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Sr QC Technician

Pharmaceutical Product Development (PPD)

Bangalore, Karnataka, India

Job Description

Job Description

We are seeking a highly skilled and meticulous professional to join as Sr. QC Technician. When you’re part of the team at Thermo Fisher Scientific, you will be surrounded by collaborative colleagues where you’ll discover meaningful work with equal opportunities that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day!

This position will be responsible for ensuring our products meet the highest quality and reliability standards. This position necessitates a keen attention to detail, problem-solving skills, and an understanding of processes and methodologies. This position is expected to collaborate and work in partnership to implement quality control measures, identify scope for improvement and implement initiatives throughout the organization.

About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our distributed team of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.

Responsibilities:

·Perform the analytical tests on the samples as per the defined specification & procedures and analyze the test results for lot disposition.

·Plan & complete the assays within the agreed turnaround time

·Maintain comprehensive documentation of quality control records, processes, and outcomes.

·Participate to identify potential quality issues, root cause analysis investigations to identify product / process failures and implement effective solutions and improvement.

·Own the responsibility of workspace safety & quality requirements.

·Maintain track of and assistance with inventory management for antigens, lysates, retains, etc to ensure timely assay completion in QC.

·Collaborate & work in team with high integrity.

·Assist in establishing Standard Operating Procedures (SOP). Assist in routine maintenance of SOPs, including periodic reviews.

Qualifications:

·Master`s degree in a life science or related fields with 1- 2 years of relevant industrial experience

·Familiarity with quality compliance standards

·Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Monitors own work to ensure quality

·Exhibits sound and accurate judgment

·Demonstrates persistence and overcomes obstacles

·Process oriented, responds to management direction; Takes ownership for own actions; Keeps commitments; Completes tasks on time

·Attention to detail and a dedication to delivering high-quality results

·Strong communication expertise (written & verbal).

·Ability to work independently and in partnership in a fast-paced and dynamic environment.

·Strong organizational and time management skills to prioritize and complete tasks.

Job posted: 2024-03-18

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