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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Required Associate QA - B. Tech. / B. E. / B. Sc. / M. Sc. Biotechnology

LEVIM LIFETECH IS HIRING ASSOCIATE QA DETAILS ARE PROVIDED BELOW  1. POSITION: ASSOCIATE QA 2. QUALIFICATION: B.TECH/ B.E BIOTECHNOLOGY, B.SC/M.SC BIOTECH 3. EXPEREINCE: 2-4 years 4. ROLES & RESPONSIBILITIES -REVIEW AND APPROVE ANALYTICAL TEST RESULTS AND REPORTS -ENSURE COMPLIANCE WITH SOPS, GLP, GMP, AND REGULATORY REQUIREMENTS -REVIEW VALIDATION PROTOCOLS AND ANALYTICAL METHOD TRANSFER ACTIVITIES -MAINTAIN ACCURATE ANALYTICAL DOCUMENTATION AND RECORDS -HANDLE DEVIATIONS, INVESTIGATIONS, AND CAPA -PARTICIPATE IN INTERNAL AND REGULATORY AUDITS -SUPPORT QC TRAINING AND CONTINUOUS QUALITY IMPROVEMENT -COLLABORATE WITH R&D, PRODUCTION, AND REGULATORY TEAMS 5. PREFERRED SKILLS:  -KNOWLEDGE OF GLP, GMP, AND REGULATORY COMPLIANCE -EXPERIENCE WITH HPLC, GC, FTIR, AND UV-VIS SPECTROSCOPY -METHOD VALIDATION AND ANALYTICAL EQUIPMENT QUALIFICATION -STRONG DOCUMENTATION AND INVESTIGATION SKILLS 6. HOW TO APPLY  CLICK ON FOLLOWING LINK FOR ONLINE APPLICATION ...
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Required Clinical Research Associate - M. Sc. / B. Pharm - 02 Vacancies

Synergen Bio is hiring for Clinical Research Associate 
Details of the available position is provided below 
1. Position: Clinical Research Associate (CRA)
2. Qualification: Msc, B.Pharm
3. Experience: 01 to 02 + year's
4. No Vacancy: 02
5. Job Location: Shivajinagar, Wakadewadi Pune.
6. Tasks Responsibilities:
a. Execute assigned BA/BE study as per SOP and applicable regulatory guideline.
b. Preparation and Compilation of Essential Document in Trial Master File, review of CRF and Raw data.
c. Responsible for assigned study documents accountability and review documents for adequacy, correctness and completeness.
d. Preparation of clinical updates and related communication to bioanalytical and statistics.
e. Provide compliance to QC and QA observation.
f. Perform informed consent presentation and obtaining in screening and study.
g. Perform registration, screening related activities.
h. Preparation and Review of SOP Responsible for training to staff as and when required.
i. Perform pharmacy related activities as and when required
j. To perform any other activity delegated by Head CR/PI/Manager Operation.
7. Interested Candidate Share CV on careers@synergenbio.com
Note: Immediate joiner preferred

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