MSc Jobs at Thermo Fisher – Life Sciences Apply Online For Production Lead Role
MSc Jobs at Thermo Fisher – Life Sciences Apply Online For Production Lead RoleProduction Lead at Thermo Fisher. Latest MSc Life Sciences Jobs. Biotechnology and Microbiology Jobs. Interested candidates can check the details below and apply online.
Job role: Production Lead at GTS Manufacturing Facility, Invitrogen BioServices India Pvt Ltd
Job ID: R-01187812
Job Location: Bangalore, Karnataka, India
Category: Operations
Job Type: Full time
About Company:
Thermo Fisher Scientific Inc. is the world leader in serving science, with revenues of more than $40 billion and approximately 70,000 employees globally. Our Mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity.
Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services – we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive services.
About Team:
Candidate will be working in GTS Manufacturing Facility, Thermo fisher Scientific, The Manufacturing Team is a strong team with 7 people, and we deliver superior quality Invitro
diagnostic products to our Indian and Southeast Asian customers/market. The team is involved in the production of covid related kit and other qPCR-based detection kits.Roles and Responsibilities for Production Lead at Thermo Fisher:
Thermo Fisher Scientific is recruiting a Production Lead who will be responsible for supervising all manufacturing and workforce performance, ensuring efficiency and timeliness. An exciting opportunity to join the Manufacturing team and the responsibilities would include.
- Lead the production team in manufacturing of the products as per ISO13485 standards and MDR2017 rules.
- In charge of the planning and execution of the semifinished goods /Finished Goods of IVD and RUO products manufactured at the site
- Should find efficient/optimal ways to use all resources: machines/tools, materials, and production executives, to ensure on-time delivery of products, and enhance manufacturing throughput.
- Lead all aspects of the day-to-day production activity. Responsible for productivity, quality, on-time delivery along with the team, and continual improvement
- Production capacity planning and identifying and calling out the bottleneck to obtain Optimal process flow.
- Interviews/Recruiting of the team members. Review performance of manufacturing supervisors and production executives
- Training of the production executives on manufacturing process and changes implemented as per ISO and GMP guidelines.
- Ensure execution of the planning, validation of new products or process as assigned to production function.
- Lead investigations to determine root cause of quality issues in manufacturing, customer complaints, and customer returns. Work closely with the Quality, IPQA and QA team to implement corrective and preventive actions.
- Initiate and Document change control (write, review and revise) in manufacturing processes ie DHR procedures, work instructions, visual aids, etc.
- Review Batch records/ DHR, ERP system – E1 entries and documents prepared by the production team
- Assist in performing periodic cycle counts on the manufacturing shop floor and reconciliation with the ERP system (E1). Monitor stock of RM finished goods at the shop floor and critical safety stock of RM.
- Support the New project introduction with the assigned tasks.
- On time submission of the production activity, its data trending, monthly review meeting and Production critical metric
- Support to internal and external audit as planned.
Candidate Requirement:
Education & Experience levels:
- Applicants should have a background in Biological /Chemical sciences, Master’s degree in microbiology/Biotechnology or related Life Science or ‘B/,BTech ,MTech in Chemical or Mechanical Engineering. Have a minimum 3-to-5-year experience
Nature of experience and Skills:
- Should have a clear understanding of manufacturing process in IVD industry.
- Previous experience in healthcare manufacturing environment would be highly suitable.
- Experience in handling Chemicals, microbes, molecular biology, qRT-PCR will be an added advantage.
- Organizational skills with attention to detail are critical.
- Candidates with strong communication skills, both oral and in scientific writing is preferred.
- Ability to apply Statistical Process Control (SPC) techniques.
- Experience with Enterprise Resource Planning (ERP) costs and how to influence them.
- An understanding of Corrective and Preventative Action (CAPA) and Change Control principles with the ability to process records within the respective databases/systems.
- The capability to contribute to and perform Risk Assessments, Risk Management/Control exercises, and Failure Mode Effect Analyses (FMEA)
- An understanding of Process Validation principles and procedures with the ability to implement.
- Candidate should be a good great teammate, ready to learn new techniques, an innovative,and problem solver
At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Apply today!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, colour, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Here are few interview questions with answers for the role of Production Lead at Thermo Fisher:
1.Can you describe your experience in managing manufacturing teams and ensuring compliance with quality standards in a healthcare manufacturing environment?
Answer: In my previous role as a Production Supervisor at XYZ Healthcare Manufacturing, I led a team responsible for producing medical diagnostic devices. I enforced strict adherence to ISO13485 standards and FDA regulations, ensuring our products met the highest quality standards. My experience involved managing the production schedule, conducting quality checks, and implementing corrective actions when needed. I believe my background in healthcare manufacturing has prepared me to excel in a similar role at Thermo Fisher Scientific.
2.How do you prioritize resources and address bottlenecks to optimize production efficiency?
Answer: To optimize production efficiency, I start by closely monitoring our manufacturing processes. I prioritize resources based on production schedules and critical demands. When bottlenecks occur, I collaborate with cross-functional teams to identify root causes and implement corrective measures swiftly. My goal is to ensure a smooth and efficient production flow, minimizing downtime and maximizing output.
3.Can you provide an example of a challenging quality issue you’ve encountered in manufacturing and how you resolved it?
Answer: In my previous role, we faced a recurring quality issue related to a specific component in our medical devices. I initiated a thorough investigation, involving the quality assurance team and production staff. We conducted root cause analysis and identified a supplier-related problem. I worked closely with the supplier to implement corrective actions, which included improved quality checks and supplier training. This resulted in a significant reduction in defects and customer complaints, showcasing my ability to tackle complex quality issues effectively.
4.How do you stay updated with industry standards and best practices in manufacturing, especially in the field of in-vitro diagnostics?
Answer: Staying current with industry standards and best practices is crucial. I regularly attend industry conferences and webinars, where I learn about the latest trends and regulations. Additionally, I am an active member of professional organizations related to in-vitro diagnostics, allowing me to network with experts and access valuable resources. By staying informed and continuously learning, I ensure that our manufacturing processes align with the most up-to-date industry standards.
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