Synokem Pharmaceuticals – Hiring for Quality Control Department

Synokem Pharmaceuticals is Established in 1983 with the core mission of protecting consumers’ health and wellbeing, Synokem Pharmaceuticals is making rapid growth with proven expertise in the field of manufacturing and marketing premium quality pharmaceutical products under the pilotage of Chairman Mr. J.M. Arora and Managing Director Mr. Abhinav Arora. Having accredited with WHO-GMP Certification, Synokem manufactures over 1000 novel DGCI-approved pharmaceutical formulations in its certified unit equipped with state-of-the-art in-house testing laboratory. Synokem Pharmaceuticals is also engaged in Contract Manufacturing of Finished Formulations in the form of Tablets, Capsules, Liquid Orals, Ointment, Hormonal Gels, Bi-layered and Sustained release preparations, which are being manufactured at its well-equipped ultra-modern three manufacturing units situated at Haridwar, Uttrakhand. These manufacturing units are WHO-GMP and ISO 9001-2008 certified.

Amneal Pharmaceuticals – Multiple Openings in Manufacturing(OSD) @ SEZ Matoda, Ahmedabad

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.

Multiple OPENINGS IN Manufacturing(OSD) @ SEZ Matoda, Ahmedabad location

Please find job details below :

Qualification : ITI, Diploma, B.Pharm

Experience : 2 to 5 years

Area Wise Requirements👇

Granulation, Coating, Compression, Packing, Capsule

*Interested candidate can share their cv on below mail chandanid@amneal.com & Jagdish.mathukiya@amneal.com

Vivimed Labs Ltd – Multiple Openings for Production / Quality Control / Plant Operations Department – Apply Now

Vivimed Labs Ltd has metamorphosed from a domestic small, entrepreneurial family-operated business to a globally renowned supplier of niche molecules and formulations across Healthcare, Pharmaceuticals and Specialty Chemicals. As a fast growing Specialty Chemicals company, we invite talented and ambitious individuals to explore an exciting career prospect at Vivimed. We offer a challenging environment where you can achieve your career goals while making a difference – through our products and its applications.

Vivimed Labs Ltd – WE ARE HIRING – Formulations (Orals/ OSD )

Requirement for Production / Quality Control / Plant Operations Department

Executive, Sr. Executive, AM, Manager, DM, GM, Sr. Manager

No. of Positions: 19

Job Location: Hyderabad

Submit your CV & Resume to careers@vivimedlabs.com

For more info, visit our website www.vivimedlabs.com

Intas Pharmaceuticals – Multiple Openings for Quality Control / QC-Micro – Apply Now

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. 

Alkem Laboratories – Freshers Walk-In on 29th June ‘ 2023 for Multiple Positions in various Departments

Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, Maharashtra, India that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally. We are a leading Indian pharmaceutical company with global operations, engaged in the development, manufacture and sale of pharma & nutraceutical products.

Zenfold Sustainable Technologies (ZST) – Walk-In on 26th June’ 2023 for B.Pharm, M.Pharm, B.Sc, M.Sc

Zenfold Sustainable Technologies (ZST) is a specialty and fine chemicals company, established in 2021. Our advanced technological capabilities and state-of-the-art infrastructure allows us to provide the entire gamut of services involved in manufacturing and contract research — from process development to scaling up.

Job Title: Chemist

Location: Pashamylaram, Hyderabad.

Date& Time: 26th June 2023,11:00 Hrs to 16:00hrs

Venue: Plot No 217, 218 & 219, Phase II, IDA Pashamylram Sangareddy.

Department: Process Research and Development

Experience – 2-6 Yrs.

Qualification: B.Sc, M.Sc, B. Pharm, M. Pharm

Interested candidates may walk in on any day between 11:00 Hrs to 16:00hrs from 26th June 2023 onwards at the above mentioned venue or drop their resume on shravankulakarni@zenfoldst.com

Metrochem API Pvt. Ltd – Walk-In on 26th – 30th June’ 2023

Metrochem API Pvt Ltd was established by Dr. N.V. Rao in the year 2004, with a grand vision of being the most preferred supply partner to pharmaceutical customers worldwide. The management aimed to achieve this vision with a clear focus on quality, affordability and products at Metrochem API Private Limited is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (APIs), Pellets (Semi finished Formulations) and Intermediates.

Metrochem API Walk In

Qualification: MS/M.Sc(Science) in Chemistry

Experience : 00-02+years

Department: API Regulatory Affairs

Role: Jr Manager/ Asst Manager

Job Location: Hyderabad/ Secunderabad,Telangana( Shapur Nagar )

No.of Openings: 02

Time and Venue

26 June – 30 June , 10.00 AM – 5.00 PM

Metrochem API -Unit-R&D, Rangabhujanag Theatre Lane, Shapurnagar, Hyderabad.

Contact – Gowtham ( 8187892413 )

Job description:

Position for – Jr Manager/ Asst.Manager – API Regulatory Affairs -Unit-R&D, Shapurnagar, Hyderabad.

Qualification – Only M.Sc. Chemistry

Experience – 7-10 years (API – RA)

Walk In

Venue – Unit-R&D, Rangabhujanga Theatre Lans, Shapurnagar, Hyderabad

Dates – 26-06-2023 to 30-06-2023

Time – 10am to 5 pm

Contact Number- 8886659021 / 8187892413

Email CV’s to – gowtham.adapa@metroapi.com

For further assistance contact – 8187888831.

JOB DESCRIPTION

1. Examining the conformity of all documents for approval must be compliant to all relevant regulations,

rules and standards and taking part in the conformity assessment procedure with coordination of all

concerned departments.

2. Developed and maintained an in dept , ongoing knowledge of Guidelines, Regulations, Directives and requirements for submission.

3. Communicate regulatory information to multiple departments and ensure that information is

interpreted correctly and support the relevant departments in fulfilling the regulatory requirements

4. Handling of Authority and Customer Queries.

5. DMF or Dossier Preparations and submission.

6. Providing the regulatory strategic note for building the product by exploring various literature and

summary basis of approval provided by various regulatory authorities.

7. To provide the regulatory in-puts for the change controls assigned.

8. Make sure the proper regulatory data base maintenance.

9. Building the regulatory awareness.

10. Genotoxic impurities assessment and control strategy.

11. Nitrosamine risk assessment evaluation.

12. New DMF and amendment review in technical aspect and regulatory compliance.

13. Serves as a liaison between the regulatory bodies and operating devisions of the company.

14. Tracking and monitoring the process of submissions.

15. Enriching the quality of documents in-line with the current regulations.

16. Regulatory Compliance Facilitate quick closure of internal and external outstanding regulatory issues.

17. Regulatory intelligence Responsible for assessment of regulatory consultants and trade consortium

18. Team empowerment Responsible for mentoring reportees

19. Team empowerment Responsible for identifying appropriate training for the team.

20. Technical and managerial skills to understand and guide cross functional teams on process development, analytical development , process scale up , product characterizations.

21. Experience and expertise to develop regulatory strategy from development stage to filing and

approval.