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

Explore R&D Opportunities: Walk-In Interview at Aurigene for Medicinal & Peptide Chemistry

 Explore R&D Opportunities: Walk-In Interview at Aurigene for Medicinal & Peptide Chemistry

Walk-In Interview at Aurigene Pharmaceuticals: Opportunities in R&D – Medicinal Chemistry & Peptide Chemistry in Bengaluru

Aurigene Pharmaceuticals, a pioneering biopharmaceutical company in drug discovery and development, is hosting a  walk-in interview for various positions in Medicinal Chemistry and Peptide Chemistry at their Bengaluru facility.

This is a unique opportunity for aspiring chemists to join a company renowned for its cutting-edge research in oncology, inflammation, and autoimmune diseases.

Aurigene is a wholly-owned subsidiary of Dr. Reddy’s Laboratories, with a mission to advance breakthrough science in small molecules and biologics. Aurigene has a rich history of successful collaborations with global pharmaceutical companies and a solid reputation for innovation in early-stage drug discovery.

The company focuses on accelerating the development of novel therapeutics in critical areas such as oncology and inflammation, providing a stimulating environment for chemists to make significant contributions to the pharmaceutical industry.

JOB AND INTERVIEW DETAILS:

R&D – Medicinal Chemistry &

Peptide Chemistry.

(Job Location – Bengaluru)

Qualification & Experience:

M.Sc. Organic Chemistry with 2 to 5 years of experience in synthetic chemistry. (Small Scale)

Date:

22nd Sept 2024 ( Sunday)

Time: 9:00 AM to 15:00 HRS

Interview Venue:

Hyderabad:

APSL Office, Bollaram Road, Jaya Prakash Narayan Nagar, Miyapur, Hyderabad

Bengaluru:

APSL Office, 39-40, Hosur Road, KIADB Industrial Area, Phase 2, Electronic City,

Bengaluru, Karnataka

AURIGENE

PHARMACEUTICAL SERVICES

Note: Please carry your updated resume along with last 3 months salary slips, salary annexure &Passport size photo.

 

Damaira Pharmaceuticals walk in interview on 22 Sep. 2024 (Sunday)

Damaira Pharmaceuticals walk in interview for Microbiologist, Regulatory Affairs, Accounts, QA, QC, Packing Production, Purchase, QMS Production on 22 Sep. 2024 (Sunday)

Damaira Pharmaceuticals Pvt. Ltd is one of its kind dedicated Carbapenem Dry Powder Injectable Manufacturing Facility which is going to revolutionize the Pharma Industry. We have top class machinery available in the market with multiple checks in place to make the Production & Quality check process Fool Proof.

Department: Microbiologist, Regulatory Affairs, Accounts, QA, QC, Packing Production, Purchase, QMS Production

Experience required: 1 to 08+ Yrs

Qualifications required: M. Pharma, B. Pharma, M.com/ MBA (Finance, Marketing), ITI, 12th, Graduate Science

Interview Date: 22 Sep. 2024 (Sunday)

Timings: 10:00-17:00

Venue Address:

HOTEL MG, REGENCY BADDI, Nalagarh Road, Near-Baddi Bus Stand, District-Solan (H.P.)

Contact us:

+91 73411-22753, +91 73411-61728

For more Information hr@damaira.com hrd@damaira.com

SMS Pharmaceuticals Ltd Walk-in Interview 20&21-09-2024 for QC, Stores & ETP Roles

 Career Alert: SMS Pharmaceuticals Ltd Walk-in Interview for QC, Stores & ETP Roles

SMS Pharmaceuticals Ltd is offering an exciting opportunity. The company, known for its excellence in producing Active Pharmaceutical Ingredients (APIs), is hosting a walk-in interview for Quality Control roles. This could be your chance to join one of the leading names in the pharmaceutical industry and secure your future with a stable and rewarding career.

SMS Pharmaceuticals Ltd is a globally recognized API manufacturer and exporter based in India. With over 30 years of experience in the industry, SMS Pharma has built a reputation for delivering high-quality APIs across the globe.

Their operations are backed by advanced manufacturing facilities, cutting-edge research, and a strong commitment to regulatory compliance

JOB AND INTERVIEW DETAILS:

1.Department: Quality Control (wet Lab )

Position: chemist to executive

Qualification: B.Sc/M.Sc/B.pharm/M.Pharm

Experience: 01 to 06 yrs wet lab analysis (RM,IM,FG,ST)

2.Department: Quality Control (instrumentation Lab)

Position: chemist to executive

Qualification: B.Sc/M.Sc/B.pharm/M.Pharm

Experience: 02 to 06 yrs wet lab analysis (HPLC handling)

3.Department: Quality Control (microbiology)

Position: chemist to executive

Qualification: B.Sc/M.Sc/B.pharm/M.Pharm (microbiology, biotechnology)

Experience: 01 to 04 yrs wet lab analysis (microbiology lab )

4.Department: Stores (RM,FG&Misc)

Position: Executive to Assistant Manager

Qualification: B.Sc/B.Com/M.com/MBA

Experience: 02 to 07 yrs ( Executive)

07 to 12 yrs (asst.Manager)

5.Department: ETP- Operations

Position: chemist to executive

Qualification: ITI/Diploma or any Degree

Experience: 02 to 06 yrs operation of strippers,MEE,ATFD

Interview Date & Time:

20th September 2024- Friday

&

21th September 2024-

Saturday

09:30 Hrs to 16:00 Hrs

Interview Venue:

SMS Pharmaceuticals Limited Unit-II

Plot No. 24 & 24B, 36&37 ,

S.V.Co-Operative T) Estate, Miyapur ,Bachupally, Hyderabad-500090

Note: Preferable for Male candidates and regulatory plant exposure will be considered.

 

Zydus Lifesciences Hiring For QC QMS

Zydus Lifesciences Hiring For QC QMS

Section Head - (QC QMS) RM/PM - Vaccines

Qualification: M. Sc. Chemistry / M. Pharm / Postgraduate with Relevant Experience

Experience: 10-15 years

Job Location : Zydus Biotech Park, Changodar, Opp. Ramdev Masala, Sarkhej Bavla, NH BA, Changodar, Ahmedabad-382213, Gujarat

Job description 

1. To be accountable as Section head in planning and supervising the sampling, testing & release of RM & PM

2. To ensure adequate number of analysts and reviewers are qualified for testing and review in chemical section (including water), ensure on job training and track to monitor the team operations.

3. To ensure analysis and release of the batches are within the defined SLA and as per standard productivity.

4. Review and Release of raw materials, packing materials, in-process and finished products in LIMS and SAP as and when required.

5. To ensure compliance with the defined cGMP and GLP requirements and to ensure revision of Specifications/ SOPs/ STPs/GTPs according to compendial requirements as and when required.

6. Act as a Super User for Laboratory Information Management System (LIMS) of QC Analysis.

7. To ensure sample management (Sample receiving and timely release of TRS)

8. To ensure zero data integrity issue within Chemical section.

9. To oversee the calibration and validation/ PM of equipment/ instrument done as per schedule, Breakdown reporting/ closure and to coordinate with engineering maintenance department or third-party lab as and when required.

10. To coordinate and ensure Installation, Qualification, Calibration and Maintenance of equipment/ instruments.

11. To ensure/procure adequate stock inventory of consumables/ reagents/chemicals/kits/stationary/ other miscellaneous items

12. To review and monitoring of Temperature/Humidity and other critical parameters

13. To execute PR/PO for CMC/AMC of instruments, Third party calibration, third party samples etc.

14. Monthly verification shall be carried out for near to expire materials of concern section and if required put the material in lock and key.

15. Ensuring cleanliness/ all-time audit readiness of the labs/ areas allocated and EHS/ Bio-safety compliance.

16. To ensure qualified third-party labs for outsourced tests

17. To oversee the manual paper-based documentation, LIMS and computerized systems for compliance

Apply Link

https://zydusgroup.darwinbox.in/ms/candidate/careers/a66dec22f71874/custom_source/QR%20CODE