Thursday, March 23, 2023

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

Wednesday, March 22, 2023

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.

Biocon – Walk In on 26th March 2023 for Engineering & Maintenance

Biocon Biologics is a subsidiary of Biocon Ltd, an innovation led global biopharmaceuticals company. Biocon Biologics is engaged in developing high quality, affordable biosimilars that can expand access to a cutting-edge class of therapies to patients globally. It is uniquely positioned as a fully integrated pure play’ biosimilars organization in the world and aspires to transform patient lives through innovative and inclusive healthcare solutions. The Company has a large portfolio of biosimilars under global clinical development with three of these commercialized in at least one of the developed markets of EU, U.S. and Japan. Biocon Biologics has a product pipeline of 28 molecules, including 11 with Mylan, several with Sandoz and is developing many independently. Biocon Biologics believes that strong partnerships offer enormous opportunities to co-create the future of healthcare, building a patient ecosystem beyond the product, which can transform millions of lives.

Biocon -Recruiting For Following
  • Qualification: B.Tech/B.E.
  • Experience : 07-12+years
  • Department : Engineering & Maintenance
  • Role: Maintenance Engineer
  • Job Location: Bangalore
  • No.of Openings: 10
Time and Venue
26 March , 8.30 AM – 1.30 PM
Bicon Campus, 20th KM, Hosur Road, Electronic City, Bengaluru-560100
Contact – Rajesh Telugunti HR

Job description:

1. Experience 7-12 Years with BE/B.Tech(Mechanical /Electrical engineering).

Skill Set:

Installation & Trouble shooting of AHU, VTD, Centrifuge, Reactor, HPLC, LYO, Clean Room equipment

2. Experience 5-7 Years with BE/B.Tech(Instrumentation/ Electronic/Electrical engineering).

Skill Set:

Automation (ABB DCS, Rockwell PLC, HPLC, LYO handling and instrument calibration and documentation

3. Experience 5-7 Years with BE/B.Tech/Dilpoma(Mechanical Engineering).

Skill Set:

Equipment qualification, QMS documentation (CAPA, RISK Assessment & Deviation).

Tuesday, March 21, 2023

Medoz Pharmaceuticals Pvt. Ltd – Walk-In Interviews - QA / IPQA / Production - on 22nd to 27th Mar’ 2023

Medoz Pharmaceutical Pvt. Ltd are one of the renowned companies engaged in the manufacturing, marketing and export of pharmaceutical drugs. These drugs contain high shelf life and are used in treatment of different ailments and therapies. Our products are manufactured in accordance with the WHO/GMP standards and we give a prime importance to the quality of our products.

WALK IN INTERVIEW @ MEDOZ PHARMACEUTICALS PVT LTD 

We are recruiting For our Tablet Capsule Manufacturing Plant at Manpura Baddi (HP)

About us: Medoz Pharmaceuticals Pvt Ltd is GMP Certified Pharmaceutical Company manufacturing of tablet, Capsule & Liquid Located in Manpura Baddi (HP).

QA Officer:

  • Officer: (Minimum Exp 1-2 Years)
  • Qualification: MSC / BSC, B Pharmacy (Responsible for Plant Documentation, SOP,OOS, CAPA, Incident, Deviation, Market Complaint, BMR, BPR, Line Clearance, Dispensing Of Raw, (Salary no issue for deserving candidate)

IPQA Officer:

  • Officer with 1-3 years Experience / in Pharmaceuticals Formulation,
  • Qualification– MSC / BSC, B Pharmacy (Responsible for Plant Documentation, SOP, BMR, BPR, LINE Clearance, Dispensing OF Raw Material. (Salary no issue for deserving candidate)

PRODUCTION TABLET / LIQUID CHEMIST:

  • (Approved or Non-approved) with minimum 1-3 years minimum Experience in Pharmaceuticals Industry.
  • Qualification: Pharmacy / BSC / MSC Tablet & Liquid manufacturing, Documentation of Online products Other related documentation (BMR,BPR,LOG BOOK PREPARATION) of Tablet Section / Liquid Section and Dry syrup section, Tablet / Liquid and Dry syrup batch processing. (Salary no issue for deserving candidate)


Date: 22/03/2023 (Wednesday) TO 27-03-2023 (Monday)

Timing: 9:00Am Onwards

NOTE: JOB LOCATION: BADDI (Preferred candidate: who are already working in Baddi)

Venue: Medoz Pharmaceuticals Pvt. Ltd Village Chanal Majra near Police Station Manpura

Interested Candidates may appear for WALK-IN at Village Chanal Majra Po Manpura (H.P.) along with update CV. Passport size photograph, bring along existing salary slips.

In case of any query please feel free to contact us at 9646926033.

Candidates unable to attend Interview can mail us CV at hr.medoz@gmail.com.

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