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Job Description

Manufacturing Coordinator 1

When you join us at Thermo Fisher Scientific, you’ll be part of an inquisitive team that shares your passion for exploration and discovery. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and chances to create significant contributions to the world.

Location/Division Specific Information

St. Louis, MO / Drug Substance Division - The Drug Substance Division is one of the five divisions that make up the Pharma Services Group. We specialize in both small and large molecule development and commercial drug substance services. This allows us to serve the needs of Small/Emerging, Mid-Sized, and Large Pharma sectors globally.

Shift Information :

This opening is for 6:00AM - 6:30 PM. This is a 12 hour, rotating 2/2/3 schedule (2 days on, 2 days off, 3 days on - you will work every other weekend).

Discover Impactful Work:

The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to preparation and organization of the downstream processing manufacturing suites.

A day in the Life:

Ensure all consumables for production processes are accounted for upon delivery to stage process consumables in an organized manner for ease of use in production set-ups

Assist with obtaining and placement of raw materials and consumables at/from the wipe-down station for entrance into the suite

Collaborate with production support groups to ensure lines, kits, and assemblies are ready when needed within manufacturing and any missing components can be acquired timely.

Ensure material kits are complete and available for manufacturing use prior to set up of process step. Confirm buffers are available prior to need. Ensure buffers move to the downstream manufacturing suites so production processing is not halted and on time processing needs are met

Support ancillary tasks on the manufacturing floor such as fit and finish, material stock/supply and equipment staging.

Assist with inventory counts within the production suites and coordinates results with Inventory Leads and Procurement.

Performs or assists with investigations when discrepancies of inventory are discovered.

Assist in all manufacturing process functions, such as maintaining suite, supplies with site SOPs and policies.

Ensure tasks are completed with a method of prioritization - interpret production schedules and complete tasks accordingly.

Participate in shift exchanges, 1-1’s, meetings, attend meetings as necessary to facilitate area needs based on changes, etc. (lean activities).

Keys to Success:

Education

High school diploma or GED is required. Associates in a relevant scientific discipline preferred.

Experience

0- 3 years of experience in a related field (regulatory cleaning/manufacturing preferred)

Science experience related to pharmaceutical industry preferred but not required.

Must be a self-starter who can take general concepts and direction and produce desirable results.

Basic knowledge of GMP/GLP regulations in cGMP/cGLP manufacturing environment preferred but not required.

Knowledge, Skills, Abilities

Knowledge

Understanding ‘why’ and not just the ‘how’ of processes and practices

Knowledge of cGMP practices, aseptic techniques, or chemical concepts seen as a plus

Skills

Proficient with PCs (Personal Computers) and use of Windows applications such as MS Excel, MS .

Word and MS PPT is required.

Inventory Management – SAP experience a plus.

Time management and prioritization.

Results driven.

Abilities

Ability to read, write and speak English fluently.

Ability to understand and carry out instructions.

Good problem-solving and critical thinking skills.

Excellent organization skills.

Effective communication (written and verbal).

Ability to function in a rapidly changing environment.

Strong attention to detail and ability to adhere to standards procedures.

Ability to recognize problems developing, not just occurring

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

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