HETERO Biopharma Ltd – Walk-In Interviews for Production – USP & DSP on 17th June’ 2023

Hetero Biopharma Limited, The leading edge of Hetero Group, Hetero Biopharma, is steadily establishing itself as a path breaking Biosimilar developer. As a strong R&D driven company offering some of the blockbuster Biosimilar Drugs, we at Hetero Biopharma are bringing about a paradigm shift in the way patients suffering from various chronic conditions are treated.

Greetings from Hetero Biopharma Limited!!!

We are conducting walk-in for the following department on 22nd April 2023 (Saturday)

Interested candidates can attend interview at Hetero Corporate office, 7-2-A2, Industrial Estate, Sanath Nagar, Hyderabad-500018

We are conducting walk-in interviews for following..!!!

Department: Production

Posts: Officer to Executives

Qualification: M.Sc / B.Sc / B.Tech Biotech / Biochem / Any Lifescience 

Experience: 2-6 yrs

Location: Jadcherla

Interview Date: 17-06-2023

Timing: 9:00 am to 04:00 pm

Venue: 

Hetero Corporate office, 7-2-A2, Industrial Estate, Sanath Nagar, Hyderabad-500018

Candidates who are not able to attend the interview can send their CV’s to praveen.ko@hetero.com with subject line as “Application Hetero Biopharma” – Drug Product – Production

Indoco Remedies Ltd – Walk-In Interviews for Multiple Positions on 18th June’ 2023 for B.Sc, M.Sc, B.Pharm, M.Pharm, D.Pharm, Diploma Candidates

Indoco Remedies Ltd., is a fully integrated, research-oriented pharma company engaged in the manufacturing and marketing of Formulations (Finished Dosage Forms) and Active Pharmaceutical Ingredients (APIs). We have seven decades of presence in the Indian Pharma market and a strong foothold in the international market across 55 countries. Indoco has carved a place for itself in the international arena and is exporting a number of generic products in the Regulated and Emerging Markets.

Walk In- Interviews @ Indoco Remedies Ltd

Below positions are for candidates to work in all shifts.

OFFICER / SR. OFFICER PRODUCTION:

Qualification : B. Pharm. / M. Pharm

Job Profile : 1 to 5 years’ experience in Granulation, Compression & Coating areas for regulated market. Experience of working in USFDA approved Tablet Manufacturing preferred.

EXECUTIVE PRODUCTION

Qualification : B. Pharm. / M. Pharm

Job Profile : 6 to 9 years’ of experience in Granulation, Compression & Coating areas for regulated market. Experience of working in USFDA approved Tablet Manufacturing preferred.

ASSOCIATE/TECHNICIAN Tablet / Capsule manufacturing

Qualification : DME / DEE / D. PHARM /B. Sc.

Job Profile : 2 to 6 years of experience in operation of machines in Granulation / Compression / Capsule / Coating areas.

OFFICER PACKING

Qualification : B. Pharm / M. Pharm

Job Profile : 2 to 4 years of experience in tablet packing department for managing routine packing activities on high speed blister packaging lines equipped with cartonators and bottle packing line. Experience in handling of Track and Trace system, coordination of shifts and batch reconciliation.

ASSOCIATE/TECHNICIAN – PACKING

Qualification : DME / DEE / D. PHARM /B. Sc.

Job Profile : 1 to 4 years of experience in Operating of Blister Machine/ Cartonator /

Bottle Packing Machines.

QUALITY CONTROL (Tablet Formulation)- ANALYSTS / REVIEWER

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

Job Profile : 3 to 8 years of experience in Tablets Formulation.

1. Analysts For HPLC/GC:

Having at least three years of work experience on these instruments.

Analyst should have handled software of Chromeleon / Empower.

Having sound knowledge on the Good Chromatographic practices.

In addition handling of troubleshoot of these instruments.

2. Reviewers For HPLC/GC:

Having overall QC experience of 5+

At least three years of work experience as a reviewer for QC analysis.

Reviewer shall be well versed with the 21 cfr instruments of QC.

Have handled HPLC software of Chromeleon / Empower.

Having sound knowledge on the Good Chromatographic practices and Good laboratory practices.

Well versed with the audit trail activities of 21 cfr instruments.

Walk-In Interview Details:

Walk-In Date: 18th June, 2023

Time: 10.30 AM – 4.30 PM

Venue:

Seasons Hotel & Resorts ,Near Jawaharlal Nehru Stadium (North Stand), Fatorda, Goa, IN 403602

SRF Limited – Walk-In Interviews on 15th & 16th June’ 2023 for B.Sc, M.Sc, B.E, B.Tech, Diploma Candidates

SRF Limited is a multi-business chemicals conglomerate engaged in the manufacturing of industrial and specialty intermediates. The company’s business portfolio covers Fluorochemicals, Specialty Chemicals, Packaging Films, Technical Textiles, Coated and Laminated Fabrics. We require deserving candidates for following positions in Chemicals Business at Dahej.

SRF Limited – Walk-In Interviews for Production / Instrumentation on 15th & 16th June’ 2023

Jr. Engineer / Sr. Executive – Production / Instrumentation

Qualification: Diploma / B.E / B.Tech / B.Sc / M.Sc Chemistry

Experience: 3 to 8 yrs

Job Location: Dahej

Walk-In Interview Details: 

Date of Interview: 15th & 16th June’ 2023

Time: 10:00 AM to 6:00 PM

Venue:

Hotel Reemz, Walope, Chiplun, Maharashtra – 415605

Interested candidates can walk for interview on below venue and also their resume mentioning Job Title to mail ID: HR.Recruitment1@srf.com

Zydus Lifesciences Ltd – Urgent Openings for Production / Quality Assurance – Apply Now

Zydus Lifesciences Ltd, 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.

Greetings from Zydus Zydus Lifesciences Ltd!!!!

We are looking for following positions for Zydus Lifesciences Ltd in Our Baddi Facility.

Department: Production / Quality Assurance

Designation: Executive / Sr. Executive / Assy. Manager

Qualification: B.Pharm / M.Pharm

Experience: 3-12 yrs

Location – Baddi

Interested candidates please share your resume at my mail id Ankit.Verma@zyduslife.com

PI Industries Ltd. – Walk-In Interview on 20th & 21st June 2023 for B.Sc / M.Sc / B.E / B.Tech / Diploma Candidates

PI Industries, a 75 years old integrated agri chemicals solution company catering to complex chemistry solutions market in agri and other fine chemicals areas across the world. Over the years, we have leveraged our capabilities and partnerships to provide value-added and innovative agri solutions to millions of farmers and partners in India and across the globe, carving a niche for ourselves built on in-depth R&D expertise, manufacturing prowess, and as a strong believer in technology, we are focusing on Industry 4.0 standards for our manufacturing plants, with strong focus on innovation.

PI Industries Ltd. – Walk-in Interview in Delhi NCR for Production Department.

Details of the job are as follows:-

Job Title: Production Supervisor / Executive

Salary Range:- Best in the Industry

Job Location: Jambusar, Gujarat.

Education: B. Sc./ M. Sc. in Chemistry /Diploma in Chemical Engineering or B.E / B. Tech in chemical

Experience: 4 – 9 years

WALK-IN INTERVIEW DETAILS: 

Venue: Park Inn by Redisson, Plot No. 6A, Extension, Pratapganj, Near Anand Vihar ISBT, New Delhi 110092.

Date:- 20th June (Tuesday) & 21st June 2023 (Wednesday)

Timings:- 10:00 a.m. to 4:00 p.m.

Gland Pharma Ltd – Hiring for Technology Transfer (Injectables) Department – Apply Now

Gland Pharma has grown over the years from a contract manufacturer of small volume liquid parenteral products, to become one of the largest and fastest growing injectable-focused companies, with a global footprint across 60 countries, including the United States, Europe, Canada, Australia, India and other markets. We operate primarily under a business to business (B2B) model and have an excellent track record in the development, manufacturing and marketing of complex injectables. This presence across the value chain has helped us witness exponential growth. We are promoted by Shanghai Fosun Pharma, a global pharmaceutical major.

Greetings from Gland Pharma Ltd!!

Dear All,

We’re hiring for Technology Transfer (Injectables) department.

Experience : 1- 3 Years

Qualification : M. Pharmacy (Pharmaceutics)

Work location : Hyderabad

Skills : Hands on experience in parenteral’ s only.

Interested with relevant experience can share resume to

hr@glandpharma.com

Milan Laboratories – Hiring for Regulatory Affairs Department – Apply Now

Milan Laboratories (India) Pvt. Ltd. is one of the leading Pharmaceutical Manufacturer and Exporter from India. An ISO 9001:2008 and WHO-cGMP certified company, is a Govt. Recognized Star Export House and a winner of various awards for Quality Excellence and Outstanding Export Performance. There is a manufacturing facility for Tablets, Capsules, Liquid Orals, Dry Syrups, Ointments and a dedicated facility for Beta Lactam Products (Penicillin Group). Our Plants are approved by drug regulatory authorities of various countries out of which, a leading few are South Africa – MCC and UK – MHRA. There is a in-house Research & Development department that develops new formulations and also modifies and improves the existing ones. A dedicated team for Regulatory Affairs prepares in-house eCTD Dossiers for filing in the Regulated markets.

Dear Candidate,

Greetings from Milan Laboratories (India) Pvt. Ltd.!!

We are looking for Regulatory Affairs Officer/Sr. Officer at our Panvel factory

Vacancies: 2

Job responsibilities:

1. Preparation & Compilation of registration dossiers for row, semi-regulated and regulated markets.

2.Collection of dossier documents from various departments like QC, QA, Stores, Production, FD, Stability and maintaining in a master document with systematic manner.

3.Submitting and reviewing the technical requirements for Tender Filing

4.Review of specifications as per monographs. (USP/Ph.Eur).

5.Review of process qualification and product development records.

6.Review of stability data.

7.Review of innovator comparative dissolution data.

8.Review of all documents related to Formulation Development.

9.Art work review and approval

10.Review, submission of quality dossiers as per the current guideline (country-specific) requirements and attending the MOH query.

11.Document follow up for FDA/Regulatory Queries

12.Raising applications for product license, COPP, FSC as per requirement.

13.Communication with customer for the country specific registration requirements.

14. Arrangement of samples for registration purpose.

Interested candidates can share their resume at talentpool@milanlabs.com