Engineer, Validation

Reckitt Benckiser

  • Salt Lake City, UT
  • $71,000-107,000 per year
  • Permanent
  • Full-time
  • 9 days ago
We are ReckittHome to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.​Supply​Our supply chain is the backbone of our business. It's how we get our trusted products to people all over the world, safely and efficiently. And it's our talented and passionate teams that make this happen. If you're looking for a career in supply chain, there's no better place to be than Reckitt. We offer a variety of exciting opportunities in all areas of the supply chain, from planning and procurement to manufacturing and logistics. You could join our Global Supply Planning team to develop and implement our global supply strategy, or work with our Procurement Centre of Excellence team to negotiate and manage our supplier relationships. Our Manufacturing Excellence team help us improve the efficiency, quality and safety of our manufacturing operations, and our Logistics Excellence team develop new and innovative ways to distribute our products to customers.About the roleSeeking an engineering leader eager to make an impact! As the Engineering Manager within one of our agile-factory teams, you'll be the spark that drives project efficiency and innovation. Be at the forefront of managing an exceptional team, turning strategic plans into reality and leading the charge in our manufacturing success. Standard engineering is not what we do - we're about pioneering. If you're passionate about leading change and enhancing how we operate, you could be the perfect fit for us.Your responsibilities
  • Support the overall validation and compliance efforts for the Salt Lake site. Generating and executing protocols, such as Installation, Operational, and Performance Qualifications (IOPQs), Process Validations (PVs) and Cleaning Validations (CVs).
  • Assists Project Engineers in defining any requirements and Factory Acceptance Test (FAT) and executes FAT is required.
  • Writes qualification documents for existing and new equipment and utilities used for manufacture and packaging of dietary supplements based on Capital Expenditure Authorization (CEA), equipment operation manuals, and physical equipment.
  • Schedules the execution with department leads and executes the protocols
  • Reviews qualification data, prepares reports, and makes recommendations for changes and/or improvements.
  • Arranges for requalification of equipments as needed.
  • Manages change control for qualification related documents and executed protocols
  • Maintains appropriate validation documentation and files.
  • Manages interaction with governmental agencies and customers, as required.
  • Investigate process and quality problems and implement corrective actions
  • Identify and define project and process improvement opportunities
  • Develop project plans and timelines. Track project goals
  • Ensure that the elements or functions that are regulated by the cGMPs for equipment, facilities, computer systems, manufacturing processes and packaging processes meet the regulatory requirements.
  • Support the site change management process by assessing the impact of changes on the validation status of the equipment.
  • Follow industry standards in generating and updating supporting documentation such as P&IDs, material and equipment specifications, and requirement specifications
  • Work within cross functional teams
  • Communicate progress effectively
  • Maintain safe working environment
Follow company policies and proceduresThe experience we're looking for
  • Must have a Bachelor's degree in a scientific field such as, but not limited to, Chemical Engineering, Chemistry, Biology, or Biochemistry, or at least three years' experience in Process Engineering, Validation, Quality Assurance or Quality Control in an FDA regulated manufacturing or processing environment.
  • Must have a minimum of 3 years of validation experience
  • Ability to work over eight hours a day when needed.
  • Computer Literacy, especially with the Microsoft Office Suite products.
  • Strong communication skills in both a written and verbal manner
  • Superior ability to analyze data and generate conclusions based upon the data
  • Excellent interpersonal and problem solving skills in dynamic environment.
  • Strong organizational skills.
  • Strong capability in the use of statistical tools to develop sampling plans.
  • Ability to manage multiple priorities within established project deadlines.
  • Ability to work/crawl in confined spaces.
  • Ability to stand, stoop, bend, sit for long periods of time.
  • Ability to work in an environment that requires a respirator.
Ability to work with other functional area team members that do not have the same business focus as the process engineeringThe skills for successPlace your text hereWhat we offerWith inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.Salary rangesUSD $71,000.00 - $107,000.00Pay transparencyThe base salary range for this role will vary based on experience in job and industry, training and education, skills relevant to the position, and other factors permitted by law. In addition to the base salary, the position is eligible for an annual discretionary bonus, which is subject to change each year. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, and life and disability insurance; paid time off for vacation, sick and Company recognized holidays; a 401(k) plan; 16-week paid parental leave or 26 weeks for the birthing parent; adoption and fertility support; tuition reimbursement; discounts; and much more. Our compensation and benefits packages aim to give our talent the reward, protection, and peace of mind they deserve. If reasonable accommodation is needed to complete your application, please contact NAtalentacquisition@reckitt.com. Reckitt is committed to the full inclusion of all qualified individuals.EqualityWe recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

Reckitt Benckiser