[ad_1]
Syngene Microbiology Vacancies – MSc Candidates Apply
Job Title: Executive – Upstream Microbial
Job 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 Expectations 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 ensure safe operations and compliance to the company’s integrity & quality standards
- Driving a corporate culture that promotes an 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 objective of the role is to handle Upstream Microbial activities.
Role Accountabilities:
- Must involve in each and every phase of commissioning and qualification activity
- Should perform all Upstream activities (Assembly preparation, media preparation, seed generation, fermenter operation, facility upkeep, etc.)
- Compliance with current good manufacturing practices
- Adherence to standard operating procedures, operational control procedures
- Maintenance and calibration of operations, equipment in coordination with the maintenance department
- Monitoring of process efficiencies
- Reporting of non-conformities and implementation of corrective/preventive actions in specific areas of operation
- Preparation, review and revision of SOPs/EOPs/IOPs
- Preparation, revision, and review of batch manufacturing records
- Preparation of general validation protocols and report, performance qualification documents
- Review of quality department protocols related to operations
- Involving in Deviations and change controls from operations to QA
- Investigation of batch failures in operations
- Handling of CAPA, change controls, and deviations
Education and Experience:
M.Sc with 1 to 3 years of relevant experience
[ad_2]