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Manufacturing Associate at Shire Human Genetic Therapies, Inc. in Cambridge, Massachusetts

Posted in General Business 30+ days ago.

Type: Full-Time





Job Description:

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Manufacturing Associate in our Lexington, MA office.

At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

Here, you will be a vital contributor to our inspiring, bold mission.

With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in Cell Culture, Purification, Solution & Equipment Prep areas. Operates production equipment according to SOPs for the production of clinical and/or commercial products.

POSITION ACCOUNTABILITIES:

This individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Records and Form Preps. Primary responsibilities include the following


  • Troubleshoot and resolve basic process related issues

  • recognize and escalate deviation

  • Execution of critical and routine activities in support of production

  • Perform Batch Record, Log Book and Form Prep requests

  • Enter data in the Laboratory Information Management System (LIMS) , MODA and or other business functions

  • Review GMP documentation

  • Sample preparation and testing

  • Identify changes needed to documentation

  • Participate in tiered visual management system and support CI initiatives

  • Complete required training on time

This individual will manage equipment and support facility related projects by


  • Initiating work orders

  • Assembly and disassembly of process equipment

  • Perform scheduled cleaning of equipment

  • Perform standardization of equipment

  • Support change over activities

  • Execution of equipment and process qualifications as well as validation

Staff Technical Training and Development


  • Maintain training requirements

  • Develop and maintain personal development plan

  • Provide annual performance self-assessment on development plan

EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS:


  • Normally requires a high school diploma and 2-4 years related industry experience or an Associate’s Degree in Life Sciences/Engineering field with 1 year of GMP Manufacturing experience.

  • Biotech Certificate preferred

  • Significant understanding of general aspects of the job with a broad understanding of the detailed aspects of the job.

  • May be required to perform as a subject matter expert for equipment and/or systems

  • The individual is proficient at following written instruction in the form of Batch Records, Form Preps, Technical Protocols and Procedures.

  • Possess excellent communication and troubleshooting skills.

  • Full awareness of current Good Manufacturing Practices.

  • Proficient computer skills.

  • Will work holidays and overtime as required.

  • May be required to adjust work schedule to meet production demands.

  • Proficient in Aseptic Technique

  • Ability to work cohesively in a team environment

  • Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes.

  • Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas.

  • Ability to lift, pull or push equipment requiring up to 25-50 lbs. of force.

  • Ability to stand for 6 hours in a production suite.

  • Ability to climb ladders and work platforms.

  • Stooping or bending to check or trouble-shoot equipment operations.

  • Ability to work around chemicals (alcohols, acids & bases).

WHAT TAKEDA CAN OFFER YOU:


  • 401(k) with company match and Annual Retirement Contribution Plan

  • Tuition reimbursement Company match of charitable contributions

  • Health & Wellness programs including onsite flu shots and health screenings

  • Generous time off for vacation and the option to purchase additional vacation days

  • Community Outreach Programs

Empowering Our People to Shine

Discover more at takedajobs.com

No Phone Calls or Recruiters Please.

Location and Salary Information:

This job posting excludes CO applicants

Locations

USA - MA - Alewife - BIO OPS

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time





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