Walk-in | Upstream manufacturing process team member

Syngene; Bengaluru; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Syngene, a leading biopharmaceutical CRO in Bengaluru, seeks a skilled professional for upstream manufacturing focused on monoclonal antibody purification using CHO-based mammalian systems. The role requires hands-on GMP knowledge and ability to ensure equipment qualification and batch records are upheld.

You will work within a cGMP environment, coordinating with QA, QC and EHS while maintaining strict documentation and data integrity throughout manufacturing operations.

Qualifications

• Relevant practical experience in upstream manufacturing, especially antibody purification.
• Need hands-on experience with CHO-based mammalian systems and purification workflows.
• Experience with equipment qualification and GMP documentation.
• Knowledge of GMP controls and regulatory requirements.
• Experience with risk assessment tools and change management.

Responsibilities

• Perform upstream manufacturing activities with focus on monoclonal antibody purification.
• Ensure process equipment is qualified and batch records are accurately maintained.
• Adhere to cGMP guidelines and safety protocols.
• Coordinate with QA/QC/EHS during manufacturing and documentation.
• Maintain accurate on-line documentation and data integrity.

Skills

Upstream ops

CHO-based systems

Mab purification

GMP awareness

Risk assessment

Equipment qualification

Change management

Education

Masters in Life Science

Microbiology

Biotechnology

Chemical Engineering

Tools

QA documentation

Regulatory compliance

Job description

Department: Biopharmaceutical Operations

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

• Active involvement in all upstream manufacturing activities.
• Perform error free operation by eliminating operational gaps in advance.
• Active trouble shooting to minimize the various risks prior to execution and during execution.
• Initiate and process upstream deviations /investigations and closure.
• Pre -execution activity: Area and equipment readiness.
• Issuance of raw material /consumables and issuance batch records.
• Upstream process execution: Batch process operation /unit operation (including CIP, SIP and preparation upstream accessories), close monitoring of batch performance and data.
• Follow and practice on-line documentation all the time.
• Follow cGMP practices during the manufacturing activity and operations associated activities with QA, QC and EAM.
• Attend the training session of EHS, cGMP and HRD.
• Ensure process equipment's/instruments are in Qualified in state.
• Verify PM, check the log books and ensure the clean room requirements in order to get line clearance from QA for batch execution.
• Active coordination with inter-depts. for sample submission, closure of documentation and timely execution and contribution for the assigned tasks.
• Perform on-line documentation, cGMP compliance in all the manufacturing activity, and timely closure of executed documents and batch records.
• Ensure the Quality system is followed in day today upstream operations. Identify the gaps in the system to improve.
• Active involvement in all upstream manufacturing activities.
• Perform error free operation by eliminating operational gaps in advance.
• Active trouble shooting to minimize the various risks prior to execution and during execution.
• Initiate and process upstream deviations /investigations and closure. .

Syngene Values

All employees will consistently demonstrate alignment with our core values

• Excellence
• Integrity
• Professionalism

Experience

• Relevant practical experience in upstream manufacturing process specifically with monoclonal antibody purification

Skills and Capabilities

• Expertise in Upstream unit operations (CHO based mammalian expression systems).
• Strong Hands on experience with SUB (Up to 2000 L scale)
• Exposure to handle of Bio-similar proteins and Mabs projects in cGMP area.
• Sound knowledge and awareness of GMP controls, Quality systems and regulatory aspects
• Experience on risk assessment tools and change management.
• Experience on the Equipment Qualification and commission aspects

Education

• Masters degree in Life Science, Microbiology, 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 law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.