Quality Control Technician

Bristol Myers Squibb; Summit (NJ); On-site; USD 44,000 - 51,000; Full time

Job summary

Bristol Myers Squibb in Summit, NJ is seeking a QC Analyst to support quality control bioanalytical testing for release of clinical and commercial products. You will interface with multiple groups, perform tasks independently, interpret results and troubleshoot.

The role requires a Bachelor's degree and 2-4 years in a regulated environment, with hands-on techniques such as ELISA, qPCR, and FACS. Strong technical writing, problem-solving, and cross-functional communication are essential.

Qualifications

• Bachelor's degree required, preferably in Science.
• 2-4 years of relevant work experience in a regulated environment.
• Equivalent combination of education and experience may substitute.

Responsibilities

• Perform testing of in-process, final product, and stability samples.
• Develop and interpret analytical methods and SOPs.
• Troubleshoot issues and recommend corrective actions.
• Train new analysts and assist with assay transfer.
• Review data per cGMP and release timelines.
• Collaborate with cross-functional teams to meet timelines.

Skills

Bioanalytical techniques (ELISA, qPCR,

Technical writing

Regulatory & cGMP knowledge

Cross-functional collaboration

Problem-solving mindset

Education

Bachelor's degree

Job description

Duration: 12 Months (Possibility of extension for right candidate depending on performance and budget)

Location: Summit, NJ 100% onsite

Pay rate: $32-$37.06/Hr

Description:

The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, when needed, this position will be able to assist with training and assay transfer.

Education:

• Bachelors degree required, preferably in Science.
• 2-4 years of relevant work experience, preferably in a regulated environment.
• An equivalent combination of education and experience may substitute.

Experience:

• Hands-on experience with various bioanalytical techniques including ELISA, qPCR and FACS.
• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
• Technical writing skills.
• Problem-solving ability/mentality, technically adept and logical.
• Ability to represent the interests of the group on cross-functional teams.
• Ability to set priorities of the group and manage timelines.
• Ability to work with management locally and globally.
• Ability to communicate effectively with peers, department management and cross-functional peers.

DUTIES AND RESPONSIBILITIES

• Perform testing of in-process, final product, and stability samples.
• Utilize scientific principles to assist in analytical testing methods and the proper use of laboratory equipment.
• Anticipate and troubleshoot problems.
• Recommend corrective actions and participate in the development of best practices.
• Understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents.
• Complete all work in a timely manner.
• Work and communicate effectively within the team to ensure timelines are met.
• Perform peer review of testing data.
• Review all data in accordance with applicable procedures and cGMP requirements.
• Apply technical knowledge and abilities to ensure all testing is performed in a compliant manner.
• Complete all review in accordance with required release timelines.
• Communicate effectively with peers, and demonstrate teamwork, with regards to results of review and corrections required.
• Train new analysts to general job duties.
• Complete necessary training to become a qualified trainer.
• Perform training effectively.
• Document training per procedural and cGMP requirements.
• Perform assigned tasks within a CAPA, deviation, or project.
• Draft and review technical documents, such as SOPs and protocols/reports.
• Communicate effectively with management regarding task completion, roadblocks, and needs.
• Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.
• Performs other tasks as assigned.

WORKING CONDITIONS (US Only):

• The incumbent should be able to distinguish colors and possess correctable vision to 20/20, annual eye exam is required.
• The incumbent must analyze numerical values on a daily basis.
• The incumbent will be working a laboratory setting up to six (6) hours per day.
• The incumbent will be working around biohazardous materials, including chemical agents, up to six (6) hours per day.
• This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.
• This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.