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Manufacturing Associate II

Job ID 1602833 Date posted12/13/2016 LocationBrooklyn Park, Minnesota, United States;
More than 30,000 Takeda employees working in more than 70 countries are committed to improving quality of life for patients, who remain at the center of everything we do. Takeda Pharmaceutical Company Limited is a global, research and development-driven organization working internally and with external partners to translate science into life-changing medicines. Takeda focuses on the core therapeutic areas of oncology, gastroenterology, central nervous system and providing vaccines that address the most important infectious diseases. Novel products, especially in oncology and gastroenterology, as well as our presence in emerging markets, fuel our growth.
While Takeda is enjoying tremendous growth as an emerging global leader in the pharmaceutical industry, we remain ever mindful of our commitment to serve people worldwide by striving toward better health through leading innovation in medicine. In short, we are a passionate team doing important work that impacts patients’ lives. If you are driven to create better health and a brighter future, join us!

OBJECTIVES:

The Manufacturing Associate II performs and documents cGMP activities to support upstream and downstream production areas and operations . This  involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed.
He or she may be responsible for training less experienced or new manufacturing associates.
He or she may be responsible for supporting deviation investigations and may participates in cross functional projects teams, may support technical transfers  with relevant teams/individuals and is involved in other assignments as directed.

ACCOUNTABILITIES:

  • Performs Processing Steps and/or Manufacturing Support activities, monitoring process against the batch record, SLR and control system.
  • Documents/Records cGMP data and information for processing steps and/or equipment activities, following standard operating procedures. Key documentation includes batch records, SLRs, and equipment logbooks.
  • Completes /reviews validation protocols, deviation reports, change controls  in accordance with cGMP’s
  • Performs the weighing, dispensing of raw materials for media and buffers
  • Performs the preparation of small and large volume media and buffer solutions, filtration and transfer of product
  • Operates bench top equipment including pH, conductivity, osmo meters, pumps, tubing welders , filter integrity testers etc.
  • Dispensing, labeling, transfer/staging of raw materials and parts
  • Assembly/disassembly, cleaning and sterilization of components, parts and equipment
  • Maintaining equipment, area and cleaning logbooks
  • Cleaning sanitizing production rooms and equipment,
  • Stocking production and cleaning supplies
  • Author/ review/improve SOP’s, batch records, protocols and technical reports
  • Actively participates in training activities, managing their individual training plan.
  • Utilizes Manufacturing knowledge to train others, improve process operations and affect positive change and demonstrates ability to troubleshoot basic mechanical operations.
  • Proficient and knowledgeable in the operation and basic to moderate troubleshooting of at least two manufacturing areas.

Qualifications

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

Knowledge, competencies and skills:

  • Advanced knowledge of current Good Manufacturing Practices (cGMP’s). Working knowledge of all relevant safety procedures  within the company. General understanding of most areas in Manufacturing and supporting functional groups.
  • Experience with cGMP Biotech or Pharmaceutical operations
  • cGMP: Understands cGMP requirements and follows those requirements, including requirements for good documentation practices.
  • Must be team-oriented (proactively builds healthy working relationships between peers, their department and other groups).
  • Possess excellent written and oral communication skills.
  • Possesses advanced knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management.
  • Possesses advanced understanding of the scientific theory of biologics manufacturing:
  • understands biotechnology processing - purpose of major unit operations and microbial control concepts
  • Actively pursues learning of required skills, new skills, and new equipment
  • Understand routine procedures upon which they have been trained.
  • Possesses advanced equipment understanding, including understanding equipment function and application.
  • Proficient and knowledgeable in the operation and basic to moderate troubleshooting of at least two manufacturing area
  • Ability to train less experienced or new manufacturing associates.
  • Proficient in MS Office and related PC skills
  • Must have the ability to work either Day or Night shift.
Education:
  • Bachelor’s Degree (BS/BA) from an accredited college or university with an emphasis in a scientific or engineering discipline and a minimum of 1-2 years relevant experience, or Associate’s Degree in a scientific or engineering discipline with a minimum of 2-4 years related experience, or High School Diploma with a minimum of 2-6 years relevant experience.

PHYSICAL DEMANDS:

  • Is required to stand, operate manufacturing equipment, computer equipment; and is required to wear personal protective equipment (PPE) such as safety shoes, safety glasses and/or hearing protection.
  • May be required occasionally to lift, push, or pull up to 50 pounds during handling of production equipment and/or materials.
  • May be required to climb occasionally (use of stepladders/stairs in production areas, or stairwells in work campus).
  • May be required to bend, kneel, or crawl rarely when troubleshooting production equipment.
  • May be required to stand and walk frequently and/or for extended periods while overseeing production activities.
  • May be required to drive rarely to attend offsite meetings and/or training.
  • May be required to use hearing occasionally when listening for production and equipment alarms.
  • Occasional movement of head/neck while using computer applications and handling of production equipment and materials.
  • May be required to perform visual inspection of production equipment, materials, and activities.
  • May be required to perform occasional overhead reaching during handling of production materials/files/supplies.
TRAVEL REQUIREMENTS:
  • On rare occasions, travel may be required to offsite meetings or training event

we are driven to improve people's lives

www.takedajobs.com

Takeda is an EEO employer of minorities, women, disabled, protected veterans. For more information, visithttp://www.takeda.us/careers/EEO_Policy_Statement.aspx

No Phone Calls or Recruiters Please.

*LI-MJ1-USA


Schedule
Full-time