Supply Chain Specialist

Raytheon Technologies Corp Andover , MA 01810

Posted 2 weeks ago

Job ID 160209BR Date posted 04/15/2020 City Andover State MA Country United States

This position supports the internal and 3rd party source inspection both in the U.S. and internationally. The individual interfaces with supply chain, 3rd party inspection agencies, suppliers, and other supplier quality team members to ensure that these inspections are scheduled and executed in a timely manner following all required quality and EXIM requirements.

This role requires daily interaction with other cross-business teams in IDS to maintain and meet organizational goals and objectives.

In addition, this individual will be responsible for processing Source Received material and transferring data into the SAP system.

Required Skills:

  • Minimum of 6 years of relevant experience in supply chain, inspection and project administration

  • Proficiency with Microsoft office and specifically excel. Including but not limited to data manipulation, vlookups, pivot tables, developing and debugging macros, etc.

Desired Skills:

  • Familiarity with SAP

  • General knowledge of Export / Import.

  • Ability to multi-task and attention to detail

Required Education (including Major):

  • High School Diploma or equivalent

  • Associates Degree (preferred)

This position requires either a U.S. Person or a Non-U.S. Person who is eligible to obtain any required Export Authorization.

160209BR 160209


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
QA Specialist

Pfizer

Posted 2 days ago

VIEW JOBS 6/3/2020 12:00:00 AM 2020-09-01T00:00 ROLE SUMMARY The QA Specialist III has knowledge of cGMPs and quality processes and procedures as well as a knowledge of scientific principles associated with development activities supported by the quality role, and has a working knowledge of principles and concepts of other disciplines. This position will initially support start up of a new manufacturing suite and then on-going support when it is in GMP production. Supports manufacturing to resolve routine quality issues related to product manufacture and testing. The position also provides Quality Assurance representation for site initiatives and acts as a liaison to various stakeholders (site functions, regulatory affairs etc.). Also acts as a point of contact and decision maker for quality and compliance issues and guidance. ROLE RESPONSIBILITIES * Represents QA on various Teams with minimal supervision. * Collaborates with a wide range of co-workers, customers and management within PGS to gather the input and background knowledge needed to complete assignments. * Anticipates issues and escalates to appropriate management attention immediately. * Provides ongoing site-based Ops support for both start up and ongoing manufacturing * Reviews and approves protocols, reports, and batch records; and authors, reviews and approves SOPs as appropriate. * Reviews and approves change controls for appropriateness, completeness and alignment with quality, validation and regulatory expectations. * Exercises judgment in resolving moderate quality issues. * Plans and executes work independently and consults with supervisor as needed. * Incumbent knows and applies technical and quality concepts, applicable guidelines of the FDA or other regulatory bodies and relevant SOPs. * Reviews and approves deviations and resulting investigation reports, corrective actions and/or preventive actions for adequacy, logic and quality/validation/regulatory impact - ensuring sound quality assurance judgement to ensure product quality. * Active participant/lead for M1s/M2s; promoting and leading adherence to the DMAIC process. Champion for implementation of sound preventative actions, leveraging the Pfizer Human Performance tools. * Maintains inspection readiness and supports internal/external audits as needed. QUALIFICATIONS Bachelor of Science Degree in Biology, Chemistry, Engineering or related Technical Physical Science. Minimum of 5-7 years' experience in GMP Pharmaceutical Manufacturing environment. PREFERRED QUALIFICATIONS Previous experience in QA preferred. Previous experience in QC, Manufacturing and/or Engineering preferred. Skilled at the use of Enterprise systems including, but not limited to site Quality Tracking System (QTS), Laboratory Information Management System (LIMS), SAP and Pfizer document repositories. Experience with quality aspects of start-up of a manufacturing facility is helpful but not required. PHYSICAL/MENTAL REQUIREMENTS Ability to gown into cGMP Manufacturing areas and adhere to governing gowning procedures as appropriate. NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Some off-shift support needed when issues arise * Last Date to Apply for Job: 06.23.2020 * Eligible for Employee Referral Bonus * #LI-PFE Sunshine Act Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative. EEO & Employment Eligibility Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. Quality Assurance and Control Pfizer Andover MA

Supply Chain Specialist

Raytheon Technologies Corp