Accuprec Research labs Hiring Regulatory affairs, Formulation development, QA professionals 2022
- Quality Assurance
- Regulatory affairs Jobs
- Biotechnology Jobs
- Formulation Development Jobs
- Assistant Manager (QAU)
ACCUPREC RESEARCH LABS hiring notification for msc, m pharm Candidates for Regulatory affairs, Formulation development, Quality Assurance, Biotechnology Departments.
Vacancy information
Quality Assurance
Role: Sr. Research Associate (QA)
Qualification: MSc / M Pharmacy
Experience: 5 to 8 years
Job Description: 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.
Regulatory affairs Jobs
Role: Sr. Research Associate (RA)
Experience: 5 to 8 years
Qualification: M Pharmacy
Job Description: Compilation, review and preparation of eCTD/CTD documents for regulatory submission. Prepare COPP, FSC application for export registration.
Prepare documentation of FDCA, CDSCO, ISO, GLP, NABL and USFDA and compliance thereof. Prepare and submit applications for Medical devices to COSCO.
Responsible for Clinical trial approval and registration -IEC, CTRI and like.
Biotechnology Jobs
Role: Sr. Research Associate (Biotech)
Qualification: MSc. (Biotech) Ph.D. desirable
Experience: 5-7 years
Job Description: 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
Formulation Development Jobs
Role: Sr. Research Associate (Formulation Development)
Qualification: M.Sc. / M.Pharm
Experience: 5-8 years
Job Description: 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) / MSc (Biology /Toxicology)
Experience: 8 to 10 years
Job Description: 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.
Positions Open For Ahmedabad Location
Interested Candidates send their resumes on mail ID : [email protected]
(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)
Senior Positions For Immediate Joining
