Manufacturing Technician 4 - Rotating Shift at Millipore S.A.S.

St. Louis, Missouri, United States -

Full Time

Start Date

Immediate

Expiry Date

04 Jan, 26

Salary

41.0

Posted On

06 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing, Quality Control, cGMP, Safety Compliance, Process Improvement, Buffer Formulation, Chromatography, Ultrafiltration, Equipment Maintenance, Training, Documentation, Good Distribution Practices, Mechanical Aptitude, Regulatory Standards, Team Collaboration, Problem Solving

Industry

Biotechnology Research

Description

Work Location: St. Louis, Missouri Shift: Department: LS-SC-POKMC3 ADC & BioCon 1 Recruiter: Erin Wilson This information is for internals only. Please do not share outside of the organization. Your Role: Join our St. Louis Cherokee facility at MilliporeSigma, a leading contract development and manufacturing organization (CDMO) and a recognized Center of Excellence for antibody-drug conjugate (ADC) manufacturing. We are seeking passionate and enthusiastic professionals to contribute to our innovative bioconjugate production, leveraging over 35 years of expertise in the field. As a vital part of our dedicated team, you will play a key role in delivering high-quality ADCs that improve the quality of life for patients suffering from cancer and other debilitating diseases. With our state-of-the-art technologies and commitment to excellence, you will ensure the highest standards of quality and compliance in our ADC manufacturing processes. As a Manufacturing Technician 4 – Rotating Shift, you will be expected to safely execute tasks, develop new approaches, and perform support operations in a cGMP regulated environment for the support of API (Active Pharmaceutical Ingredients) manufacturing teams, including maintaining equipment, preparation of solutions, staging of equipment and supplies, and other various manufacturing support activities. Job duties include: 12 hour rotating Day (6:00am - 6:30pm)/ Night (6:00pm - 6:30am) shifts including a 20% shift differential Prepare buffer formulations for Drug Substance manufacturing, ensuring safety and quality, while maintaining cleanliness in the manufacturing area. Perform routine processes, including buffer formulation, ultrafiltration, and chromatography. Maintain equipment, prepare reagents, and stock materials. Clean production equipment and spaces used in the manufacturing process. Execute daily tasks following cGMPs and quality-approved procedures, documenting all activities in compliance with GDP standards. Dispose of cleaning and process waste safely, maintain supply stock levels using the Kanban system. Ensure compliance with Safety and Quality guidelines by adhering to procedures, conducting safety inspections, performing preventive maintenance, and assisting with quality deviations. Support departmental operations by training new employees, assisting with daily functions, and contributing to process improvement, safety, quality, and 6S initiatives in collaboration with the department supervisor. Physical Attributes: Stand for extended periods of time. Lift, push, and or pull up to 50lbs. Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment. Who you are: Minimum Qualifications: Associate Degree in Biology, Chemistry, or other life science discipline OR High school diploma or GED. 1 + years’ experience in a pharmaceutical GMP operations environment (Manufacturing, Quality, MSAT, Buffers). Preferred Qualifications: Experience with Antibody Drug Conjugates (ADCs), including knowledge of their formulation and manufacturing processes. Prior experience in an API manufacturing environment. Strong mechanical aptitude. Experience in Good Distribution Practices (GDP) Demonstrated process improvement experience. Familiarity with FDA, EMA, and other regulatory standards. Demonstrated knowledge and experience in various computer skills, including Windows (Word, Excel, PowerPoint, etc.) RSREMD Pay Range for this position: $24.00 - $41.00. 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

As a Manufacturing Technician 4, you will execute tasks and support operations in a cGMP regulated environment for API manufacturing. You will ensure compliance with safety and quality guidelines while maintaining equipment and preparing solutions.