Zydus Lifesciences Walk In Interview 2022 . Zydus Lifesciences Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.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.
- Post Name: Manager / Sr Manager – Production (API) /Assistant Manager / Manager /Senior Research Associate / Associate Research Scientist
- Department: Research & Development (API)/Production (API)/Regulatory Affairs (API)
- Qualification: M Sc / M Pharm / B Pharm and / or PG Diploma/ BE / B Tech (Chemical) / M Sc (Organic Chemistry)
- Experienced: 0- 20 yrs
Job Description: Zydus Lifesciences Hiring For Manager / Sr Manager – Production (API) /Assistant Manager / Manager /Senior Research Associate / Associate Research Scientist !
Important Details :
- Location: BENGALURU & HYDERABAD
- Post of date:23/08/2022
- Selection Process: The selection will be on the basis of Interview.
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
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 firstname.lastname@example.org.
Desired Candidate Profile
Perks and Benefits