Master Batch Record (MBR) Designer (Fluent in English/Portuguese

Job Description

Salary:

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:

FormidableLeader:

GMPProsseeksanexperienced Master Batch Record (MBR) Designer

1099/Hybrid (10% travel required).

We are looking for candidates fluent inEnglish and one or more of the following languages: Spanish, French, or Portuguese.

Achieving success in this role depends on strong written and verbal communication to effectively drive global operations.

Thrive in a collaborative, inclusive, and diverse culture that champions open communication, transparency, and team connection through engaging eventswhere every voice is heard, and innovation flourishes.

LifeSciencesIndustry!

Join an innovative, fast-growing company supporting the worlds top pharmaceutical, medical device, food, animal health, and manufacturing organizations.

Here, youll experience the best of both worldsopportunities to lead impactful projects for global clients while thriving in an agile environment, supported by a highly collaborative, results-driven team.

What You'll Experience:

A fast-paced, high- energy environment with exciting challenges and the thrill of exceeding expectations.

Major recognition for your successes, and unwavering support to help you overcome any hurdles.

A journey that will expand your limits and launch you into new possibilities.

The chance to make a real, lasting impact and leave your mark on something extraordinary.

The energy and camaraderie of a passionate, driven team that thrives together.

WhatdoesitmeantobeaMasterBatchRecord(MBR)DesignerwithGMPPros?

The Essential Duties:

Proven experience (5+ years) in FDA regulated manufacturing with electronic batch record design in Werum PAS-X (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 problem-solving capabilities and a proactive approach to overcoming obstacles.

Proven ability to operate under high-pressure in a timeline constrained environment.

Ability to travel internationally.

Herearetherequirementswearelookingfor:

Proven experience (5+ years) in FDA regulated manufacturing with electronic batch record design in Werum PAS-X (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.

Strongproblem-solvingcapabilitiesandaproactiveapproachtoovercomingobstacles.

Provenabilitytooperateunderhigh-pressureinatimelineconstrainedenvironment.

Ability to travel internationally.

This position requires at least 3 years of experience in the Food, Pharmaceutical, Animal Health, Medical Device, or Bio-Pharmaceutical manufacturing sectors.

Key Words: PAS-X, GMBR Designer, MBR Designer, eBR, MES.

Pre-Employment Requirements:

Must successfully complete and maintain all pre-employment or contract requirements, including background checks, safety certifications, and verification of professional references.

Subjecttoreviewofacurrentmotorvehiclereport.

Must hold and maintain a valid drivers license and applicable endorsements based on the positions requirements.

Due to the safety-sensitive nature of this role, candidates must pass a pre-employment or contract physical, medical evaluation, and drug screening.

Required safety certifications and annual testing must be completed and maintained throughout employment.

For roles offering remote or hybrid work arrangements, candidates must ensure access to secure, high-speed internet (preferably hardwired), capable of reliably supporting video conferencing, web access, and email use simultaneouslytypically 100 Mbps or higher.

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 apply.It is the policy of GMP Pros to 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.

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This company participates in the United States Department of Homeland Security E-Verify program. The E-Verify program is an internet-based 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

Hybrid remote