift. To ensure availability of secondary packing material for packing activities. Responsible to ensure dispensing, equipment cleaning, visual inspection, vial labelling, cartonator machine,online Responsible for in process Packing activities and Finished good activities as per SOP. Planning and participation in validation of equipment. Report to Department head regarding any process or operation related problem. Manpower planning and allocation of work according to their skill.

We are having opeings in the below departments and should be expertise in the area. Department - Experience - No of openings - Positions OSD Manufacturing - 2 to 9 Yrs - 40 No's - Operator / Sr. Operator / Officer / Sr. Officer / Executive / Sr. Executive OSD & Inj Packing - 2 to 9 Yrs - 40 No's - Operator / Sr. Operator / Officer / Sr. Officer / Executive / Sr. Executive Warehouse - 2 to 9 Yrs - 45 No's - Operator / Sr. Operator / Officer / Sr. Officer / Executive / Sr. Executive IPQA Inj & OSD - 2 to 9 Yrs - 30 Nos - Officer / Sr. Officer / Executive / Sr. Executive Engineering - 2 to 7 Yrs - 45 No's - Technician / Sr. Technician / Officer / Sr. Officer / Executive

Responsibilities: It will be 6 days of working Develop injectable formulations within sterile environment Ensure compliance with regulatory standards throughout product lifecycle Collaborate cross-functionally on project delivery

Roles & Responsibilities: Position: Area Business Manager Therapy- Injectables/Gynecology/IVF Job Description: Sales Target Achievement: 1. Drive sales performance in the assigned area to meet or exceed revenue and growth targets. Implement sales strategies and initiatives to expand market penetration and boost product sales. Monitor daily, weekly, and monthly sales to track progress toward targets. 2. Team Management: Lead, manage, and develop a team of Territory Sales Executives/Managers to achieve sales goals. Conduct regular performance reviews, provide coaching, and address any performance gaps. Ensure the team follows company policies, guidelines, and ethical sales practices. 3. Customer Relationship Management: Build and maintain strong relationships with key healthcare professionals (doctors, pharmacists, hospitals) to promote product awareness. Collaborate with distributors, stockists, and retailers to ensure product availability and timely supply. Resolve customer issues and inquiries promptly to ensure high satisfaction levels. 4. Market Analysis & Strategy: Analyse market trends, competitor activities, and sales data to identify opportunities for growth. Provide feedback to senior management on market dynamics, customer preferences, and product performance. 5. Recommend adjustments to sales strategies to capitalize on market opportunities. New Product Launches: Plan and execute successful new product launches within the area. Train the sales team on new product details and competitive positioning. 6. Ensure promotional campaigns and initiatives are effectively rolled out in the field. Reporting & Compliance: Prepare and submit timely sales reports, forecasts, and market insights. Ensure compliance with industry regulations and company standards, maintaining high ethical practices in all sales activities. If Interested and have relevant experience, requesting you to share your CVs on priya.tripathi@emcure.com

Exp Req - Hospital Sales Exp of Surgical Sales OR Critical Care Division Sales Interested candidates pl. share CV on 9643975459

Biological E. Limited (BE) invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals, to join its Speciality Injectables Business located in Shamirpet, Hyderabad. The available positions are listed below: QUALITY ASSURANCE (IPQA) : Designation : Executive & Senior Executive Qualification : B. Pharm / M. Pharm / M.Sc. Experience : 3-9 Years Required Skills : Providing line clearances during the manufacturing activities like Dispensing, Manufacturing, Visual inspection, Packing and Dispatch activities, Collection and submission of in process samples, finished product samples, stability samples, control samples, cleaning samples and other samples as described in respective procedures/batch manufacturing records and packing records/protocol, Performing AQL inspection and periodic inspection of control samples, Review of the executed batch manufacturing records, batch packing records and protocols, Preparation and evaluation of the visual inspection defect set, test set and qualification of Visual inspectors, Person should have exposure on QMS elements (CAPA,Change control,Deviation). PRODUCTION PHARMA: Designation : Officer & Senior Officer Qualification : Diploma / B. Sc. Experience : 2-6 Years The candidate should possess the following skills: Hands on experience in Operation & Cleaning of Vial Washing machine, Depyrogenation Tunnel, Automatic,Terminal sterilization, Vial Filling and Vial Sealing machine & Automatic PFS filling machine. Hands on experience in Operation & Cleaning Lyophilizers with Auto Loading & Unloading Systems (ALUS). Exposure in Aseptic process activities, Aseptic Techniques, Aseptic filling & sealing activities and Media fill activities. Execution Knowledge on manufacturing and compounding activities. PRODUCTION PHARMA: Designation : Executive & Senior Executive Qualification : M. Pharmacy / B. Pharmacy /M.Sc Experience : 2-7 Years The candidate should possess the following skills: Hands on experience in Manufacturing, filtration, Filling, Lyophilization, Sealing, Pre & post Manufacturing activities. Planning and Execution of Batch Manufacturing Activities, Filling Activities, Lyophilization, sealing activities & filter Integrity. Experience on monitoring of NVPC and trending. Hands on experience in Documentation activities in shop floor. Planning & Execution of Aseptic Media Fill simulation activities & Execution of Interventions. Quality Control: Designation : Executive Qualification : B. Pharm / M.Sc. Experience : 3-6 Years (Injectables) Required Skills: Handling of HPLC/GC with empower Software is mandatory,Ion chromatograph with chromeleon software for DS & DP injectable, UV Visible Instrument, KF and Potentiometer with Tiamo Software, Analysis of In-process, Finished Product, Stability samples of injectable formulation, Knowledge on e-LIMS analysis is preferable, Analysis of AMV/AMT Activities, Analysis of diluent compatibility studies is preferable. Microbiology: Designation : Executive Qualification : M.Sc (Microbiology/Biotechnology) Experience : 3-6 Years Required Skills (EM) : Environmental Monitoring in aseptic areas, Water Sampling, Utility Monitoring, Trend Preparation. Required Skills (Testing): Culture handling , Bacterial Endotoxin Test , Sterility testing , Microbial method suitability (Sterility & BET) , Container closure integrity test , Microbial Limit testing , Water testing , Media preparation and sterilization , Regulatory Audit exposure , Good communication skills , Willing to work on shifts Engineering: Designation : Officer/Sr.Officer/Executive/Sr.Executive Qualification : Diploma/B. Tech. Experience : 3-8 Years The candidate should possess the following skills: Utilities: Candidates with the ability to handle utility equipment such as air compressors,Industrical chillers, and boilers. Candidates should also possess sound knowledge of documentation practices and Quality Management System (QMS) elements. Exposure to regulatory audits/inspections by authorities such as USFDA, MHRA, and other global agencies. HVAC: Candidates should have a strong background in the operation and maintenance of HVAC systems in a sterile/regulated environment. Experience in handling equipment such as AHUs, chillers, cold chambers, LAFs ,DPB,Walkin incubators and SPB. Strong understanding of documentation practices and Quality Management System (QMS) elements. Exposure to regulatory audits/inspections by authorities such as USFDA, MHRA, and other global agencies. Water system: Candidates must have hands-on experience with CSRO, HSRO, WFI, and PSG systems, along with knowledge of routine monitoring and GMP documentation. Familiarity with QMS elements and exposure to regulatory audits (USFDA, MHRA, etc.) is essential. Process Instrumentation - Injectables regulatory : Candidates with the ability to handle Lyophilizer, vial line, PFS line, auto claves and compounding equipments, PFS & Vial line related packing equipments. Candidates should have knowledge on SCADA,HMI and PLCs. Should have exposure in regulatory audits. Should work in shifts and should able to handle periodic activities & documentation and qualifications. Process Instrumentation API regulatory : Should handle shift instrumentation activities and have experience on handling automations that includes PLC & SCADA in API equipment. Should have experience on troubleshooting of Lyophilizer. Should handle periodic activities like data backups etc. should have exposure in regulatory audits. BMS & Outside Instrumentation: Should handle field instruments, SCADA (Honeywell) and PLC during BMS trouble shooting. Should handle shift activities for BMS & IBMS monitoring and trouble shooting. should able to handle periodic activities & documentation and qualifications. Interested Candidates may Walk-in with an updated Resume, latest increment letter, and payslips for the last 3 months on Sunday, Jun 01, 2025 from 09:00 am to 02:00 pm at Hotel Kinara Residency, Utsav Banquet Hall, 2nd Floor, 2-62/2, S.R. Chambers, beside BSNL building, Chandanagar, Hyderabad, Telangana -500050. PS: Candidates who are unable to walk-in may send in their CVs by mention subject as Applying for Department Name to careers@biologicale.com . If an individual has already attended the interview in the past 6 months or has already been offered a position with us, please do not share the profiles. - Human Resources

Location: Gandhinagar, Gujarat (On-site) Job Title: Quality Control (QC) Engineer Position Details Department: Quality Control Reporting To: Senior QC Engineer Working Days: 6 days/week Industry Preference (Mandatory) Applicants must have prior work experience in at least one of the following regulated manufacturing sectors: Sterile/Injectables Manufacturing Medical Devices Manufacturing Medicinal Equipment Manufacturing Position Overview We are looking for a proactive and detail-driven Quality Control (QC) Engineer with 3- 5 years of experience in Sterile/Injectables, Medical Devices, or Medicinal Equipment manufacturing environments. This role is critical to ensuring consistent product quality through comprehensive analytical testing and adherence to stringent regulatory standards. The ideal candidate will have hands-on expertise in chemical analysis, pharmacopeial testing, and GMP-compliant documentation, especially within a sterile or cleanroom environment. Key Responsibilities Conduct routine testing of raw materials, in-process samples, and finished products in accordance with pharmacopeial guidelines (IP/BP/USP/Ph. Eur.). Perform detailed Pharma Copea Testing including identification, assay, dissolution, impurity profiling, and other analytical parameters. Execute general wet chemistry procedures along with pH and conductivity testing . Operate and calibrate analytical instruments including IR Spectroscopy , STIR , and related chemical analysis equipment. Ensure strict compliance with Good Manufacturing Practices (GMP) , Good Laboratory Practices (GLP) , and internal Standard Operating Procedures (SOPs) . Maintain complete and accurate documentation including test reports, calibration records, instrument logs, and change control records. Support investigations related to Out of Specification (OOS) and Out of Trend (OOT) results, including root cause analysis and CAPA. Liaise with Quality Assurance (QA) , Production , and R&D teams for resolution of analytical issues and technical support. Prepare for and participate in internal and external audits, ensuring full laboratory compliance and readiness. Manage sample collection, labeling, storage, and contribute to stability studies where applicable. Candidate Requirements Educational Qualification (Preferred): B.Sc / M.Sc in Chemistry B.Pharm / M.Pharm with a focus on Pharmaceutical Chemistry Experience: 3- 5 years of relevant experience in a pharmaceutical or regulated manufacturing environment Must have worked in Sterile , Injectables , Medical Devices , or Medical Equipment manufacturing Technical Skills: In-depth knowledge of pharmacopeial testing methods and documentation practices Hands-on experience with IR Spectroscopy, STIR, pH meters, and conductivity meters Familiarity with analytical method validation and instrument calibration Strong understanding of Data Integrity , GDP (Good Documentation Practices) , and compliance in regulated cleanroom settings

Kamla Homes is looking for Officer - Sterile Ointment to join our dynamic team and embark on a rewarding career journey Oversee sterile ointment production in cleanroom settings Monitor batch records and ensure GMP compliance Perform in-process checks and manage documentation Ensure safety and quality in operations

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 from the Area Medical Head (AMH) and Area Operations Manager (AOM). Required 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. For more details contact 9908974287 or amulya.doni@olivaclinic.com

Greetings From SP Accure Labs!!! We are conducting Walk-In Interview for Production Injectables formulation department for Compounding Chemist on 30/05/2025 Friday @ our Shamirpet Plant facility. Roles and Responsibilities Conduct quality control tests on injectable products using techniques such as SIP, CIP, TOFFLON, PFS, ISOLATORS, LYOPHILIZATION. Ensure compliance with cGMP guidelines during production activities. Department - Production Role - Compounding activities like CIP, SIP Mixing & Filling Vessels. Desired Candidate Profile 4-8 years of experience in a similar role with (M.Pharmacy, M.Sc, B.Pharma / B.Sc). Strong understanding of chemistry principles applied to pharmaceuticals. Proficiency in compounding, parenteral production, sterile processing, and lyophilization techniques. Experience working with injectable products including oncology treatments. Thanks & Regards, Archana Reddy Team HR

Hospital Sales Surgical Product Sales Critical Care Division Sales Interested candidates pl. share cv on 9643975459

Hospital Sales Surgical Product Sales Critical Care Division Sales Interested candidates pl. share cv on 9643975459

Job Summary We are seeking a dynamic and experienced Formulation Scientist in Topical division for designing and development of formulation process, ensuring quality by design (QbD) implementation, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. Roles & Responsibilities You will be responsible for end to end Formulation development of Topical formulations (Creams, Ointment, Gels, Sprays and Foams) including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effectiveProof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD). You will be responsible to support in scale-up to pilot/plant scales for topicals. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible for technologytransfer and execution of the batches. You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization,processes designing and scale up). You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documentsfor drug product at every stage of development. You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materialsand ensure development studies are performed related to regulatory and internal system requirements. you will be responsible on preparation of assessments for impurities including Nitrosamine impurities and should be well versed with guidelines of India market, Russia market and US market requirements. Qualification Educational qualification: Masters in Pharmaceutical Technology/Pharmaceutics Minimum work experience: Approx. 5 years of experience in pharmaceutical company topical products. Skills & attributes: Technical Skills Have work experience on Formulation Development and expertise in Topical dosage forms Experience in areas of product development for Generic topical dosage forms Experience in Quality by Design (QbD). Experience in Process Optimization and scale up. Experience in Operational Excellence. Knowledge on Good Manufacturing Practice and Good Laboratory Practice. Experience in Technology Transfer. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Dr. Vohra's Skin Clinic is looking for Dermatologist to join our dynamic team and embark on a rewarding career journey. Evaluating the patients skin health condition and analyzing their medical history. Examine patients and determine dermatological treatments (e. g. medication, non-invasive surgeries). Prescribing medication for the treatment of skin conditions.

1. Document review and approval. 2.Deviation and non-conformance investigation. 3.Compliance with regulatory standards. 4.Process validation.

Inspection and verification of In-process activity in Manufacturing Area. Monitoring of Handover Activity of ARM/Bulk. Verification of Packing and Dispatch activity for Final ARM/Bulk. Issuance of Cell Bank / Issuance of Reference standard.

Role- AGM- International Business development- LATAM; East Europe / Russia CIS Company- A leading Biopharmaceutical Company Location- Bangalore Reporting To- VP- BD Roles and Responsibilities This role requires a dynamic individual with excellent analytical skills, strategic thinking, and the ability to manage complex projects and partnerships across semi-regulated markets, including Emerging Markets Latin America, Europe, . Expertise in sales and marketing within these regions is essential. Develop international business strategies to drive growth in overseas markets. Identify new opportunities for product launches and market expansions. Analyze market trends, competitor activity, and customer needs to inform business decisions. Deep & hands on understanding on the Documentation, Regulatory ecosystem/landscape, Dossier preparation to submission, facilitation at target market Identify and evaluate opportunities for in-licensing and out-licensing of Plasma Derived Products / Critical Care / Oncology / Vaccine / Biohpharma products across semi-regulated markets. Manage relationships with key customers, distributors, and partners. Will be responsible for managing International BD for regions such as- LATAM; East Europe / Russia CIS Desired Skills Post Graduation Degree in Business Management or Life Sciences. Total 15+ years of relevant pharmaceutical industry experience. Strong background in bio-pharmaceutical international business, particularly in semi-regulated markets such as Latin America, Europe, Emerging Market Expertise in sales and marketing within these regions. Sound knowledge of the global pharmaceutical industry (Biologics (Biopharm; Oncology. Critical Care, Vaccines. Strong analytical skills with advanced knowledge of Excel and PowerPoint. Excellent verbal and written communication skills with the ability to network effectively.

Looking for MD in Dermatology along with cosmetic training in the past, and work experience in the relevant clinic in past Able to handle independently major advanced cosmetic procedure have being preferred to work with the team in Le Gorjuss cosmetic clinic with various advanced medical cosmetology procedures Young females between the age of 25 30 years, along with enthusiasm to learn new things and being flexible are preferred Good looking and fluent English must 2 years of Contract applicable

Greetings from Kashiv Biosciences!!!! We are looking for 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 , 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 ensure for proper root cause identification and CAPA effectiveness. Responsible for technical agreements with vendors who have work at Plant premises. Responsible for preparing and review the master list of equipment, instrument along with the preventive maintenance & calibration scheduled. Responsible for change control/deviation management/CAPA Through Track wise management System. Facing the Regulatory, Customer, Internal Audits and preparation of compliance. SOPs and Protocols Training for the new personnel and refreshment training for existing team members. Co-ordination with CFT line Production, QC & QA department to execute any engineering documentation related works. Candidate Details The candidate should be from Pharma industry only having exposure to Parenteral/ Injectables. The candidate should be aware of GDP/ GMP Process. The candidate should have exposure to equipment qualification, Validation and QMS . The candidate should have good communication skills. Interested candidate please share the resume on my mail id manan.hathi@kashivindia.com Regards HR Team Kashiv Biosciences

PRODUCTION - Filling and Blending: Designation : Officer & Senior Officer, Executive, Sr. Executive. Qualification : Diploma / B. Sc/ B. Pharmacy/ M. Sc Experience : 3-10 Years The candidate should possess the following skills: BLENDING: Ability to handle shift plans for formulation Blending activities. Operate and maintain equipment like autoclave, blending vessels. Ability to handle and maintain equipment like autoclave, blending vessels, CIP and SIP skids. FILLING: Ability to handle shift plans for filling activities. Operate and maintain equipment like Vial washing, Tunnel Sterilizer, Filling and Capping, Lyo Filling & lyophilization. PACKING & LABELLING: Ability to handle shift plans for Vial Labelling Machine & VVM dot Machines with Inspection system. Operation of Videojet and Control print Printer for Batch Coding. Operation of Track & Trace System, monitoring of Cold room and Deep freezers temperatures. Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months.

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 Interview Date:- 01-06-2025 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 Washing, Sealing,Aseptic Processing Area, Tunnels, Labelling, About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.