Pharmaceutical Technology Specialist III
Pharmaceutical Technology Specialist III
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Job Description
If you want to be a difference maker our people are waiting. See the difference you can make at AbbVie.
Working at AbbVie is more than a job. Its a career with meaning. A chance to make a difference in the world and in your life. We make sure you have everything you need to reach higher ground in your career. From growing and learning together to fostering a supportive space for you to thriveat AbbVie and beyond.
AbbVie Westport has a 12 Month FTC position in our Technical Operations Department for a Pharmaceutical Technology Specialist III.
The role of Pharmaceutical Technology Specialist III will report to the Senior Manager of the NPI team as part of the Tech Center function. This role involves performing focused work to provide technical support to the business as well as specific manufacturing process tech transfers (NPIs). The staff will also support dayday operations activities within the NPI function. Other aspects of this role are QMS Instrument validation compiling and review of project documentation (e.g. SOPs methods Master records Batch Records Reports). The candidate will also be coordinating with several departments to holistically develop technical and leadership skills.
Responsibilities will include:
- of process development on existing products or new latestage clinical products including scale up to plant equipment
- Work with multiple departments as a part of routine work especially QA and validations.
- Provide onthefloor technical support to the Production Team Leaders for process/equipment optimization and troubleshooting
- Provide technical support to all manufacturing and chemistry related issues. Tasks include daily trouble shooting optimization cost reduction training and coaching of manufacturing personnel
- Support of process front runs / use tests for both NPI and commercial processes.
- Development of process control recipes for NPIs and optimization of existing commercial process recipes
- Adhere to and engage in all site Safety rules programs and initiatives.
- Authoring and reviewing batch records protocols and reports.
- Work in accordance to the AbbVie Ways We Work.
Qualifications :
- Graduate or postgraduate student in relevant science field with 3 years of experience in GMP manufacturing.
- Experience with aseptic fillfinish is preferable.
- Must be a selfstarter with the ability to work on own initiative.
- Flexibility of working hours may be required and shift work may be required upon request
- Excellent communication and interpersonal skills for interaction with internal departments (QA Validation IS EHS)
- Good time management organizational and technical writing skills.
- Able to work in a fast dynamic environment whilst being able to adjust readily to meet unexpected constraints.
Additional Information :
Interested Apply today and be part of groundbreaking work that transforms lives.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
