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Syngene BTech Biotech Job, MSc Biotechnology Executive Role, Apply Online. MSc, BTech Biotechnology Job in Syngene, Bangalore. Syngene is hiring Biotechnology candidates for Executive, Biopharmaceutical Operations job.
Don’t forget to check out possible interview questions for the role of Executive, Biopharmaceutical Operations at Syngene below
Designation: Executive, Biopharmaceutical Operations
Job Location: Bengaluru, India
Reporting to: Deputy Manager, Biopharmaceutical Operations
Job Grade: 9
Operating Unit : Biopharmaceutical
Department: Biopharmaceutical Operations
The Company
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development and manufacturing services company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical sectors. Syngene’s 4500+ scientists offer both skills and the 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 dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, as well as 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA.
The Role
Purpose of this role is to perform downstream manufacturing process at Syngene’s manufacturing facility for Cell culture products 100L,500L and 2KL scale respectively
Key Result Areas
Role-specific:
- Execution and Supervision of downstream manufacturing activities (Chromatography, filtration systems and preparation of downstream accessories).
- Manage the team and plan daily downstream execution activities.
- Active trouble shooting to minimize the various risks prior to execution and during execution.
- Planning of raw material /consumables management for production campaign.
- Maintenance of Operations equipment in coordination with Maintenance Department.
- Monitoring of process efficiencies.
- Reporting of non-conformities and implementation of corrective/preventive actions in specific areas of operation.
- Adherence to pollution control and safety requirements.
- Issue, Checking and Review of Operations documents.
- Meet training requirements.
- 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.
- Reporting Deviations and Change controls from Operations to QA.
- Investigation of Batch failures in Operations.
- Review of written Batch records, checklists and associated written documents in Operations.
- Preparation and review of Operations related documents.
- Process equipment commissioning & qualifications.
- Candidate should be ready to work in shifts
- Ability to work in a team and willingness to work in shifts including night shiftsPossess the knowledge and exposure to Environment, Health, Safety, and Sustainability (EHSS) practices.
- Follow Environment, Health, Safety, and Sustainability (EHSS) requirements at all times in the workplace ensuring individual and lab/plant safety.
- Attend training on Environment, Health, Safety, and Sustainability (EHSS)
Education and Experience
Education: M.Sc/B.Tech in Biotech
Experience: 1-6 years
Functional or Technical skills Required
- Expertise in downstream unit operations.
- Strong Hands on experience with Chromatography and filtration.
- Exposure to handle of recombinant proteins and biotheraputics projects in cGMP area.
- Sound knowledge and awareness of GMP controls ,Quality systems and regulatory aspects.
- Experience on the Equipment Qualification and commissioning aspects.
💡 Here are a few possible interview questions for the Syngene, Executive, Biopharmaceutical Operations job posting and their answers.
👍We hope this helps in giving you a rough idea as to how to prepare for the interview for this specific role. Good luck!
- What experience do you have with downstream unit operations, and what downstream manufacturing activities have you executed and supervised in the past? Answer: I have hands-on experience with downstream unit operations, including Chromatography and filtration. In my previous role, I have executed and supervised downstream manufacturing activities such as Chromatography, filtration systems, and downstream accessories preparation.
- What are the GMP controls and quality systems that you are familiar with, and how have you ensured compliance with these regulations in your previous roles? Answer: I have sound knowledge and awareness of GMP controls and quality systems. I have ensured compliance with these regulations by following standard operating procedures (SOPs), conducting regular training sessions for the team, conducting regular internal audits, and keeping up-to-date with the latest regulatory requirements.
- How have you managed raw material and consumables management for production campaigns in the past, and what challenges did you face during the process? Answer: In my previous roles, I have managed raw material and consumables management for production campaigns by maintaining accurate records of inventory levels, forecasting future requirements, and maintaining a close relationship with suppliers. One challenge I faced was coordinating with the procurement team to ensure timely delivery of materials, especially during times of high demand.
- How have you dealt with non-conformities and implemented corrective/preventive actions in specific areas of operation, and what was the outcome? Answer: In my previous roles, I have reported non-conformities and implemented corrective/preventive actions by investigating the root cause, identifying the corrective actions, and implementing them. I also monitored the effectiveness of the actions to ensure the non-conformity did not reoccur. The outcome was a reduction in non-conformities, which resulted in better process efficiency.
- How have you ensured adherence to pollution control and safety requirements, and what measures have you taken to prevent accidents in the workplace? Answer: I have ensured adherence to pollution control and safety requirements by conducting regular training sessions for the team, maintaining a safe work environment, and implementing strict safety protocols. To prevent accidents in the workplace, I have taken measures such as conducting regular safety audits, providing safety equipment and tools, and creating an open communication environment for reporting safety concerns.
About Syngene
Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries worldwide. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market, and lower the cost of innovation.
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 about 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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