600 Openings @ Aurobindo Pharma – Mega Walk-In Drive for Freshers on 31st Mar’ 2023

AP State Skill Development Corporation (APSSDC), Employment Office and Seedap – Andhra Pradesh jointly organizing Mini Job mela in Nandyala District on 31st March 2023.
Participating Companies:
1. Greentech Industries
2. CYGNI Energies Pvt Ltd
3. Aurobindo

Venue: ESC Govt. Polytechnic College, Nandyala
Time: – 09:00 am onwards
Interested candidates can register with below link.
https://rb.gy/irtfc1

Note: Candidates must attend in formal dress with copies of resumes and copies of qualification credentials.
For further details please contact:
9533631002, 8297812530
6303397635, 9440224291
or
APSSDC Helpline – 9988853335

TORRENT PHARMA – Multiple Openings - for QC / QA / Tablet / Packaging / SCM / Procurement – Apply Now

Torrent Pharmaceuticals The flagship company of the Torrent Group, Torrent Pharmaceuticals Limited is a major player in the Indian pharmaceuticals sector with the vision of becoming a global entity. Torrent Pharma enjoys dominance in the niche therapeutic areas like, cardiovascular and central nervous system, gastro-intestinal, pain management and oral anti-diabetic segments. Torrent Pharma owes its success in the domestic market to its thrust on frontline research, strategic marketing and world-class manufacturing.

Attention all job seekers!
We are currently seeking passionate individuals to join our dynamic team. If you are a driven and motivated professional looking for a challenging and rewarding career opportunity, we want to hear from you! Come be a part of our exciting journey and make an impact in your career.

• Qualification: M.Sc / B.Pharm / M.Pharm / B.E / B.Tech
• Experience : 02-12 years
• Department: QC / QA / Tablet / Packaging / SCM / Procurement
• Role: TA / Executive / Manager
• Job Location: Sikkim

Interested candidates are requested to share their CVs on anitarai@torrentpharma.com / pankajbardhan@torrentpharma.com

Contact : 9735986608 / 18 / 28 / 38

Apply now to join our team!

Zenotech Laboratories (Sun Pharma) – Multiple Openings - for QA / QA (Biotech) / QC / QC (Biotech) / Microbiology Departments – Apply Now

Zenotech Laboratories Limited is an India-based pharmaceutical company operating out of Hyderabad, India. The Company is engaged in a business of manufacture and marketing of pharmaceuticals products. The Company is a pharmaceutical specialty generic injectables company engaged in the area of manufacturing Oncology, bio-technology and General Injectables products.

We are Hiring!! Zenotech Laboratories Limited (Subsidiary of SUN PHARMA)

• Department: QA / QA (Biotech) / QC / QC (Biotech) / Microbiology
• Designation: Sr. Officer / Executive / Sr. Executive / Asst. Manager / DGM
• Qualification: M.Tech/M.Sc Biotechnology / B.Sc & M.Sc Chemistry / B.Pharm / M.Pharm
• Experience: – 3-20 years relevant experience
• Job Location: Hyderabad

Interested candidates can share their CVs to hr1@zenotech.co.in.

Zydus Biologics – Urgent Openings for Quality Control / Quality Assurance / Engineering – Apply Now

Zydus Biologics / Zydus Healthcare Limited (also known as Zydus Cadila) is an Indian multinational pharmaceutical company headquartered in Ahmedabad, Gujarat, India primarily engaged in the manufacture of generic drugs. It ranked 100th in the Fortune India 500 list in 2020. Cadila was founded in 1952 by Ramanbhai Patel (19252001), formerly a lecturer in the L.M. College of Pharmacy, and his business partner Indravadan Modi. It evolved over the next four decades into an established pharmaceutical company.

Opportunities in Quality Control / Quality Assurance / Engineering Department of Zydus Biologics, Biotech Park, Ahmedabad.
Executive / Senior Executive (Candidate must have 3 to 6 years exp.)
1. QC Chemical (M.Sc Biotech) Candidate must have hands on experience in analysis of Protein analysis/ Instrumentation, Molecular biology, Bioassay, lab activity related documents. Responsible to review all the documents, test reports, calibration reports records, logbooks, and formats in relation to the activity of Protein analysis/ Instrumentation, Molecular biology, Bioassay and filling. To carry out investigation of Incident, Deviation and OOS generated during laboratory analysis.

2. QA Analytical (M.Sc Biotech/Micro) Candidate must have experience in review of Analytical Reports, Stability Protocols and data sheets, Investigation, Review and disposition of OOS, OOT, OOG & OOE results, handling of Incidents, Deviations, and Change Controls in the Laboratory along with review of all types of Qualification documents. Review and approval of all Lab Standard Operating Procedures.

3. Electrical: (B.E Electrical) Must have experience in maintaining power supply for whole site, Manage shutdowns and load shedding independently, Able to handle preventive & breakdown maintenance of Transformer, DG set, HT & LT panels, UPS & battery for critical loads, operation of DG sets with changeover, Should have hands on experience for QMS system, track wise, SAP etc. Able to handle Fire alarm, access control & door interlock system, etc. Responsible for work permit system and safety compliance at site. Candidate having Electrical supervisor permit/license by Government office (CEE) will be given preference.
 
4. Mechanical: (B.E Mechanical) Must have experience in preventive maintenance and breakdown maintenance of utilities, water system, HVAC and plant equipment, Responsible for QMS and GMP documentation like log books, records and status labels, preventive maintenance records, deviations, change control, CAPA etc.

Candidate from Biotech, Vaccine & Injectable Pharma plants will be preferable who have knowledge of process equipment’s like as Autoclaves, Bio-reactors, fermenters, Lyophilizes etc.
Preference will be given to those who matches with above mentioned requirement and submit their CVs along with current and expected CTC to ruchi.lal@zyduslife.com by on or before 15th April 2023.

Zydus Lifesciences – Walk-In-Interview - on 26th March 2023 for QC / Production

The Zydus Group with an overarching purpose of empowering people with freedom to live healthier and more fulfilled lives, is an innovative, global lifesciences company that discovers, develops, manufactures, and markets a broad range of healthcare therapies. The group employs over 23000 people worldwide and is driven by its mission to unlock new possibilities in life-sciences through quality healthcare solutions that impact lives. The group aspires to become a global life-sciences company transforming lives through pathbreaking discoveries. The group has manufacturing sites and research facilities spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim in India and in the US and Brazil.

Zydus Lifesciences Walk In

• Qualification: B.Sc, MS/M.Sc
• Experience : 02-05+years
• Department: QC/Production
• Role: Officer / Executive
• Job Location: Vadodara

Time and Venue:

26th March, 10.00 AM – 4.00 PM

Zydus API Park, Zydus Lifesciences Ltd, (Formerly known as Cadila Healthcare Ltd) Behind Bright Day CBSE School, Next to Kishan Classic, Vasna Bhayli Canal Road, Vadodara

Contact – D K Patel ()

Job description:

We are recruiting for our API Production plant located at Dabhasa, Nr Vadodara.

Production (API) : Officer / Executive

The incumbent should be B Sc (Chemistry) / DCE with 2 to 5 years of relevant experience in API production. Should have exposure in handling reactors, centrifuges and clean room equipment with sound knowledge in cGMP and SOPs. Should have exposure to regulatory requirement of documentation. Adherence to Quality, Safety, Health and Environment measures and GMP norms.

Quality Control (API) : Officer / Executive

The incumbent should have B Sc / M Sc (Chemistry) with 2 to 5 years of Relevant experience in analyses the Raw materials, In-process and intermediates finished product and stability samples. Expertise in handling HPLC, GC, UV, IR, KF, Melting point etc. Preparation of STP / SPC / SOP for QC documentation on a routine basis. Ensure the compliance, Safety and 100% Good laboratory Practices. Having aware of the current pharma procedure of cGMP, GDP, GCP and GLP practices follows in QC laboratory.

Desired Candidate Profile:

• Candidates to have exposure in pharmaceutical company (API plant) and regulatory requirements of documentation and cGMP/GLP.
• Interested candidates may Walk-in for an interview along-with their updated CVs, CTC break up and relevant documents as per the schedule

Corona Remedies – Urgent Openings - for Quality Control Department – Apply Now

Corona Remedies Pvt. Ltd was established by a group of committed and experienced professionals who came together with “care” and “quality” as their guiding principles. Their vision was to go beyond the norm and provide the best quality affordable healthcare for all. Today, when it comes to quality, availability and affordability of medicines, we have gone beyond just growth and turned into a force to reckon within an extremely short span of time. We owe this phenomenal success to our continuous commitment to innovative product development and manufacturing facilities that adhere to strict quality control as per Schedule M, WHO-GMP guidelines. Strategic collaborations with some of the finest companies in Europe have helped us bring in a new range of world class products to India. Today Corona is poised to go beyond geographical barriers and become a true global leader. Our only desire behind all this hard work, dedication and commitment is to provide and ensure a better quality of life for all.

CORONA Remedies Private Limited is fastest growing Pharmaceutical organization based from Ahmedabad (India). We offer finest working culture to professionals. Our “Care for Coronets” is industry known.

Designation: – Officer / Senior Officer /Executive – QC

Qualification: – B. Pharm/ M.Sc (Chemistry)

Experience: – 03 to 08 Years

Job Location: – Bhayla (Near Bavla)

Expertise Area: –

1) Handling all lab instruments of HPLC, GC, Dissolution, D. T., Apparatus, Weighting balance, Friability, Hardness, Tester, FTIR, UV – Spectrophotometer.
2) Analysis of raw material, In-process, Finish products, Stability testing, Process validation.
3) Participate in Lab incident /OOS/OOT/Analysis of deviation.
4) Method Validation & Verification

Interested candidate send your latest CVs on vimalv@coronaremedies.com
Available on WhatsApp +91-9016239116
Best Regards,
Vimal Vekariya
Sr. Executive Human Resource
CORONA Remedies Pvt Ltd

INTAS PHARMA – Walk-In-Interview - for Multiple Positions in Production / QC / QA - on 26th Mar’ 2023

Intas Pharmaceuticals Ltd, Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors. A variety of initiatives in Research and Development, patents and ANDA filing, NDDS, quality manufacturing support, along with approvals by regulatory authorities of many countries has made Intas a global healthcare provider. Pioneering efforts in providing medications for both chronic and acute medical conditions, has truly led Intas live up to its corporate line Expressions for a Healthy Life.

opportunities with Intas Pharmaceuticals
Walk In Interview at Vadodara – Quality & Production Department
Date: Sunday, 26th March, 2023
Time: 10:00 AM to 04:00 PM
Venue: The Fern – An Ecotel Hotel, Vadodara, Off Dinesh Mill Road, Near Urmi Char Rasta, Purushottam Nagar, Akota Vadodara, Gujarat – 390020

Positions: Officer to Executive
Department: Solid Oral (Tablet Manufacturing)

• Qualification: B.Pharm
• Experience: 02 to 06 Years
• Having Experience in Granulation / Compression / Coating / Inspection.

Positions: Officer to Executive
Department: Quality Control

• Qualification: M.Sc. / B.Sc.
• Experience: 02 to 05 Years
• Having experience of instruments like HPLC, GC, UV, IR.

Position: Officer to Executive
Department: QA – IPQA – Validation & Qualification (Injectable)

• Qualification: M.Sc. /B.Pharm / M. Pharm
• Experience: 03 to 07 Years
• Process and Cleaning validation, validation documents, protocol report and risk assessment.
• Equipment qualification documents (URS, FAT, SAT, DQ, IQ, OQ, PQ) & Compliance mgt.
• SME in HVAC validation, temperature distribution study and Equipment Qualification.