DSP-Jr. Manager

Date: 24 Sept 2025

Location:

Bangalore, KA, IN, 560099

Division: Manufacturing Services

Designation: Jr. Manager

Job Location: Bangalore

Reporting To
Job Grade: Jr. Manager

The Company

Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene's 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA.

Key Result Areas

Role-specific

• Maintain good aseptic behaviour inside Biologics operations facility.
• Perform all the Downstream activities like Assembly preparation, accessories arrangement for step, Dispensing of raw materials and consumables, Reconciliation of excess and unused raw materials and consumables Buffer Preparation, Harvest Clarification, Chromatography operation, Low pH and Intermediate depth filtration, Viral filtration, TFF Operation and 0.2 µ filtration.
• Operating and cleaning of downstream equipment(s) as per standard operating procedures and EOP.
• Monitoring and process control of the specific Operations of the Downstream.
• Maintenance of Quality records.
• Perform In-process product sampling, sample submission and storage.
• Preparation and review of operation related documents.
• Perform room owner responsibility for the assigned DSP area.
• Perform equipment/instrument ownership related responsibilities related to DSP.
• Initiate Complaint Slips (work orders) for DSP related areas and equipment.
• Coordinate with QA for line clearance.
• Maintaining process area All-time ready for Inspection/ audit purpose.
• Maintain facility and assigned zone all-time ready for visit and audit.
• Involve and support in execution of batches as and when required and perform error free operation as per Batch Manufacturing Record (BMR).
• Involve in shipment of samples / final product as per packing and dispatch record.
• Work proactively to meet all document(s) on time closure requirement.
• Preparation of general Downstream related procedures, protocols, risk assessment and BMRs.
• Execute the protocols related to Downstream related activity and equipment / instrument qualification.
• Involve in Shipment of samples /final product as per packing and dispatch record.
• Preparation and periodic revision of equipment cleaning checklist (ECC)as ad when required.
• Execute the batch activity as per BMR and report nonconformity to the supervisor.
• Review of executed Documents on time.
• Issuance of annexures, RM, consumables and BMRs.
• Track the work order status and ensuring timely closure.
• Involve in upstream related activities under supervision of upstream supervisor.
• Responsible & accountable towards safety & compliance in all the work activities in the own responsibility area(s).
• Monitor & confirm that the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment are followed by self & direct reports.
• Monitor & confirm that self & direct reports adhere to the highest standards of quality, integrity & compliance for every work activity.
• Complete the assigned trainings in a timely manner and comply with the training procedure & training calendar and monitor & confirm the same for the direct reports.
• Attend all assigned mandatory trainings related to data integrity, health and safety measures, and monitor & confirm the same for the direct reports.
• Participate in & support the trainings on procedures, protocols and On-the-Job activities.
• Compliance to Current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP).
• Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s).
• Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls.
• Preparation, revision and review of Batch Manufacturing Records (BMR), Packing and Dispatch Record (PDR).
• Issue, Checking and Review of Operations documents.
• Preparation and review of Batch Manufacturing Records, SOPs, PDRs & Protocols.
• Conduct training for all DSP employees for prepared BMRs, PDRs and related documents.
• Review of TTD's, protocol and Quality Department Protocols related to Operations.
• Investigation of Batch failures in Operations.
• Monitor and follow good aseptic behavior inside BMP1 DSP Facility.
• Support in hiring process and bringing quality workforce to develop a team that is highly respected and engaged towards departmental goals.
• Update the batch progress in PRM's and participate in client discussions.
• Develop and implement operating methods and procedures designed to eliminate operating problems and improve manufacturing efficiency.

Education and Experience

Education
Master's degree/ bachelor's degree in pharmacy, Master's degree in Pharmaceutical Sciences.

Industry Experience
Minimum 6-8 years of relevant practical experience in mAbs downstream process.

Other Competencies Required For The Role

• Follow the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment and adhere to the highest standards of quality, integrity & compliance for every work activity.
• Complete the assigned trainings in a timely manner and comply with the training procedure & training calendar.
• Attend all assigned mandatory trainings related to data integrity, health, and safety measures.
• Compliance to Current Good Manufacturing Practices and Good Documentation Practices.
• Adherence to Standard Operating procedures, Operational control Procedures.
• Participate in & support the trainings on procedures, protocols, and On-the-Job activities.
• Follow the discipline of reporting structure at times of escalation.
• Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s).
• Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls.

Safety And DI Responsibilities

• Adhere to organizational policies & procedures on EHSS, POSH, Data Integrity and IT security.
• Always wear the applicable PPEs and adhere to any other Environment, Health, and Safety (EHS) requirements in the workplace for individuals & lab/plant safety.
• Understand all necessary safety protocols and always follow the same to ensure safety for all.
• Proactively identify near-misses & potential incidents and communicate to supervisor and/or line manager or through the respective web portals.

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.

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