Master Batch Record MBR Designer -1099 Fluent in EnglishSpanish
Master Batch Record MBR Designer -1099 Fluent in EnglishSpanish
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Wanted: Intrepid Master Batch Record (MBR) Designer
We are proud to be aGreat Place To Work US Certified company!
Check out what our employees say makes working here so great: Master Batch Record (MBR) Designer 1099/Hybrid10 travel required)
We are looking for candidates fluent in English and one or more of the following languages: Spanish French or Portuguese.
This role requires effective written and verbal communication skills to support global operations.
***This role requires a minimum of 3 years of experience in Food Pharmaceutical Animal Health Medical Device or BioPharmaceutical manufacturing industries. ***
What You Can Expect:
- Hard work relentless challenges and the pressure of high expectations.
- Generous recognition in times of success yet unwavering support during setbacks.
- A journey that will test your limits and push you to new heights.
- The opportunity to make a significant impact and leave a legacy.
- The camaraderie of a dedicated and passionate team.
Key Responsibilities:
- Author GMBRs (approx. 4900 to support client with Global deployment of MES
- Author and create GMBRs according to client design standards and best practices
- Support creation and input of Master Data
- Report to Center of Excellence project team and take direction from programlevel management
- Collaborate with individual site teams according to local deployment strategies
- Attend and support regular cadence of sitelevel meetings to include project review(s) periodic standup(s) periodic status review(s) design review(s) and working sessions.
- Give informed input on design strategy based on industry best practice
- Adhere to all design and project timelines
- Actively communicate design and project risks and escalate to relevant GMP Pros stakeholders
- Support GMP Pros governance through cascading information and project status updates
Qualifications:
- Proven experience 5 years) in FDA regulated manufacturing with electronic batch record design in Werum PASX 3.1.8 or 3.3
- Proven knowledge of FDA and CFR requirements pertaining to batch record design and documentation
- Exceptional interpersonal skills and the ability to collaborate across project teams and workstreams.
- Strong problemsolving capabilities and a proactive approach to overcoming obstacles.
- Proven ability to operate under highpressure in a timeline constrained environment.
- Ability to travel internationally
**Apply now and be part of something extraordinary.**
PreEmployment Requirements:
- Pass and maintain preemployment/contract background check and safety certification including outstanding professional references.
- Subject to motor vehicle report review.
- Maintain valid drivers license and endorsements as required per position.
- Pass preemployment/contract physical medical evaluation and drug screen due to the safety sensitive nature of this position.
- Successfully complete and maintain any required safety certification and testing annually.
- Candidates for positions that include remote or hybrid opportunities must provide their own access to a secure highspeed internet signal (preferably hard wired) at a capacity sufficient to support video web and email processing simultaneously based on their personal work environment. This is typically 100Mb and above
Key Words: PASX GMBR Designer MBR Designer eBR MES
GMP Pros is an Equal Employment Opportunity / Affirmative Employer (EEO/AA) and actively seeks to diversify its work force. Therefore all qualified applicants regardless of race color national origin religion gender gender identity sexual orientation age disability or veteran status are strongly encouraged to is the policy ofGMP Prosto provide equal opportunity in employment for all qualified individuals regardless of race color religion ethnicity national origin ancestry disability medical condition age citizenship sex sexual orientation gender gender identity gender expression marital status pregnancy genetic information military status veteran status and any other characteristic protected by law.
By submitting material for consideration for this position you are attesting that no material or interaction with GMP Pros Team Members establishes any obligation for GMP Pros to hire you. If you are hired you understand that either GMP Pros or you can terminate your employment at any time and for any reason with or without cause and without prior notice. Further you understand that no representative of GMP Pros has the authority to make any assurance to the contrary.
By submitting your application for this position you attest that you have given GMP Pros true and complete information on this application. No requested information has been concealed. You are authorizing GMP Pros to contact references provided for employment reference checks. If any information youhave provided is untrue or if you have concealed material information you understand this will constitute cause for the denial of employment or immediate dismissal.
Accessibility: If you need help accessing this page please contact:Phone:Email:If you want to view the EEO is the Law poster please choose your language:EnglishSpanishArabicChinese
This company participates in the United States Department of Homeland Security EVerify program. The EVerify program is an internetbased employment eligibility verification system operated by the U.S. Citizenship and Immigration Services. Please use the links provided for important information when applying for work with this company:Everify English / Spanish
Required Experience:
Senior IC
Employment Type
Contract
