Rajneet Kashyap on LinkedIn: **Labcorp: Hiring Clinical Research Associate in… (2024)

**Dugen Pharma Hiring: Regulatory Affairs Specialist in Pune** https://lnkd.in/gfWv8M3Z**About Company:**Dugen Pharma is seeking dedicated professionals for our regulatory affairs team. If you're located in Pune and meet the criteria, apply now!**Position Name:**Regulatory Affairs Specialist **Organization:**Dugen Pharma **Location:**S.No. 135, D-Block, Unit-203, Naren Pearl, Magarpatta Road, Hadapsar, Pune **Qualifications:**| Qualification | Experience| Salary| Preference||---------------|----------------------------------|---------------------------|-----------------------|| B.Pharm, M.Pharm | 1.5 – 3 years (CIS, LATAM, AFRICA) | 20-25 K (in-hand monthly) | Localite from Pune|**Job Details:**📢 **Joining**: Immediately📞 **Contact for Interview:**🕑 **Call Time**: 2:30 PM to 4:30 PM📱 **WhatsApp/Phone**: +91 9637454035 **How to Apply:**1. Ensure your qualifications and experience align with the job requirements.2. Prepare an updated resume highlighting your relevant experience.3. Contact via WhatsApp/Phone at the provided number within the specified call time.

**Biocon Biologics Hiring: Drug Safety Specialist**https://lnkd.in/g6zYEpzh**About the Company:**Biocon Biologics is seeking a Drug Safety Specialist with leadership skills and excellent communication abilities to oversee CRO activities. This role involves monitoring safety compliance and leading both external and internal stakeholders. The DSS will serve as a subject matter expert for drug safety, collaborating with cross-functional teams and vendors on global safety regulations and guidelines.**Position Name:**Drug Safety Specialist**Organization:**Biocon Biologics**Location:**Bengaluru**Qualifications:**🎓 Master’s degree or higher in Life Sciences, Pharmacy, or Healthcare, or equivalent🎓 Degree in alternative Medicine, BDS, or PhD🗂 Minimum five years of pharmacovigilance experience (three years in aggregate reports, safety signal, RMP) **Key Responsibilities:**✔️ Support signal management processes including detection, tracking, and evaluation✔️ Prepare and maintain Risk Management Plans (RMP)/Risk Evaluation and Mitigation Strategies (REMS)✔️ Monitor effectiveness of risk minimization measures✔️ Respond to safety questions from regulatory authorities and partners✔️ Oversee scheduling, tracking, compliance, and quality of aggregate report vendors✔️ Lead process improvement initiatives for aggregate reporting, signal management, and RMP preparation✔️ Review and input on safety sections of CCDS, local labels, health hazard analyses, and QA trend analyses✔️ Participate in pharmacovigilance audit/inspection preparation and CAPA management✔️ Prepare SOPs and working guidance ensuring pharmacovigilance compliance✔️ Oversee and mentor Drug Safety Specialists✔️ Ensure compliance and review of safety data exchange agreements✔️ Collaborate with drug safety physicians and cross-functional teams for clinical studies**Additional Responsibilities:**📊 Device safety trend analysis📝 PV safety writing for biosimilar publications📚 PV training management support for BBL employees🔍 PV vendor oversight**Skills:**🌟 Strong written and verbal communication skills🌟 Proficiency in MS Office tools (Excel, PowerPoint, Word)🌟 Leadership and collaborative interaction in team environments🌟 Strong organizational skills with the ability to prioritize independently

**Biocon Biologics Hiring: Drug Safety Specialist**https://lnkd.in/g6zYEpzh**About the Company:**Biocon Biologics is seeking a Drug Safety Specialist with leadership skills and excellent communication abilities to oversee CRO activities. This role involves monitoring safety compliance and leading both external and internal stakeholders. The DSS will serve as a subject matter expert for drug safety, collaborating with cross-functional teams and vendors on global safety regulations and guidelines.**Position Name:**Drug Safety Specialist**Organization:**Biocon Biologics**Location:**Bengaluru**Qualifications:**🎓 Master’s degree or higher in Life Sciences, Pharmacy, or Healthcare, or equivalent🎓 Degree in alternative Medicine, BDS, or PhD🗂 Minimum five years of pharmacovigilance experience (three years in aggregate reports, safety signal, RMP) **Key Responsibilities:**✔️ Support signal management processes including detection, tracking, and evaluation✔️ Prepare and maintain Risk Management Plans (RMP)/Risk Evaluation and Mitigation Strategies (REMS)✔️ Monitor effectiveness of risk minimization measures✔️ Respond to safety questions from regulatory authorities and partners✔️ Oversee scheduling, tracking, compliance, and quality of aggregate report vendors✔️ Lead process improvement initiatives for aggregate reporting, signal management, and RMP preparation✔️ Review and input on safety sections of CCDS, local labels, health hazard analyses, and QA trend analyses✔️ Participate in pharmacovigilance audit/inspection preparation and CAPA management✔️ Prepare SOPs and working guidance ensuring pharmacovigilance compliance✔️ Oversee and mentor Drug Safety Specialists✔️ Ensure compliance and review of safety data exchange agreements✔️ Collaborate with drug safety physicians and cross-functional teams for clinical studies**Additional Responsibilities:**📊 Device safety trend analysis📝 PV safety writing for biosimilar publications📚 PV training management support for BBL employees🔍 PV vendor oversight**Skills:**🌟 Strong written and verbal communication skills🌟 Proficiency in MS Office tools (Excel, PowerPoint, Word)🌟 Leadership and collaborative interaction in team environments🌟 Strong organizational skills with the ability to prioritize independently

🚀 **[Fresher] Medpace Hiring in Clinical Research!** 🚀https://lnkd.in/gNRDfZUQ**About Company:**Medpace is a full-service clinical contract research organization accelerating the global development of safe and effective medical therapeutics.**Position:** Clinical Research Associate (Entry Level)**Location:** Navi Mumbai, Maharashtra**Experience:** Fresher**Salary:** ₹4.6 LPA **Qualifications:**- Required: Bachelor’s degree in health or life science-related field- Preferred: Clinical Research Coordinator experience- Familiarity with Microsoft Office- Strong communication and presentation skills- Willingness to travel 60-80% nationally **Responsibilities:**- Conduct qualification, initiation, monitoring, and closeout visits for research sites- Communicate with medical site staff and ensure investigator compliance- Verify investigator qualifications, training, and resources- Review medical records and research source documentation- Verify subject eligibility and accurate data reporting- Assess patient recruitment and retention success- Complete monitoring reports and follow-up letters **Why Medpace:**- Support groundbreaking drug and device development- Competitive compensation and benefits- Internal growth opportunities **Application Process:**Interested candidates, apply online now! Qualified applicants will be contacted for an interview. Medpace is an Equal Opportunity/Affirmative Action Employer.🔗 **Apply Here**📢 **Join WhatsApp**📢 **Join Telegram**⚠️ **Important Notice:** Beware of phishing scams. Medpace employees will never ask for payment as part of the application process.

🚀 **Cognizant Hiring Freshers for Clinical Data Management / Pharmacovigilance!** 🚀https://lnkd.in/gUv579Dz**Position:** Trainee – Junior Data Analyst**Location:** Pune, India**Salary:** ₹25,000 – ₹35,000 /month**Eligibility:** B.Pharm, M.Pharm, Pharm.D**Experience:** Freshers💼 **Role & Department:**- Trainee – Junior Data Analyst- CDM/PV (Clinical Data Management / Pharmacovigilance)Cognizant is offering an exciting opportunity for freshers to launch their careers! If you have a degree in B.Pharm, M.Pharm, or Pharm.D, apply now!📧 **Apply Now:** pavhad103@gmail.comJoin our team and kick-start your career with us! 🌟

**Emcure Pharmaceuticals URGENT Hiring: AM-Warehouse/ Packing/ Production/ QMS/ QA/ QC**https://lnkd.in/g2MBecsP**About Company:**Emcure Pharmaceuticals, a fast-growing Indian company, develops, manufactures, and markets a broad range of pharmaceutical products globally. Our core strength lies in in-house development and manufacturing of differentiated pharmaceutical products.**Position Name:**AM-Warehouse/ Packing/ Production/ QMS/ QA/ QC**Organization:**Emcure Pharmaceuticals**Location:**Mehsana**Qualifications:**- B.Sc- M.Sc- Graduation- Post Graduation- B.Pharm- M.Pharm- ITI- Diploma**Experience:**1 to 10 years**Salary:**N/A**Job Details:**| **Position**| **Department** | **Experience Required** | **Qualification**||-----------------|----------------|-------------------------|---------------------------------------------------------|| AM-Warehouse| Warehouse| 1 to 10 years| B.Sc, M.Sc, Graduation, Post Graduation, B.Pharm, M.Pharm, ITI, Diploma || Packing| Packing| 1 to 10 years| B.Sc, M.Sc, Graduation, Post Graduation, B.Pharm, M.Pharm, ITI, Diploma || Production| Production| 1 to 10 years| B.Sc, M.Sc, Graduation, Post Graduation, B.Pharm, M.Pharm, ITI, Diploma || QMS| QMS| 1 to 10 years| B.Sc, M.Sc, Graduation, Post Graduation, B.Pharm, M.Pharm, ITI, Diploma || QA| QA| 1 to 10 years| B.Sc, M.Sc, Graduation, Post Graduation, B.Pharm, M.Pharm, ITI, Diploma || QC| QC| 1 to 10 years| B.Sc, M.Sc, Graduation, Post Graduation, B.Pharm, M.Pharm, ITI, Diploma |**Selection Process:**- **Interview Mode:** Face-to-Face- **Interview Rounds:** HR**How to Apply:**Interested and eligible candidates can attend the interview at the scheduled time and venue. Send your resume to [bhavik.parekh@emcure.com](mailto:bhavik.parekh@emcure.com).**Job Description:**Join our dynamic team and contribute to our mission of delivering quality pharmaceutical products worldwide. We look forward to meeting you!For more details, please visit our website or contact our HR department.

**Reliance Industries Hiring: Lab Analyst in Surat**https://lnkd.in/gMyYnUwB**About Company:**Motto: "Growth is Life" – At Reliance, we excel in hydrocarbon exploration, petroleum refining, petrochemicals, retail, and telecommunications. As a Fortune 500 company and India's largest private sector corporation, we lead globally in multiple sectors, including polyester yarn and fiber production.**Position:**- **Role:** Lab Analyst- **Location:** Surat**Qualifications:**- B.Sc. in Chemistry or Diploma in Chemical Engineering- Minimum 2 years of experience in QA/QC discipline**Job Details:**| **Responsibility**| **Details**||-------------------------------|---------------------------------------------------------------------|| Sample Management| Inspect and distribute routine samples, report issues|| Testing and Reporting| Follow standard test methods, validate results, report exceptions|| Emergency Response| Perform on-spot mitigation under guidance|| Laboratory Maintenance| Clean and maintain equipment, ensure good housekeeping|| Data Management| Enter test results in LIMS, record in raw data books|| Safety and Compliance| Follow HSEF procedures, report unsafe conditions|| Learning and Development| Participate in training, engage in external events|**Skills & Competencies:**- Knowledge of standard test procedures and result reporting- Ability to handle and analyze samples accurately- Effective communication for reporting abnormal results- Capability to learn various types of chemical and instrumental testing- Familiarity with fire safety management, waste management, and integrated management systems**Application:**Interested candidates, please apply now to be part of our journey.

**Hikal Limited Hiring: Jr. Officer API Production @ Bengaluru**https://lnkd.in/gc86vyQA**About Hikal:**Founded in 1988, Hikal Limited is a trusted partner in the pharmaceutical, biotech, agrochemical, and specialty chemical sectors. It stands as one of India's largest API producers.**Position:**- **Role:** Jr. Officer API Production- **Location:** Bengaluru**Qualifications:**- **Education:** BSc in Chemistry- **Experience:** 1-3 years in API manufacturing, including Intermediate & Clean Room experience**Key Responsibilities:**- Follow precise batch processing instructions- Operate processes within specified parameters- Maintain cleanliness and good housekeeping- Adhere to GMP and safety protocols- Report deviations immediately**Preferred Profile:**- Male candidates with 1-3 years of API manufacturing experience**Interview Details:**- **Mode:** Face-to-Face- **Rounds:** HR- **Date:** June 24 – June 28, 2024- **Time:** 9:30 AM – 4:00 PM- **Venue:** Hikal Limited, Unit 1, 82/A, KIADB Industrial Area, Jigani, Anekal Taluk, Bangalore – 560105- **Contact:** Ramya**Application:**Interested candidates, please send your CV to [ramya_n@hikal.com](mailto:ramya_n@hikal.com).

**Unichem Laboratories – Walk-In Interviews for Multiple Positions**https://lnkd.in/grKQm7Ws📍 **Location:** Goa**Departments:** QA / QC / Production / Engineering / Materials**Qualifications:** B.Pharm, M.Pharm, B.Sc, M.Sc, ITI, HSSC**Experience:** 2+ years**Walk-In Interview Details:**📅 **Date:** 23rd June 2024 (Sunday)🕙 **Time:** 10:00 AM to 04:00 PM📍 **Venue:** Hotel Grace Majestic, Next to Collectorate, Fatorda, Margao, Goa**Contact Information:**📞 7720031490📧 hrgoa@unichemlabs.com**Note:**- Interested freshers may apply via email: hrgoa@unichemlabs.com- Bring updated resume, passport size photo, educational certificates, previous work experience certificates, and current CTC statement.🔬🏭👩🔬👨🔬

**Hetero Labs – Walk-In Interviews for Freshers**https://lnkd.in/gCKsZJq2**Dates & Venues:**- **24th June 2024:** Govt Degree College, Salur- **25th June 2024:** Sri Sai Degree College, Bobbili**Time:** 9:00 AM - 5:00 PM**Qualifications:**- B.Sc (Chemistry)- M.Sc (Chemistry)- B.Pharm- Diploma (Mechanical)- ITI Fitters- 2020-2024 Graduates**Benefits:**- Subsidized Canteen- Transportation- ESI, EPF, Mediclaim- Retention Bonus- Monthly Variables**Note:**- Bring updated resume & documents.- Immediate joiners preferred.- Can't attend? Email resume to: Raju.g@hetero.com