Demo

Quality Control Senior Associate

Actalent
West Greenwich, RI Other
POSTED ON 2/12/2024 CLOSED ON 2/25/2024

What are the responsibilities and job description for the Quality Control Senior Associate position at Actalent?

Top Skills Details:

1. Able to work in teams and follow guidelines and procedures

2. General Chemistry knowledge

3. ELISA (testing platform) experience, general knowledge

4.. Proper Time Management skills and neat and organized worker

Description:

Quality Control Bioanalytic lab is searching is for an team member to support testing for routine, in-process, and stability samples. This person will be responsible for working in the Quality Control laboratory, using GMPs and GDPs to execute analytical testing.

The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.

Responsibilities will include, but are not limited to:

•Prepare reagents

•Performing analytical testing for general chemistry analisis (Ex.pH, Osmo, UV) and other testing such as ELISA.

•Housekeeping and landlording tasks to maintain laboratory in Inspection Ready state

•Interacting cross-functionally with a wide variety of people and teams;

•Troubleshoot, solve problems and communicate with stakeholders.

•Participate in initiatives and projects that may be departmental or organizational in scope.

•Evaluate lab practices for compliance and operational excellence on a continuous basis.

Additional Skills & Qualifications:

-High school/GED 4 years OR k experience OR Associate 2 years' work experience OR Bachelor 6 months' work experience OR Masters with no experience.

•experience in general chemistry, ELISA and/or quality control setting

•Bachelors Degree in any science field, preferred

•Demonstrated experience in investigations and QC processes

•Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision

•Strong communication skills (both written and oral), facilitation and presentation skills

•Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories, preferably with GMP experience

••Understanding of biopharmaceuticals process and related unit operations

•Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy

•Independent, self-motivated, organized, able to multi-task in time-sensitive environments.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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