ACCUPREC RESEARCH LABSPVT.LTD hiring FRESHERS & experience for multiple openings in QA, RA, R&D, PT, Pathologist, MLT & IT department
WE ARE HIRING!
Sr. Research Associate (QA)
Qualification : M.Pharm
Experience : 5 to 8years
– Review, assessment and closing of Change control, Deviations, Out of Specification, CAPA &
Investigation reports.
– Participation in Internal Audits & Compliance Activity.
– Establishing & implementing quality system.
– Co-ordinate with the cross functional department whenever required.
Sr. Research Associate (RA)
Qualification : M.Pharm
Experience : 5-8 years
-. Compilation, review and preparation of eCTD/CTD documents for regulatory submission. Prepare COPP, FSC application for export registration.
– Prepare documentation of FDCA, CDSCD, ISO, GLP, NABL and USFDA and compliance thereof.
– Prepare and submit applications for Medical devices to CDSCO Responsible for Clinical trial approval and registration-EC, CTRI and live.
Sr. Research Associate (Biotech)
Qualification : M.Sc. (Biotech), Ph.D. desirable
Experience : 5-7 years
– Experience in cell and molecular biology in an industry setting.
• Strong publication record demonstrating expertise in cell and molecular biology
– Hands-on experience in handling PCR, RT-PCR, ELISA and relevant biotechnology instruments
Sr. Research Associate (Formulation Development)
Qualification : M.Pharm/ M.Sc
Experience : 5-8 years
• Development of Formulation for ANDA and other regulatory submissions
– Should possess knowledge of Patent search, QbD, DoE etc.
– Should possess experience of preparation of MFR, PDR, TT and execution of pivotal, pilot and execute batches
Assistant Manager (QAU)
Qualification : M.Pharm. (Pharmacology) / M.Sc(Biology Toxicology)
Experience : 8-10 years
. Should possess experience of QAU as per OECD-GLP guidance documents and face
audit by NGCMA.
• It is desirable if faced audit by NABL, AAALAC, USFDA and like other regulatory
agencies.
Maintaining tes • Receipt, storage, archival and issuance of test item.
Test Item Control Officer (TICO)
Qualification : B.Sc./B.Com. or any graduate
Experience : 0-2 years
Maintaining test item utilization record.
• Verification of test item details like name, sponsor details, batch number, manufacturing and
expiry dates, quantity received, packaging, label, identification code and other important details
at the time of test item receipt. Maintain TICO facility as per regulatory norms
• Must have knowledge of Word, Excel, Mail,
Research Assistant (MB)
Qualification : M.Sc. / M.Pharm
Experience : 0-2 years
• To carry out microbiological testing, BET testing, sterility testing and like for Drug & Pharma,
Medical Device, AYUSH and Food products as per respectiva regulatory Guidelines
• Protocol preparation, report preparation, SOP Preparation pertaining to Microbiology
department
Research Assistant (PT)
Qualification : M.Pharm(Pharmacology)
Experience : 0-2 years
• To carry out pre clinic testing, toxicity testing, study plan preparation, report preparation
Veterinary Pathologist
Qualification : M.V.SC. (Pathology)
Experience : 0-5 years
•Pathological observation including gross necropsy organ weighing, histopathology examination, All activities of pathology dept should be taken care.
Research Assistant (MLT)
Qualification : DMLT/MLT
Experience : 0 to 2 years
Blood sample analysis, Clinical pathology work,
Hematology analysis Blood chemistry analysis Histopatholigical work (Tissue collection, Block preparation, section cutting and slide. preparation for Microscopic examination)
Sr. Executive (IT)
Qualification : M.Sc./BE/MCA (IT)
Experience : 5-8 years
• Should aware of ISMS policies and guidelines, Systems Management, IT infrastructure, installing & configuring servers, IT inventory, Host & manage
websites, IT deployment, IT Budgeting, Managing Web servers
• Network Management and security Management
- Positions Open For Ahmedabad Location
Interested Candidates send their resumes on mail ID:
(Mention your In-Hand Salary, Expected Salary, CTC) For any Inquiry, Contact : 90999 32105
Salary no bar for right candidate
Note: Candidates must have exposure of Pharma regulatory approved organisations (USFDA, MHRA, Eu and other Major regulatory bodies)
Interested candidates send their updated resumes to
[email protected]
Also mention the below details,
-Current CTC
-In-hand salary
-Expected Salary
-Notice Period
