Associate Quality Scientist at Millipore S.A.S.

St. Louis, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

11 Jan, 26

Salary

42.0

Posted On

13 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Control, GMP, Laboratory Techniques, Document Management, Method Development, Validation, Process Improvement, Communication, Time Management, Safety Practices, Deviation Investigations, Auditing, Testing, Microsoft Word, Microsoft Excel, Microsoft Access

Industry

Biotechnology Research

Description

Work Location: St. Louis, Missouri Shift: Department: LS-SC-POKQD2 Cherokee QC Microbiology Group 2 Recruiter: Guadalupe Barragan Hiring Manager: Chad Clutes This information is for internals only. Please do not share outside of the organization. Your Role: At MilliporeSigma, the Associate Quality Scientist will perform Quality Control activities in support of release of cGMP products, including routine testing (in-house and compendial). Perform routine testing and peer review of release samples through adherence to applicable GMP requirements. Utilize written procedures to perform routine and non-routine product testing. Revise procedures through use of the Document Management System (DMS) following Good Documentation Practices (GDP). Work in accordance with current GMPs and demonstrate proper laboratory safety and housekeeping practices. Participate in method development and validation activities to support product testing. Contribute to support function of the laboratory through participation in laboratory audits to maintain compliance. Participate in deviation investigations. Contribute to process improvement projects. Physical Attributes: Wear personal protective equipment including but not limited to: safety glasses, gloves and respirator. Who You Are Minimum Qualifications: Bachelor's Degree in Chemistry, Chemical Engineering, or other Life Sciences discipline 1+ years of GMP laboratory experience Preferred Qualifications: General laboratory techniques (theory and practice). Experience with various laboratory equipment. Working Knowledge of Good Manufacturing Practices for pharmaceutical manufacturing (21 CFR 210 & 211 and/or ICH Q7A). Knowledge of Microsoft Word, Excel and Access. Strong time management, verbal and written communication skills. Pay Range for this position: $23.00-$42.00 per hour. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Responsibilities

The Associate Quality Scientist will perform Quality Control activities in support of the release of cGMP products, including routine testing and peer review of release samples. The role involves participating in method development, validation activities, and contributing to laboratory audits and process improvement projects.