Amneal Pharma – Walk-In Interviews for Multiple Positions on 6th Aug’ 2023 for ITI / Diploma / B.Sc / B.Pharm / M.Sc / M.Pharm Candidates

Amneal Pharmaceuticals is a high-quality producer of solid and Injectable generic products and one of the fastest-growing global generics producers. We believe that the world is our family and we are committed for consistently producing high quality affordable medicines. Amneal is expanding its operations in India and invites people who share its value of relentless pursuit of quality, integrity, treating each other with respect and encouraging the very best in everyone to join the Amneal family.

Amneal Pharma Walk-in Interviews for Manufacturing (OSD/Tablet Capsules) on 6th Aug’23 (Sunday). We are looking for competent, dynamic and motivated candidates for suitable positions for OSD Manufacturing unit for SEZ Matoda Plant, Ahmedabad.

Date: 06th August, 2023 (Sunday)

Time: 9 am to 12 pm

Venue: Amneal Pharmaceuticals Pvt. Ltd.

Plot No 15,16,17 Pharmez, Sarkhej Bavla Highway,

Vil. Matoda, Ahmedabad 382213

Job Location: SEZ MATODA, Ahmedabad

(Oral Solid – OSD Requirement)

1.Manufacturing (Tablet/Capsule)

Designation: Operator/Officer/ Sr. Officer /Executive

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

Total Experience: 02 to 06 years

Area: Coating, Granulation, Compression, Packing (Bottle Packing only)

Machine Exposure along with 21 CFR compliance: RMG, FBE, Fette compression, Auto coaters, bottle packing line with Track & Trace system.

Desired Profile:

Candidates should have hands on experience along with knowledge of 21 CFR compliance in equipment’s like RMG, FBE, V-Blender, Fette compression machine, Auto coater, CVC Line and packaging line equipment with Track and Trace system.

Knowledge of Quality Management System (QMS) i.e. change control, Deviation, CAPA, and documentation in manufacturing/Packaging area of OSD.

Able to understand & have relevant knowledge of SCADA operation & 21 CFR requirements.

Able to understand & operate fluid Bed equipment

To supervise and monitor day to day activities of processing and holding of drug product as per define and approved procedures for stability batches and commercial batches.

To maintain the areas and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition.

To impart training of operation and cleaning related SOP to all subordinates and operators

Co-ordination for IQ / OQ for any new equipment / system

To perform PQ for any new equipment / system

To follow all concern departmental SOP’s for day to day operation and cleaning

To handle and manage material movement as per defined procedure and approved Batch Manufacturing Record

To perform online documentation with respect to departmental procedures as per good documentation

Maintaining the change parts for all equipment at manufacturing.

Candidate with good communication & interpersonal skills, computer knowledge, exposure to cGMP/ ALCOA, ALCOA++ & understanding of regulatory requirement will be preferred.

Note : Candidate should have 02 to 06 years of relevant experience in USFDA regulatory approved pharmaceuticals (Preferred 21 CFR compliance) organization.

Kindly carry your updated CV along with copies of CTC proof, Appointment letter, Increment letter, last 3 months salary slips, Bank statement, Education certificates & Marksheets, Aadhar & PAN card and passport size photograph, at the interview venue.

 

If you are unable to attend interview you can share CV on below email id:

chandanid@amneal.com & jagdish.mathukiya@amneal.com

Thanks & Regards

Chandani Daswani

Sr. Manager – HR

Warren Remedies – Walk-In Interviews for Production, QC, QA, Warehouse, EHS, Safety, Machine Operators on 4th Aug’ 2023

Warren Remedies Pvt. Ltd (100% Subsidiary of 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. 

Warren Remedies Pvt. Ltd (100% Subsidiary of Indoco Remedies Ltd) is conducting Walk-In Interviews for Production, QC, QA, Warehouse, EHS, Safety, Machine Operators on 4th Aug’ 2023. Looking for dynamic individuals for our Green Field project at Plot No. 17, Sector-13, AURIC City, Shendra, Dist. Aurangabad.

Job Description Details:

1) Position: Officer/ Executive/ Manager

Departments: Production, Quality Assurance, Quality Control, Warehouse, EHS/Safety, Technician (Machine Operator).

Experience: 2 to 15 years.

Qualification: B.Sc, M.Sc, B. Pharm & M.Pharm, (BE, AIDS for EHS/Safety)

 

2) Block-II API Manufacturing Facility:

Position: Officer/ Executive/ Manager

Departments: Production, Quality Assurance, Quality Control, Warehouse, EHS/Safety. Technician (Machine Operator).

Experience: 2 to 15 years.

Qualification: B.Sc, M.Sc, B. Pharm & M. Pharm, (BE, AIDS for EHS/Safety)

Walk in Interview Details: 

Date & Day: Friday, August 4, 2023

Time: 9:00 am to 5:00 pm

VENUE: Hotel Amarpreet, Amarpreet Chowk, Jalna Road, Rokda Hanuman Colony, Mondha, Aurangabad 431001.

INTAS PHARMA – Walk-In Interviews for QC / QA on 5th August’ 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.

Opportunities with Intas Pharmaceuticals,

Walk In Interview at Pharmez

Date: Saturday, 5th August

Time: 09:00 AM to 02:00 PM

Venue: Intas Pharmaceuticals Limited Plot no. 05 to 14, Pharmez Near Village Matoda, Sarkhej – Bavla Highway 8 –A, Ta – Sanand, Dist – Ahmedabad.

Position: Officer to Sr. Executive

Department: Quality Control (QC-FG/ Stability / AMV)

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

Experience: 2 to 12 Years

Analyst: Finished & Stability Section & Knowledge of Instrument – HPLC / GC / Dissolution.

Reviewer / Trouble-shooter: Chromatographic data review soft as well hard copy, must be experienced in troubleshooting of instruments.

Position: Officer to Executive

Department: Quality Assurance (IPQA Parenteral)

Qualification: B.Pharm / M.Pharm

Experience: 2 to 12 Years

Officer to Sr. Officer: Experience in IPQA Parenteral, Review of BPCR, MPCR, In Process Control Check.

Executive & Above: Preparation & Review of Process Validation, Cleaning Validation, Medial Fill, MPCR & BPCR.

FDC Limited – Walk-In Interviews on 2nd August’ 2023 for Multiple Positions in Production / Quality Control / Quality Assurance

FDC Limited carries forward the flaming spirit of its first dream, achieving accreditations from the US-FDA, UK-MHRA, MCC-RSA, and the UAE, to cite a few. FDC is a forerunner in manufacturing and marketing of Oral Rehydration Salts (ORS) and Ophthalmics. FDC has also set-up globally approved, multi-location manufacturing facilities for Active Pharmaceuticals Ingredients (APIs) as well as Finished Dosage Forms. These facilities are located at Roha, Waluj and Sinnar in Maharashtra, Verna in Goa and Baddi in Himachal Pradesh. FDC markets more than 300 products in India and exports many of these to over 50 countries.

FDC Limited, We are conducting walk-in interviews for Production, Quality Control, Quality Assurance on 2nd August’ 2023 at Khol-Bhud, Tehsil Baddi, Distt. Solan (HP) 173205.

Job Description: 

Department: Production, QC, QA

Designation: Operator, Officer/Executive

Area: MFG., MFG.(Dry Syrup Filling), HPLC/TESTING, IPQA

Qualification: B.Pharma / M.Pharm, 12th, ITI, M.sc (Chem.)

Experience: 2-8 Years

Interview Schedule Details: 

Date: 02-08-2023 

Time: 10:00 AM to 01:00 PM

Venue: FDC Limited, Khol-Bhud, Tehsil Baddi, Distt. Solan (HP) 173205

Contact Person: Mr. Sushil Kumar, Sr. Officer -HR

Contact Number: 9736880100

Note: We are required only Himachali Candidates.

MAXTAR Bio-Genics – Multiple Openings for DRA / QC / IPQA / Production / Warehouse / Stores / Engineering Departments – Apply Now

Maxtar Bio-Genics was established in the year 1991 in Delhi, India. The commencement of production was noted to be on 2007. We are a pharmaceutical company which is research based, extensively manufacturing and have the required commercial skills. Our main aim is to enhance the quality of human life with our at par quality products. We hold the ISO 9001:2000 Certification and WHO-cGMP.

VACANT POSITIONS @ Maxtar Bio-Genics

Department: DRA / QC / IPQA / Production / Warehouse / Stores / Engineering

Role: Executive / Officer / Fitter / Electrician / Operator

Qualification Required: B.Pharm, B.Sc, B.A, 10th, ITI

Experience Required: 01-07 Years

Gender: Male

Job Location: Baddi

Contact: E-Mail: maxtaradm@gmail.com

Interested can send profile at maxtaradm@gmail.com or call at 9736934896 / 9218548147

Amoli Organics – Recruiting For Multiple Positions – Submit Resume

Amoli has a successful track record in the pharmaceutical and allied industry. Making a beginning as a manufacturer of APIs and Intermediates, it made successful forays in the field of Contract Research and Custom Synthesis. Amoli has been working collaboratively with some of the leading global healthcare players. Presence in USA, EUROPE, JAPAN, RUSSIA, SOUTH EAST ASIA, MIDDLE EAST AND LATAM and it is fast growing and well integrated healthcare group.

Amoli Organics-Recruiting For Following

Qualification: M.Sc./ B. Pharm

Experience : 05-08+years

Role: Sr. Officer / Executive / Sr. Executive

Job Location: Vadodara/ Baroda,Gujarat

 Interested candidates can share their CV on pooja.patel@amoliindia.com with the below mentioned details.

Total Experience:

Current Company name where employed:

Current Designation:

Current CTC:

Expected CTC:

Notice Period:

Job description

Role & responsibilities:

Handling Chromeleon chromatographic software, Knowledge of ALCOA principle, ICH, OOS and OOT.

Responsible for analysis of Finished product (API), Stability samples, Raw material, Intermediate and In-process by HPLC as per work allocation.

Responsible for analysis as per existing release specifications and testing methods.

Responsible for timely information of OOS, OOT, Incident and deviation.

Responsible for proper (as per respective SOP) handling and storage of samples.

Responsible for calibration of instrument.

To ensure current SOP/Specification/Method of analysis is being used

Preferred candidate profile

M.Sc./ B. Pharm

Working in HPLC at least from last 3 years

Experience of working with API Industry must.

Perks and benefits

Bus & Canteen Facility Available

Ami Lifesciences Walk In On 05th August’ 2023

Ami Lifesciences was founded with the goal of changing the way in which quality medicines are delivered to people in need. We operate on the principle by extending our focus and services to maximize our impact on the global pharmaceutical industry. We have spent last two decades in building up our scientific and technological capabilities, research, and manufacturing competencies. Along the way we have earned a reputation for being innovative, inventive and resourceful. We have built long term business association pharmaceutical companies of the world.

Ami Lifesciences Walk In

Qualification: B.Sc in Any Specialization, B.Tech/B.E/ MS/M.Sc(Science)

Experience : 02-05+years

Department: Production 

Role: Chemist / Officer/ Executive

Job Location: Vadodara

No.of Openings: 10

Salary: 3-7 Lacs P.A.

Time and Venue:

5th August , 9.30 AM – 5.30 PM

Productivity House, 2nd Floor, BPD Rd, Alkapuri, Vadodara, Gujarat

Contact – Aparna Mishra/Yogita Sidhwani 

Job description:

Roles and Responsibilities

API Production, Bulk Drug,API Production

To be responsible for Batch start up activity, monitoring, calibration of balance and other instruction given by the Superior,

To review technical documents like batch records, cleaning records, validation protocols, cleaning verification protocols,

SOPs, cGMP, Reactor, BMR Review, Raw Material, Hydrogenation, batch

Desired Candidate Profile

Candidate with exposure in API Production must

Qualification: M.Sc.Chemistry / BE / B.Tech Chemical

Experience: 2 to 5 years in API Industry only