869 Pharmacy Jobs - Page 27

Roles and Responsibilities Manage pharmacy operations, including inventory management, stock control, and ordering medications. Ensure compliance with regulatory requirements and maintain accurate records of patient data and prescriptions. Supervise a team of pharmacists, technicians, and support staff to ensure efficient workflow and high-quality service delivery. Develop policies and procedures for the pharmacy department in collaboration with hospital administrators. Maintain confidentiality at all times when handling sensitive patient information.

2. Position : Dispatch Manager Job Location: Chandigarh Job Description: To perform day to day activities Maintain necessary pharma records regularly Shall be able to manage independently & well versed with pharmacy billing software Orders & purchases Education & Experience: Qualification: Graduate Shall be able to manage independently & well versed with pharmacy billing software

Platinum Hospital Pvt Ltd is looking for Maintenance - Senior Electrician to join our dynamic team and embark on a rewarding career journey Perform inspections and electrical maintenance tasks Ensure compliance with safety protocols Troubleshoot wiring and control systems Maintain logs and equipment reports

Brief team/department description: The Associate, Documentation Management plays a key role in maintaining a robust and inspection-ready Quality Management System (QMS) within a regulated pharmaceutical environment. This position supports integrity, compliance, and continuous improvement of controlled documentation and electronic quality systems, ensuring adherence to GxP and regulatory requirements such as 21 CFR Part 11 and EU Annex 11. Principle Responsibilities: Maintain and support a compliant, inspection-ready Quality Management System (QMS) in accordance with industry regulations and internal procedures. Support the validation, integrity, and ongoing compliance of electronic quality systems, including document management platforms. Support the Documentation Management System, ensuring all controlled documents (e.g., SOPs, policies, work instructions) are accurately authored, reviewed, approved, and updated per lifecycle requirements. Oversee document lifecycle activities, ensuring all documentation meets GxP and regulatory standards. Support the development, maintenance, and delivery of a GxP training program to ensure relevant personnel remain current with quality and compliance standards. Participate in continuous improvement initiatives aimed at enhancing the effectiveness of quality systems and documentation processes. Assist in the management and execution of the Computer System Validation (CSV) program, ensuring alignment with 21 CFR Part 11, EU Annex 11, and applicable internal validation policies. Support internal and external audits and regulatory inspections by ensuring documentation and systems are readily accessible and compliant. Qualifications and Education Requirements Bachelor s degree in Life Sciences, Pharmacy, Quality, or a related field. 1-3 years of experience in documentation management, quality assurance, or regulatory compliance within the pharmaceutical or biotech industry. Understanding of GxP principles, 21 CFR Part 11, EU Annex 11, and other applicable regulations. Familiarity with electronic Document Management Systems and Computer System Validation practices. Strong attention to detail and organizational skills By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

Brief team/department description: To support and maintain a robust, inspection-ready Quality System in alignment with global regulatory standards, ensuring operational excellence, data integrity, and continuous improvement in GxP environments. This role encompasses management of key quality processes including Change Control, Product Quality Reviews, and Risk Management. Principle Responsibilities: Maintain an efficient, compliant, and inspection-ready Quality System aligned with applicable GxP regulations and industry best practices Oversee the end-to-end change control process, ensuring timely assessment, approval, and implementation in compliance with applicable regulations. Coordinate and ensure timely completion of PQRs for all marketed products, including data collection, trending, evaluation, and final review. Support the implementation and monitoring of quality metrics and KPIs to assess system performance and identify areas for improvement. Provide governance for quality risk management processes and ensure timely escalation of significant issues to senior management. Manage Quality Risk Escalation and Quality Council meetings Identify and drive continuous improvement initiatives in quality systems and processes. Regularly report quality system metrics, status of change controls, and PQRs to the Head of Quality Compliance. Prepare dashboards and presentations as needed. Qualifications and Education Requirements Bachelor s or Master s degree in Life Sciences, Pharmacy, or a related discipline. Minimum 5 years of experience in pharmaceutical/biotech quality systems or quality assurance roles. Experience in PQR and change control management. Excellent communication, leadership, and problem-solving skills. Experience with quality audits and regulatory inspections is an advantage. By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.

About the Role: As a Regulatory Affairs Specialist, you will play a crucial role in ensuring that our products comply with all applicable regulations and standards. You will work closely with various departments to prepare and submit regulatory documents, manage communications with regulatory agencies, and keep abreast of the latest regulatory requirements. Key Responsibilities: Monitoring authorities websites for updates and regulatory requirements. Creating product information, including EU Common Submission Information (EUCSI), Summary of Product Characteristics (SmPC), Patient Information Leaflet (PIL), and labels. Providing support for user testing of product information. Preparing dossiers for regulatory submissions, including eCTD format. Conducting compliance audits and drafting detailed audit reports. Drafting documentation for EU regulatory procedures, such as Decentralized Procedure (DCP), Mutual Recognition Procedure (MRP), and Centralized Procedure (CP). Performing life-cycle maintenance tasks, including safety variations, XEVMPD updates, and preparation of protocols for user testing. Maintaining and comparing core product texts to ensure consistency and compliance. Training the team on regulatory processes and industry best practices. Undertaking any additional services mutually agreed upon in writing. Preferred Qualifications: Bachelor s degree in a scientific discipline (e.g., Biology, Chemistry, Pharmacy) or a related field. Minimum of 3 years of experience in regulatory affairs, preferably within the [specific industry, e.g., pharmaceutical, medical device, biotechnology] sector. Strong knowledge of regulatory requirements and guidelines (e.g., EMA, ICH). Excellent written and verbal communication skills. Attention to detail and strong organizational skills. Ability to work independently and as part of a team. Proficiency in Microsoft Office Suite and regulatory databases.

Job Description Comply with all cGMP, GxP and any other applicable regulatory requirement, including EH&S requirements. Complete training on relevant SOPs and develop an understanding of the activities to be conducted prior to undertaking any task. Conduct all tasks/activities as per the applicable SOPs. Report any difficulty or deviation in following the procedure/instruction to immediate supervisor/managers. Report any quality concern or suggestion for improvement to supervisors/ managers. Packing and documentation of assigned products as per instruction given in the BPR, SOP and cGMP. Handling the movement of bulk, packing material, semi-finished and finished goods as per SOP. Maintaining Overall equipment efficiency (OEE)/Productivity. To up keep cleanliness of area and machine as per GMP requirement. Operation, washing and cleaning of equipment and accessories used in related production activities as per SOP. Monitoring and recording of differential pressure, temperature & relative humidity as per SOP. Ensure calibration and preventive maintenance of equipment and instrument as per approved schedule and the results of same meeting the standards. Performing in-process checks as per respective BPR and recording of results of in process checks in BPR. Receipt, issuance, retrieval, maintenance and disposal of change parts. Area and Equipment Usage documented as per SOP. To attend the required cGMP/On job/Functional training activities as per planner. To ensure proper self - hygiene before entering in the production area and follow all the rules and regulation set by HR department. To initiate and review the request like additional material requisition, material return note, packing material carry forward Stereo request and screen request etc. To ensure the effective control on usage of manpower, machine and material in the department and maintain proper inventory of operating supplies in the department. To support Quality Management system and to report any discrepancy, abnormality, non -conformance or any incidence observed to the department head. Handling of Omnidoc, Data Acquisition system (DAS). Checking of strip/blister foil proof with batch packing record and also retention of all required packing material proof with batch packing record for packing section. To attend the trouble shooting of machine. Trouble shooting: Handling, ensuring, verifying and trouble shooting of software like, Blister inspection system, inkjet coding. Any additional responsibility delegated by department head. Work Experience 2 to 5 years of experience Education Diploma in Pharmacy Graduation in Science Competencies Strategic Agility Process Excellence Innovation & Creativity Developing Talent Customer Centricity Collaboration Result Orientation Stakeholder Management

Apollo is Hiring for ANM/GNM, Pharmacist - Chatrasala,Sedam, Gulbarga , Karnataka ANM/GNM Qualification: ANM/GNM Salary : upto 24k ctc per month Experience : 1-3yrs Pharmacist : Qualification : D Pharma/B pharma / M pharama Salary : upto 24k ctc per month Experience : 1 - 3yrs Interested candidates can share resume to mohan_mochi@apollohospitals.com contact to Mr. Mohan: 7981876842 for further queries Thanks & Regards Mohan . M

Role & responsibilities: Job Requirements: Cases will be assigned through the system, where you will be required to call the patients, the pharmacist should be able to read the prescriptions which are attached to the order. The pharmacist should build a rapport with the patient and observe the medicines that were ordered by the customer. Based on the medicines orders by the patient, you will be required to pitch the substitutes of the same salt & and strength for the medicines that they have ordered. All the substitutes that are recommended are doctor-recommended substitutes. An Integral part of this job will be to explain & and convince the customer to take the substitutes & to explain to them how much they can save on their medicines if they opt for the same. Must have sound medical knowledge, like the difference between pediatrics & and geriatrics or the difference between an SR & PR & other relevant clinical responsibilities

Job Title : Assistant Professor / Associate Professor, Doctor of Pharmacy (Pharm.D.) Department Responsibilities: Educate: Teach Pharm.D. students in various pharmacy fields using innovative methods. Research: Conduct and publish research, securing funding and advancing knowledge. Serve: Contribute to the department, college, and profession through various activities. Qualifications: Doctor of Pharmacy (Pharm.D.) degree from an accredited institution. Demonstrated experience in teaching at the graduate level in a Pharm.D. program. Phd in Doctor in pharmacy A distinguished record of scholarly research and publications in peer-reviewed journals. To Apply: Please submit a resume and curriculum vitae to krisha.raval27133@paruluniversity.ac.in before 17/10/24

Position Title: Assistant Professor, Associate Professor, or Professor (Department of Pharmaceutical Sciences) Job Summary: We are seeking dynamic and experienced individuals to join our esteemed faculty in the Department of Pharmaceutical Sciences. The successful candidates will be responsible for delivering high-quality education, conducting research, and contributing to the academic and professional development of our students. Candidates should possess a strong background in pharmaceutical sciences and technology. Responsibilities: Teaching: Deliver lectures, seminars, and practical training sessions on topics and update course materials to reflect advances in the field; provide mentorship and academic guidance to students. Research: Conduct innovative research in pharmaceutical science , publish findings in peer-reviewed journals, and present at conferences; seek external funding opportunities to support research initiatives. Administration: Participate in departmental meetings and committees; contribute to curriculum development and program assessment; assist with accreditation processes and compliance with regulatory requirements; provide support to students regarding academic advising and career development. Professional Development: Stay informed about the latest developments and trends in pharmaceutical sciences; pursue opportunities for professional growth and continuing education; collaborate with industry partners to address current challenges and opportunities in the field. Qualifications: Assistant Professors: M.Pharm. and B.Pharm. degrees in pharmacy & Sciences or a similar discipline, or comparable training. Relevant teaching or research experience is preferred; candidates with exceptional academic credentials will also be considered. Associate Professors: Ph.D. in a related field with a specialization in pharmaceutical science. Demonstrated effectiveness in teaching, research productivity, and scholarly publications in the field. Professors: Ph.D. in pharmaceutical sciences with significant expertise in pharmaceutical science. Proven leadership in research, teaching, and academic or professional service; a distinguished record of scholarly achievements and contributions to the advancement of the field. Applications should be sent to krisha.raval36516@paruluniversity.ac.in along with a resume, curriculum vitae (CV), statement of teaching philosophy, research statement, and contact details. Applications will be accepted for 7 days from the date of the job advertisement.

Job Title : Assistant Professor / Associate Professor, Doctor of Pharmacy (Pharm.D.) Department Responsibilities: Educate: Teach Pharm.D. students in various pharmacy fields using innovative methods. Research: Conduct and publish research, securing funding and advancing knowledge. Serve: Contribute to the department, college, and profession through various activities. Qualifications: Doctor of Pharmacy (Pharm.D.) degree from an accredited institution. Demonstrated experience in teaching at the graduate level in a Pharm.D. program. Phd in Doctor in pharmacy A distinguished record of scholarly research and publications in peer-reviewed journals. To Apply: Please submit a resume and curriculum vitae to krisha.raval36516@paruluniversity.ac.in before 22-November-2024

Vice Principal - Faculty of Pharmacy Vice Principal: Parul University is seeking candidates who will be responsible for driving academic and administrative excellence within the faculty. Key responsibilities include ensuring the efficient conduct of classes, examinations, and technical training programs, fostering innovation and research, strengthening industry partnerships, and promoting international collaborations and exchange programs. Eligibility criteria PhD degree with Minimum 15 years experience in Teaching/industry/Research out of which 5 years must be at the level of Professor. Administrative experience is desirable.

Associate Dean - Faculty of Pharmacy Associate Dean: Parul University is seeking experienced individuals to support the Dean in managing academic, research, and extension programs, assisting in curriculum development, guiding Board of Studies, and ensuring efficient operations in alignment with the Dean's strategic vision. Eligibility criteria : PhD degree with Minimum 15 years experience in Teaching/industry/Research out of which 5 years must be at the level of Professor. Administrative experience is desirable

PREFERRED QUALIFICATIONS - D.PHARM / B. Pharm 1)To ensure the requirements are always in stock / working condition as per the practical designed for respective labs. 2) To have minimum knowledge about the chemicals and reagents for practical. 3) To ensure proper maintenance of all amenities including glassware, equipment and chemicals are in proper place and condition at all times. 4) To assist students during practicals for proper conduct of experiments. 6) To process for replacement of broken / not working glassware and equipment appropriately 7) Equipment maintenance/ follow up/ servicing of various instruments in the lab which is assigned to them. 8) Working in association with exam departments during university external as well as internal examinationary examinations. 9) To maintain the lab upkeep in clean conditions 24X7 11) To maintain all lab records uptodate and to assist any other college related work as and when assigned by the Principal of the college

We are looking for an Assistant Professor in Pharmaceutical Chemistry who will be responsible for teaching and mentoring pharmacy students, developing educational content, and participating in research activities related to Pharmaceutical Chemistry.

Check prescriptions for proper dosage; dispense prescribed pharmaceuticals to customers or other healthcare professionals and advise them on indications, contraindications, adverse effects, drug interactions, and dosage Maintain medication profiles of customers, including a registry of poisons, narcotics, and controlled drugs; order and maintain stock of pharmaceutical supplies; advise customers on the selection and use of non-prescription medications; renew existing prescriptions in limited circumstances. Exp.- Both freshers and experienced candidates are eligible to apply for this position.

Immediate Hiring !! Designation: Medical Coder Trainee . Salary: Upto 20k PM + Incentives. Shift : General, Day. Skills: Anatomy, Physiology, Pathology. Location: Chennai, Coimbatore, Bangalore. Required Candidate profile Eligibility: UG or PG or Diploma ( 3 Years) Specialization: Life Science, Non - Life science , Para-Medical & Medical Studies. Passout: 2023- 2025

Job Summary: We are seeking an experienced and detail-oriented Hospital Pharmacy Manager for our Ortho-One. The ideal candidate will be responsible for overseeing the operations of the OP, IP, and OT Pharmacy, ensuring adherence to NABH standards, conducting medication audits, managing pharmaceutical dispensing, and leading a team of pharmacy professionals. The Pharmacy Manager will also play a key role in maintaining the quality, safety, and compliance of medications used in patient care. Key Responsibilities: Manage the daily operations of the OP, IP, and OT pharmacies to ensure medications are dispensed accurately and safely in all patient care areas. Ensure pharmacy operations comply with NABH standards and regulations. Conduct regular audits to verify proper medication documentation, accurate dispensing, and regulatory compliance. Stay updated on OT implants used in orthopaedic surgeries and manage their proper handling and distribution. Prepare and dispense prescribed medications, ensuring accuracy in formulas, ingredients, and prescriptions. Follow standard procedures for compounding medications, including measuring and mixing ingredients. Supervise pharmacy staff in tasks such as mixing, packaging, labeling, and dispensing medications. Educate patients and pharmacy staff about drug interactions, side effects, proper dosage, and medication storage. Ensure proper handling and security of controlled substances, as well as safe disposal of hazardous medications. Maintain accurate records of prescriptions, medication costs, and inventory in the pharmacy system. Check the medications to ensure their identity, purity, and strength meet the required standards. Train and guide pharmacy interns and other medical staff on pharmacy practices, safety measures, and medication knowledge. Candidate Profile: Education: B.Pharm Experience: Minimum of 5 years of experience as Pharmacy Manager or In-charge in a hospital (orthopaedics exposure is preferable). Skills & Knowledge: Strong understanding of NABH standards and hospital pharmacy operations. Extensive knowledge of medication audits, OT implants, and pharmacy compounding processes. Leadership skills and experience managing pharmacy staff. Excellent communication skills, both with patients and healthcare professionals. Ability to manage inventory and ensure accurate record-keeping.

Responsibilities: * Dispense medications accurately and efficiently * Ensure compliance with pharmacy laws and standards * Manage inventory and order supplies Contact below number to apply for the job. +91-9820280109 (Dr. Jagdish Dubey)

Greetings from Scorelabs ! Hiring Pharmacists Handle range of prescriptions for both Semi-controlled and un- controlled drug in the hospital. Maintain the records for semi control drugs. Supervise the dispensing of drugs through Asst. Pharmacy. Required Candidate profile Qua - B Pharmacy Freshers & Exp Both are Eligible Hr Gowthami - 7842272470

Needed a skilled pharmacist who have a good knowledge of medicines and marketing of medicines

We are looking Pharmacy Manager In Our Hospital

As a leading financial services and healthcare technology company based on revenue, SSC is headquartered in Windsor, Connecticut, and has 27,000+ employees in 35 countries. Some 20,000 financial services and healthcare organizations, from the worlds largest companies to small and mid-market firms, rely on SSC for expertise, scale, and technology. DomaniRx is a newly formed organization focused on shaping the future of Pharmacy Benefit Management by delivering a cloud-native, API-driven claims adjudication platform. Our team is made up of engineers with varying levels of professional experience and backgrounds, from new graduates to 20-year veterans of the healthcare industry. We are looking for creative engineers and technologistsrelevant industry experience is important, but less so than your demonstrated abilities, passion and attitude. We re always improving and looking for individuals that enjoy being challenged and have a strong desire to make the engineering experience better for our users.

As a leading financial services and healthcare technology company based on revenue, SSC is headquartered in Windsor, Connecticut, and has 27,000+ employees in 35 countries. Some 20,000 financial services and healthcare organizations, from the worlds largest companies to small and mid-market firms, rely on SSC for expertise, scale, and technology. DomaniRx is a newly formed organization focused on shaping the future of Pharmacy Benefit Management by delivering a cloud-native, API-driven claims adjudication platform. Our team is made up of engineers with varying levels of professional experience and backgrounds, from new graduates to 20-year veterans of the healthcare industry. We are looking for creative engineers and technologists: relevant industry experience is important, but less so than your demonstrated abilities, passion and attitude. We re always improving and looking for individuals that enjoy being challenged and have a strong desire to make the engineering experience better for our users. Unless explicitly requested or approached by SSC Technologies, Inc. or any of its affiliated companies, the company will not accept unsolicited resumes from headhunters, recruitment agencies, or fee-based recruitment services. SSC Technologies is an Equal Employment Opportunity employer and does not discriminate against any applicant for employment or employee on the basis of race, color, religious creed, gender, age, marital status, sexual orientation, national origin, disability, veteran status or any other classification protected by applicable discrimination laws.