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Manufacturing Operator

Company: Thermo Fisher Scientific
Location: Bend
Posted on: February 13, 2019

Job Description:

With 70,000 extraordinary minds on our global team, each one of us at Thermo Fisher has an important story to tell. Whether we---re helping customers to fight disease, making sure our air is clean, or solving cold cases, our stories involve thousands of important projects that improve millions of lives. Our dedicated sales professionals are laser focused on delivering our customer value proposition---accelerating innovation and enhancing productivity. With talented managers and inspiring coworkers to support you, you---ll find the resources and opportunities to make significant contributions to the world.

Performs current Good Manufacturing Practices (cGMP) production of pharmaceutical Spray Dried Intermediates (SDI) and Solid Dosage Forms (tablets, capsules, granules). Executes process documentation in a fast-paced manufacturing environment.Essential Functions:Maintains cleanliness and safety required of equipment, work areas, and facility with assistance of assigned personnel. Prepares manufacturing suites and components for Production Batch Record execution. Executes Production Batch Records. Keeps proper Personal Protective Equipment (PPE) and gowning materials supplied in gowning suite. Maintains cGMP materials inventory according to applicable Standard Operating Procedures (SOP---s). Complies with established waste disposal operations. Cleans and visually inspects the processing equipment, tools, and utensils for cleanliness per the appropriate SOP and documents those activities. Monitor manufacturing operations including all procedures, batch records, and components, to see that cGMP requirements are met. Train personnel in manufacturing techniques and other support aspects of Manufacturing. Document manufacturing technician training. Support all aspects of manufacturing and help ensure personnel are following SOPs. Review Master Batch Records. Review Production Batch Records and all other documentation prior to submitting to QA. Performs other Manufacturing operator responsibilities as necessary.Education:Bachelor---s degree and/or military experience preferred; HS degree required.Experience:Three-Five (3-5) years of production experience in the pharmaceutical industry preferred.Equivalency:Equivalent combinations of education, training, and relevant work experience may be considered.Competencies:Good knowledge of current Good Manufacturing Practices (cGMP) and experience with cGMP documentation, spreadsheets and software applications preferred. Pharma or biotech experience highly preferred. Proven track record of producing an excellent work product with a high degree of accuracy. Ability to multi-task and handle shifting priorities in a fast-paced manufacturing environment. Strong proficiency in Microsoft Office Suite (Word and Excel). Effective written and interpersonal skills.Physical Requirements:Work setting: Production of pharmaceutical dosage forms in a small-scale manufacturing suite setting. Position requires frequent standing (up to 8 hours) as well as ordinary ambulatory skills and physical coordination sufficient to move about office, laboratory & manufacturing locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of medium to heavy weights of 35-50 pounds; arm, hand and finger dexterity, including ability to grasp and move for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate laboratory equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.Disclaimer:This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.Nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.Please take note that we require a negative drug screen, administered by our third-party vendor, as a condition of employment.

If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here for further assistance.

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.

Keywords: Thermo Fisher Scientific, Bend , Manufacturing Operator, Other , Bend, Oregon

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