Los Angeles Manufacturing Development Program Associate

Takeda Pharmaceutical Company Ltd Los Angeles , CA 90009

Posted 2 months ago

Summary:

The Los Angeles Manufacturing Development Program (LAMDP) is designed to attract the best talent and provide a solid career foundation that will assist the incumbents in becoming outstanding leaders. An LAMDP Associate will gain valuable experience in various manufacturing departments/ functions across the Los Angeles Site. Selecting a full-time role with a company that will invest in you is critical. That is why Takeda is an excellent choice.

LAMDP consists of (4) rotational assignments in a 24-month period through the Fractionation and Purification Manufacturing Business Units. The first 2 rotations will be on the manufacturing floor as a technician in training. The third rotation will be dedicated to working on continuous improvement initiatives/ projects. The final rotation will be in a leadership or a technical, individual contributor role. The LA Site is a 24/7 facility and the LAMDP will be required to work a variety of shifts through the program. The incumbent will be responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines, and any other related regulations, which could apply.

Expected to fully participate in both departmental projects and any other quality working team that may be acceptable. Under the general direction of the lead operator and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The incumbent shall troubleshoot existing procedures, equipment, etc.

LAMDP Associates have the opportunity to develop their skills through rigorous, hands-on experience coupled with specific technical and leadership training and mentoring. LAMDP Associates are eligible to participate in the developmental programs targeted for this level of position.

Essential Duties and Responsibilities:

LAMDP Associates can be assigned positions in various segments of our manufacturing facility in the first year, which may include:

  • Clean manufacturing and associated support areas

  • Clean equipment, which may include tanks

  • Provide critical process monitoring and trouble-shooting of minor problems, may use measuring devices to make product/process quality decisions

  • Follow departmental safety procedures, may conduct cGMP audits of department areas

  • Assist in updating SOPs

  • Maintain awareness of proper handling and removal of hazardous wastes

  • Ensure assigned projects and deliverables are completed by assigned commitment date

  • Perform the operations he/she is qualified on, which may include the following

  • Process Monitoring

  • Additions

  • Buffer/Solution make up

  • Set up and operation of various equipment

  • Centrifugation and Filter Press operations

  • Perform precipitate and paste collection from Westfalia centrifuges and filter presses

  • Perform alcohol and or buffer additions and take manual sight glass readings from stationary tanks

  • Ensure 100% compliance with established department procedures and regulations in producing high-quality therapeutic products

  • Interface with computerized (automated) manufacturing control system

  • Other duties as assigned

The second-year assignments will require focus on continuous improvement initiatives and lean manufacturing methodologies, and exploring a technical discipline or a manufacturing leadership opportunity.

Qualifications:

  • Strong influencing skills, with the ability to multi-task effectively and solve technical problems

  • Flexibility to work in assignments across functions and locations in a fast-paced environment

  • Must be able to work any shift in 24/7 environment

  • Demonstrate leadership skills to include personal accountability, quality decision making, customer focus, drive for results, integrity, and trust

  • Excellent communication and interpersonal skills

  • Strong motivation skills

  • Ability to solve technical problems

  • Must have good written and verbal communication skills and understanding of cGMP regulations

  • Proficient in a variety of mathematical disciplines and be able to work with both metric and USA standards of measurement

  • Must be able to read and follow detailed written instructions

  • May require immunization before performing work within the manufacturing area

  • Must be able to perform all three-step and five-step cleaning operations as per current equipment cleaning procedure at the plant

  • Must have good computer skills

  • Must have strong aptitude for operation and controls of manufacturing equipment and processes

Education and/or experience:

  • Candidates must already be authorized to be legally employed on an on-going basis in the United States

  • Bachelor's Degree in Engineering (Chemical, Electrical, Mechanical) or Hard Sciences (Biochemistry, Chemistry, Microbiology) required

  • Demonstrated leadership experience required

Physical Demands:

  • Must be able to lift, push, pull, and carry up to 50 lbs

  • Variety of physical demands referenced on job analysis

Working Environment:

  • Must be able to work in controlled environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body

  • No make-up, jewelry, contact lenses, nail polish, or artificial fingernails may be worn in the manufacturing environment

  • Will work in a cold, wet environment, and climb up into large processing tanks

  • Will work in a loud area that requires hearing protection and other protective equipment to be worn

  • Will work around chemicals such as alcohol, acids, buffers, and, celite that may require respiratory protection

  • Must be able to work multiple shifts, including weekends

  • Must be able to work overtime as required

  • May be required to work in a confined area

  • Some clean room and cool/hot storage conditions

Notice to Employment / Recruitment Agents:

Employment / Recruitment agents may only submit candidates for vacancies only if they have written authorization to do so from Shire, a wholly-owned subsidiary of Takeda's Talent Acquisition department. Any agency candidate submission may only be submitted to positions opened to the agency through the specific Agency Portal. Shire, a wholly-owned subsidiary of Takeda will only pay a fee for candidates submitted or presented where there is a fully executed contract in place between the Employment / Recruitment agents and Shire, a wholly-owned subsidiary of Takeda and only if the candidate is submitted via the Agency Portal. Candidates submitted or presented by Employment / Recruitment Agents without a fully executed contract or submitted through this site shall not be deemed to form part of any Engagement for which the Agency may claim remuneration.

Equal Employment Opportunity

Shire, a wholly-owned subsidiary of Takeda, is an Equal Opportunity Employer committed to a diverse workforce. Shire, a wholly-owned subsidiary of Takeda, will not discriminate against any worker or job applicant on the basis of race, color, religion, gender, national origin, ancestry, age, sexual orientation, marital or civil partnership status, pregnancy, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, application for military service, or membership in any other category protected under law.

EEO is the Law - https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf

EEO is the Law - Supplement - https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCP_EEO_Supplement_Final_JRF_QA_508c.pdf

Pay Transparency Policy - https://www.dol.gov/ofccp/pdf/pay-transp_formattedESQA508c.pdf

Reasonable Accommodations

Shire, a wholly-owned subsidiary of Takeda, is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please call 484-595-8400 and let us know the nature of your request and your contact information.

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Los Angeles Manufacturing Development Program Associate

Takeda Pharmaceutical Company Ltd