Syngene MSc Biochemistry Research Associate Job Opening – Apply Now
Senior Research Associate (56057)
Requisition ID 56057 –
Posted 05/23/2024 – India
Job Description
Job Title: Clinical Pathology Analyst
Department: Safety Assessment
Location: Bangalore
About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit.
Mandatory expectation for all roles as per Syngene safety guidelines
- Overall adherence to safe practices and procedures of oneself and the teams aligned
- Contributing to the development of procedures, practices and systems that ensures safe operations and compliance to the company’s integrity & quality standards
- Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
- Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
- Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
- Compliance to Syngene’s quality standards at all times
- Hold self and their teams accountable for the achievement of safety goals
- Govern and Review safety metrics from time to time
Core Purpose of the Role: The purpose of this role is to perform hematology, coagulation, clinical chemistry and urine analysis in automated instruments.
Role Accountabilities:
- Preparation of anticoagulant, vials for sample collection and separation of plasma/serum
- Performing the analysis of clinical chemistry, hematology, coagulation and urine parameters using automated analyzers
- Microscopic examination of urine sediments
- Preparation of blood smears and staining.
- Manual DLC count and morphological examination of blood smears
- Recording, verification and compilation of raw data
- Online data entry using data capture software
- Performing qualification instruments/ computerized system validation
- Standardization and validation of additional parameters
- Coordination in maintenance and calibration of various equipment in clinical pathology
- QC management of clinical pathology parameters.
- Effectively troubleshooting in case of QC failure and instrument malfunctioning.
- Preparation and revision of standard operating procedures.
- Receipt, labeling of chemicals and maintaining the chemical stock register
- Ensuring proper documentation as per regulatory requirements.
- Ensure that work performed is in accordance with the requirements of the study plan and in full compliance with GLP
- Comply with EHS policy without deviation
Syngene Values
All employees will consistently demonstrate alignment with our core values:
- Excellence
- Integrity
- Professionalism
Specific requirements for this role
Experience: 3-6 years in GLP lab.
Skills and Capabilities:
- Proficiency in handling and troubleshooting various automated clinical pathology instruments
- Knowledge on GLP, CLIA, WHO guidelines on clinical laboratory and 21 CFR-part-11
- Working experience in GLP environment
Education: M.Sc in Biochemistry
Keywords: Senior Research Associate, Clinical Pathology Analyst, Syngene, Safety Assessment, Bangalore, Biochemistry, GLP. Syngene MSc Biochemistry Research Associate Job Opening – Apply Now. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebook
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