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Parexel Work from home Hiring Regulatory Affairs Consultant

Parexel Work from Home Hiring Regulatory Affairs Consultant Join Parexel as a Regulatory Affairs Consultant – Work Remotely in India Are you an experienced Regulatory Affairs professional looking for a flexible remote job? Parexel, a leading global clinical research organization, is hiring a Regulatory Affairs Consultant to support regulatory strategies and compliance processes for biopharmaceutical and medical device companies. This work-from-home opportunity offers a chance to collaborate with industry leaders and contribute to global regulatory initiatives. About Parexel Parexel is a globally recognized clinical research organization (CRO) specializing in regulatory affairs, clinical trials, and pharmaceutical consulting. With a strong commitment to innovation, patient safety, and regulatory excellence, Parexel helps pharmaceutical companies bring their products to market efficiently and in compliance with global regulations. Regulatory Affairs Consultant – Job Overview Current Vacancies in Department: Regulatory Affairs – Labeling and Safety Compliance Job Location: Remote – Work from Home (India) Required Education: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or a related field Experience Required: Minimum 5 years of experience in Regulatory Affairs Expertise in safety labeling changes, CCDS (Company Core Data Sheet) creation or updates, and change control assessments Prior experience with Centralized Products is a plus Proficiency in Veeva RIMS and TVT Tool is preferred Key Responsibilities Manage safety labeling changes impacting Product Information Create and update Company Core Data Sheets (CCDS) Conduct regulatory impact assessments for product modifications Oversee change control processes in compliance with regulatory requirements Work collaboratively with cross-functional teams, ensuring timely and efficient regulatory submissions Maintain up-to-date knowledge of EU, UK, CH, AU, and NZ regulatory frameworks Skills & Qualifications Needed  Strong understanding of global regulatory requirements Experience handling safety labeling changes Knowledge of Centralized Products regulations Proficiency in Veeva RIMS & TVT Tool Excellent communication and problem-solving skills How to Apply? Don’t miss this opportunity to work with Parexel, a leading name in regulatory affairs consulting. If you meet the above qualifications, apply now using the link below: 🔗 Apply Here

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Novo Nordisk Hiring Medical Writers Bangalore | Apply Now

Novo Nordisk Hiring Medical Writers Bangalore – Apply Now! Are you an experienced medical writer looking for an opportunity to work with a globally renowned pharmaceutical company? Novo Nordisk is hiring Medical Writers in Bangalore, Karnataka. This is an excellent opportunity for candidates with a PhD, MSc, MPharm, or PharmD and at least 2 years of relevant experience. Read on to explore the role, responsibilities, and how to apply! Why Join Novo Nordisk? Novo Nordisk is a global healthcare leader with over 100 years of legacy in defeating serious chronic diseases. With over 72,000 employees worldwide, Novo Nordisk is known for its commitment to innovation and excellence. This role offers a chance to contribute to impactful clinical research and regulatory documentation. Job Details Medical Writer – Bangalore, Karnataka Department: Clinical Reporting Unit Novo Nordisk’s Clinical Reporting Unit plays a crucial role in medical writing, document control, and regulatory submissions. The team consists of experienced medical writers, publishers, and regulatory experts working on diverse therapeutic areas. Key Responsibilities Prepare clinical trial protocols, reports (CTRs), non-interventional study reports (NSRs), investigator brochures (IBs), and regulatory response documents. Communicate clinical data in a clear and concise manner. Collaborate with cross-functional teams across different time zones. Ensure compliance with global regulatory requirements. Contribute to knowledge sharing and process improvements within the department. Required Qualifications Education: PhD, MSc, MPharm, PharmD, or equivalent in life sciences, pharmacology, medicine, or related fields. Experience: Minimum 2+ years of experience as a medical writer in a pharmaceutical or CRO setting. Strong understanding of regulatory requirements and clinical data interpretation. Excellent analytical and communication skills. Ability to work independently while managing multiple tasks effectively. About the Clinical Reporting Unit The Clinical Reporting Unit at Novo Nordisk has grown significantly since its inception in 2011. The team includes skilled medical writers, document controllers, and regulatory experts with deep knowledge of different therapeutic areas. They play a vital role in global regulatory submissions and public disclosure activities. Work Culture & Growth Opportunities Novo Nordisk is committed to fostering a collaborative and inclusive work environment. Employees benefit from: Career growth opportunities in a global organization. Exposure to cutting-edge clinical research and regulatory writing. A dynamic work culture that values innovation and professional development. How to Apply If you meet the qualifications and are excited about this opportunity, apply now through the official Novo Nordisk career portal: 👉 Apply Here Application Deadline: March 6, 2025 Beware of Fraudulent Job Offers Novo Nordisk does not charge applicants any fees or request payments for recruitment. Be cautious of fraudulent job offers that may require personal information or funds.

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Work from Home Opportunity at Parexel - Audit Coordinator | B Pharm, M Pharm, MSc

Work from Home Opportunity at Parexel - Audit Coordinator Are you looking for a work-from-home opportunity in the pharmaceutical industry? Parexel, a leading global clinical research organization, is hiring an Audit Coordinator for its Quality Management team. This is a remote role available across India, including Hyderabad and Mohali. If you have a background in pharmacy, life sciences, or related fields, this could be the perfect career opportunity for you! Job Overview Company Name: Parexel Job Title: Audit Coordinator Location: Remote (India), Hyderabad, Mohali Department: Quality Management Education Required: B.Pharm, M.Pharm, MSc (Life Sciences, Biological Sciences, or related fields) Experience Required: 1-2 years in Quality Assurance, Quality Management, or Clinical Trial Support Job ID: R0000031037 Key Responsibilities General Administrative Duties Organize meetings and business trips, draft minutes, and process travel expenses Download and distribute reports using appropriate systems Provide support in generating and analyzing reports and questionnaires Assist in client deliverables, including audit reports and metrics Maintain and update departmental organization charts Manage SharePoint folders and access permissions Oversee SOP reviews and stakeholder assignments Audit and Compliance Support Extract and compile awarded signed audit reports Assist in sponsor audits and regulatory inspections (SAI), including documentation support Gather essential documents such as CVs, job descriptions, and training packages Schedule and coordinate global QA meetings Assist in GxP audits, including sample selection and coordination Maintain compliance with Parexel’s international SOPs and GxP requirements Data Analysis and Reporting Collect, analyze, and interpret data for quality metrics Generate reports and visual presentations of key performance indicators (KPIs) Identify trends in quality metrics to improve processes Required Skills and Qualifications Education & Experience Bachelor's or Master’s degree in Pharmacy (B.Pharm, M.Pharm), Life Sciences (MSc), or related disciplines 1-2 years of experience in Quality Assurance, Quality Management, or Clinical Trial Support Knowledge of GxP guidelines and industry standards Technical & Soft Skills Strong Microsoft Office skills (Word, Excel, PowerPoint, Outlook) Expertise in Microsoft Excel (formulas, pivots, lookups, and chart generation preferred) Excellent written and verbal communication skills Ability to prioritize workload and meet deadlines Attention to detail and problem-solving skills Ability to work in a matrix environment with a global mindset How to Apply? Interested candidates can apply directly through the Parexel Careers Portal using the link below: Apply Here

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Puerto Life Sciences Hiring for Quality Assurance, Production, and Quality Control Roles

Puerto Life Sciences Private Limited, a leading pharmaceutical company specializing in sterile manufacturing, is looking for skilled professionals for its Neemrana, Rajasthan facility. With cutting-edge technology and global GMP standards, Puerto offers exceptional career opportunities for candidates in Quality Assurance (QA), Production, and Quality Control (QC). Job Openings and Details 1. Quality Assurance (QA) Designation: Assistant Manager/Manager Qualification: B. Pharma / M. Pharma 2. Production Designation: Assistant Manager/Manager Qualification: B. Pharma / M. Pharma 3. Quality Control (QC) Designation: Assistant Manager/Manager Qualification: MSc in Microbiology, Chemistry, or Biotechnology Location Details Facility: Puerto Life Sciences Pvt. Ltd., Neemrana, Rajasthan (Sterile Facility). Focus Area: Aseptic manufacturing with strict compliance to global GMP standards. Application Process Interested candidates should email the following details to hr@puerto.in: Updated resume Current CTC Notice period

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TechObserver india Hiring Clinical Research Associate Noida

TechObserver india Hiring Clinical Research Associate Noida https://pharmastuff.org.in/job/cra-tech-observer-india?fsp_sid=19

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Hospital Pharmacist Job Vacancies Recruitment Notification The recruitment drive is organized by M/s. Principle Security & Allied Services Pvt. Ltd. on behalf of Homi Bhabha Cancer Hospital, Sangrur, Punjab. The pharmacist positions are purely contract-based. Walk-in Interview Details Date: 29th November 2024 (Friday) Reporting Time: 9:30 AM to 11:00 AM Venue: Auditorium, 3rd Floor, New Building, Homi Bhabha Cancer Hospital, Sangrur, Punjab – 148001 Pharmacist Job Role and Requirements Job Title: Pharmacist Vacancies: 03 Salary: ₹25,000 per month Age Limit: Up to 30 years Qualifications: Educational Background: B. Pharm: Minimum 1-year experience in the dispensary/pharmacy of a hospital with at least 100 beds. D. Pharm: Minimum 3 years of experience in the dispensary/pharmacy of a hospital with at least 100 beds. Registration: Must have a valid State Pharmacy Council Registration with an allotted registration number. Preferred Skills: Experience working in a computerized pharmacy system. Willingness to work in shifts, including night duties. Required Documents for the Interview Candidates attending the interview must bring the following documents: Updated resume. Passport-size photograph. Originals and photocopies of: PAN card and Aadhaar card. Educational and academic certificates. Experience certificates. Note: An MCQ test may be conducted if there are a large number of applicants, and only shortlisted candidates will proceed to the interview. [caption id="attachment_47862" align="aligncenter" width="930"] Pharmacist Walk-in-Interview at Homi Bhabha Cancer Hospital, Punjab[/caption] Application Process For candidates unable to attend the walk-in interview, queries can be addressed to the following: Email: bo.jalandhar@psas.in, hbchs.hrd@gmail.com Helpline: 18005721201 or 01672-223941 Full Detailed Notification: Click Here

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Labcorp Clinical Report Writer Coordinator Job Vacancies Labcorp, a global leader in life sciences and healthcare solutions, is hiring a Clinical Report Writer Coordinator in Bangalore, India. This entry-level position offers an exciting opportunity to develop expertise in clinical trial documentation, working within a dynamic team environment. If you have a passion for clinical writing and are ready to kick-start your career, this role is for you! Labcorp Hiring Clinical Report Writer Coordinator Labcorp is actively seeking a dedicated and detail-oriented individual to join their LMVRS (Labcorp Medical Writing and Reporting Services) team. As a Clinical Report Writer Coordinator, you will contribute to producing high-quality clinical trial documentation that supports research and innovation in healthcare. Key Job Details Job Title: Clinical Report Writer Coordinator I Category: Clinical Location: Bangalore, India Job ID: 2444315 Job Type: Full-Time Job Responsibilities As a Clinical Report Writer Coordinator, you will: The Report Writer Coordinator is an entry level position in the LMVRS group, learning the Labcorp writing standard and learning to draft and edit reports to promote product consistency. Learns to use software tools to efficiently and accurately complete job duties. Learns and understands any new/changed conventions or standard language. Creates report folders and requests all needed information, documentation and any other relevant information from the respective departments. Creates part of the initial draft of lower complexity clinical trials internal or client facing documents using pre-defined templates or client-supplied information with guidance from more senior colleagues and using study protocol information, SOPs and/or lab data. Creates data tables, as needed, using the corresponding database(s). Performs review and quality control (QC) as applicable. Edits internal or client facing documents, as needed, after review, ensuring that company convention, style, format and terminology have been used. Independently utilizes workload management tool to track and document data and report completion activities. Ensures compliance to applicable departmental Standard Operating Procedures and Work Instructions. Maintains/develops training manuals. Effectively manages own time and deadlines. Effectively manages task status tracking and time recording. May provide backup assistance to colleagues, as appropriate. Performs other duties as assigned. [caption id="attachment_111808" align="aligncenter" width="1200"] Labcorp Hiring Clinical Report Writer Coordinator – Entry-Level Opportunity in Bangalore[/caption] Eligibility Criteria To apply for this role, candidates must possess: Strong writing and communication skills. Proficiency in using software tools for data management and document creation. Excellent time management abilities. This position is ideal for individuals eager to grow in the field of clinical writing within a supportive and innovative organization. How to Apply To apply for the Clinical Report Writer Coordinator role, visit the official Labcorp careers page at the link below: Apply Here Equal Opportunity Employer Statement Labcorp is proud to be an Equal Opportunity Employer. Employment decisions are based on qualifications and business needs, without discrimination based on race, gender, religion, or other protected characteristics.

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NIPER Pharmacovigilance Job Vacancies If you’re passionate about drug safety and pharmacovigilance, here’s an exciting opportunity for you! The National Institute of Pharmaceutical Education and Research (NIPER), Hajipur, is hiring for the role of Junior Pharmacovigilance Associate. This is an excellent opportunity to contribute to healthcare safety while gaining valuable experience in the pharmaceutical domain. Pharmacovigilance Hiring at NIPER Hajipur The National Institute of Pharmaceutical Education and Research (NIPER), Hajipur, a premier institute in pharmaceutical sciences, invites applications for a contractual role as Junior Pharmacovigilance Associate. Job Overview Job Title: Junior Pharmacovigilance Associate Organization: NIPER Hajipur Location: Hajipur, Vaishali District, Bihar Job Type: Contractual Number of Posts: 1 (Unreserved) Eligibility Criteria Candidates applying for this position must meet the following qualifications: Essential Qualifications: M.Pharm or Pharm.D with specialization in Clinical Pharmacology, Pharmacy Practice, or Clinical Research. MBBS or BDS from a recognized University/Institute. Desirable Experience: 1 year of experience in pharmacovigilance or related fields. Strong communication and computer skills are preferred. Age Limit: Maximum age of 28 years as of the application deadline. Key Responsibilities As a Junior Pharmacovigilance Associate, your primary responsibilities include: Collecting and processing Adverse Drug Reaction (ADR) reports. Managing Individual Case Safety Reports (ICSRs) using VigiFlow. Conducting quality, clinical, and statistical reviews of ICSRs. Assisting with tasks assigned by the Competent Authority. This role involves working closely with healthcare and pharmacovigilance professionals to enhance drug safety monitoring systems. Salary and Benefits Salary: ₹26,250 per month. The contract tenure is for 1 year, subject to satisfactory performance. Application Process Interested candidates are required to follow these steps to apply: Application Submission: Send a letter of intent along with your updated CV to the AMC Coordinator at amc@niperhajipur.ac.in. Address for Correspondence: Dr. Sameer Dhingra, Department of Pharmacy Practice, NIPER Hajipur, District Vaishali, Bihar. Important Dates: Application Deadline: November 25, 2024. Shortlisting Date: November 29, 2024. Interview Date: December 3, 2024 (Tentative). The interview will be conducted online, and details will be communicated to shortlisted candidates. [caption id="attachment_111752" align="aligncenter" width="1200"] Job as Junior Pharmacovigilance Associate at NIPER Hajipur[/caption] Important Notes The appointment and salary processing will be handled by NCC-PvPI through an authorized outsourcing agency. The Competent Authority reserves the right to accept, reject, or modify the terms of the recruitment process. Ensure all documents and communication are submitted accurately to avoid disqualification.

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Teva Pharmaceuticals is hiring experienced Pharmacovigilance Professionals for their office in Bangalore, India (560052). With over 200 million people worldwide taking Teva’s medicines daily, this is your chance to contribute to global health. Job Overview – Pharmacovigilance Professional Location: Bangalore, India (560052) Position: Pharmacovigilance Professional Experience Required: 3-4 years in pharmacovigilance, including experience in Individual Case Safety Report (ICSR) processing and literature review. Qualification: Any life sciences/pharmaceutical/healthcare professional graduate (B. Pharmacy, M. Pharmacy, Pharm D, BDS). Solid understanding of pharmacovigilance concepts, regulations, and procedures Advanced proficiency in Microsoft Office platforms Minimum of 02 to 04 years of experience in pharmacovigilance including literature review process in ICSR Experience in patient safety/pharmacovigilance: solid knowledge in pharmacovigilance concepts, regulations, and procedures. Advanced knowledge of Microsoft Office platforms. Flexible to adapt to shifting team priorities. Excellent communication skills including written, verbal, and non-verbal. Excellent Interpersonal and people skills. Good analytical skills and problem-solving skills. Key Responsibilities: As a Pharmacovigilance Professional at Teva Pharmaceuticals, you will: Processing serious & non-serious adverse events from various post-marketing sources. Ensure accurate and consistent medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in Safety Database. Data verification between source documents and entered data in Safety Database for evaluation of events/suspect drug coding, seriousness, causality, listedness and narrative writing. Evaluate the need for follow-ups, queries with various stakeholders for correct and accurate data transfer to various parties Ensure that quality data is analyzed for any trending and to prepare team for process stabilization. Providing administrative support by taking up complete responsibility of assigned case processing related activities on day-to-day basis. Coordinate with internal/ external stakeholders to obtain necessary information required for day-to­ day operations and to update the reporting manager on status reports on real time basis. Effective communications to be maintained with internal (related departments and units) & external (partners, authorities, vendors) stake holders in order to run the process as transparent as possible. Pharmacovigilance Associate-Patient Safety Operations Perform the case processing and related activities in alignment with patient Safety Operations. Extensive knowledge of Medical Terminology, clinical pharmacology, patient treatment, diagnostic investigations & pathology. Exp in medical coding through MedDRA (Medical Dictionary for Regulatory Activities) for all events in safety database. Pharmacovigilance Associate - Literature Review Relevant experience in Pharmacovigilance including Literature review process in ICSR Experience in Patient Safety/ solid knowledge in Pharmacovigilance concepts, regulations & procedures. Knowledge of database: Embase, Medline, Pubmed, Ovid, etc. Support PV teams like case processing, training teams, Quality assurance, audits & inspection etc [caption id="attachment_102197" align="aligncenter" width="640"] Pharmacovigilance Professionals Wanted at Teva Pharmaceuticals – Bangalore[/caption] Teva Pharmaceuticals’ Equal Employment Commitment Teva Pharmaceuticals is committed to diversity and equal employment opportunities. We ensure that employment decisions are made without regard to race, age, gender, disability, or any other legally protected status. We encourage candidates who require accommodations to apply and will provide support throughout the recruitment process. How to Apply Ready to take the next step in your career? Apply online for the Pharmacovigilance Professional role at Teva Pharmaceuticals via the link below:

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GSK is hiring Pharmacovigilance Literature Specialists to join their esteemed team in Bangalore. This role is perfect for professionals with a background in Life Sciences, Pharmacy, or related fields and a keen eye for detail. If you're ready to make an impact, keep reading to explore the job responsibilities, qualifications, and why GSK is the right place for you. About GSK GSK (GlaxoSmithKline) is a global biopharmaceutical company driven by its mission to unite science, technology, and talent to tackle diseases worldwide. With a strong focus on innovation, GSK aims to improve the health of billions by advancing solutions in vaccines, specialty medicines, and general healthcare. At GSK, employees thrive in a culture of inclusivity, growth, and innovation, making it a prime destination for professionals seeking meaningful and impactful careers. Key Responsibilities As a Pharmacovigilance Literature Specialist, your role will encompass: Key Responsibilities: Core Activities Provide support for Global Safety literature screening activities for both ICSR and signal detection purposes in accordance with their procedures and regulatory requirements. Support SERM product specialists by identifying articles of interest for relevant safety information from screened publications for all of GSK’s product portfolio. Perform PV literature surveillance activities according to regulations and agreed processes Ensure timely production of key deliverables including but not limited to: Screen and review literature search results (articles/abstracts/citations) for purposes of ICSR identification Triage literature search results for potential articles of interest with relevant safety information concerning both GSK marketed and GSK products in development, for signal detection/periodic reporting purposes using defined algorithms and criteria. Demonstrate GSK values. Literature Specialist, PV Operations – Literature Surveillance Review (Grade 9) Maintain and document up-to-date product knowledge for literature review. Possess working knowledge of the maintenance of product knowledge and Master drug list. Demonstrate working knowledge in quality checks for literature articles triaged by team. Education Requirements (minimum expected) : Bachelor’s Degree - Life sciences, Pharmacy, Medical or pharmacology degrees. Preferred: Master’s degree or higher in Health Sciences. Job Related Experience (minimum requirements): Pharmaceutical industry experience (e.g., drug safety (desired), regulatory, clinical development, medical affairs) Working knowledge of key pharmacovigilance regulations and methodologies Good English language skills – written and verbal particularly in scientific/medical terminology Ability to evaluate data and draw conclusions with appropriate guidance from senior team members or manager Good attention to detail. Service-oriented attitude and ability to be a team player and interact effectively with all levels of personnel in an interdisciplinary and matrix environment. Computer proficiency, IT skills, the expertise and ability to work with web-based applications Good level of flexibility and ability to prioritize work Good/Highly developed interpersonal, presentation and communication skills. Qualifications and Skills Educational Requirements: Mandatory: Bachelor’s Degree in Life Sciences, Pharmacy, Pharmacology, or related fields. Preferred: Master’s Degree or higher in Health Sciences. Experience: 2-4 years of experience in the pharmaceutical industry, with exposure to pharmacovigilance, regulatory affairs, or medical affairs. Familiarity with pharmacovigilance regulations and methodologies. Strong analytical and communication skills, with proficiency in medical and scientific terminology. Expertise in handling web-based applications and data evaluation tools. Job Details Job Title: Pharmacovigilance Literature Specialist Location: Bangalore, India Experience Level: 2-4 years

Job Type: Full-time Department: Medical and Clinical [caption id="attachment_111627" align="aligncenter" width="1200"] GSK Hiring Pharmacovigilance Literature Specialist Recruitment[/caption] How to Apply Take the next step in your career by applying for this exciting opportunity with GSK. Click the link below to submit your application: Apply for GSK Pharmacovigilance Literature Specialist Application Deadline: Rolling applications—apply soon to avoid missing out! Important Notes GSK does not charge any fees during the recruitment process. Be cautious of fraudulent job postings and verify information through official channels. If you have questions or concerns, contact askus@gsk.com for confirmation regarding the job’s authenticity.

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Maithri Drugs Hiring for Quality Control (Documentation) in Bonthapally | BSc & MSc Chemistry Roles Looking for a career in Quality Control (Documentation) within the pharmaceutical industry? Maithri Drugs Private Limited, a leading name in pharma manufacturing, is conducting interviews for skilled professionals in Bonthapally, Telangana. If you have a BSc or MSc in Chemistry and 4–9 years of relevant experience, this is your chance to advance your career. About the Role Position: Quality Control (Documentation) Department: Quality Control Experience: 4–9 years Qualification: BSc & MSc (Chemistry) Key Responsibilities Ensure accurate preparation and maintenance of quality documentation as per regulatory guidelines. Perform audits and monitor compliance with quality standards. Collaborate with cross-functional teams for timely resolution of documentation issues. Assist in developing and implementing quality control procedures. This role is ideal for individuals who are detail-oriented, experienced in handling documentation for quality control, and have a strong understanding of industry practices. [caption id="attachment_66262" align="aligncenter" width="930"] Maithri Drugs Recruitment Alert[/caption] Interview Details Date: November 23, 2024 Time: 10:00 AM – 3:00 PM Interview Venue & Work Location Maithri Drugs Private Limited Sy. No. 205, 222 to 226, Bonthapally(V), Gummadidala(M), Sangareddy(D), Telangana, India – 502313 How to Apply Apply now through the official Maithri Drugs career portal: Click Here to Apply

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Quality Control Senior Officer Job Vacancies Looking to advance your career in pharmaceutical quality control? Sun Pharmaceutical Industries Ltd., a global leader in the pharma industry, is seeking talented professionals for the position of Quality Control Senior Officer at their Mohali facility. Sun Pharma Recruitment Job Overview As a Senior Officer in Quality Control, you will play a crucial role in ensuring product quality and compliance with industry standards. This position offers the opportunity to work with advanced analytical techniques and contribute to the success of a world-class pharmaceutical company. Key Responsibilities Analyze Finished Product/Stability/Validation/In-process/Swab Samples as per approved specification and standard test procedures. Recording the analytical data in raw data sheet/protocol. Ensure standardization of working standards and conduct, preventive maintenance, calibration, qualification of laboratory instruments as and when required. Ensure accuracy of document and maintain neat/concise/organized stability record. Follow the EHS policy, Laboratory procedure and maintain the compliance to cGMP requirements. Initiate the OOS, OOT and deviation & CAPA in Trackwise software. Destruction of Finished Product/Stability/Validation/In-process/Swab samples after completion of analysis and review of the data. Ensure integrity, accuracy and adequacy of the analysis performed. Recording of instrument and standard usage in the respective log books/registers. To perform the analytical method transfer activity. Preparation of eCOA /SAP COA/ Regulatory COA as per requirement. Any other Assignment given by Lab in charge/ Manager Quality Control from time to time. [caption id="attachment_56281" align="aligncenter" width="930"] Sun Pharmaceutical Recruitment Notification[/caption] Qualifications Education: Bachelor’s degree in Pharmacy, Chemistry, or related sciences. Experience: Prior experience in a pharmaceutical quality control environment is an advantage. Location Details This opportunity is based in Mohali, a prime location offering a thriving pharmaceutical hub and excellent career growth prospects. How to Apply Ready to take the next step in your career? Submit your application through the official Sun Pharma careers portal. Don’t miss the chance to be part of a globally respected organization.

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Explore exceptional career opportunities with Pfizer, a global leader in the pharmaceutical industry. Pfizer Healthcare India Private Limited invites qualified professionals to join their team in injectable manufacturing as Junior/Assistant Associates. Job Details: Junior/Assistant Associates Roles Position: Junior/Assistant Associates – Injectable Manufacturing Location: Pfizer Healthcare India Pvt Ltd, Visakhapatnam Eligibility Criteria: Qualification: Diploma or BSc (Full-time) Experience: 1–5 years in an injectable manufacturing facility Regulatory Knowledge: Hands-on experience with USFDA-regulated environments and processes is mandatory. Key Responsibilities As a Junior/Assistant Associate in Pfizer’s injectable manufacturing team, you will: Operate and Maintain Equipment: Work with sterile and injectable machinery, including formulation, filling, sealing, and packing machines. Monitor Production: Ensure that all processes meet Good Manufacturing Practices (GMP) standards. Data Management: Maintain accurate production records and conduct routine equipment maintenance. Collaborate: Coordinate with team members to resolve issues and optimize efficiency. Quality Control: Monitor product quality and adhere to strict regulatory standards. Skills and Attributes Strong knowledge of injectable production processes. Familiarity with sterile environments and equipment operation. Detail-oriented, with excellent problem-solving and teamwork skills. Commitment to maintaining the highest standards of GMP compliance. [caption id="attachment_94691" align="aligncenter" width="930"] Pfizer Career Opportunities in Injectable Manufacturing: Junior/Assistant Associates Roles[/caption] How to Apply Interested and eligible candidates are encouraged to apply by sending their resumes to: 📧 Email: pgsindiacxteam@pfizer.com

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Pharmacovigilance Executive Opportunity at Jubilant Pharma Jubilant Pharma Limited, a global pharmaceutical company, is offering an exciting opportunity for a Pharmacovigilance Executive to join their dynamic team. This role involves crucial responsibilities in ensuring regulatory compliance and maintaining high standards of pharmacovigilance. LOCATION : Greater Noida, Uttar Pradesh Job Description Overview: In this role, you will be responsible for various pharmacovigilance activities, including case processing, data entry, regulatory compliance, and communication with internal and external stakeholders. Here's a detailed look at the scope of work and key accountabilities: Scope of Work: Accountabilities Scope of work: Perform literature search and identify the safety information present in the article with regard to Jubilant’s products Perform quality check of the ICSR in the safety database to ensure accurate and consistent data entry and processing from adverse event reports/source document following the Company’s Data Entry Conventions. Principle Accountabilities Timely allocation of ICSRs for data entry, quality review, medical review and its distribution in the safety database. Preparation of PADERs and other aggregate reports as per the company’s SOP and regulatory guidelines. Compilation of data and preparation of RMPs as per the company’s SOP and regulatory guidelines. Timely updation of literature tracker as per the exclusion and inclusion criteria of the safety information. Documentation: Updating the QC checklist for the reviewed ICSRs on real time manner. Archival of relevant documents and e-mail communications related to RMPs and update the RMP details in the RMP tracker. Maintain an awareness of current legislation associated with the Worldwide Regulatory Pharmacovigilance requirements. Statutory Compliance: Stay updated with current legislation related to worldwide regulatory pharmacovigilance requirements. Provide timely and quality information for aggregate reports and signal review, ensuring regulatory compliance. [caption id="attachment_56204" align="aligncenter" width="1200"] jubilant pharmacovigilance jobs[/caption] Key Responsibilities: Conduct case processing and data entry activities within specified timelines. Participate in triaging and book-in of various types of reports, including regulatory, EMA MLM ICSR, and literature reports. Ensure accurate coding of adverse reactions using PV-MedDRA. Maintain documentation of pharmacovigilance SOPs, procedures, and guidelines. Communicate effectively with internal and external stakeholders as per requirements. Stay informed about current pharmacovigilance regulations and ensure compliance. How to Apply: If you have a minimum of [mention years of experience required], relevant qualifications in pharmacovigilance, and are looking to advance your career in a globally renowned pharmaceutical company, we encourage you to apply now. Apply now

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GSK Internship M Pharm | Publications Writing Intern Are you an M. Pharm graduate looking for a rewarding career opportunity? GSK is offering an internship as a Publications Writing Intern at their Bengaluru office. This position is ideal for fresh graduates passionate about medical writing, technical documentation, and project management in the pharmaceutical industry. M. Pharmacy Fresher Pharma Jobs About GSK GSK (GlaxoSmithKline) is a global biopharmaceutical leader driven by the mission to unite science, technology, and talent to combat diseases. With an extensive portfolio of vaccines, specialty medicines, and therapeutic solutions, GSK positively impacts billions of lives globally. GSK emphasizes creating an inclusive, growth-oriented workplace where employees can thrive. The company is now inviting applications from M. Pharm 2024 pass-outs for its Publications Writing Internship in Bengaluru. Key Highlights of the Internship Location: GSK Luxor North Tower, Bengaluru, India Role: Publications Writing Intern This role offers an incredible opportunity for M. Pharm graduates to gain hands-on experience in scientific writing and publication management while adhering to global standards of integrity and compliance. Key Responsibilities Technical Writing and Project Management Support: Provide support for technical writing tasks and project management activities related to specific publication deliverables in collaboration with publication writing team Participate in the execution of encore publications, ensuring consistency and compliance with guidelines Asist in the consolidation and review of content pre- and post-submission Contribute to ensuring the timely delivery of impactful and high-quality publications Quality Assurance and data QC: Perform data quality control (QC) checks to ensure accuracy and integrity of publication data Help to ensure all project management tools (e.g., Datavision, tracking sheets) are updated in a timely manner Assist in the preparation of briefing packages and review drafts to ensure they meet quality standards Adherence to Publication Practices: Learn and apply good publication practices and principles to ensure compliance with GSK’s policies and guidelines (GPP/ICMJE) Support the team in maintaining high scientific integrity of data interpretation Training and Development: Participate in training sessions and seek mentorship from senior publications writers Take initiative to learn and develop skills in medical writing and publication management [caption id="attachment_111479" align="aligncenter" width="1200"] GSK Internship Opportunity for M Pharm | Publications Writing Intern[/caption] Qualifications Educational Requirements M. Pharm graduates (2024 pass-outs preferred). Basic understanding of scientific research and data interpretation. Key Skills Strong technical writing and communication skills. Ability to maintain accuracy and attention to detail in all tasks. Familiarity with data quality checks and regulatory guidelines. Note: GlaxoSmithKline does not charge any fee whatsoever for recruitment process. Please do not make payments to any individuals / entities in connection with recruitment with any GlaxoSmithKline (or GSK) group company at any worldwide location. Even if they claim that the money is refundable. Application Process Interested candidates can apply directly through the official GSK Careers portal. Verify all communications and avoid fraudulent recruitment attempts. Apply Here: GSK Careers - Publications Writing Intern

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Accuprec Research Labs Pvt. Ltd., a leading organization in the pharmaceutical and research industry, is seeking talented professionals for multiple roles, including Quality Control, Quality Assurance, GLP, Accounts, and Microbiology. This hiring drive is for various levels of expertise, ranging from entry-level to managerial positions. The roles are based in Ahmedabad, Gujarat, a hub for pharmaceutical innovation. Job Openings and Details 1. Analytical Development & Quality Control (AD & QC) Role: Assistant Manager (GC, GC-MS) Qualification: MSc, M Pharm Experience: 8-10 years 2. GLP Department Study Director (In-Vitro) Qualification: MSc (Biotech/Micro/Toxicology) Experience: 2-5 years Study Director (In-Vivo) Qualification: M Pharm (Pharmacology & Toxicology) Experience: 2-5 years Veterinary Doctor Qualification: M.V.Sc. (Pharmacology & Toxicology) Experience: 0-2 years Document Control Officer (DCO) Qualification: Any Graduate (Preferably BSc, B Pharm) Experience: 0-2 years 3. Quality Assurance (QA) Assistant Manager (Corporate Quality Assurance) Qualification: MSc, M Pharm Experience: 8-10 years Research Associate/Sr. Research Associate Qualification: MSc, M Pharm Experience: 2-7 years Research Assistant Qualification: MSc, M Pharm Experience: 0-2 years 4. Accounts (AC) Manager Qualification: B Com, M Com, MBA (Finance) or equivalent Experience: 15+ years Purchase Executive Qualification: B Com, M Com, MBA (Finance) or equivalent Experience: 5-10 years Sales Executive Qualification: B Com, M Com, MBA (Finance) or equivalent Experience: 1-3 years 5. Microbiology (MB) Role: Research Assistant Qualification: MSc (Microbiology) Experience: 0-2 years [caption id="attachment_99455" align="aligncenter" width="930"] Accuprec Hiring for Quality Control, Quality Assurance, GLP, Accounts, and Microbiology Roles[/caption] Application Process Interested candidates are encouraged to send their resumes to: 📧 Email: career@accuprec.in 📞 Contact Numbers: +91 90999 32105 | +91 90999 37398

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Thermo Fisher Scientific, a global leader in scientific research services, is seeking a talented Regulatory Affairs Specialist to join their remote team in India. This is a perfect opportunity for professionals with a background in regulatory science, especially M.Sc. graduates, to contribute to life-changing therapies and innovations. With a fully remote work setup, you can make a significant impact while working from the comfort of your home. About Thermo Fisher Scientific: At Thermo Fisher, we are committed to enabling our customers to make the world healthier, cleaner, and safer. Our work spans across laboratory research, clinical trials, and regulatory affairs. The Regulatory Affairs team plays a critical role in accelerating product development and ensuring compliance with global regulations. If you are passionate about science and regulatory standards, this role could be a great fit for you. Job Role: Regulatory Affairs Specialist As a Regulatory Affairs Specialist at Thermo Fisher, you will be responsible for ensuring regulatory compliance across clinical trials and product development. Working within our PPD® clinical research portfolio, you will provide regulatory expertise and guidance to clients, assisting in the preparation of documentation, submissions, and project management. Location: Remote, India Job Type: Full-time Category: Clinical Research Work Schedule: Monday to Friday (Standard hours) Job ID: R-01285926 Key Responsibilities: Supports the preparation of documentation and submissions under guidance. Coordinates and manages client deliverables supporting regulatory compliance. Liaises with internal and external clients in the tracking and status update of project plans and overall support of projects. Assists with project budgeting/forecasting. Maintains knowledge and understanding of SOPs, client SOPs/directives, and current regulatory guidelines. Assists in business development and pricing of projects for the department. Evaluates client needs in relationship to overall project timelines, quality and delivery. Engages other project team members, functional units and/or management as necessary to deliver final product, and resolve/mitigate identified issues or barriers to delivery as needed. Knowledge, Skills, Abilities Good English language (written and oral) communication skills as well as local language where applicable Good attention to detail and quality as well as editorial/proofreading skills Good interpersonal skills to work effectively in a team environment Good computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies Basic organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects Good negotiation skills Capable of working independently with direction and exercising independent judgment Capable of independently assessing sponsor regulatory needs and working with project team members in producing compliant deliverables Basic knowledge of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management Basic understanding of medical terminology, statistical concepts, and guidelines Good analytical, investigative and problem-solving skills Capable of interpreting data [caption id="attachment_107789" align="aligncenter" width="640"] Work from Home Regulatory Affairs Specialist Hiring | Thermo Fisher[/caption] Qualifications: Educational Background: Bachelor's degree or higher (preferably in life sciences or related fields such as M.Sc.). Experience: Minimum of 2 years of relevant experience in regulatory affairs, ideally within clinical research or pharmaceuticals. Why Thermo Fisher? Thermo Fisher offers an inclusive work culture that values diversity and empowers individuals to contribute their unique perspectives.

This role is ideal for candidates looking to work remotely while contributing to a dynamic, innovative global team. You'll have the chance to engage in clinical research projects that positively impact patient outcomes and make a real difference in the world. How to Apply: Interested candidates can apply directly through the official Thermo Fisher career portal. Apply Here