Validation Scientist Position Available In Harrison, Mississippi

Validation Scientist
Gulfport, Mississippi (On-Site)
Permanent
Job Description
Validation Scientist
Full-time, permanent position
Gulfport, Mississippi, USA
Enjoy coastal living
Are you a seasoned Validation Scientist? Are you looking for an opportunity to join a team of experienced professionals and work for a stable and quality-focused company?
If this sounds like you, we want to hear from you!
We’re Raise, and we’ve joined forces with our client, a world-leading manufacturer of liquid antacids. Their high-volume capacity and superior quality control make them the first choice for discerning private-label brands. They offer state-of-the-art technology, unparalleled service, economical pricing, and a professional team that is dedicated to servicing over-the-counter and personal health needs.
What you’ll be doing
As the new Validation Scientist, you’ll be responsible for the technical ownership and successful execution of the Validation Program. TS (Technical Services) Validation personnel provide stewardship of the site’s Validation Program, including assessment of and improvement in existing controls.
Responsibilities
Establishes equipment qualifications by performing IQ (Installation Qualification, OQ (Operational Qualification), and PQ (Performance Qualification) on new and existing manufacturing equipment and processes
Designs, authors, and executes protocols
Develops and implements process validations
Prepares cleaning validations
Presents validation packages during regulatory/internal/customer audits
Writes risk assessments
Completes maintenance and continuous improvements of the Validation programs
Writes validation protocols and reports in support of the site’s validation programs
Plans and executes validation activities, including cross-functional coordination and internal coordination with Validation Specialists
Prepares and provides technical review of completed/executed validation packages by compiling and analyzing validation data for submittal for review and approval
Leads resolution of validation deviations through technical knowledge, execution of supporting validation studies, and manufacturing documentation review and approval
Maintains an up-to-date knowledge of validation requirements, practices, and procedures
Writes and reviews policies and procedures (SOPs)
Performs risk assessments for validation programs
Performs and/or coordinate validation studies, testing, verification, and sampling
Represents/defends validation strategies during internal assessments / audits and external regulatory inspections
The ideal candidate will possess exceptional attention to detail, thoroughness, and recent experience in independently writing and executing validation protocols. They are dedicated to meeting deadlines in a fast-paced environment while maintaining a strong focus on delivering high-quality work and products. Additionally, they demonstrate strong interpersonal and teamwork skills, along with excellent self-management and organizational abilities, ensuring effective collaboration and efficient task management.
The Details
This is a full-time, permanent position located in the vibrant city of Gulfport, Mississippi, where you can enjoy the charm of coastal living. Gulfport offers a diverse range of activities and attractions for everyone. You will work from the Gulfport facility, Monday through Friday. Relocation assistance is available on a case-by-case basis. In addition to a competitive base salary in the range of $70,000 – $100,000 per year (commensurate with experience), you will also a benefits package and vacation time.
Qualifications
B.S. in Science discipline preferably in a scientific discipline (Chemistry, Biology, Pharmacy, Engineering or a related field)
Experience with a variety of pharmaceutical manufacturing equipment
3 years of experience in Validation within the Pharmaceutical industry
Superior writing skills, strong accuracy, attention to detail, and technical knowledge
Knowledge of computer software, including relevant applications such as Microsoft Office
Knowledge of cGMPs regulations
Ability to handle multiple tasks concurrently and complete tasks in a timely manner
Attention to detail, excellent review skills and analytical skills
Experience in Operations, TS, QA, QC, Regulatory, or Supply Chain within pharmaceutical manufacturing
Demonstrated understanding reviewing/writing technical documents, risk assessments/impact assessments, validation documents, IOQ protocols and final reports
Hands-on experience supporting/executing qualifications related to various processes and activities
Ability to drive change and motivate others toward a common vision including the ability to effectively influence others and lead others that are not direct reports
Your Application
We value diversity and inclusion and encourage all qualified people to ; however, only those selected for an interview will be contacted.
Looking for meaningful work? We can help
Raise is an established hiring firm with over 65 years of experience. We believe strongly in making the world a better place through work, which is why we’re a certified B Corporation and donate 10% of our profits to charity.
We strive to build teams that reflect the diversity of the communities we work in. We encourage all qualified applicants to , including people from traditionally underrepresented groups such as women, visible minorities, Indigenous peoples, people identifying as LGBTQ2SI, veterans, and people with visible/nonvisible disabilities.
We have a dedicated webpage for accommodations where you can learn more about what we offer, and request accommodation: https://raise.jobs/accommodations/
In order to submit candidates for roles, our clients will sometimes require personal information to confirm the identity of applicants and their legal status to work. Raise will never ask you for personal or banking information unless you have been selected for a job. If you are ever unsure about the legitimacy of this or another job posting by Raise (or have any other questions),