Hetero Labs Ltd – Walk-In Interview for - QC / QA / Production / Packing on - 15th Apr’ 2023

Hetero Labs Limited is one of India’s generic pharmaceutical companies and the “world’s largest producer of anti-retroviral drugs”. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. HETERO is one of the India’s leading generic pharmaceutical companies and is one of the world’s largest producer of anti-retroviral drugs for the treatment of HIV/AIDS. With more than 25 years of expertise in the pharmaceutical industry, Hetero’s strategic business areas include API’S, generic and biosimilar. Hetero also offers custom pharmaceutical services to its partners around the world. The company is recognized for its strengths in Research and Development, manufacturing and commercialization of a wide range of products.

Greetings from Hetero!
We are expanding our team and we are hiring for our Unit-III which is located in Jeedimetla.
Interested candidates can attend interviews on  15th Apr’ 2023(Saturday) at Jeedimetla, Hyderabad

Greetings for the day from Hetero Labs Limited.

We are looking for Experienced Candidates for Following departments..

• Department : QC / QA / Production / Packing
• Designation: Officer / Jr. Officer / Executive / Jr. Executive / Operator / Jr. Operator 
• Experience: 1 to 5 yrs
• Qualification: B.Sc, B.Pharm, M.Sc, M.Pharm, ITI, Diploma
• Location : Unit-III, Jeedimetla

Walk-In Interview Details: 

Date of Interview: 15th Apr’ 2023(Saturday)

Time: 9:00 am to 03:00 pm

Venue:

Hetero Labs Limited, Unit-III, 22-110, Phase-III, IDA, Jeedimetla, Hyderabad

Please forward your CV to hrd@hetero.com, in case you are not able to attain the interview

Vital Pharma – Walk In Interviews for QA / QC / Store / Maintenance /Production Departments on 14th & 15th April’ 2023 @ Hyderabad

Vital Pharma is an endeavour to offer trustworthy partnership comprising superior quality products and services par excellence in Contract Manufacturing, Animal Nutrition, Human Nutrition, Aquaculture and Vitamin pre-mixes. Vital Therapeutics & Formulations is designed to meet International Regulatory requirements such as CGMP, WHO, ISO 9001 & FSSC 22000 and recognised for abiding to vigorous quality and service standards for product development, analytical services, packaging and regulatory services.

Vital Pharma – Walk In Interviews for QA/ QC/ Store / Maintenance/Production Department on 14th & 15th April’ 2023 @ Hyderabad’ Cherlapally.

1) Dept: QA – Analytical Document Review – Male/Female
Qly: M. Pharmacy /MSc – Analytical
Exp: 2 – 4 years
JD: For Analytical documents review
Skills: Good Communication

2)Dept: QC – Male
Qly: B. Pharmacy / M Pharmacy/ MSc
Exp: 2 – 4 years
Skill: Handling of HPLC and Wet / GC

3)Dept: Store – Male
Qly: B.Sc / B.Com
Exp: 1 – 2 years
Skill: Take care of Inward Entry, RM, PM, Dispatch & Dispensing Activities

4.Dept: Maintenance – Male
Qly: Diploma/B-tech – Mechanical
Qly: 4 – 5 years
JD: OSD/OLD-Manufacturing (Formulation), maintenance management, Production, Utility Management, HVAC, Water system, EHS knowledge, Air compressor, Documentation, vacuum pumps. Industry: Pharmaceutical Formulation.

5.Dept: Production – Blister Packing Operator
Qly: ITI/Diploma- Any
Exp: 1 – 3years
JD: Rapid Pack 240 – Double Track
Pack size- 10’s, 15’s, 30,s and 4’s Pack Change over, Faming rolls, Cad map,
Cutting rolls, Change Gear, Change holograms,

6.Dept: Production /Maintenance -Male
Qly: ITI/Diploma- Any
Exp: Fresher’s
Passed Out: 2019 to 2022

Dt: 14th & 15th April’ 2023
Time: 9:30am to 12:30pm
*Venue: Vital Therapeutics & Formulations Pvt Ltd.
Plot No:47 B/2, St.No.4, Phase-I, IDA, Cherlapally, Secunderabad.*
Interested candidates send CV to hr@vitalpharma.in

Walk-In Drive for FRESHERS – QC / QA / ARD / FARD / Stability on 12th Apr’ 2023 @ Aurobindo Pharma Foundation

AUROBINDO PHARMA LTD’ (APL). APL is a growing Indian multinational pharmaceutical manufacturing firm with turnover of over US$2.8 Billion revenues for 2018-19, with presence in more than 34 countries fronted presence with products exported to 155 nations. APL is 2nd Largest Generic Company as per Rx dispensed in the USA.APL is Amongst Top 10 Generic player in France, Germany, Portugal, UK, Italy, Czech Republic, Netherlands & Belgium.

We are conducting a walk-in drive for the  M.Sc. and B.Pharmacy freshers passed out in 2021, 2022 and 2023 for our Aurobindo Pharma Foundation Training program located at Hyderabad. Interested candidates can scan the QR code for registration and attend the interview as per the details mentioned

AUROBINDO PHARMA LTD – Hiring for FRESHERS

• Department: QC / QA / ARD / FARD / Stability
• Experience: Freshers
• Division: Skill Development
• Qualification: M.Sc / B.Pharm
• Passouts: 2021, 2022 & 2023 Batch
• Location: Hyderabad

Date of Interview: 12th Apr’ 2023

Time: 9:30 AM to 11:00 AM

Venue: Aurobindo Pharma, Research Centre-II, Skill Development Centre, Pashamylaram, Indrakaran Village, Sangareddy, Hyderabad

For Further queries Contact: E-Mail: apfsdc@aurobindo.com

Registration Link: Registration Form for SDC 2023 Walk-in drive (google.com)

Gland Pharma – Walk-Ins for B.Sc, B.Pharm, M.Sc, M.Pharm Candidates – Quality Control / Microbiology on 12th Apr’ 2023

Gland Pharma Limited is Established in Hyderabad, India in 1978, 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.

Walk-in interviews for Experienced Quality Control candidates on 12th April (Wednesday) @ Gland Pharma Ltd Unit 2, Pashamylaram | Experience: 1-5 years | Immediate Joiners Preferred | Parenteral Experience Mandatory 

DEPARTMENT: QUALITY CONTROL

• Sterile injectable experience is mandatory.
• Willing to work in any shifts
• Education – B.Sc, B.Pharma, M.Sc, M.Pharm candidates can apply. 

WALK-IN INTERVIEW DETAILS: 

• Walk-in Venue – Gland Pharma Unit 2, Plot No: 42-52., Phase III, TSIIC. Pashamylaram. Patancheru, Hyderabad, Medak, Telangana, India
• Walk-in Date & Time – 12th April (Wednesday) b/w 9:00 AM-12:30 PM
• Work location Pashamylaram (Sangareddy)
• HR POC – (9100964561)

Mandatory Documents: 10th, 12th, UG, PG marks memo, Last three months’ Salary slips, Latest Increment Letter/CTC letter, Last three months Bank Statement.

Please Note : Candidates interviewed within the last 6 months are not eligible. Non Local candidates with relevant skillsets and experience can mail their resumes to Hrd.pmy@glandpharma.com

Hy-Gro Chemicals – Walk-Ins for - Freshers & Experienced in - Production / Quality Control on - 11th & 12th April’ 2023

Hy-Gro Chemicals Pharmtek Pvt. Ltd came into existence in the early 1970s first as a trading company and then ventured into the manufacturing of bulk drugs as an associate company in 1980. Hy-Gro’s dream of having its manufacturing operations was realized with the setting up of its first manufacturing facility in Bollaram – Telangana State – India in 1995 (Unit-I) for manufacturing Active Pharmaceutical Ingredients (APIs), Advanced Intermediates and Speciality fine chemicals. Hy-Gro Chemicals Pharmtek Pvt. Ltd. is a Leading Bulk Drugs& APIs manufacturer, Approved by USFDA & KFDA, looking for suitable candidates for various Departments at our Vizag Location.

Walk-in Interviews for  Production / QC

• Department: Production / QC
• Designation: Chemist / Sr, Chemist / Executive / Trainees
• Experience: 2 to 10 yrs / Freshers
• Location:  Parwada, Vizag

Hy-Gro Chemicals Pharmtek Pvt. Ltd. (Unit-III)

Plot No. 51A&51B, Jawaharlal Nehru Pharma City,

Parawada(M), Visakhapatnam(D), AP–531019.

Contact:7331185503

Walk Ins Date & Time:

Production – 11^thApril, 2023 (Tuesday) @ 10:00 AM – 01:00 PM

QC  – Walk ins:12^thApril, 2023 (Wednesday)@ 10:00 AM – 01:00 PM

Note: Candidates must carry the following documents to eligible for interview.

1 Applicants preferred Male Candidates willing to join immediately.

2 Passport Size Photo.

3 Present CTC /Present Increment Letter / Previous Appointment Letter.

4 Three Months Pay Slips along with Bank Statement.

Saurav Chemicals Limited – Walk-In Interviews - on 12th April 2023

Saurav Chemicals Limited is established in the early 90’s SCL offers a wide range of Active Pharmaceutical Ingredients and Intermediates to its customers worldwide. SCL’s products are exported to Europe, Japan, Russia, South and Central America, ASEAN, W.Asia, MENA regions. SCL’s manufacturing facilities have been built to comply with EU GMP and U.S. FDA norms. Besides manufacturing; SCL also operates a pharmaceuticals trading and distribution business offering Generic Finished Dosages and Pharmaceutical Ingredients.

Saurav Chemicals Limited Walk-In Interviews 

• Qualification: Any Graduate
• Experience : 02-07+years
• Department: Production
• Role: Technician
• Job Location: Dera Bassi
• Salary: 1-3.5 Lacs P.A.
• No.of Openings: 20

Job description:

• Carrying out production activity as per the applicable procedure.
• Responsible for recording the observation of reaction parameters on the batch card as per the approved procedure.
• Filling of the entire batch card as per approved instruction.
• Maintain work procedure, safety precautions and cGMP.
• Exposure of operations of Clean room.
• Ensure housekeeping of plant and cleanliness of the equipment, update the equipment.
• Report accidents and irregularities at the workstation to the shift offers.
• Prepare the production batch card, protocol and another relative document of production.
• ERP operation related to production activities.

Time and Venue

12th April , 11.00 AM – 4.00 PM

SAURAV CHEMICALS LIMITED, DERABASSI BARWALA ROAD, VILLAGE-BHAGWANPURA, Punjab, India,

Contact – Aruna Thakur ( 9875901857 )

Troikaa Pharmaceuticals - Walk In on - 13th April 2023 for - B. Pharm, M. Pharm, MS/M.Sc

Troikaa is a young and fast growing system oriented pharmaceutical company. Troikaa is recognized as a discovery company, manufacturing innovative products based on varied Novel Drug Delivery Systems. The company has developed through in-house R&D, unique patented technology platforms for intra-oral, parenteral, sustained release and topical drug delivery. All these innovations are backed by requisite clinical trials. The company has two state of the art manufacturing facilities in India. The plants are designed for approvals in regulated markets. The company has a near zero product failure record. Plants are equipped to manufacture tablets, capsules, liquicaps, parenterals (including parenteral emulsions), topical and inhalation anesthetic products. We have marketing networks in India, South East Asia, Latin America & Africa. Company intends to enter the highly regulated markets by year 2009.

Job Vacancy Details: 

• Department: R&D Analytical
• Qualification: B. Pharm, M. Pharm, MS/M.Sc
• Experience: With 1-6 years of experience
• Job Location: Virochannagar, Sanand
• Salary: 2-6 Lacs P.A.

Time and Venue

13th April , 09:30 AM – 05:00 PM

Troikaa Pharmaceuticals Ltd. ‘Troikaa House-1’, Satya Marg, Bodakdev, Ahmedabad -380054, Gujarat

Contact – Pankaj Gupta ( 9099901634 )

Job description

1. Method developments and validation of analytical method on said sophisticated instruments like HPLC , Gas chromatograph UV Spectrophotometry , autititratour , dissolution etc. as per ICH / Pharmacopeia guideline.
2. Preparation of protocol and report there off.
3. Very well versed with the sample preparation on Microwave digestion system
4. Creating and executing method development and method validation test protocols for finished products and generating the appropriate analytical methods.
5. Stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, UV, Dissolution) techniques, as appropriate.
6. Writing analytical specifications using current pharmacopoeias and reviewing existing analytical specifications.
7. Writing/reviewing Standard Operating Procedures (SOPs),
8. Ensuring that procedures are carried out carefully and accurately to eliminate errors.
9. Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
10. Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).