Zydus Lifesciences – Walk-In Interviews for R&D / Production / Regulatory Affairs on 27th – 28th Aug’ 2022
Zydus Lifesciences Limited (Formerly known as Cadila Healthcare Limited), a leading Indian Pharmaceutical company is a fully integrated, global healthcare provider. With in-depth domain expertise in the field of healthcare, it has strong capabilities across the spectrum of the pharmaceutical value chain. From formulations to active pharmaceutical ingredients and animal healthcare products to wellness products, Zydus has earned a reputation amongst Indian pharmaceutical companies for providing comprehensive and complete healthcare solutions. One of the salient features of Zydus is its rich history and lineage. The origin of the company dates all the way back to the 1950s. The company was founded in the year 1952 by Mr. Ramanbhai B. Patel (late), a first-generation entrepreneur and a doyen in the field of Indian Pharmaceuticals.
ZYDUS LIFESCIENCES – WALK-IN INTERVIEW – BENGALURU & HYDERABAD
Roles and Responsibilities:
Research & Development (API) Location: Vadodara
Senior Research Associate / Associate Research Scientist
- Candidates should have Ph D in Organic Chemistry with 0 5 years of relevant experience in handling multistage reactions with knowledge of analytical data interpretation, literature search, developing routes of synthesis and in-depth knowledge of chemistry.
Regulatory Affairs (API)
Assistant Manager / Manager Location: Vadodara
- M.Sc / M Pharm / B Pharm and / or PG Diploma in Regulatory Affairs with 5 12 years of experience in regulatory affairs (API).
- The job requires preparation and submission of drug master files and certificate of suitability application (CEP) for Active Pharmaceutical Ingredients for submission to various regulatory authorities. The job requires to file amendments and deficiency response within timelines with a go getter approach, to review documents related to DMF submission against predefined checklists and submission to various agencies globally.
- Candidates are required to prepare and review high-quality Drug Master File and certificate of suitability application (CEP) for submission to various regulatory authorities. Candidates should draft regulatory write up for various sections like process description, validation, stability protocols and reports with special emphasis on regulatory ramifications. Should also review master documents and should possess regulatory skills i.e. impact assessment on cross linked sections and data. Must have an experience and should possess the skills in eCTD.
Production (API)
Manager / Sr Manager – Production (API) Location: Dabhasa and Ankleshwar
- Candidates should be BE / B Tech (Chemical) / M Sc (Organic Chemistry) with 10 – 20 years of relevant experience in handling multipurpose an API production facility.
- Candidate should have at least 3 – 5 years in a managerial role with all-round and independent operational / Plant management responsibilities.
- Candidate must have in depth exposure in resource planning and managing productivity as per organisational objectives. Must be well versed with regulatory including cGMP requirements and capacity enhancement processes,
- Candidate should have good exposure in handling various regulatory and quality audits and proficient in adhering to Safety, Health and Environment measures.
Note : For Production – Separate time slot will be given individually for interview.
Interested candidates should walk in with their updated CVs and can also share their CVs with dkpatel@zyduslife.com.
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