Job Description
Target PR Range : 19-22 / hr
Duties :
Job Title : Tech, Product Engr
Working with our Engineering and Quality Departments, this individual will be creating change orders, revising existing documentation, inspecting and post-approving artwork, and documentation associated with lab el changes to our product packaging. This position supports one or more mid to senior-level managers and works in a diverse and complex environment inclusive of some customer and executive contact. This role creates red line documents and enters into the AGILE Document Control Program and routing for approval. Duties may include more complex administrative activities including managing project tasks, composing letters and reports, preparing / editing presentations, critical thinking / investigative skills, and recommending or making purchase decisions are included in the responsibilities of this role. This role is responsible for the comparison of approved graphics to vendor proof's and the review / comparison of graphic files to technical documentation as defined by the Documentation Center.
Skills :
Essential Functions Attention to detail including Graphic, Alpha and Numeric. Manage and track Graphics and their approvals. Edit and revise Tech. Spec. using Word, Excel and AGILE. Manage and track revised spec. and their approvals. Organize and maintain work flow to establish priorities. Possesses strong written and verbal communication skills. Intermediate to advanced computer skills including word processing, spreadsheet, and basic presentation or database applications and may train others. Must be able to work autonomous with limited direction. Preferred Skills / Qualifications Experience using Microsoft Office Software Skills / Competencies Ability to express ideas both in written and oral communications.
Education :
Education required / preferred High School Diploma required preferred Associates Degree from a two-year college or technical school or equivalent experience. Experience Three years of experience preferably in a medical manufacturing industry. Understanding of FDA regulations surrounding the manufacture of medical devices and GMPs
Equal Opportunity Employer : We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
Fraud Alert : Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
Product Engineer • El Paso, TX, United States