Lead Downstream Development
Job Summary
JOB DESCRIPTION
Job Title: Lead Downstream Process Development
Job Location: Bangalore
Department: Biopharmaceutical Development
About Syngene: Syngene () 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 reporting in.
- Contributing to development of procedures practices and systems that ensures safe operations and compliance to companys integrity & quality standards.
- Driving a corporate culture that promotes environment health and safety (EHS) mindset and operational discipline at the workplace always.
- Ensuring safety of self teams and labs by adhering to safety protocols and following environment health and safety (EHS) requirements always 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.
- Always Comply to Syngenes quality standards.
- Hold self and their teams accountable for the achievement of safety goals.
- Govern and Review safety metrics from time to time.
Syngene Values
All employees will consistently demonstrate alignment with our core values
- Excellence
- Integrity
- Professionalism
Experience
- Good experience to lead downstream process development specifically with monoclonal antibody purification
Skills and Capabilities
- Working knowledge of downstream purification principles is essential for this role.
- Proficient in operation maintenance of downstream process equipment like AKTA Pure AKTA Pilot TFF systems column packing buffer preparation and inventory management.
- Execution of laboratory experiments and documenting them in detail as per Good Documentation Practices
- Compilation of data Interpretation and preparation of development report TTD BPR SOP EOP IOP and technical presentations.
- Preparation of draft experimental protocol and getting it reviewed by the team lead.
- Experience in scale-up and tech transfer is preferable
- Knowledge on Process characterization control strategy and PPQ batch is preferable not mandatory.
- Experience in using electronic lab notebook Electronic Database Management System (EDMS) TrackWise is preferable not mandatory.
Education
- Masters degree (M. Tech/) in Life Science Chemical Engineering Biotechnology or related field.
Equal Opportunity Employer:
It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age color national origin citizenship status physical or mental disability race religion creed gender sex sexual orientation gender identity and/or expression genetic information marital status status with regard to public assistance veteran status or any other characteristic protected by applicable legislation or local addition Syngene will provide reasonable accommodations for qualified individuals with disabilities.
About Company
We are an innovation-led contract research, development and manufacturing organization offering end-to-end solutions to fulfil R&D and manufacturing requirements of our clients