Join CORONA Remedies for a Walk-In Interview – 22nd Sept 2024

CORONA Remedies is organizing a Walk-In Interview for positions in Quality Assurance (QA) and Quality Control (QC) on Sunday, 22nd September 2024 in Ahmedabad. This is an exciting opportunity for professionals in the pharmaceutical sector looking to join a leading Indian company known for its quality products.

QUALITY ASSURANCE

Designation: Officer / Officer/ Executive

Qualification: B. Pharm / M. Sc

Experience: 03 to 06 Years

Job Description:

Person should know QMS, IPQA, validation, Qualification, Cleaning Validation, Risk Assessment, CSV, regulatory requirements, Market Complain, Vendor Qualification, OOS, OOT, Product Recall, Investigation, Regulatory requirement, audit & response

QUALITY CONTROL

Designation: Officer / Officer/ Executive

Qualification: B. Pharm / M. Sc

Experience: 03 to 06 Years

Job Description:

Handling the Lab instruments of HPLC, Dissolution, D. T., Apparatus, Weighting Balance, Friability, Hardness Tester, FTIR, UV-Spectrophotometer. Analysis of Raw Material, In-process, Finish Products, Stability Tastings, Process Validation, Participate in Lab incident/ OOS/ OOT/Analytical Deviation.

Job Location:

CORONA Remedies Private Limited, Near Super Gas Pump. Bavla-Bagodara Road, Vill- Bhayla, Tal. Bavla, Dist.: Ahmedabad

Date: 22nd September, 2024 Sunday

Timing: 10:00 AM to 02:30 PM

Interview Venue :

Mondeal Business Park “CORONA House”, Block C, S. G Highway, Nr. Gurudwara, Ahmedabad.

APPLY NOW!

Interested candidates who are unable to attend walk in may share CV on

sagart@coronaremedies.com

CORONA Remedies is a well-established pharmaceutical company based in Ahmedabad, Gujarat, specializing in the production and distribution of high-quality healthcare products. The company focuses on therapeutic segments such as cardiovascular, diabetes,

 

Join PI Industries Walk-In in Vadodara on Sunday, 22 Sept 2024!

PI Industries is conducting a Walk-In Interview in Vadodara on Sunday, 22nd September 2024. This is a great opportunity for professionals in the chemical, pharmaceutical, and manufacturing industries who are looking to join a leading agrochemical company.

Positions Available: PROCESS INNOVATION, TECHNOLOGY TRANSFER, KILO LAB / PILOT PLANT

PROCESS INNOVATION

Position: EXECUTIVE

Qualification: M.Sc / Ph.D in Chemistry / Organic Chemistry or M.Pharma in Pharmaceutical Chemistry

Experience: Ph.D with 1 to 5 years & M.Sc with 1 to 12 years in chemical process development / process optimization

TECHNOLOGY TRANSFER

Position: EXECUTIVE

Qualification: B.Tech/BE/M.Tech in Chemical Engineering

Experience: 2 to 8 years of relevant experience in scale-up of processes from laboratory scale to pilot to plant scale, technology absorption from laboratory, preparation of BFD / PFD, mass balance, utility calculations

KILO LAB / PILOT PLANT

Position: PRODUCTION SUPERVISOR

Qualification: B.Sc / M.Sc in Chemistry / Diploma in Chemical Engineering

Experience: B.Sc OR Diploma in Chemical Engineering with 5 years of experience. M.Sc in Chemistry with 2 years of experience

Date: SUNDAY 22 SEPT

10am – 5pm

Venue: Hotel Four Points by Sheraton 1275 Ward, No. 7, Fatehgunj, Vadodara, Gujarat 390002

Send your resume to deepanshu.bhattl@piind.com

Preferred Industries:

Agro Chemicals / Fine Chemicals / Pharma-API /Specialty Chemicals

Why Join PI Industries?

PI Industries is a well-established name in the agrochemical industry with a reputation for innovation and growth. The company offers a stimulating work environment with opportunities for career development and growth.

 

Venus Remedies Ltd– Hiring Alert for Quality Control Positions!

VENUS, a leader in healthcare innovations, is expanding its team and currently hiring for Quality Control positions.

This is an excellent opportunity for quality-focused professionals to join a dynamic, cutting-edge company that’s redefining healthcare solutions.

At VENUS, the work culture is all about innovation, collaboration, and continuous improvement.

As part of the Quality Control team, you will have the opportunity to contribute to groundbreaking healthcare solutions that impact people’s lives.

Venus Remedies Ltd hiring for below mentioned position at Baddi- Injectable Plant

📢Department – Quality Control

Section – FG/ Stability/ GLP

Qualifications – M.Sc Chemistry

✈️Experience – 2 to 4 yrs

💼Job location – Baddi

Must have skills on – HPLC

Candidate must have exposure of injection plant

interested candidates can share their resume on 📧- hra_staff5@venusremedies.com WhatsApp -9882859675

This is an excellent opportunity to join a reputable company like Cipla and grow in the pharmaceutical sector. Prepare well, and don’t miss this chance!

We're Hiring SARTHI PHARMA

 We're Hiring SARTHI PHARMA

Positions:

1) IMPORT EXPORT EXECUTIVE-1

Qualification: Any Graduate

Experience 1-2 Years Manage Import & Export Documentation and Logistics(City office)

2) GRAPHIC DESIGNER-2

Qualification: Qualified Designer

Experience 6 Months-2 Years Designing in Coral Draw, Photoshop Eto(City office).

3) COA EXECUTIVE-2

Qualification: B. Pharm or M. Pharm or MSc

Experience 1-3 Years To Evaluate & Monitor the Product Quality at Various Manufacturing Sites (City office).

4) STORE OFFICER-2

Qualification: Any Graduate Experience 1-3 Year

5) PRODUCTION OFFICER-5

Qualification: BSc or MSc or B. Pharm

Experience 1-3 Years To Handle the Production Activities at plant.

6) REGULATORY AFFAIRS EXECUTIVE-2

Qualification: B. Pharm or M. Pharm or Msc

Experience 1-3 Years To Prepare Dossiers in CTD Formates for ROW Market (City office).

7) QA OFFICER-2

Qualification B. Pharm or M. Pharm or Msc

Experience 1-3 Years To Work in Prodcution QA at Plant.

To Manage the Inward & Outward of Goods at Plant.

WE ARE HIRING! Join with CUREFOX TEAM Vacancy for 'Officer/Executive' in Warehouse Department

 WE ARE HIRING Join with CUREFOX TEAM Vacancy for 'Officer/Executive' in Warehouse Department

We "CUREFOX HEALTHCARE PVT LTD", is looking for candidates for WHO- EU GMP Compliance, Pharmaceutical Injectable Small Volume Parenteral manufacturing facility located at Chacharvadi Vasana Ahmedabad Gujarat.

No. Of Vacancies:01

Department:Warehouse (Injectable)

Designation:Officer/Executive

Experience:3 to 6 years

Place Of Work:

Chacharvadi Vasna, Ahmedabad- Gujarat 382213

Min. Qualification

B.Sc

Interested candidates can share their CV along with CTC details on hr@curefox.in.

CUREFOX HEALTHCARE PVT. LTD.

 

Become a Drug Safety Associate at Novotech – Apply Today!

Novotech is actively seeking candidates for the role of Drug Safety Associate at its Bengaluru location. This is a key position for individuals passionate about pharmacovigilance and ensuring the safety of pharmaceuticals in clinical trials.

Drug Safety Associate

Job Description

 Brief Position Description:

“Drug Safety Associate” will be responsible for complete and accurate case processing of adverse event reports following company standard operating procedures, internal business practices and regulatory guidance documents, to ensure compliance with worldwide safety regulations. 

Minimum Qualifications & Experience:

• Registered nurse/pharmacist or with health/biomedical degree or other related scientific degree/ qualification is required. 
• A minimum of 2 years safety-related experience in a pharmaceutical company/CRO environment is required. 
• At Novotech, the individual should have completed a minimum of 2 years in Drug safety associate role. 
• Have understood the processes and are ready to take on additional responsibilities. 

Responsibilities:

Overall responsible for drug safety reporting aspects of Novotech’ s business including.

Configuring/ reviewing of applicable safety database with study-specific information.

Preparing and reviewing study-specific safety management plan and related tools per client requirements, SOP, and guidelines.

Case processing: completion of full case information on the database, including quality review to ensure accuracy and completeness, triage of incoming cases to prioritize for daily workflow management, completion of narrative, manual coding, approval, and reconciliation of safety data.

Liaison with medical monitors/drug safety physicians, clients, and study teams as appropriate to clarify appropriate information required for case processing.

Prioritization of data entry activities for cases by reference to the date of receipt in accordance with SOPs and guidelines.

Apply for Job Click hear..https://fa-euzi-saasfaprod1.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/2650?utm_medium=jobboard&utm_source=linkedin

 

Join Teva Pharmaceutical as a PV Professional in Bangalore, India

Teva Pharmaceutical is offering an exciting opportunity for Pharmacovigilance (PV) Professionals at their Bangalore, India location. This position is ideal for professionals with expertise in pharmacovigilance and a passion for drug safety.

PV Professional

Date:  Sep 17, 2024

Location: Bangalore, India, 560052

Company:  Teva Pharmaceuticals

Job Id:  58156

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

How you’ll spend your day

• 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.

to be contd.

Assist in Safety Database related administrative and procedural activities as required or requested and to ensure that all assigned tasks are performed in compliance in accordance to the work instructions and GVP modules.

Ensure that quality of case processing and assigned tasks are evaluated and trends are identified for process improvement.

Various compliance metrics like case timelines, assigned trainings, and TAT for assigned activities are met.

Provide the analytical support to the peers and managers for investigations & analysis of various trends as a part of audits, and inspections.

Mentoring/Training the new hires with case processing knowledge transfer, evaluating their progress close to perfection during their initial phases of learning curves.

Your experience and qualifications

 M.Pharm/ Pharm.D/ BDS Postgraduate in registered life Sciences

Min 2 – 4 years relevant experience into Pharmacovigilance case processing and related activities in alignment with patient safety operations

Click hear 
https://careers.teva/job/Bangalore-PV-Professional-Indi-560052/1213750200/?mode=job&iis=Job+Board&iisn=LinkedIn&utm_source=linkedin&jobPipeline=LinkedIn