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Aembic Pharmaceuticals Walk-In Drive for Freshers in Vadodara Aembic Pharmaceuticals Pvt. Ltd. invites freshers with a Diploma in Mechanical or Electrical Engineering to join our esteemed team. We are conducting a walk-in drive at our Panelav site near Vadodara, Gujarat. This is an excellent opportunity for entry-level professionals to kickstart their careers in a reputable pharmaceutical company known for its commitment to quality and innovation. About Aembic Pharmaceuticals Aembic Pharmaceuticals is dedicated to producing high-quality, affordable medicines. Our company has been recognized as a Great Place to Work, thanks to our focus on employee growth, innovation, and a collaborative work environment. Walk-In Drive Details Location: Alembic Research Centre, Opp. Alembic Cricket Ground, Near In-Orbit Mall, Alembic Road, Vadodara Date: Saturday, 25th May 2024 Time: 09:00 AM to 11:00 AM Open Positions and Qualifications 1. Production (Oral Solid Dosage & Injectables) - Trainees Qualifications: Diploma in Mechanical or Electrical Engineering Batch: 2022, 2023, 2024 Eligibility Criteria: No active backlog or ATKT. Proficient in English (written and oral communication). Willing to work in rotational shifts. Must clear technical and English proficiency tests. Recruitment Process Written Test: All candidates will undergo a written test to assess their technical and language skills. Personal Interview: Candidates who pass the written test will be invited for a personal interview after five days. Note: Candidates who have appeared for a written test or interview in the last three months are not eligible. How to Apply If you are unable to attend the walk-in drive, please send your updated resume to [email protected]. Ensure your resume includes details of your total experience, current CTC, expected CTC, and notice period. Beware: Aembic Pharmaceuticals does not hire through consultants or agents who promise interviews or jobs for monetary consideration or registration fees. Beware of fraudulent calls. Venue: Alembic Research Centre Opp. Alembic Cricket Ground, Near In-Orbit Mall Alembic Road, Vadodara Date: Saturday, 25th May 2024 Time: 09:00 AM to 11:00 AM Key Responsibilities As a trainee in the Production (Oral Solid Dosage & Injectables) department, you will: Operate and maintain production equipment under the supervision of senior staff. Ensure compliance with cGMP and regulatory standards. Participate in process improvement initiatives and contribute to maintaining a safe work environment. By joining Aembic Pharmaceuticals, you will be part of a team that values excellence, innovation, and continuous learning. We look forward to welcoming dynamic and talented individuals to our organization. [caption id="attachment_68256" align="aligncenter" width="930"] Alembic Pharma Recruitment Notification[/caption]

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Aembic Pharmaceuticals Walk-In Drive in Vadodara Aembic Pharmaceuticals Pvt. Ltd. is inviting talented professionals to join their team at a walk-in drive in Vadodara. This event provides an excellent opportunity for candidates with qualifications in M. Pharm, B. Pharm, and M.Sc. to advance their careers in the pharmaceutical industry. We are looking for individuals with experience in Production (OSD/API) and Quality Control (OSD/Injectable/API). About Aembic Pharmaceuticals Aembic Pharmaceuticals is committed to producing high-quality, affordable medicines. We are a rapidly growing company known for our innovative approach and dedication to excellence. Our team is comprised of skilled professionals who work collaboratively to deliver the best outcomes. Walk-In Drive Details Location: Aembic Vidyalaya, Alembic City, Opposite Bhailal Amin General Hospital, Alembic Road, Vadodara Date: Sunday, 26th May 2024 Time: 09:00 AM to 03:00 PM Open Positions and Qualifications 1. Production (OSD) - Technical Officer/Junior Executive/Executive Core Areas: Granulation, Compression, Coating, Pelletization, Capsule Filling Qualifications: M. Pharm, B. Pharm, DME, ITI Experience: 2-7 years Responsibilities: Manage production processes in granulation, compression, coating, and capsule filling areas. Ensure adherence to cGMP and regulatory requirements. Maintain accurate production records and documentation. 2. Production (API) - Junior Executive/Executive/Senior Executive Core Areas: Operating machinery, documentation, compliance Qualifications: Diploma in Chemical Engineering, B.Sc. Experience: 2-7 years Responsibilities: Operate reactors, centrifuges, dryers, and filtration systems. Maintain detailed records of production activities. Ensure compliance with regulatory standards. 3. Quality Control (OSD/Injectable) - Executive Core Areas: QC instruments, lab records, compliance Qualifications: M. Pharm, B. Pharm, M.Sc. Experience: 2-5 years Responsibilities: Handle QC instruments like HPLC, LCMS, GC, UV-spectrophotometer, and dissolution apparatus. Manage QMS activities and maintain lab records. Ensure QC compliance and GLP activities. 4. Quality Control (API) - Executive Core Areas: Analysis, instruments, stability samples Qualifications: M.Sc. in Organic/Analytical Chemistry Experience: 2-5 years Responsibilities: Conduct analysis for finished products, stability samples, and raw materials. Handle instruments such as HPLC, GC, and UV-Visible/IR Spectrophotometer. Ensure adherence to GLP and QMS guidelines. How to Apply Interested candidates are encouraged to attend the walk-in interview with their updated resumes and relevant documents. If unable to attend, please send your resume to the following email addresses based on your area of expertise: Production (OSD): [email protected] Production (API): [email protected] Quality Control (OSD/Injectable): [email protected] Quality Control (API): [email protected] Note: Aembic Pharmaceuticals does not hire consultants or agents who promise interviews or jobs for monetary consideration or registration fees. Beware of fraudulent calls. [caption id="attachment_68256" align="aligncenter" width="930"] Alembic Pharma Recruitment Notification[/caption] Why Join Aembic Pharmaceuticals? Competitive Salary and Benefits: We offer attractive compensation packages and comprehensive benefits. Professional Growth: Opportunities for continuous learning and career development. Innovative Work Environment: A collaborative workplace that encourages creativity and excellence. Venue: Aembic Vidyalaya Alembic City, Opposite Bhailal Amin General Hospital Alembic Road, Vadodara Date: Sunday, 26th May 2024 Time: 09:00 AM to 03:00 PM

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Centaur Pharmaceuticals Recruitment Drive Centaur Pharmaceuticals Pvt. Ltd., a leading specialty drug manufacturing organization, is conducting a recruitment drive for talented professionals in Quality Assurance (QA) and Quality Control (QC). This drive is open to candidates with qualifications in B. Pharm, M. Pharm, and M. Sc., and offers exciting career opportunities at our Pune site. About Centaur Pharmaceuticals Centaur Pharmaceuticals is renowned for providing high-quality, affordable medicines trusted by healthcare professionals worldwide. With regulatory approvals from USFDA and MHRA, we are one of the fastest-growing pharmaceutical companies in India. Our commitment to excellence drives us to continuously seek dedicated and skilled professionals to join our team. Recruitment Drive Details Location: Centaur Pharmaceuticals Pvt. Ltd., Pune Date: Sunday, 26th May 2024 Time: 10:00 AM to 04:00 PM Venue: St Laurn Koregaon Park, 15 A, Koregaon Road, Pune - 411001 Open Positions and Qualifications Quality Assurance (QA) - Officer/Executive/Sr. Executive Core Areas: QMS, Validation, Investigation, APQR, Stability Study, Auditing, Compliances, Training, IPQA Qualifications: B. Pharm, M. Pharm Experience: 4-8 years for Officer/Executive/Sr. Executive, 12-14 years for Asst. Manager Quality Control (QC) - Officer/Executive/Sr. Executive Core Areas: Raw Material, In-Process, Finished Product, Stability, AMV, AMT Qualifications: M. Sc. (Chemistry) Experience: 5-10 years for Officer/Executive/Sr. Executive, 10-15 years for Asst. Manager Job Responsibilities Quality Assurance (QA) Officer/Executive/Sr. Executive: Initiate, review, and track QMS elements like deviation, change control, and CAPA market complaints. Ensure compliance with regulatory requirements and cGMP. Prepare, review, and implement QA SOPs and CQA SOPs. Conduct internal and external audits to assess QMS effectiveness. Oversee the review and approval of manufacturing batch records and analytical data. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Quality Control (QC) Officer/Executive/Sr. Executive: Analyze raw materials, in-process materials, and finished goods. Conduct stability testing and handle stability samples. Operate and maintain HPLC, dissolution, and other sophisticated instruments. Develop and implement LIMS modules and integrate instruments with LIMS. Conduct OOC, OOT, OOE, and deviation investigations. Plan and execute work related to the GLP and stability sections. [caption id="attachment_56437" align="aligncenter" width="930"] Centaur Pharmaceuticals Recruitment Notification[/caption] Requirements Location Flexibility: Willingness to relocate to Pune or nearby locations. Shift Work: Ability to work in shifts. Documentation: Carry CV, educational certificates, experience letters, salary slips, and address & photo proof to the walk-in interview. What We Offer Competitive Salary and Benefits: Attractive compensation packages and comprehensive benefits. Professional Growth: Opportunities for continuous learning and career development. Innovative Work Environment: A collaborative workplace that encourages creativity and excellence. How to Apply Interested candidates are invited to attend the walk-in interview with their updated resumes and relevant documents. Alternatively, candidates can send their profiles to [email protected]. Note: Centaur Pharmaceuticals follows a formal recruitment process through its HR Department and does not outsource the final selection to any individual, agency, or consultant. We do not charge any registration fees or security deposits at any stage of the recruitment process.

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Exciting Opportunity at IQVIA - Biostatistics Techn (Campus) - India IQVIA is offering exciting opportunities for freshers in the field of biostatistics at our Kochi location. If you are passionate about statistics, clinical research, and making a difference in healthcare, this is your chance to join a leading global company dedicated to transforming the industry. At IQVIA, you will have the opportunity to work with experienced professionals, gain hands-on experience, and contribute to meaningful projects that impact healthcare outcomes worldwide. Job Type: Full-Time Location: Kochi, IN Referred By: Niranjan M Job Overview: As a Biostatistics Techn at IQVIA, you will provide statistical support for the production and checking of statistical outputs and the development of analysis plans under the guidance of the project team lead. Job Responsibilities: Job Overview With appropriate support and guidance, provide statistical support for the production and checking of statistical outputs and the development of analysis plans, under the direction of the project team lead. Essential Functions Production of High-Quality Deliverables:  Completes, and reviews, assignments on time. Clearly follow instructions of project lead in the execution of project assignments. Seeks assistance and guidance when needed. AIQVIA for 'Right the First Time'. Timelines and Communication:  Attends internal project team meetings.  Accountable for speaking up if a task takes longer than expected to complete. Provides timely progress updates to team lead.  Supports colleagues as requested. Technology:  Awareness and utilization of technology offerings (Biostatistical Tools) rolled out by the Global business unit. Under Supervision Specifications:  Writes and maintains specifications for assigned datasets and TLFs, where applicable.  Datasets:  Programs datasets to industry standards, with mentor/manager support. Tables, Listings and Figures (TLFs): Programs tables, listings and figures, checks output for format and content, and questions specifications, as needed. Ensures consistency across TLFs. Documentation:  Create and/or review documentation as requested including but not limited to  statistical analysis plans, data review, specifications and statistical analyses. Risk Management:  Identifies risks to project delivery and/or quality to team lead. [caption id="attachment_66320" align="aligncenter" width="1200"] Biostatistics Fresher Jobs Kochi[/caption] Qualifications:  High School Diploma or equivalent Active enrollment in a biostatistics or related field degree program at an accredited college or university Req Active enrollment in a biostatistics or related field degree program at an accredited college or university No experience required. Requires knowledge of basic principles, theories, and concepts of a job area, typically obtained through advanced education or prior relevant experience. Excellent written and oral communication skills including grammatical/technical writing skills. Excellent attention and accuracy with details. Basic knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Familiarity with basic statistical methods that apply to Phase I-IV clinical trials. Strong individual initiative. Strong organizing skills. Aptitude for SAS computing package skills. Strong commitment to quality. Ability to effectively manage multiple tasks and projects. Ability to accept direction of lead team members. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Apply Now: If you are ready to kick-start your career in biostatistics and make a difference in the healthcare industry, apply now

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Exciting Opportunity at IQVIA - Biostatistics Techn (Campus) - India IQVIA is offering exciting opportunities for freshers in the field of biostatistics at our Kochi location. If you are passionate about statistics, clinical research, and making a difference in healthcare, this is your chance to join a leading global company dedicated to transforming the industry. At IQVIA, you will have the opportunity to work with experienced professionals, gain hands-on experience, and contribute to meaningful projects that impact healthcare outcomes worldwide. Job Type: Full-Time Location: Kochi, IN Referred By: Niranjan M Job Overview: As a Biostatistics Techn at IQVIA, you will provide statistical support for the production and checking of statistical outputs and the development of analysis plans under the guidance of the project team lead. Job Responsibilities: Job Overview With appropriate support and guidance, provide statistical support for the production and checking of statistical outputs and the development of analysis plans, under the direction of the project team lead. Essential Functions Production of High-Quality Deliverables:  Completes, and reviews, assignments on time. Clearly follow instructions of project lead in the execution of project assignments. Seeks assistance and guidance when needed. AIQVIA for 'Right the First Time'. Timelines and Communication:  Attends internal project team meetings.  Accountable for speaking up if a task takes longer than expected to complete. Provides timely progress updates to team lead.  Supports colleagues as requested. Technology:  Awareness and utilization of technology offerings (Biostatistical Tools) rolled out by the Global business unit. Under Supervision Specifications:  Writes and maintains specifications for assigned datasets and TLFs, where applicable.  Datasets:  Programs datasets to industry standards, with mentor/manager support. Tables, Listings and Figures (TLFs): Programs tables, listings and figures, checks output for format and content, and questions specifications, as needed. Ensures consistency across TLFs. Documentation:  Create and/or review documentation as requested including but not limited to  statistical analysis plans, data review, specifications and statistical analyses. Risk Management:  Identifies risks to project delivery and/or quality to team lead. [caption id="attachment_66320" align="aligncenter" width="1200"] Biostatistics Fresher Jobs Kochi[/caption] Qualifications:  High School Diploma or equivalent Active enrollment in a biostatistics or related field degree program at an accredited college or university Req Active enrollment in a biostatistics or related field degree program at an accredited college or university No experience required. Requires knowledge of basic principles, theories, and concepts of a job area, typically obtained through advanced education or prior relevant experience. Excellent written and oral communication skills including grammatical/technical writing skills. Excellent attention and accuracy with details. Basic knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Familiarity with basic statistical methods that apply to Phase I-IV clinical trials. Strong individual initiative. Strong organizing skills. Aptitude for SAS computing package skills. Strong commitment to quality. Ability to effectively manage multiple tasks and projects. Ability to accept direction of lead team members. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Apply Now: If you are ready to kick-start your career in biostatistics and make a difference in the healthcare industry, apply now

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Encube Ethicals Fresher Recruitment Drive in Pune Encube Ethicals Pvt. Ltd., a leader in topical formulations, is conducting a fresher recruitment drive for various positions in production and manufacturing. This walk-in drive is scheduled for May 26, 2024, in Pune. We are looking for enthusiastic candidates with qualifications in B.Pharm, M. Pharm, Diploma Chemical, D. Pharm, ITI, B.E. - Mechatronic/Elect./Mech. About Encube Ethicals Pvt. Ltd. Encube Ethicals is an integrated pharmaceutical company dedicated exclusively to topical formulations such as creams, ointments, gels, lotions, and solutions. With 24 years of experience in contract development and manufacturing, Encube Ethicals defines excellence in the field of semisolid formulations. Walk-In Drive Details Date: Sunday, May 26, 2024 Time: 10:00 AM to 04:00 PM Venue: St Laurn Koregaon Park, 15 A, Koregaon Road, Pune - 411001 Open Positions and Qualifications Production - Filling & Packing Qualifications: B.Pharm, Diploma in Electrical/Mechanical, B.Sc., ITI Experience: 0-7 Years Manufacturing - Bulk Manufacturing Qualifications: B.Pharm, M. Pharm, Diploma in Chemical, D. Pharm, ITI, B.E. - Mechatronic/Elect./Mech. Experience: 0-5 Years Job Responsibilities Production - Filling & Packing: Operate and maintain filling and packing equipment. Ensure the accuracy and quality of packaging. Adhere to production schedules and timelines. Maintain cleanliness and safety standards in the production area. Manufacturing - Bulk Manufacturing: Participate in bulk manufacturing processes. Work with chemical formulations and handle raw materials. Ensure compliance with GMP and safety standards. Collaborate with the quality control team to maintain product quality. Requirements Willingness to relocate to Goa, Ponda, or nearby locations. Flexibility to work in shifts. Carry CV, educational certificates, experience letters, salary slips, and address & photo proof to the walk-in interview. [caption id="attachment_77731" align="aligncenter" width="930"] Encube Ethicals Pvt Ltd Recruitment - Job vacancies[/caption] What We Offer Competitive Salary and Benefits: We provide an attractive compensation package and comprehensive benefits. Professional Growth: Opportunities for continuous learning and career development. Innovative Work Environment: A collaborative and innovative workplace that encourages creativity and excellence. How to Apply Interested candidates are invited to attend the walk-in interview with their updated resumes and relevant documents. Alternatively, candidates can send their profiles to [email protected]. Note: Encube Ethicals follows a formal recruitment process through its HR Department. We do not outsource the final selection to any individual, agency, or consultants. We do not charge any registration fees or security deposits at any stage of the recruitment process. Venue: St Laurn Koregaon Park 15 A, Koregaon Road, Pune - 411001

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Join Aizant Drugs & Pharmaceuticals Hyderabad Walk-In for Synthesis & Analytical R&D Positions in Vizag Aizant Drugs & Pharmaceuticals is conducting a walk-in interview for talented professionals in the fields of Synthesis and Analytical R&D. This exciting opportunity is open for candidates with M.Sc in Organic Chemistry and Analytical Chemistry. The walk-in interview will be held on June 14, 2024, at our Hyderabad location for positions based at our API R&D Center in Visakhapatnam. About Aizant Drugs & Pharmaceuticals Aizant is a leading integrated drug development solutions provider. Our state-of-the-art facilities and innovative approach to pharmaceutical research and development make us a preferred partner for clients worldwide. We are committed to fostering a collaborative and growth-oriented work environment. Walk in interview Details Location: API R&D Center, Visakhapatnam Interview Location: Aizant Drug Research Solutions Pvt Ltd, Sy. No. 172 & 173, Apparel Park Rd, Dulapally, Quthbullapur Mandal, Hyderabad, Telangana 500100 Date: June 14, 2024 Time: 9:00 AM Open Positions and Qualifications Scientist - Synthesis R&D Qualifications: M.Sc in Organic Chemistry with 10-15 years of experience or Ph.D. with 5-6 years of experience Chemist - Synthesis R&D Qualifications: M.Sc in Organic Chemistry with 1-4 years of experience Scientist - Analytical R&D Qualifications: M.Sc in Analytical Chemistry with 10-15 years of experience or Ph.D. with 5-6 years of experience Chemist - Analytical R&D Qualifications: M.Sc in Analytical Chemistry with 1-4 years of experience Key Responsibilities Project Management: Oversee and manage R&D projects, ensuring timely delivery and compliance with industry standards. Synthesis R&D: Conduct research and development in synthetic organic chemistry, focusing on innovative solutions and methodologies. Analytical R&D: Perform analytical testing and research, developing new analytical methods and ensuring accuracy and precision in results. Team Collaboration: Work collaboratively with cross-functional teams to drive project success and innovation. Client Interaction: Prepare for and participate in client meetings, addressing queries and providing project updates. What We Offer Competitive Salary and Benefits: Attractive compensation packages and comprehensive benefits. Professional Growth: Opportunities for continuous learning and career development. Innovative Environment: A collaborative and innovative workplace that encourages creativity and excellence. [caption id="attachment_57327" align="aligncenter" width="930"] Aizant Drugs Research Solutions Recruitment Notification[/caption] How to Apply Interested candidates are invited to attend the walk-in interview with their updated resumes and relevant documents. If you are passionate about pharmaceutical research and development and looking to make a significant impact, we want to meet you! Venue: Aizant Drug Research Solutions Pvt Ltd Sy. No. 172 & 173, Apparel Park Rd, Dulapally, Quthbullapur Mandal, Hyderabad, Telangana 500100

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Aragen Lifesciences Hiring Project Management Professionals for M.Sc. Organic Chemistry, MBA/PMP in Bangalore Are you an experienced project management professional with a background in M.Sc. Organic Chemistry or an MBA/PMP qualification? Aragen Lifesciences, a leading player in the CRO, CDMO, and Pharma sectors, is hiring talented individuals to join their team in Bangalore. This is an exciting opportunity to advance your career and contribute to groundbreaking projects in the pharmaceutical industry. About Aragen Lifesciences Aragen Lifesciences is dedicated to providing high-quality contract research and manufacturing services to the pharmaceutical and biotechnology industries. Our commitment to excellence and innovation makes us a preferred partner for companies worldwide. Job Details Location: Bangalore, India Position: Project Management Professional Qualifications: M.Sc. in Organic Chemistry, MBA/PMP Experience: 2-7 years in CRO, CDMO, or Pharma sectors Key Responsibilities Project Management: Understand and apply key project management practices and methodologies. Productivity Measurement: Measure key productivity parameters regularly and report findings to the appropriate hierarchy. Operational Challenges: Resolve routine operational challenges efficiently. Compound Delivery: Supervise and ensure the delivery of compounds to designated destinations. Client Interaction: Assist in preparing for client meetings and visits. Shipment Handling: Manage complex shipments and generate shipment databases. LNB Audits: Conduct LNB audits and report observations accurately. Timeline Management: Escalate any deviations from timeline deliverables promptly. Action Items: Capture and follow up on action items from client meetings. Training: Attend mandatory training sessions and implement learnings effectively. [caption id="attachment_77668" align="aligncenter" width="930"] Aragen Lifesciences Recruitment - Job vacancies[/caption] Why Join Aragen Lifesciences? Innovative Environment: Work on groundbreaking projects in a leading pharmaceutical company. Professional Growth: Enhance your skills and career prospects with continuous learning and development opportunities. Collaborative Culture: Join a team of dedicated professionals committed to excellence and innovation. How to Apply Interested candidates can share their profiles with Rajkumar Selvaraj at [email protected].

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Internship Opportunity: Intern Research & Development for B.Tech/M.Sc/M.Tech in LifeScience, Biotech, Biomedical Engg, Chemistry, Nanotechnology Are you passionate about working on breakthrough diagnostics and contributing to solving the problem of Anti Microbial Resistance (AMR)? Module Innovations is offering an exciting internship opportunity for B.Tech, M.Sc, and M.Tech students in LifeScience, Biotech, Biomedical Engineering, Chemistry, and Nanotechnology. Join our team and be part of innovative solutions in the field of infectious diseases. Internship Details Company: Module Innovations Location: Pune, Maharashtra, India Application Deadline: 30th May 2024 Available Positions 1. Research & Development Internship Qualifications: B.Tech/M.Sc/M.Tech in LifeScience, Biotech, Biomedical Engineering, Chemistry, Nanotechnology Responsibilities: Develop novel materials Conduct microbial testing Optimize new chemistries for bio-conjugation and their applications Compensation: This is an unpaid internship, offering valuable hands-on experience, mentoring, independent decision-making opportunities, and networking. A recommendation and experience letter will be provided upon completion. 2. Marketing & Sales Internship Qualifications: MBA Responsibilities: Meet stakeholders and drive product and service sales Create market reports and conduct product research Identify market trends 3. Graphic Design Internship Qualifications: Relevant degree or experience in graphic design Responsibilities: Develop content for public showcases Build product usage documentation Create instructions for use (IFU) and other related content [caption id="attachment_77665" align="aligncenter" width="1200"] Internship Opportunity: Intern Research & Development for B.Tech/M.Sc/M.Tech in LifeScience, Biotech, Biomedical Engg, Chemistry, Nanotechnology[/caption] About Module Innovations Module Innovations is a leading startup focused on developing breakthrough diagnostic technologies for infectious diseases and combating Anti Microbial Resistance (AMR). We are recognized and funded by top investors and funders globally. Our innovative approach and dedication to addressing critical healthcare challenges make us a dynamic and rewarding place to work. Why Join Us? Innovative Projects: Work on cutting-edge diagnostic technologies. Mentorship: Receive guidance from industry experts. Networking: Connect with professionals and stakeholders in the field. Experience: Gain practical, hands-on experience in a fast-paced environment. How to Apply Interested candidates can apply online through the following application form. Application Deadline: 30th May 2024

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Zydus Lifesciences is excited to announce a Walk-in Drive for various positions at our SEZ 1 Manufacturing Unit in Ahmedabad. This drive is a fantastic opportunity for candidates with qualifications ranging from B.Sc and M.Sc to ITI and Diploma. Join us on 25th May 2024 and take your career to the next level! Job Details Company: Zydus Lifesciences Limited (Formerly known as Cadila Healthcare Limited) Location: SEZ 1 Manufacturing Unit, Sarkhej-Bavla N.H. 8A, At – Matoda, Ta – Sanand, Dist – Ahmedabad, Gujarat - 382213 Date: 25th May 2024 (Saturday) Time: 9:00 AM to 3:00 PM Available Positions and Qualifications Quality Control (QC) – Officer/Executive Qualification: B.Sc/M.Sc Experience: 3 to 7 years in a USFDA-approved facility Skills: HPLC, GC, dissolution apparatus, UV-visible spectrometer, weight analysis, stability, GLP Engineering – Technical Assistant/Plant Operator Qualification: ITI (Fitter/Refrigeration/Electrician) or Diploma (Instrumentation/Mechanical/Electrical) Experience: 2 to 7 years Responsibilities: Process equipment maintenance, breakdown maintenance, HVAC/BMS, instrument calibration Manufacturing – Production (OSD) Designation: Plant Operator/Technical Assistant/Apprentice Qualification: B.Pharm/BE Responsibilities: Handle production processes, ensure compliance with GMP and safety standards Packing – Tablet/Capsule Designation: Plant Operator/Technical Assistant Responsibilities: Manage packing operations, maintain equipment, ensure quality control Key Responsibilities QC Officer/Executive: Conduct quality control tests using HPLC, GC, and other laboratory equipment Ensure compliance with GLP and regulatory standards Maintain stability studies and perform weight analysis Technical Assistant/Plant Operator: Perform maintenance and calibration of process equipment Manage HVAC and BMS systems Handle breakdown maintenance to ensure minimal downtime [caption id="attachment_77610" align="aligncenter" width="930"] Zydus Lifesciences limited Fresher Recruitment - Job vacancies[/caption] Why Join Zydus Lifesciences? Zydus Lifesciences is a leading pharmaceutical company known for its innovative and high-quality products. Working with us means being part of a dynamic team that values excellence, integrity, and growth. We offer ample opportunities for professional development and a supportive work environment. How to Apply Unable to attend the walk-in interview? Apply online at Zydus Careers. Interview Venue: Zydus Lifesciences Limited Plot No 1A/1 & 2, Pharmez – SEZ, Sarkhej – Bavla N.H. 8A, At – Matoda, Ta – Sanand, Dist – Ahmedabad, Gujarat - 382213

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At Brooks Steriscience Limited, we are committed to excellence in pharmaceutical manufacturing and quality assurance. Located in the vibrant region of Vadodara, Gujarat, our state-of-the-art facility specializes in API and Sterile API production, adhering to the highest standards of GMP and FDA regulations. Brooks Steriscience Limited Block No 61/62, Village Manglej, Nareshwar Road, Tal Karjan, Dist: Vadodara, Gujarat Position: Executive (Documentation) - Production Department Qualification: MSc/BSc (Familiarity with GMP, FDA regulations, and other relevant quality standards) Experience Required: 5 to 8 years in Pharma Industry (API Plant) Key Responsibilities: Manage Drug product manufacturing and QMS compliance Prepare and revise Master Production/Formula Records (MFR/MPR), Batch Manufacturing/Production Records (BMR/BPR), SOPs, Trend, Qualification documents, Protocols, and Reports Manage the change control process for production documentation, ensuring changes are properly documented, approved, and communicated Effectively implement CAPA Proficiency in SAP system Prepare for and participate in internal and external audits and inspections related to production documentation and implement audit CAPAs Experience in USFDA approved site Application: Interested candidates should share their most updated CV with the HR Department at [email protected] Position: Executive (Sterile API) - Production Department Qualification: B.E. / B.Tech. / B. Pharma / MSc. Experience Required: 5 to 8 years in Pharma Industry (Sterile API) Key Responsibilities: Lead and supervise production teams during assigned shifts, ensuring the effective operation of Sterile API manufacturing processes Ensure compliance with Sterile processing procedures, including aseptic techniques, cleanroom protocols, and environmental monitoring Implement and maintain practices that uphold the sterility of the production environment Enforce adherence to GMP and other relevant quality standards specific to Sterile API manufacturing Work closely with the Production Planning team to ensure accurate scheduling and sequencing of Sterile API production activities Proficiency in handling critical equipment (Reactors, Filters, ANFD, Powder Filling, Autoclave) and working in a batch process, cGMP environment Experience in USFDA approved site and SAP system Application: Interested candidates should share their most updated CV with the HR Department at [email protected] [caption id="attachment_77605" align="aligncenter" width="930"] Brooks Laboratories limited Recruitment - Job vacancies[/caption] Position: Officer - Production Department Qualification: MSc/BSc Experience Required: 2 to 5 years in Pharma Industry (API Plant) Key Responsibilities: Execute API manufacturing processes under the guidance of senior production staff Follow GMP and SOPs to maintain high-quality production Accurately document production activities, including batch records, logbooks, and other required paperwork Adhere to safety protocols and guidelines to ensure a secure working environment Report safety concerns or incidents promptly to the supervisor Identify and report deviations, abnormalities, or issues during production processes Monitor environmental conditions within the production area to meet specified requirements Proficiency in handling critical equipment (Reactors, Centrifuges, Dryers, FBD, Filters, ANFD, Hydrogenator) and working in a batch process, cGMP environment Application: Interested candidates should share their most updated CV with the HR Department at [email protected] Position: Officer/Operator (Sterile API) - Production Department Qualification: MSc/BSc Experience Required: 5 to 8 years in Pharma Industry (Sterile API) Key Responsibilities: Execute Sterile API manufacturing processes according to SOPs and aseptic processing guidelines

Operate and monitor equipment and machinery involved in Sterile processing Adhere to Sterile processing protocols, including gowning procedures, cleanroom behavior, and environmental monitoring Maintain awareness of aseptic techniques and contribute to the maintenance of sterility Follow GMP and quality standards specific to Sterile API manufacturing Proficiency in handling critical equipment (Reactors, Filters, ANFD, Powder Filling, Autoclave) and working in a batch process, cGMP environment Contribute to environmental monitoring activities to meet Sterile processing specifications Work in shifts and report to the Shift Incharge Application: Interested candidates should share their most updated CV with the HR Department at [email protected] Position: Executive (Shift In Charge) - Production Department Qualification: B.E. / B.Tech. / MSc/BSc Experience Required: 5 to 8 years in Pharma Industry (API Plant) Key Responsibilities: Supervise and lead production teams during assigned shifts, ensuring smooth and efficient operation of API manufacturing processes Collaborate with other shift incharges and production managers to facilitate seamless transition between shifts Proficiency in SAP system Proficiency in handling critical equipment (Reactors, Centrifuges, Dryers, FBD, Filters, ANFD, Hydrogenator) and working in a batch process, cGMP environment Provide training and mentorship to production staff on API manufacturing processes, safety protocols, and regulatory compliance In-depth knowledge of GMP, safety regulations, and quality standards in API production Knowledge and compliance of clean room equipment and area Experience in USFDA approved site Application: Interested candidates should share their most updated CV with the HR Department at [email protected] For all positions, please ensure your CV includes relevant experience and clearly outlines your qualifications and responsibilities in previous roles. We look forward to welcoming dedicated and skilled professionals to our team.

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Amneal Pharmaceuticals Walk-in Drive for Injectable Manufacturing Plant in Pipan Are you looking for a career in the pharmaceutical industry? Amneal Pharmaceuticals is conducting a Walk-in Drive for various positions at their Injectable Manufacturing Plant in Pipan. This is a fantastic opportunity for candidates with qualifications ranging from ITI and Diploma to B.Sc, B.Pharm, and M.Sc. Join us on 26th May 2024 and take the next step in your career! Job Details Company: Amneal Pharmaceuticals Pvt. Ltd Location: Pipan, Sanand, Ahmedabad, Gujarat Date: 26th May 2024 (Sunday) Time: 9:00 AM to 2:00 PM Available Positions and Qualifications Injectable Manufacturing Department: Designation: Assistant/Associate Qualification: ITI/Diploma/B.Sc Experience: 1 to 10 years of hands-on experience in handling processes for aseptic and controlled areas of injectable/sterile manufacturing (production). Exposure to handling of Isolator-based filling lines is preferred. Designation: Officer/Sr. Officer/Executive Qualification: B.Sc/B.Pharm/M.Sc Experience: 1 to 10 years of hands-on experience in handling processes for aseptic and controlled areas of injectable/sterile manufacturing (production). Exposure to handling of Isolator-based filling lines is preferred. Key Responsibilities Assistant/Associate: Manage production processes in aseptic and controlled areas. Operate and maintain isolator-based filling lines. Ensure compliance with GMP and safety standards. Officer/Sr. Officer/Executive: Oversee aseptic manufacturing operations. Lead quality control and assurance activities. Maintain and improve production efficiency and safety. [caption id="attachment_49554" align="aligncenter" width="930"] amneal pharmaceuticals recruitment notification[/caption] Why Join Amneal Pharmaceuticals? Amneal Pharmaceuticals is a leading global pharmaceutical company committed to delivering high-quality products. Working with us means being part of a dynamic team that values innovation, integrity, and excellence. We offer ample opportunities for professional growth and development in a supportive and collaborative environment. How to Apply Unable to attend the walk-in interview? Share your CV with us at [email protected]. Interview Venue: Amneal Pharmaceuticals Pvt. Ltd. Plot No: 161/1, Sanand Bavla Highway Road, Village: Pipan, Sanand, Ahmedabad, Gujarat – 382110

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Join Cohance Lifesciences: Microbiology Job Openings for Freshers Are you a recent graduate with a degree in Microbiology or Biotechnology? Cohance Lifesciences has exciting job openings for freshers in the field of Microbiology. This is an excellent opportunity to start your career with a leading company in the pharmaceutical industry. Job Details Position: Microbiologist Experience: 0-1 Years Qualification: MSc in Microbiology/Biotechnology Location: Jaggaiahpet, Andhra Pradesh Preferred Candidates: Immediate joiners Key Responsibilities Microbiological Testing: Perform routine microbiological testing of samples. Quality Control: Ensure compliance with quality standards and protocols. Sample Analysis: Analyze samples to detect and identify microbial contamination. Documentation: Maintain accurate records of tests and results. Equipment Maintenance: Ensure proper functioning and calibration of laboratory equipment. [caption id="attachment_58501" align="aligncenter" width="930"] cohance lifesciences Recruitment Notification[/caption] Why Join Cohance Lifesciences? Cohance Lifesciences is committed to innovation and excellence in the pharmaceutical industry. As a fresher, you will have the opportunity to work in a dynamic environment, gain hands-on experience, and grow your career in microbiology. Our team is dedicated to fostering a collaborative and supportive work culture. How to Apply Interested candidates are encouraged to send their resumes to [email protected]. Immediate joiners are highly preferred, so apply now to take the first step towards a rewarding career in microbiology.

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Cronus Pharma Specialities Hyderabad Walk-in Interview for Microbiology Positions Are you a skilled microbiologist seeking new career opportunities? Cronus Pharma Specialities invites you to their Hyderabad walk-in interview for multiple microbiology positions. This event is an excellent chance to join a leading pharmaceutical company and contribute to groundbreaking work in injectable formulations. Walk-in Interview Details Date: 22nd, 23rd, 24th May 2024 Time: 09:30 AM to 2:00 PM Location: Cronus Pharma Specialties India Pvt Ltd, GMR Hyderabad Aviation SEZ, Mamidipally (V), Balapur (M), RR (D) Contact: HR 7337445157 / 7337445197 Available Positions 1. Jr. Executive/Executive/Sr. Executive Experience: 3 - 6 Years Qualification: Relevant qualifications in microbiology or related fields Location: Hyderabad Key Responsibilities Environmental Monitoring: Oversee the environmental monitoring of aseptic processing areas. Microbial Limit Testing: Conduct microbial limit tests to ensure product safety. Isolate Identification: Use Vitek-2 instruments for microbial isolate identification. Bacterial Endotoxin Testing: Perform bacterial endotoxin tests on water for injection (WFI) and finished products. Culture Handling: Manage culture handling techniques to maintain sample integrity. Sterility Testing: Conduct sterility testing using both closed and open methods. Particulate Matter Testing: Handle liquid-borne particulate testing using PAMAS instruments. [caption id="attachment_63821" align="aligncenter" width="930"] Cronus pharma Recruitment Notification[/caption] Why Join Cronus Pharma? Cronus Pharma Specialities is a leader in the pharmaceutical industry, known for its innovative approaches and commitment to quality. Joining their team means working in a state-of-the-art facility with opportunities for professional growth and development. You will be part of a dynamic team dedicated to improving healthcare through advanced microbiological techniques. How to Apply Interested candidates are encouraged to attend the walk-in interview on the specified dates. Please bring your updated CV to the interview or send it in advance to [email protected] or [email protected]. For more information, contact the HR team at 7337445157 / 7337445197.

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Are you an experienced professional in injectable formulation and quality control? Cronus Pharma Specialities is hosting a walk-in interview in Hyderabad for multiple positions in their quality control department. This is a fantastic opportunity to join a leading pharmaceutical company and advance your career. Walk-in Interview Details Date: 22nd, 23rd, 24th May 2024 Time: 09:30 AM to 2:00 PM Location: Cronus Pharma Specialties India Pvt Ltd, GMR Hyderabad Aviation SEZ, Mamidipally (V), Balapur (M), RR (D) Contact: HR 7337445157 / 7337445197 Available Positions 1. Jr. Executive/Executive/Sr. Executive Experience: 5 - 7 Years Qualification: Relevant qualifications in pharmaceutical sciences or related fields Location: Hyderabad Key Responsibilities IP, FP, RM, PM, Stability, and Analytical Validations: Preparation of protocols and reports for injectable formulations. Compliance Sampling and Analysis: Responsible for sampling, analysis, and release of raw materials and packing materials. Review and Release: Oversee the review and release of in-process, finished products, and stability products. Documentation: Preparation and review of SOPs, GTPs, STPs/Specification water-related documents. Method Validation: Involvement in method validation protocols, method transfer protocols, method validation reports, and method verification. [caption id="attachment_63821" align="aligncenter" width="930"] Cronus pharma Recruitment Notification[/caption] Secondary Responsibilities Inventory Management: Ensure sufficient inventory of consumables, chemicals, HPLC, GC columns, and other laboratory instrument spare parts. Why Join Cronus Pharma? Cronus Pharma Specialities is committed to innovation and quality in the pharmaceutical industry. By joining their team, you will be part of a company that values expertise, collaboration, and professional development. Their state-of-the-art facility in Hyderabad offers a dynamic work environment where you can make a significant impact. How to Apply Interested candidates can attend the walk-in interview on the specified dates. Please bring your updated CV to the interview or send it in advance to [email protected] or [email protected]. For more information, contact the HR team at 7337445157 / 7337445197.

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Sun Pharmaceutical Jobs in Dewas - Apply Now! Are you looking for a rewarding career in the pharmaceutical industry? Sun Pharmaceutical Industries Ltd, Dewas, is currently hiring for various positions in their engineering and manufacturing departments. This is an excellent opportunity to join a leading global pharmaceutical company and advance your career. Available Positions 1. Engineering Supervisor (Executive/Sr. Executive) Experience: 6 - 10 Years Qualification: B.E. in Electronics & Instrumentation Location: Dewas Responsibilities: Oversee engineering activities in supporting facility blocks, including warehouse, PM Lab, Stability & Microbiology, CQC-Admin, OSD, Hazardous waste storage, process area, and GSC export warehouse. Promptly attend to equipment and system breakdowns. Ensure compliance with preventive maintenance, facility maintenance, and calibration of plant and machinery. Review and approve HVAC documents. Ensure QMS activities for engineering. Provide engineering support to other blocks. Skills Required: Pharmaceutical background preferred. Strong knowledge of maintenance and block management. Good communication skills. 2. Manufacturing Supervisor Experience: 4 - 7 Years Qualification: B.Pharm Location: Dewas Responsibilities: Hands-on experience in granulation, compression, and coating. Good knowledge of QMS. Strong communication skills. 3. Primary Packing Supervisor/Executive Experience: 3 - 6 Years Qualification: B.Pharm Location: Dewas Responsibilities: Hands-on experience in blister sealing, strip sealing, and dry syrup. Good knowledge of QMS. Strong communication skills. [caption id="attachment_56281" align="aligncenter" width="930"] Sun Pharmaceutical Industries recruitment notification[/caption] Why Join Sun Pharmaceutical Industries Ltd? Sun Pharmaceutical Industries Ltd is a leading global pharmaceutical company known for its commitment to quality and innovation. By joining Sun Pharma, you will have the opportunity to work in a dynamic environment that encourages professional growth and development. The Dewas facility is equipped with state-of-the-art technology, and you will be part of a team that strives to make a difference in the healthcare industry. Application Process Interested candidates are encouraged to apply by sending their resumes to [email protected]. If you know someone who is actively looking for a job, please refer them to these exciting opportunities.

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IQVIA Medical Data Reviewer in Chennai Are you a fresh graduate with a background in life sciences or engineering? IQVIA is seeking dedicated individuals to join their team as Medical Data Reviewers in Chennai. This is an excellent opportunity to start your career with a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. Job Overview As a Medical Data Reviewer at IQVIA, you will play a crucial role in ensuring the accuracy and completeness of key opinion leader (KOL) profiles. Your responsibilities will include: Extracting and verifying details of KOL profiles for the life sciences industry. Identifying and profiling KOLs for various disease areas globally. Understanding project requirements and scope to provide accurate data. Collecting information on KOLs’ publications, meetings, clinical trials, and other relevant data. Entering KOL details into the Profiling Tool Application. Key Responsibilities Extract and verify KOL profiles from various web sources. Ensure no data gaps in the collected profiles. Profile KOLs for specific disease areas worldwide. Gather and input data on KOLs’ publications, meetings, and clinical trials. Understand project requirements and adhere to specified scopes. Qualifications To be eligible for the Medical Data Reviewer position, you should have a background in one of the following: MPharma DPharma BE-Bio BTech-Bio MSc MTech Additionally, the ideal candidate will possess: Excellent web researching skills. Proficiency in MS Office. Good communication skills. Knowledge of medical terminology. [caption id="attachment_77581" align="aligncenter" width="1200"] IQVIA Hiring Freshers Medical Data Reviewer in Chennai[/caption] Why Join IQVIA? IQVIA is committed to pushing the boundaries of human science and data science to create a healthier world. Joining IQVIA means being part of a company that values innovation, collaboration, and the development of its employees. You will have the opportunity to work with cutting-edge technology and contribute to significant advancements in the life sciences industry. Application Process Interested candidates are encouraged to apply online through the official IQVIA referral link: Apply Now.