Senior Laboratory Analyst I (Bio)

Allergan; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading company in the pharmaceutical industry is seeking a Quality Control Analyst. The role involves providing comprehensive testing services in compliance with GMP standards. Candidates should have a strong background in QC laboratories, excellent problem-solving abilities, and the capacity to mentor colleagues. This position offers the opportunity for professional growth in an innovative environment dedicated to quality and integrity.

Qualifications

• Requires at least 5 years of experience in a QC Lab.
• 1-3 years experience in pharmaceutical manufacturing is essential.
• Candidates should have a strong GMP background.

Responsibilities

• Responsible for testing of raw materials and final products.
• Maintain and verify laboratory records and equipment.
• Lead laboratory investigations and support method validations.

Skills

GMP knowledge

Analytical skills

Problem-solving

Interpersonal skills

Communication skills

Education

Bachelor of Science in Biology, Chemistry, Biochemistry or related field

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

Purpose:

The primary function is to support the Quality Control Laboratories with independent, effective and timely testing services and able to ensure that tasks are performed according to requirements with review/verification of results and problem solving for issues identified.

Major Responsibilities:

• Responsible for the timely completion and data verification of all testing of raw material, intermediates, in-process control samples and final product
• Maintain up-to-date, complete and precise records of all tests performed
• Ensure that all test equipment is used and maintained properly in GMP environment
• Acts as an SME for simple to complex instruments and techniques where needed
• Lead and perform any method transfer or method validation protocols or equipment qualifications and support the transfer of new products
• Understands, implements and maintains cGMP and 6S concept
• Able to present clearly and lead confidently during audits and site leadership inquiries
• Write/revises procedures as necessary and make recommendations for process improvement
• Effectively perform a multitude of laboratory techniques for which they are trained on with minimal error
• Trains new analysts and technicians on all instruments/techniques, as well as routinely reviewing that all API lab personnel are adhering to proper GMP standards
• Responsible for assisting the lab supervisor in following up with corrective actions
• Responsible for ownership of laboratory investigation - Able to lead the whole laboratory investigation and work alongside with QA for success closure of investigation
• Participate in tier meeting for manufacturing updates on incoming raw materials/in-process samples and final API
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements by driving all EHS standards, procedures and policies

Qualifications

• Bachelor of Science majoring in Biology, Chemistry, Biochemistry or related scientific degree
• At least 5 years of experience in a QC Lab
• At least 1-3 years of experience in a pharmaceutical manufacturing environment
• Strong GMP background and proficient with using laboratory equipment
• Highly motivated, independent and able to work under pressure
• Possess good interpersonal and communication skills
• Strong analytical, problem solving and writing skills
• Team motivator – able to motivate and be role model for less experienced peers
• Total commitment to quality and maintaining a high standard of work at all times

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html