Accuprec Research Labs Pvt Ltd. is FDCA approved, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA. Accuprec provides all type of Pharmaceutical testing solutions to its domestic and MNC clients.
HIRING FOR FOR GLP TEST FACILITY
Study Director
Department : Pharmacology and Toxicology (In Vivo)
Qualification : M.Pharm (Pharmacology & Toxicology) / M.V.Sc. / M.Sc. Toxicology or relevant
Experience : 2+ years
Job Description :
• Knowledge of Good Laboratory Practices for Nonclinical Laboratory Studies highly desirable
• Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed.
• Evaluates, analyzes and interprets data and presents in a clear, well-organized, scientifically sound report.
• Prepares protocol submissions for IAEC review and responds to committee comments/questions as necessary.
• Other duties as assigned.
Study personnel
Department : Pharmacology and Toxicology (In Vivo)
Qualification : M.Pharm (Pharmacology & Toxicology) / M.V.Sc. / M.Sc. (Toxicology)
Experience : 0-2 years
Job Description : Assist to study director in preclinical toxicology studies for handling pre-clinical testing, toxicity testing, study plan preparation, report preparation etc.,
Study Director
Department : Pharmacology and Toxicology (In Vitro)
Qualification : M.Sc. (Biotech / Micro / Toxicology) or relevant
Experience : 2+ years
Job Description :
• Maintain overall scientific responsibility for the In Vitro study design, interpretation, and reporting of study results.
• Manages studies in accordance with established protocols, SOPs, and pertinent regulatory requirements.
• May develop and review new procedures, technologies, and SOPs as required.
• Hands on experience in cell line and microbial culture handling and maintenance.
• Development and validation of new in vitro model studies
• Other duties as assigned.
Study personnel
Department : Pharmacology and Toxicology (In Vivo)
Qualification : M.Sc. (Biotech / Micro / Toxicology)
Experience : 0-2 years
Job Description : Assist to study director in preclinical toxicology studies for handling pre-clinical testing, toxicity testing, study plan preparation, report preparation etc.,
Research Associate / Sr. Research Associate
Department : Quality Assurance Unit (QAU)
Qualification : M.Pharm (Pharmacology & Toxicology/ Quality Assurance) / M.Sc. (Life Science) with GLP experience
Experience : 2+ years
Job Description :
• Should possess experience of QAU as per OECD GLP.
• Preferred to have faced audit by NGCMA. It is desirable if faced audit by AAALAC, NABL, CDSCO etc.,
• Plan and perform study, process and facility based insections, vendor audit and validation activity (CSV) etc.,
• Liase with study team for various inspections
• Effective in verbal and written communication skills including correct grammar, spelling, and punctuation.
Research Assistant
Department : Quality Assurance Unit (QAU)
Qualification : M.Pharm (Pharmacology & Toxicology/ Quality Assurance) / M.Sc. (Life Science)
Experience : 0-2 years
Job Description : Assist QAU team in conducting various day to day activities including inspections (study, process, facility, vendor audit etc.,)
* Positions Open For Ahmedabad Location
Interested candidates send their resumes on email ID with clearly mentioned the post applied career@accuprec.in (Mention your In-Hand Salary, Current CTC, Expected CTC, Notice Period)
Note : Short listed candidates will be contacted after 16th January 2023
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